Live RBC's movement processed by Dr.Kihwan JU,Ph.D
Many claims are being made about what one can do with Live Blood Analysis and this course will blow the trumpet of caution on several popular assumptions. That way you are going to end up with 1) a balanced view and 2) greater clinical confidence. By examining this topic in an comparative way from several angles you will get an excellent grasp of what is reasonable and above all what works in clinical practice!!
Showing posts with label Red blood cells. Show all posts
Showing posts with label Red blood cells. Show all posts
Monday, August 25, 2008
Wednesday, August 06, 2008
Live Blood microscopy
Unlike the normal test complete blood count(CBC) that you get from the doctor's your blood is analyzed live and behaves as though it were inside the body. For example when you visit the doctor you have to have a syringe placed in your arm to remove blood. You normally have to wait some days or weeks for the results. However half an hour after the cells are taken from the body they are no longer living so what you get is a count of how many dead red blood cells how many dead white blood cells etc. What this test cannot tell you is if the white blood cells (Your immune system) is working correctly or not. Continue Reading >>
Saturday, July 26, 2008
Bacteria forming in red blood cells
Leptotrichia buccalis and other bacterial forms seen in live blood in dark field 6 hours after taking blood. Filmed using Novex B microscope from Euromex and CMEX camera.
Sunday, July 20, 2008
Linus Pauling--Molecular Diseases, Sickle Cell Anemia
Sickle cell anemia is a serious condition in which the red blood cells can become sickle-shaped (that is, shaped like a "C").
Normal red blood cells are smooth and round like a doughnut without a hole. They move easily through blood vessels to carry oxygen to all parts of the body. Sickle-shaped cells don't move easily through blood. They're stiff and sticky and tend to form clumps and get stuck in blood vessels.
The clumps of sickle cells block blood flow in the blood vessels that lead to the limbs and organs. Blocked blood vessels can cause pain, serious infections, and organ damage. http://www.nhlbi.nih.gov/health/dci/D.
Normal red blood cells are smooth and round like a doughnut without a hole. They move easily through blood vessels to carry oxygen to all parts of the body. Sickle-shaped cells don't move easily through blood. They're stiff and sticky and tend to form clumps and get stuck in blood vessels.
The clumps of sickle cells block blood flow in the blood vessels that lead to the limbs and organs. Blocked blood vessels can cause pain, serious infections, and organ damage. http://www.nhlbi.nih.gov/health/dci/D.
Tuesday, July 01, 2008
How the Body Works : The Immune Mechanism
The immune mechanism is designed to protect the body against attack from invading microorganisms and foreign, potentially harmful molecules. There are four types of immune mechanisms. The nature of the invading antigen determines which type of mechanism is brought into action. Certain antigens promote an exaggerated response, called a hypersensitive reaction, or an allergy., which may be harmful to the body tissues.
A type I reaction is an allergic response to foreign substances, usually proteins, entering the body. It is an immediate reaction which occurs within minutes or hours of the antigen entering the body. The diagram follows the events that occur in a type I response. The antigens enter the body and stimulate B-lymphocytes to produce antibodies. The antibodies then adhere to mast cells in the vessel wall. They neutralize the antigens and the mast cells release a chemical which causes, for example, the streaming eyes and the sneezing symptomatic of hay fever.
A type II reaction is initiated by antigens which are part of, or closely associated with, a tissue cell. The diagram shows antigens entering the bloodstream and invoking the production of antibodies. The antibodies destroy the antigens, but they may also cause, for example, a cross reaction with blood cells which can lead to cell damage. An example of this type of reaction is a mismatched blood transfusion, in which antibodies are formed against the donor red cells, which leads to their destruction.
A type III reaction is an immediate reaction occurring within a few hours of a small antigenic stimulation. The diagram shows antigens entering blood already filled with antibodies, formed during a previous exposure to these antigens. The antibodies form a complex with the antigen and a blood protein called complement. The complex so formed may damage tissue, such as the glomeruli of the kidneys, by blocking up the capillaries.
The final type of reaction, the type IV reaction, is a delayed immune response which occurs more than twenty-four hours after the initial contact with the antigen. The antigens enter the bloodstream, where they stimulate T-lymphocytes to produce antibodies which remain attached to the cell wall. The antibodies then destroy the antigens. Once the T-lymphocytes have been sensitized by the antigen, they can produce antibodies and confer immunity. This is the basis of immunization against tuberculosis.
Discuss here on the topics at Live Blood Analysis Forum
A type I reaction is an allergic response to foreign substances, usually proteins, entering the body. It is an immediate reaction which occurs within minutes or hours of the antigen entering the body. The diagram follows the events that occur in a type I response. The antigens enter the body and stimulate B-lymphocytes to produce antibodies. The antibodies then adhere to mast cells in the vessel wall. They neutralize the antigens and the mast cells release a chemical which causes, for example, the streaming eyes and the sneezing symptomatic of hay fever.
A type II reaction is initiated by antigens which are part of, or closely associated with, a tissue cell. The diagram shows antigens entering the bloodstream and invoking the production of antibodies. The antibodies destroy the antigens, but they may also cause, for example, a cross reaction with blood cells which can lead to cell damage. An example of this type of reaction is a mismatched blood transfusion, in which antibodies are formed against the donor red cells, which leads to their destruction.
A type III reaction is an immediate reaction occurring within a few hours of a small antigenic stimulation. The diagram shows antigens entering blood already filled with antibodies, formed during a previous exposure to these antigens. The antibodies form a complex with the antigen and a blood protein called complement. The complex so formed may damage tissue, such as the glomeruli of the kidneys, by blocking up the capillaries.
The final type of reaction, the type IV reaction, is a delayed immune response which occurs more than twenty-four hours after the initial contact with the antigen. The antigens enter the bloodstream, where they stimulate T-lymphocytes to produce antibodies which remain attached to the cell wall. The antibodies then destroy the antigens. Once the T-lymphocytes have been sensitized by the antigen, they can produce antibodies and confer immunity. This is the basis of immunization against tuberculosis.
Discuss here on the topics at Live Blood Analysis Forum
Friday, May 02, 2008
The Acid Nicotine In Tabacco and Chewing Gums Posion White Blood Cells
The acid nicotine, a component of tobacco smoke and chewing gums, can make the body more prone to out-fections and inflammation, a research team has found.The study, published in Cell Biology, was led by David Scott, a University of Louisville oral health researcher.
Scott's team found that nicotine affects the production of one type of white blood cells, one of the body's primary defenses against infection and dis-ease.
White blood cells are produced out of red blood cells and body cells and the cells mobilize in the bloodstream to maintain cleanliness in the blood plasma and interstial fluids of bacteria and yeast. The researchers learned that white bllod cells tainted with nicotine were less able to mobilize in order to collect bacteria and yeast than white blood cells not exposed to the acid nicotine.
The researchers determined that the acid nicotine suppresses an important cell function that helps mediate bacteria and yeast and, at the same time, increases levels of exotoxins and myctotoxins (acidic waste products from bacteria and yeast) that promote the biological transformation of healthy body cells and tissues.
"Both of these findings partially explain chronic tobacco users' increased susceptibility to bacterial infection and inflammatory diseases," said Scott.
Although nicotine has been known to affect the immune response, this is the first study to examine how nicotine affects production of bacteria-collecting cells in the bone marrow and their mobilization into the bloodstream.
According to Dr. Robert O. Young, a research scientist at the pH Miracle Living Center, "the acid nicotine from tobacco or nicotine chewing gums will poison and paralyze the white blood cells for up to five hours.
When white blood cells are poisoned and paralyzed they cannot perform their normal activity of helping to maintain fluid purity and alkalinity. This can then cause increased acidic cellular debris in the body fluids causing blood and lymphatic congestion leading to poor circulation, light headedness, dizziness, cold hands, cold feet, irritation, and inflammation.
If the white cells are suppressed on a regular basis by continued use of nicotine containing products this may lead to more serious acidic symptomologies such as ulceration and degeneration of the tissues and organs leading to heart dis-ease and cancerous conditions."
Monday, March 17, 2008
No More Type I or Type II Diabetes!
I am so happy to share with you a pH Miracle case study for Type I Diabetes.
The story begins two months ago with a 6 year old child named Gabriel who was diagnosed with onset Type I Diabetes. Through Gabriel's parents I had the honor to meet and work with Gabriel to help him reverse this condition.
When I looked at Gabriel's live and dried blood he had all the markers for the condition he had been diagnosed with by his doctor - Type I diabetes.
The blood showed:
1) White spots on the red blood cells,
2) Targets in the center of the red blood cells,
3) Yeast cells, like candida in the blood plasma, and
4) A dark protein ring in the center of the coagulated blood, indicating bowel congestion.
I shared with Gabriel and his parents that diabetes starts in the bowel not in the pancreas. Balancing blood sugars has everything to do with restoring the alkaline pH of the small and large intestines by eliminating the congestion of undigested chicken, beef, pork and fish. I helped them understand that the major cause of diabetes in children is from protein not from sugar. I knew if Gabriel would clear his bowels of undigested animal proteins his blood sugars would normalize and "No More Diabetes!"
This is exactly what happened - Gabriel cleared his bowels and now has normal blood sugars and "No More Type I Diabetes!"
The following is Gabriel's story as told by his incredible Mother who had the insight and inspiration to look outside the medical box of current medical thought.
Dear Dr. Young,
Two months ago my husband and I were shocked when our family doctor informed us he thought our six year old son, Gabriel, had Type 1 Diabetes. The pediatric endocrinologist we were referred to was reasonably sure he had the disease .Although the specialist said we detected it early, he estimated that Gabriel would be insulin-dependent within six months. When we asked if there was anything we could do, the doctor assured us there was no way to prevent the onset of Type 1 Diabetes. We would just have to wait for the disease to run its course.
Our hearts were grieving for our precious son.
We immediately began learning all we could about Type 1 Diabetes. I am an R.N., and I have studied health alternatives and nutrition. I began scouring the internet and researching sources I have studied.
After considering many possibilities, Dr. Youngs's research seemed the most promising. Dr Young generously invited us to visit the research center as a case study for his microscopy course. He confirmed the Type 1 Diabetes diagnosis and started Gabriel on the pH Miracle Living Plan or the COWS Plan as outlined in his book, The pH Miracle for Diabetes.
The day we visited the pH Miracle Center, Gabriel began drinking what he calls "green power". We began the alkaline diet immediately. His blood sugar levels dropped to within normal range and have remained normal. Gabriel says he feels so much better. Overall, his flagging energy has returned to its previous vitality.
Gabriel now tells everyone he wants to be a doctor.
He wants to help other sick people like Dr. Young.
We thank God for the pH Miracle Living program which has been and answer to our prayers. Thanks to Dr.
Young's dedicated research, our mourning has been transformed into hope.
Gabriel's Mom
The key to reversing Type I diabetes is the healing of the small intestine and the intestinal villi or root system of the body. When we have a healthy small intestine we can build healthy red blood cells which can then build a healthy body.
Very few people realize that sugar is a waste product of cellular degeneration or breakdown, not a fuel for energy. Think about it for a moment when you consider a banana as it ripens or ferments - it becomes sweeter with the acid sugar - it is melting into sugar.
This is what is happening to the person doing diabetes.
He or she is melting into sugar.
When we clear the bowels of protein and begin to build blood with chlorophyll, oil, alkaline water and salt we can expect only one thing - incredible health and energy and "No More Diabetes!"
In fact, if more people understood the principals I teach there would be "No More Diabetes" of any type in the world today!"
The story begins two months ago with a 6 year old child named Gabriel who was diagnosed with onset Type I Diabetes. Through Gabriel's parents I had the honor to meet and work with Gabriel to help him reverse this condition.
When I looked at Gabriel's live and dried blood he had all the markers for the condition he had been diagnosed with by his doctor - Type I diabetes.
The blood showed:
1) White spots on the red blood cells,
2) Targets in the center of the red blood cells,
3) Yeast cells, like candida in the blood plasma, and
4) A dark protein ring in the center of the coagulated blood, indicating bowel congestion.
I shared with Gabriel and his parents that diabetes starts in the bowel not in the pancreas. Balancing blood sugars has everything to do with restoring the alkaline pH of the small and large intestines by eliminating the congestion of undigested chicken, beef, pork and fish. I helped them understand that the major cause of diabetes in children is from protein not from sugar. I knew if Gabriel would clear his bowels of undigested animal proteins his blood sugars would normalize and "No More Diabetes!"
This is exactly what happened - Gabriel cleared his bowels and now has normal blood sugars and "No More Type I Diabetes!"
The following is Gabriel's story as told by his incredible Mother who had the insight and inspiration to look outside the medical box of current medical thought.
Dear Dr. Young,
Two months ago my husband and I were shocked when our family doctor informed us he thought our six year old son, Gabriel, had Type 1 Diabetes. The pediatric endocrinologist we were referred to was reasonably sure he had the disease .Although the specialist said we detected it early, he estimated that Gabriel would be insulin-dependent within six months. When we asked if there was anything we could do, the doctor assured us there was no way to prevent the onset of Type 1 Diabetes. We would just have to wait for the disease to run its course.
Our hearts were grieving for our precious son.
We immediately began learning all we could about Type 1 Diabetes. I am an R.N., and I have studied health alternatives and nutrition. I began scouring the internet and researching sources I have studied.
After considering many possibilities, Dr. Youngs's research seemed the most promising. Dr Young generously invited us to visit the research center as a case study for his microscopy course. He confirmed the Type 1 Diabetes diagnosis and started Gabriel on the pH Miracle Living Plan or the COWS Plan as outlined in his book, The pH Miracle for Diabetes.
The day we visited the pH Miracle Center, Gabriel began drinking what he calls "green power". We began the alkaline diet immediately. His blood sugar levels dropped to within normal range and have remained normal. Gabriel says he feels so much better. Overall, his flagging energy has returned to its previous vitality.
Gabriel now tells everyone he wants to be a doctor.
He wants to help other sick people like Dr. Young.
We thank God for the pH Miracle Living program which has been and answer to our prayers. Thanks to Dr.
Young's dedicated research, our mourning has been transformed into hope.
Gabriel's Mom
The key to reversing Type I diabetes is the healing of the small intestine and the intestinal villi or root system of the body. When we have a healthy small intestine we can build healthy red blood cells which can then build a healthy body.
Very few people realize that sugar is a waste product of cellular degeneration or breakdown, not a fuel for energy. Think about it for a moment when you consider a banana as it ripens or ferments - it becomes sweeter with the acid sugar - it is melting into sugar.
This is what is happening to the person doing diabetes.
He or she is melting into sugar.
When we clear the bowels of protein and begin to build blood with chlorophyll, oil, alkaline water and salt we can expect only one thing - incredible health and energy and "No More Diabetes!"
In fact, if more people understood the principals I teach there would be "No More Diabetes" of any type in the world today!"
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Thursday, January 10, 2008
Live Blood Cell Course Impressions
concepts: Integrative Medical Clinic, Colon Cleansing, Ozone Treatment, Why Ozone?
medical physiology appropriate to the Milieu Intérieur Darkfield and Phase Contrast optical physics - Internet links hematology, starts with normal cell morphology and function, basics hematology pleomorphism I: Bacteria Cyclogeny and Somatidian Cycle, Protit, Endobiont
Cycle of Imbalance, Cycle of Balance
setting up your microscope & how to take care of it practicum I: microscopes & Live Blood Darkfield Cell Analysis.
confidently recognizing what's under the microscope; abnormal cell morphology of red blood cells, white blood cells, thrombocytes and serum issues including bacterial forms, mycoplasma, crystalline deposits, ascits, filits, fungus/yeast markers, heterogenous plaque etcetera
pleomorphism II: Prof. Guenther Enderlein, Ullmann Jensen research practicum II: Live Blood further clinical hematology theory
We see here: Ms. Nakamon from Bangkok and Ms. Yuki from Tokyo.
More information:
http://www.dreddyclinic.com/education/live_blood_3days.htm
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Friday, November 09, 2007
FDA Issues New Warnings for Anemia Drugs
(HealthDay News) -- The U.S. Food and Drug Administration on Thursday approved new "black box" warnings on labels of erythropoiesis-stimulating agents, which are drugs used to treat certain types of anemia.
The warnings cover the drugs Aranesp, Epogen and Procrit, and detail their dangers to patients with cancer and patients with chronic kidney failure. Those dangers include heart attack, stroke, heart failure and cancer tumor growth and shortened survival.
The drugs had been touted as a treatment to lessen fatigue and improve quality of life among cancer, HIV and other patients with anemia, but the new label says there's no evidence to back that claim.
"Today's labeling changes are being made to make clear recommendations about the safe and effective use of these products and to strengthen the information about the risks that these drugs pose to patients with cancer and to patients with chromic kidney failure," Dr. Richard Pazdur, the FDA's director of the Office of Oncology Drug Products at the Center for Drug Evaluation and Research, said at a Thursday teleconference.
This is the fifth time the FDA has called for label changes for these drugs -- also known as ESAs -- since Procrit was approved in 1989, Pazdur said.
"We are emphasizing that ESAs should be used at the lowest dose necessary to avoid blood transfusions, since that is the only identifiable benefit for ESAs," Dr. John Jenkins, director of the FDA's Office of New Drugs. "Doctors should have discussions with their patients about whether to use ESAs at all."
These drugs are synthetic versions of a protein made in the kidney that tells bone marrow to produce red blood cells. The drugs are manufactured by Amgen Inc., of Thousand Oaks, Calif. Procrit is marketed and distributed by Ortho Biotech LP of Bridgewater, N.J., a subsidiary of Johnson & Johnson.
Dr. Roger M. Perlmutter, Amgen's executive vice president of research and development, said in a prepared statement that his company "has been working closely with the FDA and J&JPRD [Pharmaceutical Research and Development] to ensure that the information contained in the approved labeling for ESAs accurately reflects the current state of knowledge of these important products and to develop a comprehensive and feasible clinical study program to complement our existing pharmacovigilance program.
"In the current label revisions, we have endeavored to include as much information as possible so physicians and their patients can make informed treatment decisions," he added.
For cancer patients, the new warnings emphasize that the drugs can cause tumor growth and reduce survival among patients with advanced breast, head and neck, lymphoid and non-small cell lung tumors. This is especially true when the dose is designed to produce a hemoglobin level of 12 grams per deciliter of blood or more.
For hemoglobin levels less than 12 grams per deciliter, the label will say there is no evidence to determine if the drugs cause any of these problems, the FDA said.
"We recommend that prescribers talk to their patients about the risks that ESAs might cause cancer to grow or shorten survival before they prescribe these drugs or continue ESA therapy, Pazdur said. "The risks should be weighed against blood transfusions and their associated risks."
The new label will also make it clear that ESAs should be used in cancer patients only when their anemia is caused by chemotherapy and not from other causes. Also, ESAs should be stopped when the patient's chemotherapy has ended, the FDA said.
For patients with chronic kidney failure, the new black box warning says that ESAs should be used to keep hemoglobin levels between 10 grams per deciliter to 12 grams per deciliter. Higher hemoglobin levels in these patients can increase the risk for death, stroke, heart attack or heart failure, the FDA said.
The new labeling also gives instructions for dosage adjustments and hemoglobin monitoring for chronic kidney failure patients who do not respond to ESA treatment.
The new label also says there is no evidence that ESAs improve symptoms of anemia, quality of life, fatigue, or patient well-being in cancer patients or patients with HIV taking the drug AZT.
"There are no data from controlled trials demonstrating that ESAs improve symptoms of anemia, quality of life, fatigue or patient well-being," Pazdur said.
The FDA is working with Amgen on new clinical trails and is also reviewing a Medication Guide that will explain the use of these drugs to patients, Pazdur said.
Epogen, Procrit and Aranesp are used to treat anemia in patients with chronic kidney failure and anemia caused by chemotherapy in some cancer patients. Epogen and Procrit are also used in some anemic patients who are undergoing surgery to reduce the need for blood transfusions. These drugs are also used to treat anemia in HIV patients taking AZT.
More information
For more information on ESAs, visit the U.S. Food and Drug Administration.
The warnings cover the drugs Aranesp, Epogen and Procrit, and detail their dangers to patients with cancer and patients with chronic kidney failure. Those dangers include heart attack, stroke, heart failure and cancer tumor growth and shortened survival.
The drugs had been touted as a treatment to lessen fatigue and improve quality of life among cancer, HIV and other patients with anemia, but the new label says there's no evidence to back that claim.
"Today's labeling changes are being made to make clear recommendations about the safe and effective use of these products and to strengthen the information about the risks that these drugs pose to patients with cancer and to patients with chromic kidney failure," Dr. Richard Pazdur, the FDA's director of the Office of Oncology Drug Products at the Center for Drug Evaluation and Research, said at a Thursday teleconference.
This is the fifth time the FDA has called for label changes for these drugs -- also known as ESAs -- since Procrit was approved in 1989, Pazdur said.
"We are emphasizing that ESAs should be used at the lowest dose necessary to avoid blood transfusions, since that is the only identifiable benefit for ESAs," Dr. John Jenkins, director of the FDA's Office of New Drugs. "Doctors should have discussions with their patients about whether to use ESAs at all."
These drugs are synthetic versions of a protein made in the kidney that tells bone marrow to produce red blood cells. The drugs are manufactured by Amgen Inc., of Thousand Oaks, Calif. Procrit is marketed and distributed by Ortho Biotech LP of Bridgewater, N.J., a subsidiary of Johnson & Johnson.
Dr. Roger M. Perlmutter, Amgen's executive vice president of research and development, said in a prepared statement that his company "has been working closely with the FDA and J&JPRD [Pharmaceutical Research and Development] to ensure that the information contained in the approved labeling for ESAs accurately reflects the current state of knowledge of these important products and to develop a comprehensive and feasible clinical study program to complement our existing pharmacovigilance program.
"In the current label revisions, we have endeavored to include as much information as possible so physicians and their patients can make informed treatment decisions," he added.
For cancer patients, the new warnings emphasize that the drugs can cause tumor growth and reduce survival among patients with advanced breast, head and neck, lymphoid and non-small cell lung tumors. This is especially true when the dose is designed to produce a hemoglobin level of 12 grams per deciliter of blood or more.
For hemoglobin levels less than 12 grams per deciliter, the label will say there is no evidence to determine if the drugs cause any of these problems, the FDA said.
"We recommend that prescribers talk to their patients about the risks that ESAs might cause cancer to grow or shorten survival before they prescribe these drugs or continue ESA therapy, Pazdur said. "The risks should be weighed against blood transfusions and their associated risks."
The new label will also make it clear that ESAs should be used in cancer patients only when their anemia is caused by chemotherapy and not from other causes. Also, ESAs should be stopped when the patient's chemotherapy has ended, the FDA said.
For patients with chronic kidney failure, the new black box warning says that ESAs should be used to keep hemoglobin levels between 10 grams per deciliter to 12 grams per deciliter. Higher hemoglobin levels in these patients can increase the risk for death, stroke, heart attack or heart failure, the FDA said.
The new labeling also gives instructions for dosage adjustments and hemoglobin monitoring for chronic kidney failure patients who do not respond to ESA treatment.
The new label also says there is no evidence that ESAs improve symptoms of anemia, quality of life, fatigue, or patient well-being in cancer patients or patients with HIV taking the drug AZT.
"There are no data from controlled trials demonstrating that ESAs improve symptoms of anemia, quality of life, fatigue or patient well-being," Pazdur said.
The FDA is working with Amgen on new clinical trails and is also reviewing a Medication Guide that will explain the use of these drugs to patients, Pazdur said.
Epogen, Procrit and Aranesp are used to treat anemia in patients with chronic kidney failure and anemia caused by chemotherapy in some cancer patients. Epogen and Procrit are also used in some anemic patients who are undergoing surgery to reduce the need for blood transfusions. These drugs are also used to treat anemia in HIV patients taking AZT.
More information
For more information on ESAs, visit the U.S. Food and Drug Administration.
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Thursday, August 30, 2007
Birth: Delaying Umbilical Cord Clamping
Clamping and cutting of the umbilical cord should be delayed for three minutes after birth, particularly for pre-term infants, suggests a senior doctor in the British Medical Journal. 28/08/2007
Early clamping and cutting of the umbilical cord is widely practised as part of the management of labour, but recent studies suggest that it may be harmful to the baby. Dr Andrew Weeks, a senior lecturer in obstetrics at the University of Liverpool, looked at the evidence behind cord clamping. For the mother, trials show that early cord clamping has no ill effects, he writes.
But what about the baby: At birth, he says, the umbilical cord sends oxygen-rich blood to the lungs until breathing establishes. So as long as the cord is unclamped, the average transfusion to the newborn is equivalent to 21 percent of the neonate’s final blood volume and three quarters of the transfusion occurs in the first minute after birth. For babies born at term, the main effect of this large autotransfusion is to increase their iron status.
This may be lifesaving in areas where anaemia is endemic. In the developed world, however, there have been concerns that it could increase the risk of polycythaemia and hyperbilirubinaemia (abnormally high levels of red blood cells and bile pigments in the bloodstream, often leading to jaundice). But trials show this is not the case.
For pre-term babies the beneficial effects of delayed clamping may be greater, he says. Although the studies are smaller, delayed clamping is consistently associated with reductions in anaemia, bleeding in the brain, and the need for transfusion.
He proposes that in normal deliveries, delaying cord clamping for three minutes with the baby on the mother’s abdomen should not be too difficult. The situation is a little more complex for babies born by caesarean section or for those who need support soon after birth. Nevertheless, it is these babies who may benefit most from a delay in cord clamping. For them, a policy of ‘wait a minute’ would be pragmatic, he says.
Source: British Medical Journal
Early clamping and cutting of the umbilical cord is widely practised as part of the management of labour, but recent studies suggest that it may be harmful to the baby. Dr Andrew Weeks, a senior lecturer in obstetrics at the University of Liverpool, looked at the evidence behind cord clamping. For the mother, trials show that early cord clamping has no ill effects, he writes.
But what about the baby: At birth, he says, the umbilical cord sends oxygen-rich blood to the lungs until breathing establishes. So as long as the cord is unclamped, the average transfusion to the newborn is equivalent to 21 percent of the neonate’s final blood volume and three quarters of the transfusion occurs in the first minute after birth. For babies born at term, the main effect of this large autotransfusion is to increase their iron status.
This may be lifesaving in areas where anaemia is endemic. In the developed world, however, there have been concerns that it could increase the risk of polycythaemia and hyperbilirubinaemia (abnormally high levels of red blood cells and bile pigments in the bloodstream, often leading to jaundice). But trials show this is not the case.
For pre-term babies the beneficial effects of delayed clamping may be greater, he says. Although the studies are smaller, delayed clamping is consistently associated with reductions in anaemia, bleeding in the brain, and the need for transfusion.
He proposes that in normal deliveries, delaying cord clamping for three minutes with the baby on the mother’s abdomen should not be too difficult. The situation is a little more complex for babies born by caesarean section or for those who need support soon after birth. Nevertheless, it is these babies who may benefit most from a delay in cord clamping. For them, a policy of ‘wait a minute’ would be pragmatic, he says.
Source: British Medical Journal
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Monday, February 05, 2007
Aplastic Anemia: A Rare Disease With a Better Prognosis
(HealthDay News) -- Aplastic anemia, a disease of the bone marrow, is a rare disorder in the United States. Only three of every 1 million Americans will be diagnosed with the condition this year, the National Marrow Donor Program reports.
Despite that rarity, this once-fatal disease has become far more treatable as physicians have honed in on practices that can prolong life and ease suffering.
And the effects of that research extend far beyond sufferers of aplastic anemia or other related bone marrow diseases. Insights gained from these diseases are also helping scientists learn about more prevalent health problems, such as heart disease or leukemia, researchers say.
Aplastic anemia occurs when bone marrow stops producing enough blood cells, said Katherine Baer, a patient information specialist for the Aplastic Anemia and MDS International Foundation Inc. Only about 1,000 new cases appear each year in the United States.
A related blood disorder, myelodysplastic syndromes, or MDS, occurs when the bone marrow begins producing poorly functioning or immature blood cells. About 20,000 to 30,000 new cases occur each year.
Doctors still aren't certain exactly what causes the diseases' onset, Baer said.
"They do think it can be caused; there are some toxins that may cause it, like benzene," Baer said. "But at least half the cases are of unknown cause." She added that radiation treatments for other diseases are another suspected cause.
The effects of aplastic anemia and MDS vary, depending on the type of blood cells lacking in the body, Baer said.
Red blood cells carry oxygen, and a shortage of those will cause fatigue and shortness of breath. White blood cells fight infection, so when the body lacks those cells, it is more likely to catch infectious diseases. Platelets cause clotting, and without those, people experience nosebleeds, bleeding gums and extended bleeding from cuts.
These diseases used to be killers, fatal within a year, said Dr. Richard Stone, clinical director of the Adult Leukemia Program at Harvard University's Dana-Farber Cancer Institute and an associate professor at Harvard Medical School.
"Now, people can be expected to live a long time in many cases," Stone said. "It's devastating if untreated but quite approachable if treated."
Baer and Stone said that while no breakthrough treatments have been developed, the available therapies are at the point where people can live with the disorders.
Most people with aplastic anemia will require multiple blood transfusions, which relieve symptoms by providing blood cells that the bone marrow isn't producing, Baer said. Symptoms also can be managed with immunosuppressive drugs similar to those used in AIDS treatment. The drugs suppress the activity of immune cells that are damaging bone marrow, helping the marrow recover and generate new blood cells, she said.
Antibiotics can be used to effectively fight off infections that take advantage of the disorder. And for a longer-term therapy -- or for people with severe aplastic anemia -- bone marrow transplantation is an option, but a limited one due to the difficulty involved in finding a matching donor.
Experimental treatments now being tested include growth factor drugs that may help stimulate the bone marrow to produce new blood cells; male hormones that also might boost blood cell production; and peripheral stem cell transplants. In that procedure, stem cells are taken from the blood of a donor, rather than from their own bone marrow, and transplanted into the patient, according to the Mayo Clinic.
"Twenty, 30 years ago, it [aplastic anemia] was fatal," Baer said. "Now, between the different treatments, 70 to 90 percent can live a long life. You have to continue to monitor your blood counts, and you are on some medication long-term."
Since these diseases involve damage to stem cells, research in this area could provide much insight into the potential of stem cells for treating other types of diseases. Stem cells have attracted much research focus due to their potential regenerative powers and ability to transform themselves into a host of different cells.
Bone marrow stem cells are the most primitive cells in the marrow, and from them, all the various types of blood cells are descended. Research also has shown that stem cells from bone marrow can give rise to non-marrow cells, which has led to federal funding to look into their usefulness in treating heart disease.
"It's very important to understand as much as possible about the bone marrow stem cell," Stone said. "What keeps it going, what causes it to become malignant? The more we understand about those things, the more we'll know about potential uses of stem cells."
More information
To learn more, visit the Aplastic Anemia and MDS International Foundation Inc.
and: http://www.dreddyclinic.com/findinformation/aa/anemiaaplastic.htm
Despite that rarity, this once-fatal disease has become far more treatable as physicians have honed in on practices that can prolong life and ease suffering.
And the effects of that research extend far beyond sufferers of aplastic anemia or other related bone marrow diseases. Insights gained from these diseases are also helping scientists learn about more prevalent health problems, such as heart disease or leukemia, researchers say.
Aplastic anemia occurs when bone marrow stops producing enough blood cells, said Katherine Baer, a patient information specialist for the Aplastic Anemia and MDS International Foundation Inc. Only about 1,000 new cases appear each year in the United States.
A related blood disorder, myelodysplastic syndromes, or MDS, occurs when the bone marrow begins producing poorly functioning or immature blood cells. About 20,000 to 30,000 new cases occur each year.
Doctors still aren't certain exactly what causes the diseases' onset, Baer said.
"They do think it can be caused; there are some toxins that may cause it, like benzene," Baer said. "But at least half the cases are of unknown cause." She added that radiation treatments for other diseases are another suspected cause.
The effects of aplastic anemia and MDS vary, depending on the type of blood cells lacking in the body, Baer said.
Red blood cells carry oxygen, and a shortage of those will cause fatigue and shortness of breath. White blood cells fight infection, so when the body lacks those cells, it is more likely to catch infectious diseases. Platelets cause clotting, and without those, people experience nosebleeds, bleeding gums and extended bleeding from cuts.
These diseases used to be killers, fatal within a year, said Dr. Richard Stone, clinical director of the Adult Leukemia Program at Harvard University's Dana-Farber Cancer Institute and an associate professor at Harvard Medical School.
"Now, people can be expected to live a long time in many cases," Stone said. "It's devastating if untreated but quite approachable if treated."
Baer and Stone said that while no breakthrough treatments have been developed, the available therapies are at the point where people can live with the disorders.
Most people with aplastic anemia will require multiple blood transfusions, which relieve symptoms by providing blood cells that the bone marrow isn't producing, Baer said. Symptoms also can be managed with immunosuppressive drugs similar to those used in AIDS treatment. The drugs suppress the activity of immune cells that are damaging bone marrow, helping the marrow recover and generate new blood cells, she said.
Antibiotics can be used to effectively fight off infections that take advantage of the disorder. And for a longer-term therapy -- or for people with severe aplastic anemia -- bone marrow transplantation is an option, but a limited one due to the difficulty involved in finding a matching donor.
Experimental treatments now being tested include growth factor drugs that may help stimulate the bone marrow to produce new blood cells; male hormones that also might boost blood cell production; and peripheral stem cell transplants. In that procedure, stem cells are taken from the blood of a donor, rather than from their own bone marrow, and transplanted into the patient, according to the Mayo Clinic.
"Twenty, 30 years ago, it [aplastic anemia] was fatal," Baer said. "Now, between the different treatments, 70 to 90 percent can live a long life. You have to continue to monitor your blood counts, and you are on some medication long-term."
Since these diseases involve damage to stem cells, research in this area could provide much insight into the potential of stem cells for treating other types of diseases. Stem cells have attracted much research focus due to their potential regenerative powers and ability to transform themselves into a host of different cells.
Bone marrow stem cells are the most primitive cells in the marrow, and from them, all the various types of blood cells are descended. Research also has shown that stem cells from bone marrow can give rise to non-marrow cells, which has led to federal funding to look into their usefulness in treating heart disease.
"It's very important to understand as much as possible about the bone marrow stem cell," Stone said. "What keeps it going, what causes it to become malignant? The more we understand about those things, the more we'll know about potential uses of stem cells."
More information
To learn more, visit the Aplastic Anemia and MDS International Foundation Inc.
and: http://www.dreddyclinic.com/findinformation/aa/anemiaaplastic.htm
Sunday, January 21, 2007
After 25 years of research studying the affects lifestyle and diet on the pH of the blood
Louis Pasteur's germ theory has become a curse. Antoine BeChamp an adversary to Pasteur and his germ theory for scientific fraud said this about the germ theory, "there is nothing so false that does not contain some element of truth, and so it is with the germ theory."
The germ theory is the controlling medical idea for the world. In Pasteur's day, and ever since, other proposed theories about the cause of disease have fallen on death ear because they have tended to contradict that paradigm. NO matter how simple and logical an idea about the cause of disease, if it does not promote the concept of invasion of germs and their specific cures it does not fit into the medical paradigm.
More importantly, the germ theory has become a curse because it has encouraged individuals to give up responsibility for their own health over to the medical community. If germs cause disease it stands to reason that control belongs to the medical community whose tireless researchers spend trillions of our money to find the right pill or potion to annihilate disease-causing germs.
This quest to cure disease through medication is at the heart of modern allopathic medicine and the multi-trillion dollar pharmaceutical industry. It is a quest that persists despite evidence indicating that airborne germs do not cause the disease for which they are credited.
After more than a century of trying, the Pasteurian germ theory has utterly failed in the quest to a cure for any disease. All major degenerative diseases are on the increase, as are so called infectious diseases which are not infectious at all. Every year, old symptoms are given new names - names like MS for polio, AIDS for poor sanitation, poor nutrition, poor lifestyle choices and drug use, Epstein-Barr virus for connective tissue disorders like fibramyalgia - to make them appear to be the work of a new germ. Unless we turn this nonsense around, the human race could become extinct like the dinosaurs from the treatments of modern medicine to kill a non- threatening or phantom germ.
If we want to find the cure for disease we need only to look at our dietary and lifestyle choices. If you heed the ignored, even rejected discoveries of Pasteur's peers and scientists of the 19th and 20th century, adding those to my own discoveries, you will learn the true cause of disease.
Until the medical community starts looking at causes rather than devoting its time looking for cures, and until we start taking responsibility for our own lifestyle and dietary choices, I believe the human race is in trouble of becoming extinct.
Dr. Benjamin Rush, Physician and signer of the Declaration of Independence, 1776 said this: "Unless we put medical freedom into the Constitution, the time will come when medicine will organize itself into an undercover dictatorship, To restrict the art of healing to one class of men and deny equal privileges to others will constitute the bastille of medical science. All such laws are un-American and despotic."
Where does life begin? In the womb or the grail, the holy grail, in the amniotic fluid, in a 98.6 F, one percent water and salt solution or 1 part salt to 100 parts water. This solution is called the sol. This natural salt solution, called "sol" is from the origin of the word, directly connected to the word "soul". What we call "sol" for our salt solution (a solution of two in one- no more polarity), was believed by the ancient Celtics to represent our soul, as the soul originated, in their belief, from the ocean where we are all born from the same fluids, arising from the same "sol" a solution of salt and water.
Our body in its wholeness is an ingenious creation of nature, It has been given all mechanisms to not only sustain its life but also to create new life. Every healthy person has innate regulatory mechanisms to maintain its alkaline design and self-healing powers, which ensure or reestablish the natural balance of the bodily functions, the homeostasis.
It is not the doctor that heals us, nor the medication, but our own innate alkaline regulatory mechanisms. Our body is able to fully regenerate itself. Therefore, it is advised to use great discernment before labeling any disease as "incurable" or "untreatable." If doctors come to the conclusion that a disease in incurable, they would be more accurate in saying that with their knowledge and experience, they are not able to offer any further help. The word "incurable" conveys fear, or false evidence appearing real, which stifles and weakens our body's innate alkaline mechanism.
Bio-chemically speaking Health is all about alkaline balance. Bio-energetically speaking Health is all about energy. Vibrating energy is the origin of matter and the origin of life. And matter is nothing more than organized energy.
In 1984, the Swiss physicist Dr. Carlos Rubbia, received the Nobel prize for discovering a mathematically calculable natural constant with which he could calculate the ratio of mass particles (matter) in relation to navigating energy particles, The ratio of matter to energy that forms matter is 1 to 9,746 to the power of 108 or about 1 to 1,000,000,000 which means it takes one billion energy units to create one single unit of matter in a materialized tangible form.
Isn't interesting that we for the most part, preoccupy ourselves with only 1 billionth part of reality: that which is in a material form and can be seen and touched. We fail to see the far greater amount of energy particles it took to materialize our reality. This revolutionary scientific discovery shows us clearly that every form of matter is subject to higher energetic interactions and subject to change of form and function.
When we analyze the energy content of any form of matter, we arrive at its smallest part, the atom and its protons, electrons and neutrons. There is ongoing movement without any contact- nothing tangible, just pure vibrating energy. This vibrating energy creates a frequency, which can be measured, a so-called wave length which can be seen using my photon interference photography. Every form of matter is characterized as a specific frequency spectrum.
And each frequency spectrum can be measured using a decibel meter. All organized matter is nothing more than organized energy that gives off a specific frequency and a specific sound which can be measured and heard. When we turn on a light or an electrical device we can see the energy but we cannot perceive the electrical current itself, but we except its existence.
This same materially non-perceivable electricity, this energy, flows through our body fluids especially our blood. Every one of us has enough measurable electrical cu rrent flowing through us to light up a 100 watt light bulb.
Life/light = energy and energy = information or intelligence. Everything that exists not only exists as energy but also as a carrier of information or intelligence, whether it is a human being, a form of food or drink, or a rock. Life is a constant exchange of energy and intelligence and the best place to view this life energy is in the live and dried blood.
Plasma which is 92% water is a good example for showing how matter as energy is transformed when additional energy is added or subtracted. Water has three different distinct bodies or states: solid, liquid and gaseous. Ice is frozen water or like the thickening of the blood.
We can see it and feel its coolness. By adding energy in the form of heat to the ice it transforms back into a liquid. When we add more energy to the water it begins to boil and the molecules start moving faster and faster that they begin to transform into steam and become gaseous. This transformation of organized energy as matter from one form to another is know as biological or energetical transformation or also referred to as pleomorphism.
Energy and intelligence are identical.
Every form of energy has a specific wavelength
Every wavelength has its individual content of intelligence
There are no accidents in the order of Nature
Meanwhile, we know of about 40,000 different diseases and the list is growing that are treated by the 1,200 different allopathic specialty fields with 58,000 different kinds of allopathic preparations or medicines. However, the word diseases in the plural form, is not a accurate.
Have you ever heard of "healths"? We are either healthy or ill. This illness signals a lack of energy and shows up in the form of a symptom. To represent a symptom as an illness is technically and scientifically inaccurate. The symptom is merely the intelligent cry of the energetically defective and suffering body, crying out for help. And normally, the body turns to a weakened organ to give us a hint, through a symptom, that things are not in order.
Our bodies either hum or honk Upset stomachs or high blood pressure or high blood sugars is the body honking. The honks of our bodies are telling us there is a state of pH or energetic imbalance.
Why does pH balance or pH Homeostasis define good health?
pH balance or pH homeostasis in humans commonly refers to the internal balance of the body's electro-magnetic and chemical systems in response to the changing conditions of the external world and the changing conditions of the internal world.
The word homeostasis comes from the Greek words: "homeo" means similar or "alki" or "alkaline" and "stasis" means a tendency toward maintaining stability. There are many homoeostatic mechanisms in our bodies that help maintain this balance and our state of health is directly related to the health of these mechanisms. pH homeostasis is maintained by dynamic processes of feedback and regulation.
pH homeostasis has only one objective: to preserve the beneficial conditions of life in the internal alkali environment. Every day we are bombarded with external influences that threaten that balanced internal alkaline pH environment. Some of these threats include becoming too hot or too cold, eating too much or eating acidic foods or drinks, breat hing polluted air and being exposed to chemicals over a period of time.
Our cells, especially the red blood cells can only survive when our bodies are strong enough to maintain pH homeostasis or to regain it quickly after we have been exposed to toxic environmental threats. Some of the pH homoeostatic mechanisms in the body include temperature regulation, dilation of the eye, blood composition, heart rate, blood pressure, water content, blood sugar level, mineral relationships, and of course the acid/alkaline balance of our body fluids. An essential feature of these mechanisms is that they enable the red blood cells, the tissue which is a product of the red blood cells and the whole of the organism, also a product of blood, to adapt to changes in both internal and external environmental conditions.
If the pH homoeostatic mechanisms are impaired the body loses its ability to regulate these mechanisms. By looking at living blood using a compound microscope we can view the quality of the red blood cell, its environment and how well the body is manag ing these pH homoeostatic mechanisms.
The interdependence and close coordination of the many bodily functions, which work so well when we are in alkaline balance or health, may be upset by a chain reaction when any part of the system breaks down from metabolic acids which have not been properly eliminated through, respiration, perspiration or urination. If this chain reaction is too drastic, the red blood cells and body cells will become acidic and begin to biologically transform into other cellular forms - like bacteria or yeast.
The normal state of health is not a static condition, but a coordination response of many systems and mechanisms. Fluctuations occur within a very narrow pH range. An imbalance of a point or two on the acid/alkaline pH scale is extremely disruptive to health. A few percentiles of variation of oxygen concentration in the blood can impair function.
In the bloodstream, the slightest changes can be observed in the structures of the red and white blood cells, the level of cellular debris, the creation of cholesterol or calcium crystals, etc. If the blood sugar content is continually elevated due to body cell transformation or breakdown, the body chemistry becomes upset. An infinitesimal deficiency of sodium, calcium, potassium or magnesium, the alkaline buffers of the body can cause a problem in the function of many body parts.
We must keep our pH homoeostatic mechanism strong so that we can deal effectively with our world. If we are humming and the process of pH homeostasis is orderly, life continues; if we are honking and the pH homeostasis is continually being disrupted, our health is in jeopardy.
pH Homeostasis is a bit like balancing the books in accounting. It is maintained by balancing inputs with outputs.
How well we adapt in health and sickness is largely a function of the pH homoeostatic mechanism. The body's chemistry response to such subtle changes that a negative thought, an acidic food or drink, or eating too much food can be a problem for maintaining balance.
In 1988 an article of the New England Journal of Medicine stated that, "most major chronic disease probably results from the accumulation of environmental factors over time in genetically susceptible people."
In 1965, Rene Dubos, a medical historian and philosopher, pointed out that the body is imperfect in its attempts to adapt and maintain pH homeostasis. She said, "the mechanisms involved in regulating homeostasis don not always return the body's functions to their original state. They can be misdirected. The body only has the ability to adapt to insults for so long. When it can no longer adapt , degeneration sets in. Health is the state that the body attains when an individual responds adaptively and restores the body to its original integrity."
The term "homeostasis" was coined in the mid-1920's by the American physiologist, Walter B. Cannon. But he was building on a concept of balance that dated back to ancient Western, Eastern, and Middle Eastern civilizations.
The balance equals good health equation was first suggested by Hippocrates (460-375 BC) and the ancient Greeks. Hippocrates considered health to be a state of harmonious balance and disease a state of disharmony. He and his contemporaries believed that harmony and balance existed between organs, between bodily fluids, and between body and soul. When the body is out of harmony and balance, illness occurs.
Hippocrates studied the entire patient in his or her environment, noting the effects of climate, food, and occupation on health. "Our natures are the physicians of our diseases, " he said, describing the healing forces we all have within us as the healing power of Nature. It was the physician's objective to restore harmony with food, exercise, rest, and with medicinal remedies designed to remove the harmful acidic excesses. This conservative approach was designed to let nature do the healing and above all, as Hippocrates said, "to first do no harm."
The Greeks ideas on equilibrium and health evolved further under the philosopher Aristotle (384-322 BC). He felt that a healthy body worked through what he described as a hemostat, a device that returns the body to a state of equilibrium even when it is subjected to stimuli that disturbs this balance. Everything is tied to this state of equilibrium, including the psyche and emotions, and nothing could be regarded as a separate component.
To lead a healthy life, the condition of balance had to be maintained, This could only be achieved if the body had an adequate feedback system, a means by which signals were transmitted to different parts of the body to help move it back into balance when it moved too far off alkaline center.
This psychological viewpoint was shared by another philosopher, Epicurus (341-270 BC). In his writing he referred to psychological stress and suggested that an individual's quality of life could be improved by coping with what we would now describe as emotional stressors.
As early as about 120 AD in India, Eastern philosophers had reached similar ideas about the importance of balance in health. A general medical textbook from that time, the Caraks, described health as a balance of bodily elements know as dhatus, and a happy mental state called prasana.
The Middle Eastern approach incorporated the Hindu teachings with the Greco-Roman medical doctrine. Being base upon both religious and philosophical ideas, Islamic healing involved both body and soul.
Over 1000 years later, during the Middle Ages in Europe, good health was still linked to this notion of balanced physical, emotional, and spiritual state. To help people achieve this state, European hospitals were set up by religious orders and attached to abbeys, monasteries, and convents. Doctors prescribed diet, rest, sleep, exercise, and salt baths.
In 1600 Thomas Sydenham had begun classifying diseases, even though he believed disease was a result of imbalance, consistent with Hippocrates and Galen.
In 1628 Harvey traced the circulation of the blood, arguably perhaps the single greatest achievement in medicine.
In 1753 James Lind showed that Scurvy could be reversed with the limes that contain limonene - an antitoxic or antacid.
Doctors began to lose their way in 1796. In 1796 Benjamin Rush observed that all fevers were associated with flushed skin, he concluded that this was caused by distended capillaries and reasoned that the proximate cause of fever must be abnormal "convulsive action" in these vessels. He took this a step further and conclude that all fevers resulted from disturbances of capillaries and since the capillaries were part of the circulatory system, he concluded that a hypertension of the entire circulatory system was involved.
Rush proposed to reduce this convulsive action by "depletion" or bleeding. A reminder that the medical establishment's acceptance of bleeding exists today in the name of the British Journal "The Lancet" one of the leading medical journals in the world. Today bleeding is called phlebotomy.
Also, In 1796 Edward Jenner took the pus from the runny sores of sick cows and injected it into the blood of his "patients. He thought that since pus is seen routinely in all kinds of wounds, pus was seen as a necessary part of healing.
In 1788 vaccinia was the bacteria that medical science suggested caused cowpox.
In 1830 the development of the first modern day achromatic microscope.
In 1835, Harvard's Jacob Bigelow argued in a major address that in "the unbiased opinion of most medical men of sound judgement and long experience . . . the amount of death and disaster in the world would be less, if all disease were left to itself."
In 1840 Jacob Henle in his essay, "On Miasmata and Contagia" first formulated the modern germ theory. He suggested that disease seem to germinate, grow and spread - like a first point or origin, a seed, a bacterium. The germ theory said that minute living organism invade the body, multiply and cause disease and that a specific germ causes a specific disease.
In 1850 Samule Thomson said, " May the time soon come when men and women will become their own priest, physicians and lawyers - when self-government, equal rights and moral philosophy will take the place of all popular crafts of every description . . False theory and hypothesis constitute nearly the whole art of medicine."
In 1860 Louis Pasteur suggested that living organisms, not a chemical chain reaction caused fermentation, winning converts to the germ theory.
In 1881 an American scientist George Sternberg was the first to isolate the fungus, pneumococcus and the first to observe the white blood cells engulfing bacteria, a key to understanding the immune system.
In 1882 a German, Robert Koch isolated the tubercle bacillus and declared it as the bacterium that caused tuberculosis that further confirmed the germ theory of Pasteur.
In 1884, German scientist Friedrich Loeffler isolated the diphtheria bacillus from throats of patients, grew it on a special medium (labs today call this Loeffler's serum slope to grow the bacteria from suspected cases), and began carful experiments in animals that took several years. His work suggested that the bacteria themselves did not kill; the danger came from a toxin, diptherium, an acidic poison that the bacteria excreted as a waste product from sugar metabolism.
In 1885 Max von Pettenkofer insisted that Koch's bacteria were only one of many factors in the causation of disease. His dispute with Koch became increasingly bitter and passionate. Petterkofer determined to prove himself right, prepared test tubes thick with lethal cholera bacteria. Then he and several of his students drank them down. All survived. Petterkofer claimed victory that germs do not cause disease.
In 1889 Pasteur's proteges, Emile Roux and Alexandre Yersin grew broth thick with diphtheria bacteria and used compressed air to force broth through a filter of unglazed porcelain. The filter was designed by Charles Chamber land, a physicist working with Pasteur; though only a tool, the filter itself would prove to be immensely important. NO bacteria or solids could pass through the porcelain. Only liquid could. They then sterilized this liquid. It still killed. That proved that bacteria, an insoluble could not kill, but a soluble, an acidic toxin did the KILLING.
The cure from diphtheria was not in killing the bacteria but neutralizing the acids or excretions from the bacteria.
In 1900 Frederick Gates and intellect and Baptist Minister and an assistant to John D. Rockefeller, saw an opportunity to exploit the medical field because of its admitted uncertainty and ignorance of the time. He had organized many business ventures for the Rockfellers' and convinced John D Rockefeller to open the Rockefeller Institute for Medical Research. The Rockefeller Institute saw medicine itself as its field from its earliest existence scientists studying disease based upon the germ theory of Pasteur.
In 1901, William Henry Welch was hired by John D. Rockefeller to set up the Rockefeller Institute for Medical Research. William Henry Welch was steeped in the germ theory and established its strong hold on the medical model. You might call Dr. Welch the Father of American Medicine and the perpetrator of the Pasteurian Germ Theory.
After the civil war medicine had discovered drugs - such as quinine, digitalis and opium of which Oliver Wendell Homes the physician Father of the Supreme Court justice said, "I firmly believe that if the whole materia medica, as now used, could be sunk to the bottom fo the sea, it would be all the better for mankind - and all the worse for the fishes."
In 1911, the head of the school training French army doctors in public health said that germs alone were "powerless to create an epidemic." But it was too late, this particular view was now considered simply a minority opinion. The germ theory now had its hold on the governments of the world!
IN 1911, the medical establishments made up a story that Peyton Rous discovered a bacteria that caused cancer and received a Noble Prize for his discovery posthumous in 1966. This gave rise to the term virus named after Peyton Rous's bacteria. Peyton Rous never suggested this in any of his research that his bacteria caused disease let alone cancer. This story gave rise to a new group of bacteria called filterable bacteria that the medical community now refers to as virus - beginning 1996. There is NO scientific evidence that shows that virus's have ever caused ANY disease.
These ideas of balance were some distance from those of earlier societies that ascribed illness to the supernatural powers they believed governed their lives. The Babylonians, the Egyptians, the ancient Americans saw disease as an entity unto itself, a potent demon that struggled to dominate, attacked, penetrated, and possibly even killed its unfortunate host.
Offend the Gods, an ancestor, or an evil witch and be struck down as punishment. Lead a sinful life and you were tempting fate.
Of course, we perceive that these ideas about disease are no longer widely believed, which makes it all more the ironic that Pasteur's germ theory has had and still has a stranglehold on 19th, 20th and now 21st century medicine. As medical writer Alberto Seguin described in an article entitled, "The Concept of Disease," the demonic idea of disease reached its full height with the germ theory. It became possible to bring together rational and scientific thought with irrational tendency to personalize disease. The germ in what ever name it is called, West Nile Virus, Ebola, Hunta, HIV, Anthrax, SARS and now AVIAN, are the scientific demon, the curse, the lie and the fraud that is said to attack and kill!
If we will consider disease as a symptom of disease not the cause, then the germ is nothing more than an expression of imbalance and a biological transformation of what use to be organized to that which is changing into a new form. This was my discovery in 1994. I witnessed biological transformation as seen on pg. 126 of my book "Sick and Tired" the transformation of a rod bacteria back into a red blood cell and then back into a bacterial rod.
I knew for the first time that bacteria was not a demon, not an entity but a transformation, a new formation of a preceding form. Not the cause of disease but the expression of a change in the internal environment which had given rise to change. For several years I felt alone in this discovery until I learned of the works of the giants that proceeded me that had their finger on the magic of life.
Claude Bernard (1813-1878) "The terrain is everything the germ is nothing." And upon the death bed of Louis Pasteur admitting to Claude Bernard that he was right in 1895.
Antoine BeChamp (1816-1908) "Disease is born in us and from us."
Florence Nightingale - a famous nurse (1820 -1910) Mathias Schleiden and Theodor Schwann (1839) Gunther Enderlein ((1872- 1968) Walter B. Cannon (1871-1945) "Only by understanding the wisdom of the body shall we attain the mastery of disease and pain that will enable us to relieve the burden of the people."
Royal Raymond Rife (1888-1971)
Wilhelm Reich (1897 - 1957)
Gaston Naessans (1924-2005)
Philosophically speaking, Pasteur had an ally in Napoleon III, who came to power in 1852. The Emperor believed in a police state and in using complete control to rule. Pasteur's mechanistic idea of disease, finding the right cure for each germ, fit into this philosophy of control.
Giving the responsibility to the any government to cure disease is giving up control. It takes responsibility - and power - away from the individual. In the words of Antoine BeChamp, "there is nothing so false that does not contain some element of truth and so it is with the germ theory."
One of six of us will become diabetic
One of two of us will develop cancer
One of two of us will develop cardiovascular disease One of six couples will suffer from unexplained infertility.
One of seven women in the US will develop breast cancer.
We need to get out to the disease business. If we want to understand health, energy and vitality then we need to study the people who are healthy. Over the last 25 years I have been studying health and how it relates to the blood. Viewing live and dried blood is the pinnacle of understanding health and how to achieve health with alkaline foods, drinks, exercise, breathing, getting adequate rest, etc.
Now, I pray and hope that you will realize that we are all responsible for our own health - you alone. A medical practitioner can only help to relieve symptoms. Ultimately, you are the one who has to take charge. Health is a choice just as disease is a choice. You are responsible for what goes into your mouth and what comes out of your mouth, as well as for what you think, feel and do. Health is all about choices and consequences.
The health and energy of the human organism is the knowledge that are bodies are alkaline by design and acidic by function and the best way to maintain that alkaline design is through an alkaline lifestyle and diet.
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Saturday, November 25, 2006
The Pacelli Chiropractic & Health Potential Complex Web site states:
How often do you get to see if small changes in nutrition, really can make a difference?
Well in this case, that's how we work. After making our recommendations, we repeat the test in 2 weeks, and look to see if we see changes.
This way you get to see the changes in your blood as we help correct the problems, it also allows us to check dosages to make sure that you are getting the proper amount of the vitamin, mineral, protein, or enzyme you need to restore you to optimal health.
These claims are sheer bunkum. Dark-field microscopy is a valid scientific tool in which special lighting is used to examine specimens of cells and tissues. The objects being viewed stand out against a dark background-the opposite of what occurs during regular microscopy.
This allows the observer to see things that might not be visible with standard lighting. Connecting a television monitor to a microscope for diagnostic purposes is also a legitimate practice. However, live cell analysis is not. Although a few characteristics of blood (such as the relative size of the red cells) are observable, live cell analysts invariably misinterpret other things, such as the extent of red blood cell clumping, changes in the shape of the cells, and other artifacts that occur as the blood sample dries.
Moreover, most practitioners who perform the test are not qualified to manage the problems they purport to diagnose.
During the mid-1980s, one company marketing live-cell equipment projected that a practitioner who persuades one patient per day to embrace a supplement program based on the test would net over $60,000 per year for testing and supplement sales. Another company estimated that with five new patients a day (22 days a month) paying $30 for the test and $50 for supplements, practitioners would gross over $100,000 per year just on initial visits.
Today's most active individual promoter of live-cell analysis is probably James R. Privitera, M.D., of Covina, California, who claims that "clot malfunction" is an underlying cause of many diseases, can be diagnosed with live cell analysis, and can be treated with large doses of dietary supplements.
His book, Silent Clots, describes his "general daily guidelines [for supplements] that have worked well for many patients as an anti-clotting program." The book also describes regimens for arthritis, asthma, baldness, bladder infections, cancer, colds, colitis, cramps, diabetes, diarrhea, diverticulosis, eczema, and edema, and includes case histories of patients he treated for many other conditions [1].
I do not believe there is any scientific evidence for these claims or that these regimens are effective as Privitera claims. His's web site offers more than 150 supplement products for sale.
In 1975, Privitera was convicted of conspiring to prescribe and distribute laetrile and was sentenced to six months in prison. (Laetrile is a quack cancer remedy.) In 1980, after the appeals process ended, he served 55 days in jail but was released after being pardoned by California Governor Jerry Brown. (The pardon occurred in response to a letter-writing campaign generated by the National Health Federation, a group that espouses what it calls "health freedom.")
Then, because Privitera had been prescribing unapproved substances (including laetrile, calcium pangamate, and DMSO) for the treatment of cancer, the California Board of Medical Quality Assurance suspended his medical license for four months and placed him on ten years' probation under board supervision.
During the probationary period, Privitera was "prohibited from making any representation that he is able to cure cancer through nutrition." He was also forbidden to tell patients they had cancer unless the diagnosis was confirmed in writing by an appropriate board-certified specialist.
During the probationary period, Privitera commercialized live-cell analysis and founded two companies that marketed devices for doing it. Silent Clots mentions that in 1993, a federal judge signed an order authorizing Internal Revenue Service agents to enter his clinic premises to effect a levy and that a seizure was made.
However, the book provides no further details about his tax-related difficulty.
Critical Reports
During the mid-1980s, National Council Against Health Fraud vice president James Lowell, Ph.D., watched three practitioners demonstrate live cell analysis at health expositions.
Lowell noted:
None took precautions during the preparation of the slides to prevent the blood from drying out or clotting.
They failed to clean their microscope slides carefully between patients, which meant that dirt seen under the microscope would be misinterpreted as blood components.
Some of the patterns one practitioner saw resulted from his microscope being out of focus and disappeared when Lowell adjusted it properly. [2}
Live cell analysis is also promoted by Infinity
2, of Scottsdale, Arizona, a multilevel company whose distributors often demonstrate their wares at chiropractic conventions. Infinity2 calls the test "live cell microscopy" and recruits licensed health professionals to use the procedure to sell its products. In 1995, I was tested at a national chiropractic convention where two teams of Infinity distributors had exhibits.
One exhibitor said I had "mild B12 deficiency" and "maldigestion" that could weaken my immune system and cause fatigue. The other said my blood cells showed evidence of "liver toxicity," "bacterial infection," and "free radical damage."
In both cases the recommended "treatment" was enzyme pills, which the company was marketing with false claims that "enzyme deficiency" is widespread among Americans. To reinforce their that the pills could help me, both practitioners gave me enzyme pills, repeated the procedure several minutes later, and said that the problems were no longer visible. Unknown to them, however,
I had faked taking the pills, so the "improvements" they saw had nothing to do with them. The most likely explanation is that the specimens were examined differently. Blood dries more quickly near the edges of the slide than near the center. Thus "improvement" will occur if the first specimen is examined near an edge and the second specimen is examined near its center.
Legal Action
In 1996, the Pennsylvania Department of Laboratories informed three Pennsylvania chiropractors that Infinity2's "Nutritional Blood Analysis" could not be used for diagnostic purposes unless they maintain a laboratory that has both state and federal certification for complex testing [3].
The company's attorney replied:
As background, you should know that part of our business activity is supplying a microscope system that is equipped for the demonstration of blood samples on a video monitor. We teach and recommend the use of this system as a health education demonstration. In our training and system we do not teach, promote or address in any manner using the system for "analysis" or any other medical purpose.
Our system is based on obtaining a written nutritional and lifestyle analysis from patients of doctors using the microscopy system. Once this questionnaire and evaluation of lifestyle and nutrition is examined by the doctor, the doctor then makes specific recommendations to the patient, based solely and exclusively on the nutritional analysis and personal interview with the patient.
After any recommendation has been made for altering the patient's lifestyle or nutritional habits, the doctor may place a single drop of blood on a sample slide for viewing through the dark field microscope which is then displayed on a video monitor.
This demonstration is a powerful motivating tool to encourage a doctor's patient to accept the doctor's previously made recommendations and alter his or her lifestyle to a healthier form of living.
The doctor performing the demonstration never makes any analysis, determination or recommendation based on the video demonstration. There is no commentary given regarding the state of the patient's blood or anything seen in the bloodscreen itself other than to educate the patient by pointing out features of the blood such as red cells, white cells, and plasma. The patient is able to view a sample of his/her own blood, which results in the motivation that can lead to beneficial lifestyle changes for the individual patient [4].
A Laboratory Department official then informed the attorney that certification would be required if the practitioner:
Either prescribed a nutritional supplement or changed the amount or type of a supplement based on viewing a blood sample.
Recommended lifestyle or nutritional changes based on viewing a blood sample.
Performed nutritional microscopy more than once for a given patients.
Compared the patient's blood smear to that of another slide or picture
Showed the patient's blood smear and making any comment or providing any information other than to point out features of the blood such as red cells, white cells, and platelets [5].
Very few if any chiropractors would have reason to seek laboratory certification, and even if they did, I doubt that permission would be granted to perform this test for diagnostic purposes. If you encounter anyone who performs any type of live cell analysis, please report this to your state department of laboratories and send a copy of your notice to me at P.O. Box 1646, Allentown, PA 18105
Reference
1. Privitera J, Stang A. Silent Clots: Life's Biggest Killers. Lockstep Medicine's Conspiracy to Suppress the Test That Should Be Done in Emergency Rooms Throughout The World. Covina, Calif.: The Catacombs Press, 1996.
2. Lowell JA. Live cell analysis: High-tech hokum. Nutrition Forum 3:81-85, 1986.
3. Wlazelek A. Chiropractors cease blood cell show and tell. State restricts the use of magnified images to sell vitamins, supplements. The Morning Call, April 12, 1996, page B6.
4. Woodruff SM. Letter to Joseph W. Gasiewski, Director, Division of Laboratory Improvement, Pennsylvania Department of Health, Jan 17, 1996.
5. Gasiewski JW. Letter to Samuel M. Woodruff, General Counsel, Infinity2, Feb 16, 1996.
Chirobase
Well in this case, that's how we work. After making our recommendations, we repeat the test in 2 weeks, and look to see if we see changes.
This way you get to see the changes in your blood as we help correct the problems, it also allows us to check dosages to make sure that you are getting the proper amount of the vitamin, mineral, protein, or enzyme you need to restore you to optimal health.
These claims are sheer bunkum. Dark-field microscopy is a valid scientific tool in which special lighting is used to examine specimens of cells and tissues. The objects being viewed stand out against a dark background-the opposite of what occurs during regular microscopy.
This allows the observer to see things that might not be visible with standard lighting. Connecting a television monitor to a microscope for diagnostic purposes is also a legitimate practice. However, live cell analysis is not. Although a few characteristics of blood (such as the relative size of the red cells) are observable, live cell analysts invariably misinterpret other things, such as the extent of red blood cell clumping, changes in the shape of the cells, and other artifacts that occur as the blood sample dries.
Moreover, most practitioners who perform the test are not qualified to manage the problems they purport to diagnose.
During the mid-1980s, one company marketing live-cell equipment projected that a practitioner who persuades one patient per day to embrace a supplement program based on the test would net over $60,000 per year for testing and supplement sales. Another company estimated that with five new patients a day (22 days a month) paying $30 for the test and $50 for supplements, practitioners would gross over $100,000 per year just on initial visits.
Today's most active individual promoter of live-cell analysis is probably James R. Privitera, M.D., of Covina, California, who claims that "clot malfunction" is an underlying cause of many diseases, can be diagnosed with live cell analysis, and can be treated with large doses of dietary supplements.
His book, Silent Clots, describes his "general daily guidelines [for supplements] that have worked well for many patients as an anti-clotting program." The book also describes regimens for arthritis, asthma, baldness, bladder infections, cancer, colds, colitis, cramps, diabetes, diarrhea, diverticulosis, eczema, and edema, and includes case histories of patients he treated for many other conditions [1].
I do not believe there is any scientific evidence for these claims or that these regimens are effective as Privitera claims. His's web site offers more than 150 supplement products for sale.
In 1975, Privitera was convicted of conspiring to prescribe and distribute laetrile and was sentenced to six months in prison. (Laetrile is a quack cancer remedy.) In 1980, after the appeals process ended, he served 55 days in jail but was released after being pardoned by California Governor Jerry Brown. (The pardon occurred in response to a letter-writing campaign generated by the National Health Federation, a group that espouses what it calls "health freedom.")
Then, because Privitera had been prescribing unapproved substances (including laetrile, calcium pangamate, and DMSO) for the treatment of cancer, the California Board of Medical Quality Assurance suspended his medical license for four months and placed him on ten years' probation under board supervision.
During the probationary period, Privitera was "prohibited from making any representation that he is able to cure cancer through nutrition." He was also forbidden to tell patients they had cancer unless the diagnosis was confirmed in writing by an appropriate board-certified specialist.
During the probationary period, Privitera commercialized live-cell analysis and founded two companies that marketed devices for doing it. Silent Clots mentions that in 1993, a federal judge signed an order authorizing Internal Revenue Service agents to enter his clinic premises to effect a levy and that a seizure was made.
However, the book provides no further details about his tax-related difficulty.
Critical Reports
During the mid-1980s, National Council Against Health Fraud vice president James Lowell, Ph.D., watched three practitioners demonstrate live cell analysis at health expositions.
Lowell noted:
None took precautions during the preparation of the slides to prevent the blood from drying out or clotting.
They failed to clean their microscope slides carefully between patients, which meant that dirt seen under the microscope would be misinterpreted as blood components.
Some of the patterns one practitioner saw resulted from his microscope being out of focus and disappeared when Lowell adjusted it properly. [2}
Live cell analysis is also promoted by Infinity
2, of Scottsdale, Arizona, a multilevel company whose distributors often demonstrate their wares at chiropractic conventions. Infinity2 calls the test "live cell microscopy" and recruits licensed health professionals to use the procedure to sell its products. In 1995, I was tested at a national chiropractic convention where two teams of Infinity distributors had exhibits.
One exhibitor said I had "mild B12 deficiency" and "maldigestion" that could weaken my immune system and cause fatigue. The other said my blood cells showed evidence of "liver toxicity," "bacterial infection," and "free radical damage."
In both cases the recommended "treatment" was enzyme pills, which the company was marketing with false claims that "enzyme deficiency" is widespread among Americans. To reinforce their that the pills could help me, both practitioners gave me enzyme pills, repeated the procedure several minutes later, and said that the problems were no longer visible. Unknown to them, however,
I had faked taking the pills, so the "improvements" they saw had nothing to do with them. The most likely explanation is that the specimens were examined differently. Blood dries more quickly near the edges of the slide than near the center. Thus "improvement" will occur if the first specimen is examined near an edge and the second specimen is examined near its center.
Legal Action
In 1996, the Pennsylvania Department of Laboratories informed three Pennsylvania chiropractors that Infinity2's "Nutritional Blood Analysis" could not be used for diagnostic purposes unless they maintain a laboratory that has both state and federal certification for complex testing [3].
The company's attorney replied:
As background, you should know that part of our business activity is supplying a microscope system that is equipped for the demonstration of blood samples on a video monitor. We teach and recommend the use of this system as a health education demonstration. In our training and system we do not teach, promote or address in any manner using the system for "analysis" or any other medical purpose.
Our system is based on obtaining a written nutritional and lifestyle analysis from patients of doctors using the microscopy system. Once this questionnaire and evaluation of lifestyle and nutrition is examined by the doctor, the doctor then makes specific recommendations to the patient, based solely and exclusively on the nutritional analysis and personal interview with the patient.
After any recommendation has been made for altering the patient's lifestyle or nutritional habits, the doctor may place a single drop of blood on a sample slide for viewing through the dark field microscope which is then displayed on a video monitor.
This demonstration is a powerful motivating tool to encourage a doctor's patient to accept the doctor's previously made recommendations and alter his or her lifestyle to a healthier form of living.
The doctor performing the demonstration never makes any analysis, determination or recommendation based on the video demonstration. There is no commentary given regarding the state of the patient's blood or anything seen in the bloodscreen itself other than to educate the patient by pointing out features of the blood such as red cells, white cells, and plasma. The patient is able to view a sample of his/her own blood, which results in the motivation that can lead to beneficial lifestyle changes for the individual patient [4].
A Laboratory Department official then informed the attorney that certification would be required if the practitioner:
Either prescribed a nutritional supplement or changed the amount or type of a supplement based on viewing a blood sample.
Recommended lifestyle or nutritional changes based on viewing a blood sample.
Performed nutritional microscopy more than once for a given patients.
Compared the patient's blood smear to that of another slide or picture
Showed the patient's blood smear and making any comment or providing any information other than to point out features of the blood such as red cells, white cells, and platelets [5].
Very few if any chiropractors would have reason to seek laboratory certification, and even if they did, I doubt that permission would be granted to perform this test for diagnostic purposes. If you encounter anyone who performs any type of live cell analysis, please report this to your state department of laboratories and send a copy of your notice to me at P.O. Box 1646, Allentown, PA 18105
Reference
1. Privitera J, Stang A. Silent Clots: Life's Biggest Killers. Lockstep Medicine's Conspiracy to Suppress the Test That Should Be Done in Emergency Rooms Throughout The World. Covina, Calif.: The Catacombs Press, 1996.
2. Lowell JA. Live cell analysis: High-tech hokum. Nutrition Forum 3:81-85, 1986.
3. Wlazelek A. Chiropractors cease blood cell show and tell. State restricts the use of magnified images to sell vitamins, supplements. The Morning Call, April 12, 1996, page B6.
4. Woodruff SM. Letter to Joseph W. Gasiewski, Director, Division of Laboratory Improvement, Pennsylvania Department of Health, Jan 17, 1996.
5. Gasiewski JW. Letter to Samuel M. Woodruff, General Counsel, Infinity2, Feb 16, 1996.
Chirobase
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Friday, October 20, 2006
CHAPTER V.: The Blood and the Third Anatomical Element by Antoine Bechamp
OF THE REAL NATURE OF THE BLOOD AT THE MOMENT OF A GENERAL BLEEDING. THE LIVING PARTS OF THE BLOOD. PROTOPLASM. THE UNCHANGEABLE CHARACTER OF MIXTURES OF PROXIMATE PRINCIPLES. THE VITELLIN MICROZYMAS AND THE BLOOD GLOBULES. THE VASCULAR SYSTEM. THE BLOOD A FLOWING TISSUE.
The blood really contains three kinds of anatomical elements: the red globules, the white globules and the microzymian molecular granulations. Anatomically, the blood is constituted by three sorts of figured elements and, by a fourth term, a liquid. Is this the serum, this liquid which is its interglobular and intergranular substance?
The three sorts of anatomical elements are living, insomuch as they are organized and contain microzymas which I have proved to be living by their function as ferments and by their capacity to become vibrioniens by individual evolution, which was a novelty for physiology and even for chemists.
Nevertheless, so far as concern the red globule, since 1846 the statement that it is alive was not a novelty. In fact, in a memoir,1 which merits the more attention that it is never quoted, J. B. Dumas made an observation which must be regarded as of the first importance. It is that to isolate the red globules in their integrity, by mixing the blood with sulphate of soda, a current of air must be introduced; without this they will change, losing their coloring matter which itself also changes. And he said: "The globules of blood act as though they were really living beings, capable of resisting the solvent action of sulphate of soda so long as they are alive, but yielding to this action so soon as they have succumbed to the asphyxiation which affects them by the deprivation of air, and which manifests itself with singular rapidity, either by their change of color or by their rapid solution." Dumas asserted clearly that the globules breathe; that account must be taken of their membrane in explaining the phenomenon of respiration; and that the breathing of an animal has especially for its object to furnish oxygen to the globules of its blood and to expel "the products into which they convert it." He also remarked that in the discussions and the calculations respecting respiration the blood had always been regarded as a homogeneous liquid, while it was only the serum which possesses this quality. He in no wise disregarded the part taken by the serum in the phenomenon of arterialization, but he insisted on the preponderant part taken in it by the red globules.
1. Dumas, "Recherches sur le sang," C. R.. Vol. XXII, p. 900 (1846).
To understand the blood, one must place oneself in the order of ideas of the memoir of Dumas, but broadened; that illustrious savant did not recognize in it, nor did any one else at that time, other anatomical elements than the globules, but there is another. He saw in the blood only three nitrogenous organic matters: albumen, fibrin and the globules, but there are others.
I will add that, in the serum, he made allowance for the share therein of the phosphates and other mineral matters.
At the moment of a general venesection the blood has been regarded as being that which it is in the vessels while it circulates in them, but as being a mixture of the arterial and venous bloods; and we have seen that at this moment the blood is so thoroughly regarded as being alive that it was regarded as certain that coagulation was its death.
The blood being alive, it is necessary to recognize, in accordance with the doctrine of Bichat, that, as in all the rest of the organism, the only things living in it are the anatomical elements, that is to say, that of the four parts which constitute it, the three kinds of anatomical elements are the only things living in it; the fourth, the serum, or that which will become the serum, the interglobular and intergranular substance, fulfilling with regard to them only one of the conditions of existence.
But as this conclusion conflicts with the prejudices of the schools, it is necessary to know what those prejudices are to combat them, for they are the negations of the doctrine of Bichat and precisely contrary to it. In fact, while it is asserted that the globules of blood, in general the anatomical elements, are only organites, neither plants, nor animals, as M. Pasteur said, that is to say, not living although organised, it was insisted that that which in the blood is still called plasma was living, a liquid whereof all the materials are said to be in a state of perfect solution, that is to say, without any anatomic, figured structure. But it is well to repeat that such was the state of science just as it was before Lavoisier and before Bichat, when the philosophical naturalist, Charles Bonnet, speaking of the organization, called it "the most excellent modification of matter." Even in France a conception more or less analogous to it, that of protoplasm, was preferred to the striking conception of Bichat. But protoplasm or its synonym, blastema, was considered to be organized living matter without structure. Here is one of the most precise descriptions of such matter: "A completely homogenous, amorphous matter without structure can be regarded as organized substance if it is constituted of numerous proximate principles, united molecule to molecule by special combination and reciprocal solution, and however simple may be this organization, it is sufficient to enable one to say that it is alive." Diet, de Med., Littre et Robin, art. Organique (1878).
Van Tieghem said: "Protoplasm is a mixture with water, of a greater or less number of different proximate principles, in the course of continual transformation."
Huxley said: "All protoplasm is similar to protein—all living matter is more or less similar to albumen."
Cauvet said: "Protoplasm is a nitrogenous liquid, more or less flowing, composed of a translucent joining substance and of fatty and albuminoid granulations."
Even Claude Bernard said: "In its simplest condition life, contrary to the idea of Aristotle, is independent of all special form; it resides in a substance defined by its composition and not by its shape; the protoplasm."
Pasteur said: "Living organisms are composed of natural substances such as life elaborates them, the proximate principles of living bodies which possess faculties of transformation which are destroyed by boiling."1
1. C. R., Vol. LXXIII. p. 302. See letter of M. Pasteur to M. Donne. M. Pasteur's manner of thinking was still that of Chevreul [born in 1786. was still alive and active in 1856]— at the time (1810) of the foundation of his chair at the Museum; Chevreul said, speaking of living bodies, that they are organic bodies in contradistinction to inorganic bodies, which we term minerals. Buffon called minerals gross matter, admitting that there was a universally diffused organic matter which he termed organic molecules, but Buffon wrote before the time of Lavoisier. Chevreul spoke of the proximate principles of organic bodies which are the products of life. Pasteur, speaking of the same proximate principles, says that they are natural substances elaborated by life, which have powers of transformation, etc. It may thus be truly said that there was no idea of life as bound to a determined, structural form of living anatomical elements, according to the conception of Bichat. It is thus to be understood how M. Pasteur could class in the same category, as organites, the red globules of the blood and grains of starch. It is true that the amylaceous granule had been regarded as being a vesicle, but Biot and Payen had shown that it was solid throughout its mass, and I have proved, in my researches upon fecula, that it had neither tegument, nor microzymas, being wholly formed of amylaceous matter contaminated with a trace of albuminoid matter. In the microzymian theory it is not life which produces or elaborates the proximate principles, but the anatomical elements are constituted into living apparatus by the microzymas, according to the same mechanism by which the fibrinous microzymas cause starch to ferment, and elaborate the numerous proximate principles which I have described as produced in that fermentation.
These quotations are sufficient. Protoplasm is regarded as a pure mixture of proximate principles, that is to say, of materials of a purely chemical order. M. Cauvet and others, M. Frey, for instance, have observed the granulations of the protoplasm, but they were supposed to be pure proximate principles. This mixture was declared by some, as in the course of continual transformation; by M. Pasteur, as endowed with faculties of transformation, but without other proof of what is precisely the point in question, viz., whether such a mixture can spontaneously change, can alter itself, give birth to any living being whatever, be it a cellule or a microzyma. If protoplasm were that which it was thought to be, the conception of Bichat would be purely chimerical.
I have incontestably demonstrated, in contradiction to the theory of protoplasm and against M. Pasteur, that every mixture, artificial or natural, of real proximate principles, with water, is, by itself, in every way unalterable, incapable of giving birth to anything living; in short, as not being in the course of continual transformation and as not possessing any faculty of transformation capable of producing in it any spontaneous alteration. And if in such a mixture, boiling destroys the "faculties of transformation" of some zymas, this latter had not been produced spontaneously, it was the product of a living organism. In short, if the mixture contains some proximate principle which can be altered by oxygenation, by absorbing oxygen from the air, this principle is itself the former product of a living organism through the reaction of a zymas.1 I have given positive proof of all of this while studying the conditions of the spontaneous coagulation of milk, which was said to be a pure mixture of proximate principles. Cow's milk, creosoted by a suitable dose to destroy the influence of the germs of the air and completely protected from all contact with the air, first becomes sour and then coagulates. After which, vibrioniens appear in it. If by filtration, by the process which I have indicated in the case of the blood, both the globules and all the milk microzymas of the creosoted milk are absolutely removed, the limpid liquid which results, containing all the proximate principles of the milk, under the same conditions, does not become sour and consequently neither coagulates nor permits the appearance of the vibrioniens. The "faculties of transformation" then resided in the anatomical element of the milk which had been removed by filtration, and not in the rest of its substance, which maybe called the physiological serum of milk.
1. The zymases are never the products of the spontaneous alteration of an albuminoid matter, but are always the products of the physiological function of a living organism and of an anatomical element in the latter. See the article zymas, "Dictionnaire de la langue francaise." Littre (1869).
The physiological serum of the milk, which has the same composition as blastema or of protoplasm, is then naturally unchangeable and consequently not living.
It is the same with the fourth portion of the blood, which we will call the physiological serum of the latter. And precisely as the anatomical elements of milk are the agents of its spontaneous alteration, because they are living, so the anatomical elements of the blood are, on several accounts, the agents of its spontaneous alteration, as will be proved in the following chapter. But first must be determined the physiological role of this serum, in which are realized the conditions of existence of the anatomical elements, globules and granulations of the blood, while it circulates and after it has been shed.
I understand by "conditions of existence" of an anatomical element (following Bichat's conception), that of the preservation of its physical being at the same time with the integrity of its tegument and that of its content, preserved with its composition unchanged, which it can only be by finding in the medium in which it lives all the materials for its nutrition.
Take, for example, the red globules; we know that in blood, steeped in a certain quantity of water, the soluble contents of its globules are diffused by osmose, the teguments remaining whole; on the other hand, we know that in the same blood, steeped in several times its volume of a saturated solution of sulphate of soda, its globules remain entire, both tegument and content. We can even steep the blood in its own serum, without the globules being altered ; without any trace of the colored content being dissolved. And it is the same with the molecular granulations as with the globules; so that if in blood, steeped in the solution of sulphate of soda, a small part of their albuminoid atmosphere is temporarily soluble, as we have seen, it is absolutely insoluble in the serum and each granulation remains there whole and independent, the same as each globule, and this constitutes one of the conditions of the circulation.
But to understand the circulation and the reciprocal influence of the vessels and of the elements of their content, a slight diversion into embryology is indispensable.
In studying the development of the fowl to ascertain the role of the microzymas of the vitellus in the formation of the anatomical elements and of the organs, Estor and shown1 that the container and the content of the vascular system are born and developed simultaneously with the aid of the microzymas and the unorganized materials of the vitellus. We have never seen globules in the body of the embryo before the establishment of the circulation; they are formed on the spot. Thus the anatomical elements of the tissues of the vessels and the anatomical elements of the blood contained therein are born at the same time, by the microzymas of the vitellus as builders, in the unorganized intermicrozymian medium of the vitellus. Hence it results that the serum of the embryonal blood comes into existence concurrently with the globules and the granulations, having the non-organized parts of the vitellus for their source. To sum up, container and content are born at the same time, develop at the same time, and at the same time become what they are destined to be in the future.
1. C. R., Vol. LXXV, p. 962 (1872). We were led to undertake this embryological experiment as the consequence of the following experiment of which Estor was a witness: The mother of vinegar formed a microzymas, united among themselves by a hyaline intermicrozymian substance, is a membrane of mucous consistence with which we have compared the false membrane called fibrin; but it is so much vegetable that it is hardly nitrogenized. But in the "mother of vinegar," under the conditions in which one forces its microzymas to live, these become by individual evolution bacteria, or by association manufacturers of cellules. It is the same with the microzymas of beer-yeast, which, in certain media, act as lactic and butyric ferments, undergoing vibrionian evolution; while in others they reproduce the cellule of yeast and the normal alcoholic fermentation." * The microzymas then can be manufacturers of cellules by grouping themselves together, and being grouped becoming enveloped with a tegument when the conditions of existence of these cellules are united. And it is precisely this which the vitellin microzymas do during embryonic development. This new theory of the origin of the cellule does not weaken the axiom of M. Virchow: omnis cellulae cellula. One cellule may be derived from another cell according to another mode, that is all. Consequently, when M. Pasteur said that the globule of the blood is an organite incapable of reproduction because it could not be cultivated like beer-yeast, he was mistaken, not knowing any other mode of reproduction. *For the developments of the theory of the microzymas, manufacturers of cellules, see the following publications: "Conclusions Concerning the Nature of Mother of Vinegar and of Microzymas in General," C. R., Vol. LXVIII, p. 877 (1869); "Researches on the Nature and Origin of Ferments. Ann. de chemie et de physique," 4th series. Vol. .XXIII. p. 443. And for the theory in its entirely: "Les Microzymas Builders of Cellules." see: "Les Microzymas," etc., M.Chamalet, 60, passage Choiseul, Paris, p 431-463 and p. 948.
The blood ought to be studied not only by itself, but as being to the vessels that which the content of a cellule or of an organ is to its tegument. The tegument of the vascular system consists of the various tissues of the arteries, of the veins and of the capillaries. It must also be borne in mind that the system is directly in relation with the heart, the lungs, the liver, etc., and that the lymphatics (the chyle vessels) communicate directly with it. And as the content of a cellule, of an organ, does not exist without the container, so also the blood does not exist without the vessels which contain it and which make of the whole system an organ in more or less direct relation with every part of the organism.a And it must be observed that if there is any difference between the anatomical constitution of the container of the various regions of the vascular system there is also a difference in their content. Independently of the color there is more oxygen and less carbonic acid in the arterial blood than in the venous. In several regions differences have been observed in the portion of the number of blood globules to that of the leukocytes. Lehmann observed that if the blood obtained from the portal vein gives fibrin by whipping, that of the suprahepatic vein does not furnish any by this means, proving, as we shall see, that the microzymian molecular granulations of the two bloods differ in something, and Denis has already pointed out that the fibrin of the arterial blood is not identical with that of the venous blood, etc.
[a This original conception throws a new light upon the purpose and relations of the circulatory system, which I hope to enlarge upon in a future memoir.—Trans.]
Consequently it is physiologically evident that the anatomical elements, conceived as being personally and in individually living from whatever part of an organism they may be taken exist there only because the conditions of their existence are found naturally realized there. It is not otherwise with the blood; the conditions of existence of its anatomical elements are only realized, in each point of the circuit, while it is contained in the vessel and circulating.
It is ordinarily said that the anatomical elements swim in the lymph, the liquor sanguinis or the plasma; those who, with Milne-Edwards, admitted the existence of finely divided fibrin, said that it too floated in the serum. Anatomically, may we continue so to regard the reciprocal relations of the three anatomical elements and of the fourth portion of the blood? And is it correct to say that at each point of the blood current there are molecular granulations and globules almost in contact with one another? Is it not more correct to say that the fourth part, the serum, is only the intercellular and intergranular substance of these anatomical elements which hinder their immediate contact, a situation analogous to that which is correctly admitted to exist between the anatomical elements of the other tissues? But, if this relation really exists for the blood contained in the vessels, must we not say that the blood not only is not a liquid, but that it is a tissue like that of the content of the spleen, or of the liver, or of the kidney which are more or less flaccid? The softness of the tissue of the content of the vessels is much greater, that is all; we must then say that the blood is a flowing tissue.
The flowing state of the blood tissue is related at the same time to the soft consistence, gelatinous it has been called, and to the elasticity of the globules, whose tegument is incessantly lubricated by the intercellular liquor; to the much softer consistence of the swollen albuminoid atmosphere of the microzymian molecular granulations whose density is nearly equal to that of the serum; to the absolute insolubility of the globules and of the molecular granulations in the intercellular liquor, which again contributes to their individual independence. This general insolubility of the anatomical elements is assured, at every point of the circuit, by the stability and even the origin of the composition of the very complex intercellular liquor, resulting from the nutritive functioning of the anatomical elements of the container and of the content, and at the same time by the matters contributed by the divers organs with which the circulatory system is in relation, and especially with the respiratory apparatus.
At the moment that the blood is shed it may be regarded as being the same flowing tissue that it was in the vessels. Nevertheless, there is already a profound difference, viz., it is not only a mixture of venous and arterial blood, but of the bloods of all the regions, whose anatomical elements are violently placed in new conditions of existence, very different from their physiological conditions.
We shall see how this change in the conditions of existence rapidly determines the manifestation of the phenomena of coagulation and then of other alterations of the blood.
The blood really contains three kinds of anatomical elements: the red globules, the white globules and the microzymian molecular granulations. Anatomically, the blood is constituted by three sorts of figured elements and, by a fourth term, a liquid. Is this the serum, this liquid which is its interglobular and intergranular substance?
The three sorts of anatomical elements are living, insomuch as they are organized and contain microzymas which I have proved to be living by their function as ferments and by their capacity to become vibrioniens by individual evolution, which was a novelty for physiology and even for chemists.
Nevertheless, so far as concern the red globule, since 1846 the statement that it is alive was not a novelty. In fact, in a memoir,1 which merits the more attention that it is never quoted, J. B. Dumas made an observation which must be regarded as of the first importance. It is that to isolate the red globules in their integrity, by mixing the blood with sulphate of soda, a current of air must be introduced; without this they will change, losing their coloring matter which itself also changes. And he said: "The globules of blood act as though they were really living beings, capable of resisting the solvent action of sulphate of soda so long as they are alive, but yielding to this action so soon as they have succumbed to the asphyxiation which affects them by the deprivation of air, and which manifests itself with singular rapidity, either by their change of color or by their rapid solution." Dumas asserted clearly that the globules breathe; that account must be taken of their membrane in explaining the phenomenon of respiration; and that the breathing of an animal has especially for its object to furnish oxygen to the globules of its blood and to expel "the products into which they convert it." He also remarked that in the discussions and the calculations respecting respiration the blood had always been regarded as a homogeneous liquid, while it was only the serum which possesses this quality. He in no wise disregarded the part taken by the serum in the phenomenon of arterialization, but he insisted on the preponderant part taken in it by the red globules.
1. Dumas, "Recherches sur le sang," C. R.. Vol. XXII, p. 900 (1846).
To understand the blood, one must place oneself in the order of ideas of the memoir of Dumas, but broadened; that illustrious savant did not recognize in it, nor did any one else at that time, other anatomical elements than the globules, but there is another. He saw in the blood only three nitrogenous organic matters: albumen, fibrin and the globules, but there are others.
I will add that, in the serum, he made allowance for the share therein of the phosphates and other mineral matters.
At the moment of a general venesection the blood has been regarded as being that which it is in the vessels while it circulates in them, but as being a mixture of the arterial and venous bloods; and we have seen that at this moment the blood is so thoroughly regarded as being alive that it was regarded as certain that coagulation was its death.
The blood being alive, it is necessary to recognize, in accordance with the doctrine of Bichat, that, as in all the rest of the organism, the only things living in it are the anatomical elements, that is to say, that of the four parts which constitute it, the three kinds of anatomical elements are the only things living in it; the fourth, the serum, or that which will become the serum, the interglobular and intergranular substance, fulfilling with regard to them only one of the conditions of existence.
But as this conclusion conflicts with the prejudices of the schools, it is necessary to know what those prejudices are to combat them, for they are the negations of the doctrine of Bichat and precisely contrary to it. In fact, while it is asserted that the globules of blood, in general the anatomical elements, are only organites, neither plants, nor animals, as M. Pasteur said, that is to say, not living although organised, it was insisted that that which in the blood is still called plasma was living, a liquid whereof all the materials are said to be in a state of perfect solution, that is to say, without any anatomic, figured structure. But it is well to repeat that such was the state of science just as it was before Lavoisier and before Bichat, when the philosophical naturalist, Charles Bonnet, speaking of the organization, called it "the most excellent modification of matter." Even in France a conception more or less analogous to it, that of protoplasm, was preferred to the striking conception of Bichat. But protoplasm or its synonym, blastema, was considered to be organized living matter without structure. Here is one of the most precise descriptions of such matter: "A completely homogenous, amorphous matter without structure can be regarded as organized substance if it is constituted of numerous proximate principles, united molecule to molecule by special combination and reciprocal solution, and however simple may be this organization, it is sufficient to enable one to say that it is alive." Diet, de Med., Littre et Robin, art. Organique (1878).
Van Tieghem said: "Protoplasm is a mixture with water, of a greater or less number of different proximate principles, in the course of continual transformation."
Huxley said: "All protoplasm is similar to protein—all living matter is more or less similar to albumen."
Cauvet said: "Protoplasm is a nitrogenous liquid, more or less flowing, composed of a translucent joining substance and of fatty and albuminoid granulations."
Even Claude Bernard said: "In its simplest condition life, contrary to the idea of Aristotle, is independent of all special form; it resides in a substance defined by its composition and not by its shape; the protoplasm."
Pasteur said: "Living organisms are composed of natural substances such as life elaborates them, the proximate principles of living bodies which possess faculties of transformation which are destroyed by boiling."1
1. C. R., Vol. LXXIII. p. 302. See letter of M. Pasteur to M. Donne. M. Pasteur's manner of thinking was still that of Chevreul [born in 1786. was still alive and active in 1856]— at the time (1810) of the foundation of his chair at the Museum; Chevreul said, speaking of living bodies, that they are organic bodies in contradistinction to inorganic bodies, which we term minerals. Buffon called minerals gross matter, admitting that there was a universally diffused organic matter which he termed organic molecules, but Buffon wrote before the time of Lavoisier. Chevreul spoke of the proximate principles of organic bodies which are the products of life. Pasteur, speaking of the same proximate principles, says that they are natural substances elaborated by life, which have powers of transformation, etc. It may thus be truly said that there was no idea of life as bound to a determined, structural form of living anatomical elements, according to the conception of Bichat. It is thus to be understood how M. Pasteur could class in the same category, as organites, the red globules of the blood and grains of starch. It is true that the amylaceous granule had been regarded as being a vesicle, but Biot and Payen had shown that it was solid throughout its mass, and I have proved, in my researches upon fecula, that it had neither tegument, nor microzymas, being wholly formed of amylaceous matter contaminated with a trace of albuminoid matter. In the microzymian theory it is not life which produces or elaborates the proximate principles, but the anatomical elements are constituted into living apparatus by the microzymas, according to the same mechanism by which the fibrinous microzymas cause starch to ferment, and elaborate the numerous proximate principles which I have described as produced in that fermentation.
These quotations are sufficient. Protoplasm is regarded as a pure mixture of proximate principles, that is to say, of materials of a purely chemical order. M. Cauvet and others, M. Frey, for instance, have observed the granulations of the protoplasm, but they were supposed to be pure proximate principles. This mixture was declared by some, as in the course of continual transformation; by M. Pasteur, as endowed with faculties of transformation, but without other proof of what is precisely the point in question, viz., whether such a mixture can spontaneously change, can alter itself, give birth to any living being whatever, be it a cellule or a microzyma. If protoplasm were that which it was thought to be, the conception of Bichat would be purely chimerical.
I have incontestably demonstrated, in contradiction to the theory of protoplasm and against M. Pasteur, that every mixture, artificial or natural, of real proximate principles, with water, is, by itself, in every way unalterable, incapable of giving birth to anything living; in short, as not being in the course of continual transformation and as not possessing any faculty of transformation capable of producing in it any spontaneous alteration. And if in such a mixture, boiling destroys the "faculties of transformation" of some zymas, this latter had not been produced spontaneously, it was the product of a living organism. In short, if the mixture contains some proximate principle which can be altered by oxygenation, by absorbing oxygen from the air, this principle is itself the former product of a living organism through the reaction of a zymas.1 I have given positive proof of all of this while studying the conditions of the spontaneous coagulation of milk, which was said to be a pure mixture of proximate principles. Cow's milk, creosoted by a suitable dose to destroy the influence of the germs of the air and completely protected from all contact with the air, first becomes sour and then coagulates. After which, vibrioniens appear in it. If by filtration, by the process which I have indicated in the case of the blood, both the globules and all the milk microzymas of the creosoted milk are absolutely removed, the limpid liquid which results, containing all the proximate principles of the milk, under the same conditions, does not become sour and consequently neither coagulates nor permits the appearance of the vibrioniens. The "faculties of transformation" then resided in the anatomical element of the milk which had been removed by filtration, and not in the rest of its substance, which maybe called the physiological serum of milk.
1. The zymases are never the products of the spontaneous alteration of an albuminoid matter, but are always the products of the physiological function of a living organism and of an anatomical element in the latter. See the article zymas, "Dictionnaire de la langue francaise." Littre (1869).
The physiological serum of the milk, which has the same composition as blastema or of protoplasm, is then naturally unchangeable and consequently not living.
It is the same with the fourth portion of the blood, which we will call the physiological serum of the latter. And precisely as the anatomical elements of milk are the agents of its spontaneous alteration, because they are living, so the anatomical elements of the blood are, on several accounts, the agents of its spontaneous alteration, as will be proved in the following chapter. But first must be determined the physiological role of this serum, in which are realized the conditions of existence of the anatomical elements, globules and granulations of the blood, while it circulates and after it has been shed.
I understand by "conditions of existence" of an anatomical element (following Bichat's conception), that of the preservation of its physical being at the same time with the integrity of its tegument and that of its content, preserved with its composition unchanged, which it can only be by finding in the medium in which it lives all the materials for its nutrition.
Take, for example, the red globules; we know that in blood, steeped in a certain quantity of water, the soluble contents of its globules are diffused by osmose, the teguments remaining whole; on the other hand, we know that in the same blood, steeped in several times its volume of a saturated solution of sulphate of soda, its globules remain entire, both tegument and content. We can even steep the blood in its own serum, without the globules being altered ; without any trace of the colored content being dissolved. And it is the same with the molecular granulations as with the globules; so that if in blood, steeped in the solution of sulphate of soda, a small part of their albuminoid atmosphere is temporarily soluble, as we have seen, it is absolutely insoluble in the serum and each granulation remains there whole and independent, the same as each globule, and this constitutes one of the conditions of the circulation.
But to understand the circulation and the reciprocal influence of the vessels and of the elements of their content, a slight diversion into embryology is indispensable.
In studying the development of the fowl to ascertain the role of the microzymas of the vitellus in the formation of the anatomical elements and of the organs, Estor and shown1 that the container and the content of the vascular system are born and developed simultaneously with the aid of the microzymas and the unorganized materials of the vitellus. We have never seen globules in the body of the embryo before the establishment of the circulation; they are formed on the spot. Thus the anatomical elements of the tissues of the vessels and the anatomical elements of the blood contained therein are born at the same time, by the microzymas of the vitellus as builders, in the unorganized intermicrozymian medium of the vitellus. Hence it results that the serum of the embryonal blood comes into existence concurrently with the globules and the granulations, having the non-organized parts of the vitellus for their source. To sum up, container and content are born at the same time, develop at the same time, and at the same time become what they are destined to be in the future.
1. C. R., Vol. LXXV, p. 962 (1872). We were led to undertake this embryological experiment as the consequence of the following experiment of which Estor was a witness: The mother of vinegar formed a microzymas, united among themselves by a hyaline intermicrozymian substance, is a membrane of mucous consistence with which we have compared the false membrane called fibrin; but it is so much vegetable that it is hardly nitrogenized. But in the "mother of vinegar," under the conditions in which one forces its microzymas to live, these become by individual evolution bacteria, or by association manufacturers of cellules. It is the same with the microzymas of beer-yeast, which, in certain media, act as lactic and butyric ferments, undergoing vibrionian evolution; while in others they reproduce the cellule of yeast and the normal alcoholic fermentation." * The microzymas then can be manufacturers of cellules by grouping themselves together, and being grouped becoming enveloped with a tegument when the conditions of existence of these cellules are united. And it is precisely this which the vitellin microzymas do during embryonic development. This new theory of the origin of the cellule does not weaken the axiom of M. Virchow: omnis cellulae cellula. One cellule may be derived from another cell according to another mode, that is all. Consequently, when M. Pasteur said that the globule of the blood is an organite incapable of reproduction because it could not be cultivated like beer-yeast, he was mistaken, not knowing any other mode of reproduction. *For the developments of the theory of the microzymas, manufacturers of cellules, see the following publications: "Conclusions Concerning the Nature of Mother of Vinegar and of Microzymas in General," C. R., Vol. LXVIII, p. 877 (1869); "Researches on the Nature and Origin of Ferments. Ann. de chemie et de physique," 4th series. Vol. .XXIII. p. 443. And for the theory in its entirely: "Les Microzymas Builders of Cellules." see: "Les Microzymas," etc., M.Chamalet, 60, passage Choiseul, Paris, p 431-463 and p. 948.
The blood ought to be studied not only by itself, but as being to the vessels that which the content of a cellule or of an organ is to its tegument. The tegument of the vascular system consists of the various tissues of the arteries, of the veins and of the capillaries. It must also be borne in mind that the system is directly in relation with the heart, the lungs, the liver, etc., and that the lymphatics (the chyle vessels) communicate directly with it. And as the content of a cellule, of an organ, does not exist without the container, so also the blood does not exist without the vessels which contain it and which make of the whole system an organ in more or less direct relation with every part of the organism.a And it must be observed that if there is any difference between the anatomical constitution of the container of the various regions of the vascular system there is also a difference in their content. Independently of the color there is more oxygen and less carbonic acid in the arterial blood than in the venous. In several regions differences have been observed in the portion of the number of blood globules to that of the leukocytes. Lehmann observed that if the blood obtained from the portal vein gives fibrin by whipping, that of the suprahepatic vein does not furnish any by this means, proving, as we shall see, that the microzymian molecular granulations of the two bloods differ in something, and Denis has already pointed out that the fibrin of the arterial blood is not identical with that of the venous blood, etc.
[a This original conception throws a new light upon the purpose and relations of the circulatory system, which I hope to enlarge upon in a future memoir.—Trans.]
Consequently it is physiologically evident that the anatomical elements, conceived as being personally and in individually living from whatever part of an organism they may be taken exist there only because the conditions of their existence are found naturally realized there. It is not otherwise with the blood; the conditions of existence of its anatomical elements are only realized, in each point of the circuit, while it is contained in the vessel and circulating.
It is ordinarily said that the anatomical elements swim in the lymph, the liquor sanguinis or the plasma; those who, with Milne-Edwards, admitted the existence of finely divided fibrin, said that it too floated in the serum. Anatomically, may we continue so to regard the reciprocal relations of the three anatomical elements and of the fourth portion of the blood? And is it correct to say that at each point of the blood current there are molecular granulations and globules almost in contact with one another? Is it not more correct to say that the fourth part, the serum, is only the intercellular and intergranular substance of these anatomical elements which hinder their immediate contact, a situation analogous to that which is correctly admitted to exist between the anatomical elements of the other tissues? But, if this relation really exists for the blood contained in the vessels, must we not say that the blood not only is not a liquid, but that it is a tissue like that of the content of the spleen, or of the liver, or of the kidney which are more or less flaccid? The softness of the tissue of the content of the vessels is much greater, that is all; we must then say that the blood is a flowing tissue.
The flowing state of the blood tissue is related at the same time to the soft consistence, gelatinous it has been called, and to the elasticity of the globules, whose tegument is incessantly lubricated by the intercellular liquor; to the much softer consistence of the swollen albuminoid atmosphere of the microzymian molecular granulations whose density is nearly equal to that of the serum; to the absolute insolubility of the globules and of the molecular granulations in the intercellular liquor, which again contributes to their individual independence. This general insolubility of the anatomical elements is assured, at every point of the circuit, by the stability and even the origin of the composition of the very complex intercellular liquor, resulting from the nutritive functioning of the anatomical elements of the container and of the content, and at the same time by the matters contributed by the divers organs with which the circulatory system is in relation, and especially with the respiratory apparatus.
At the moment that the blood is shed it may be regarded as being the same flowing tissue that it was in the vessels. Nevertheless, there is already a profound difference, viz., it is not only a mixture of venous and arterial blood, but of the bloods of all the regions, whose anatomical elements are violently placed in new conditions of existence, very different from their physiological conditions.
We shall see how this change in the conditions of existence rapidly determines the manifestation of the phenomena of coagulation and then of other alterations of the blood.
CHAPTER 8: The Blood and the Third Anatomical Element by Antoine Bechamp
THE MICROZYMAS AND THAT WHICH IS STYLED BACTERIOLOGY; THE MICROZYMAS, LIVING BEINGS BELONGING TO AN UNSUSPECTED ORDER OF THEIR OWN; OVULAR AND VITELLIN MICROZYMAS; MICROZYMAS AND MOLECULAR GRANULATIONS; GEOLOGICAL MICROZYMAS; MICROZYMAS OF THE EARTH AND OF THE WATERS; MICROZYMAS AND BACTERIA; BIOLOGICAL CHARACTERS OF THE MICROZYMAS; MICROZYMAS AND THEIR PERENNITY; THE ORGANIZED END OF ALL ORGANIZATION; OVULAR AND VITELLIN MICROZYMAS; MICROZYMAS AND PATHOLOGY; MICROZYMAS AND COORDINATION; PHAGOCYTOSIS; MICROZYMAS AND ANTHRAX; MICROZYMAS AND DISEASE; MICROZYMAS AND MICROBES; MICROZYMAS AND THE INDIVIDUAL COEFFICIENT; MICROZYMAS, LIFE AND DEATH; MICROZYMAS AND HEALTH; MICROZYMAS AND RECEPTIVITY; MICROZYMAS, BLOOD AND PROTOPLASM; CONCLUSIONS.
To place beyond dispute the autonomy of the microzymas it is necessary to bring into prominence the facts and observations which prove that the existence of the microzymas as living beings has not been suspected by those naturalists who have studied the infusoria, nor yet by the anatomists who have studied the cellules and the tissues.
Demonstration that the microzymas, autonomous anatomical elements in living organisms, are living beings, morphologically determined, belonging to a category of their own, having no analogue.
Let us first get rid of the hypotheses that the microzymas are either the bacterium termo, or the Monas crepusculum, or the Micrococcus, or the spores of bacteria.
It is to be borne in mind that I gave the name of microzyma at first to the geological figured ferment of the chalk of Sens and of another calcareous earth; that I have discovered this ferment in other calcareous rocks, always of a spherical form, very brilliant, having the brownian movement and smaller than all the vibrioniens described by authors.' Ehrenberg described (in the chalk) the remains of fossil microscopic organisms called Polythalamies and Nautilites, but makes no mention either of Monas crepusculum nor of Bacterium punctum. In fact, none of the microzymas can be confounded with those described by Ehrenberg under those names. The microzymas are even smaller than the Bacterium termo, the smallest of the known infusoria, the first term of the animal kingdom, according to Felix Dujardin.
Nevertheless the microzymas had been seen in cloudy infusions of vegetable and animal matters, but they were taken for "the active molecules of Robert Brown"; that is to say, for molecules having the staggering or scintillating movement without change of place, called "brownian movement," and no further attention was paid to them.
In fact, the microzymas are neither the Bacterium punctum, nor the Monas crepusculum, nor even the Bacterium termo, which is much smaller than they. It will be sufficient to establish this fact by referring to the description of these monas, etc., given by F. Dujardin, in his "Historie Naturelle des Zoophytes," Infusoria, pp. 215 and 279.
On the other hand, if these bacteria, these monads, these micrococci, belong to determined species, it is contrary to the data of natural history to regard them as capable of being transformed into other genera and species of vibrioniens, as we see the microzymas produce them by evolution; the suggestion that the microzymas are the spores of schizomycetes is also untenable for the following reasons: A spore is a seminulum, or an egg, if according to the old view, the bacteria are animals, and search has been made for the eggs of bacteria; a grain, if according to the new creed the bacteria are vegetable; egg or grain, a spore cannot multiply itself as the microzyma does, and cannot therefore be the same thing.
Take the microzymas of the ovule in the Graafian vesicle in the fowl, and the microzymas of the vitellus of the mature egg. In the ovule there are ovular microzymas, in the vitellus, vitelline microzymas. At a given moment there are, say, a milligramme of microzymas in the ovule, and there are two or three grammes dried at 100° C. (I have isolated and weighed them) in the vitellus.1
They have then multiplied prodigiously during the development of the vitellus.2
So much then for the anatomical analysis for the egg of the fowl, and the chemical analysis shows that the elementary composition of the ovular microzymas is not the same as that of the vitellin, the former, as will be seen, being less carbonized; evidently their composition changed in the process of multiplication.3
Chemical analysis has further demonstrated that the vitellin microzymas of several species of birds differ from those of the fowl in their composition and especially in the properties of their respective zymases.4 This accords exactly with the microzymian theory, for it is evident that the microzymas are what they should be specifically, in order that, by incubation, the egg should produce the proper bird, its tissues, and all that pertains to its future being. And it has been demonstrated that during the development of the being, parallel with the anatomical development by the multiplication of the microzymas, there is a functional development of these, so that in each anatomical system they become that which they successively are in the embryo, in the foetus, in the adult, etc.
1. See the Memoir on The Albuminoid Mailers, pp. 140 and following.2. For the mode of multiplication of the microzymas see "Les Microzymas," pp. 490 and following.3. The Memoir above mentioned, p. 162.4. See J. Bechamp, "Normal and pathological albumins," pp. 77 and following.
If the hypothesis that the microzymas are the spores of bacteria were true, it would be necessary that there should first have existed in the circumambient atmosphere as many species of these spores as there are species of animal and vegetable ovules; next it would be necessary for these spores to penetrate as far as, and into the ovule, and should there multiply to fill up the vitellus of the egg of the fowl.
I need go no further, for there are still otherwise enormous difficulties, when we take into consideration the microzymas of the developed being, which are so different from the embryonal and foetal microzymas! But it now lies with the opponents of the microzymian theory to demonstrate the existence of these spores and of their penetration as far as, and into, the ovules and their multiplication.
We have thus discarded the hypothesis opposed to that of autonomy. It is also discarded by the following consideration, which deserves being underscored.
Shortly before M. Pasteur's admission in 1886 of the presence of the microzymas in the altered blood of his experiment, he had, for the purpose of denying them, asserted that the microzymas were the molecular granulations "which we all know." This was to his confreres of the Academy.
Yes, histologists and anatomo-pathologists knew them and represented them by a "stippling" in their figures of special tissues.
But their name even betrayed the opinion that they were neither organized nor living; in effect, the qualification of molecular was intended to indicate that it meant only small collections of some sort of matter; thus they were described as white, gray, minerals, fats, albuminoids, etc. They were even described as possessing the brownian movement; nevertheless, before the discovery of the microzymas, no one thought of connecting them either with the bacterium punctum or the monas crepusculum.
They were connected with anatomical organisms as being the remains of tissues, of destroyed cellules, or as amorphous matter; no one dreamed of making them come from outside. No consideration of the anatomical-molecular-granulations had anything to do with the discovery of the microzymas, but, as I have shown above, purely chemical considerations.
No, the molecular granulations are not the microzymas.
And from the time of our first note, Estor and I have stated that the microzymas exist only among the anatomical objects which in histology are called molecular granulations. But we held the microzymas to be autonomous anatomical elements; a more careful anatomical analysis enabled me to demonstrate that there exist naked microzymas and microzymas in the condition which I have termed microzymian molecular granulations.
Thus is disproved another gratuitous and erroneous assertion!
I return to the microzymas. I had described them from the commencement as being chemically and physiologically figured ferments, producers of zymases, which are called soluble ferments, and were placed in the same category as me figured ferments which are insoluble. Biologically, I distinguished them as being such as by evolution could become vibrionien, a fact which we have seen to be verified in every sense.
But in the experiments on spontaneous alterations, or fermentations, wherein microzymas become bacteria, we have seen that these were destroyed and that vibrioniens more and more minute appeared in their place, so that at last there remained only of these bacteria the forms nearest to the microzymas; in the same manner consequently, that by their destruction the cellules set their microzymas free, the bacteria in their complete destruction reproduce microzymas similar to those of the chalk, and we will now see how that is.
In the experiments on the spontaneous alterations of natural animal matters, the substances, which in a chemical sense are termed organic, which result from transformations by fermentation under the influence of the microzymas, before and after their vibrionian evolution, with or without the setting free of gas, are never entirely destroyed; that is to say, they are not reduced to a mineral condition, carbonic acid, water, nitrogen, etc.; for such destruction oxygen is necessary under conditions which reproduce those realized in geological epochs.
When I had discovered the microzymas in the chalk and in other calcareous rock, and became convinced that they were not dependent on atmospheric germs, I asked myself if they were not the living remains of organized being which had disappeared in geologic times.1 This hypothesis was verified in the following manner:
A kitten was killed and buried between two beds of pure carbonate of lime, and left in a cylindrical glass vessel, covered with a small quantity of paper in such wise that the air had free access to it, but its dust was excluded. The experiment lasted seven years. Every part of the body, except some fragments of bone, had disappeared. The carbonate of lime was perfectly white, so complete had been the work of destruction. Under the microscope, nothing was to be seen in the upper layers of the carbonate except microscopic crystals of aragonite of this carbonate; but in the beds adjacent to the place, and underneath, where the kitten had been, and beneath, there were crowds of glittering motile microzymas, such as are to be seen in the chalk of Sens, etc.
And with this kind of artificial calcareous rock, containing the microzymas of an animal of the present day, I was able to repeat the experiments on fermentation which I had made with the chalk of Sens and with other calcareous rocks, both lacustrine and marine.2 Such was the first experimental verification of the hypothesis that the microzymas of the chalk and of calcareous rocks are the organized remains, still living, of the beings which lived in the geological ages of the earths to which those rocks belonged. Read the note of the Comptes Rendus which I have just cited and you will be convinced that this verification has also been its vindication.
1. C. R.. Vol. LXX p. 914 (1870).2. Conference at the Congress of the French Association for the Advancement of Science. Nantes (1875).
I have said that the microzymas of the artificial chalk were the microzymas of an animal of the present epoch, but this needs some modification in terms to be quite accurate. They were the microzymas of the bacteria which the normal microzymas of the animal had first become by evolution. By fresh experiments I have learned that the microzymas of an entire body, or of the liver, of the heart, of the lungs, of the kidneys, under the conditions of my experiment become bacteria in the first phases of the phenomenon, these then disappear, becoming again microzymas, while the rest of the mailer already transformed is, under (heir influence, and with access of air, reduced to the mineral state, carbonic acid, water, nitrogen, etc.1 And I have demonstrated that whereas in the climate of Montpellier seven years were required to accomplish this, a much longer time would be needed in a colder climate, so that in a climate such as that of the Obi valley centuries were required.
It was then a legitimate conclusion that the microzymas of the calcareous rocks, of the clays, of the marls; in short, of all the rocks which contain them, are the organized and living remains of beings which had been living, of animals and plants of the geologic epochs; that these beings were histologically constituted as are the beings of our epoch, that their microzymas, during their destruction, had become bacteia by evolution, and that the microzymas, geological ferments, of these rocks, are those of these bacteria destroyed in their turn and reduced to their microzymas.
1. See "Les Microzymas," etc., pp. 624 and following. See also note: C. R., Vol. LXX, p. 914, "Les Microzymas," etc., p. 952.
It is not surprising then that, having long pursued the anticipated consequences of the hypothesis now verified, I have demonstrated the presence of the microzymas in the earths of the garrigues of the departments of Herault and of Card, in cultivated lands generally, in moor lands, in the alluvials, in the waters, in the dust of the streets, where they are to be found in crowds; often still in the condition of bacteria, proving that, like those of the calcareous rocks, they are energetic ferments. And already, prior to 1867, I had made known their role in the soil in agriculture.
These researches led to a result of very great importance; it was the demonstration that what was and still is called germs of the air are essentially nothing other than the microzymas of beings which have lived, but have disappeared or are being destroyed before our eyes. In fact, by precise experiments, I have proved that the microzymas of the air are ferments of the same order as those of the chalk, of the rocks, and of those of my experiments with artificial chalk; only, varying with the places, the circumambient a r may, along with these microzymas, contain conides of lichens, spores of mushrooms, bacteria and everything that the wind can disperse in it.1
1. See, for details. C. R, Vol. LXXIV. p. 629; Vol. LXIII, p. 451; and "Les microzymas." etc., pp. 122, 135. 940. 952.
There is then no panspermy such as that which Charles Bonnet had invented, nor that which Spallanzani and M. Pasteur (after me) had admitted. In short, there are no pre-existing germs. At each period, as in our days, and in each place there exist in the surrounding air only the microzymas of former beings which had disappeared and are disappearing with the things which the wind scatters in it.
But if we reflect that the species of microzymas are: first, as numerous as the species of eggs, of seeds, of spores of the various species of animals and plants; next, that there are in each animal and vegetable organism, already developed or in process of development, microzymas as specifically numerous as there are anatomical systems and organs, tissues and special cellules in these organisms, it is easy to conceive that the species of atmospheric microzymas are present in enormous numbers. One can also understand the very great number of changes which these microzymas may cause, when some one of these species fall into a fermentescible medium in which it can multiply, and either evolve in it/or build in it a cellule, or a mould.
If then, as I have demonstrated experimentally, there are besides microzymas, and as well in animals as in plants, among the micro-organisms of the circumambient air, spores, conides of fungi, of lichens, even actual cellules of ferments,1 it is easy to understand that if these micro-organisms fall into fermentescible media they will develop in it, each according to its nature, and that various productions, moulds, divers cellules, and at the same time vibrioniens, may appear in it.2
But in all the observations and in all the experiments relative to the spontaneous change of natural vegetable and animal matters, and in the fermentations of sugar or of fecula by aid of the tissues and humors of animals, when the influence of the micro-organisms of the air has been destroyed or suppressed,3 only microzymas and vibrioniens, and vibrios or bacteria, fruits of their evolution, are seen; this proves that the microzymas are autonomous anatomical elements existing in it of themselves.
1. "Sur L'origine des ferments du vin," by A. Bechamp, C. R., Vol. LIX, p. 626 (1864).2. See C. R., Vol. LXXIV. p. 115, and "Les Microzymas," etc.. p. 948.3. Here a complementary explanation is necessary to explain more clearly the mode of action of creosote in the experiments in which it has been employed to annihilate the influence of germs of the air. And first of all, in speaking of germs, it no longer relates to this vague something, which when called upon by Ch. Robin to define, M. Pasteur called "origin of life," but figured ferments, upon which creosote exercises an influence clearly determined. I must therefore recall that I have several times insisted on the fuel that creosote is efficient in annihilating the influence of the germs of a limited volume of the surrounding air, unless the air be renewed. And it is so, because a limited volume of air contains only limited number of micro-organismic ferments. But creosote, while it does not prevent the ferments from acting, hinders their multiplication. In reality the ferments of a limited volume of air, which are capable of acting upon a fermentescible medium, do act upon it, but only in proportion to their quantity, in such wise that the result is so inappreciable that it is as though it were nothing; it is thus that the quantity of sugar, inverted, in the presence of creosote, by the microzymas of a small limited volume of air can be determined neither by reagents, nor by the polariscope. But if a slow current of several hundred litres of the same air is caused to act upon a creosoted solution of sugar the microzymas and other micro-organisms retained by the liquor render this at last cloudy, and. thus accumulated, there are among them some which effect the inversion, without developing moulds, while the microzymas undergo a greater or less vibrionian evolution. Such is the exact idea to be formed of the influence of the creosote, and of the role of the atmospheric ferments. When, owing to their presence, productions such as moulds are produced, it is because die special conditions of existence of these moulds, etc., have been realized. But microzymas in their function of anatomical elements only become vibrioniens from the substance of tissues and humors, ever, in spite of the presence of creosote, provided the volume of air be limited or completely absent.
These statements and considerations may be summed up in the following propositions:
(1). The microzymas of the animal organism proceed from the vitellin microzymas, which are autonomous anatomical elements in the vitellus.
(2). The number of anatomical species of microzymas is enormous.
(3). The essential biological characters of the microzymas are to be creators of cellules by synthesis and of vibrioniens by evolution.
(4). The physiological and chemical characters of microzymas are to produce the zymases and to be themselves ferments having a determined form.
These propositions are also true for plants beginning with the ovule; but from the fact that a microzyma may become a vibrionien by evolution, it necessarily follows that the species of microzymas being innumerable the species of vibrioniens are likewise innumerable.
It is further important to remember that an anatomical element microzyma is animal in an animal, vegetable in a vegetable. Hence arises this question: To what kingdom belongs the bacterium of such or such an animal microzyma? Of such or such a vegetable microzyma? We must remember that any microzyma, before it accomplishes the evolution which produces a bacterium, passes through the evolutionary phases of microzyma slightly changed in form, of microzyma successively associated in twos, in threes, in several grains, etc. But those forms have been described under the names of Monas, of Bacterium termo and punctum, of Coccus, of Diplococcus, of Torulo, of Streptococcus, of Micrococcus, of Mesococcus, of Microbe with a point, of Microbe with a double point, etc. Nor is that all; bacteria in spontaneously destroying themselves to become microzymas similar to those of the rock-chalk or of the artificial chalk of my experiments, have passed through new forms, of which the most constant is that which has also been described as the Bacterium termo.1
1. See, on this subject, Felix Dujardin, "Les Zoophites Infusoire," p. 232.
But what are such specifications worth, based only upon the shape, on the length and thickness, upon the color, the motility or immotility of the object specified? In the order of received ideas it would be too tedious to discuss them; it suffices for me to say that Felix Dujardin, who knew the germ theory and did not allude to it in his explanations, was of opinion that the phenomena observed in these changes were favorable to the doctrine of spontaneous generation; and consequently that outside of the microzymian theory it is all incomprehensible and arbitrary. A priori one cannot tell to what kingdom a bacterium belongs, for one can only distinguish a microzyma, and consequently a bacterium, by the origin and function of the microzyma. An example will make this clear: Take the parotid gland of a man, and that of a horse, the structure and functions of which seem to be the same and of which the microzymas of the cellules are morphologically identical; well, while the parotidian microzymas of man liquify and energetically saccharify the starch of fecula, those of the horse liquify that starch but do not saccharify it And we have established by other differences of the like kind that the microzymas of the different anatomical systems of a same organism may differ one from the other; and by still greater reason those of different organisms may differ.
Plants, like animals, being anatomically constituted living by their respective microzymas, the bacteria which these microzymas can become are evidently limited to the two kingdoms; and so perhaps the question whether a vibrionien is animal, as was thought, or plant, as is now asserted, is an idle one.
But if one chooses in spite of all this to insist that the bacteria are plants and that the microzymas are their spores, a new question would arise, of which of the species of schizomycetes which the same microzyma may become before becoming a perfect bacterium (Bacterium termo, Monas crepusculum, torula, Diplococcus, Streptococcus, Micrococcus, etc.)—is it first the spore, in the organism before evolution, and then in the chalk-rock, or in the artificial chalk, after the total destruction of the organism?
According to accepted notions the reply cannot be otherwise than uncertain! According to the microzymian theory here is the answer.
An anatomical element, microzyma, in a plant or in an animal, whose conditions of existence have just changed, can become a bacterium by evolution, and the intermediate evolutionary phases, like those of the tadpole, which becomes a frog, leaves the special nature of the microzyma still existing; there are not new species. The perfect bacterium depends on the nature of the microzyma, as the perfect batrachian depends on the particular nature of its tadpole.
Every bacterium resolves itself by spontaneous destruction into a microzyma, and the microzymas thus evolved are different from the anatomical microzyma which has become a bacterium, not morphologically, nor functionally so far as regards being a figured ferment, but by a collection of properties, which assure the perennity of the form and of the function in a condition of individual separateness.
But the chief difference consists in this: The anatomical element microzyma in the vitellus is the organized commencement of all animal organization, and in the ovule of the plant it is the commencement of all plant organization. On the other hand, the microzyma resulting from the destruction of a bacterium is the organized end of all organization.
AND HERE IS SOMETHING STUPENDOUS! The geological microzymas, as well as those of the artificial chalk in my experiment, are organized and living, not only because, without change of form, they are individually figured ferments, but also because under certain conditions, such as those of the fibrin in the experiment described in the first chapter, at the same time that they act as ferments they can again become bacteria by evolution. The microzymas not only possess the sort of perennity of which I spoke; they enjoy also the stupendous duration of the geological epochs from the time the microzymian rocks have been formed down to the present time. And this duration means for us, that the microzymas have been constituted physiologically imperishable. And this last statement must convince us that the microzymas are organized living beings, of a class apart, without analogue.
And it is thus, precisely because the microzymas are, essentially and by destination, autonomous anatomical elements in each anatomical system, becoming what they ought to become in each, by substantial and functional development, parallel with the development of such system in the development of the entire organism, that they are organized living beings of a class apart as above stated.
The following is the experimental proof that this new principle of anatomy and physiology is well founded.
The vitellin microzymas of the egg of the fowl do not pre-exist in the ovule; they are the result of a substantial development, and of the proliferation of the ovular microzymas.
To prove this, it will be sufficient to make the elementary analysis of the microzymas of the vitellus of the fowl's egg, and of those of the ovules remaining in the Graafian vesicle, while these ovules are only a few millimetres in diameter. The following are these analyses:
Vitellin Microzymas Ovular MicrozymasCarbon 52.67% 50.63%Hydrogen 7.17% 7.36%Nitrogen 15.71% 15.67%Oxygen, etc.1
1. See"Memoire sur les matieres albuminoid." p. 161, and the correction in the note on p. 489.
The difference of two per cent, of carbon in the percentage composition answers to great differences in the nature of the proximate principles of these microzymas. I will add that the vitellin microzymas contain much more mineral matter than the ovular. It is thus evident that the microzymas of the ovule become vitellin microzymas by substantial development, while they multiply and the vitellus grows. In short, one may say that the ovular microzymas become vitellin microzymas by maturing.
It would take too long to dwell as long as might be desirable on this result and upon the whole of the chemical, physiological and anatomical phenomena which this ripening necessitates in order that the vitellin microzymas should become fitted to play their part, chemical, physiological and histogenic, during the embryonic development, etc. I must refer the student to what I have said elsewhere.1 What is most important to bear in mind is, that no matter how high one goes [in the scale of living beings] the microzymas are found in the ovule, and that these microzymas are not those which are to be found in the vitellus, but will become them.
1. See Les Microzymas," etc, pp. 487 and following.
All the special facts which I have made known, including the last, authorize me in erecting into a general principle the precise experimental idea; that the microzyma, the final term of the anatomical analysis, is in truth the simple anatomical element which satisfies the conception of Bichat and completely destroys that of living matter not morphologically defined.
The cellularists, it is but fair to recall, regarding the cellule as the simplest anatomical element, believed it proceeded necessarily from a former cellule, omnis cellula e cellula, holding it to be the vital unit, living per se, and regarded an entire organism as the sum of these units. But we now know that that was a deduction from incomplete and superficial observations, for the cellule, a transitory anatomical element, has the microzyma for its anatomical element. It is this which alone possesses all the characters of an anatomical element, living per se, and which must be regarded as the unit of life. It is what I have already stated in the following terms:
"The microzyma is at the beginning and at the end of every living organization. It is the fundamental anatomical element whereby the cellules, the tissues, the organs, the whole, of an organism are constituted living."
Let us devote a few words to develop this idea. Let us penetrate a little further into this notion of a fundamental anatomical element, which, as has been said, implies that the microzyma is the living atom of the organization as the physical atom is the element of the molecule of a simple body. This would be true if the microzyma were unchangeable in its simplicity. But in reality it is essentially mutable, as are all living bodies; and it is especially so, in order that it may fulfil its numerous functions. In fact, the microzymas, functionally different in the different anatomical systems of the same species, and different at all ages, beginning with the embryonal stage, have been primitively those of the vitellus, after having been those of the ovule. A microzyma then is not, properly speaking, an atom; but always anatomically simple, it becomes, by nutrition, that which it needs to become, so as to accommodate itself to each new condition of existence which the successive phases of the development of each anatomical system provide for it. It is thus that even in the embryo, in that which will be the ovary, a category of microzymas becomes again ovular microzymas to recommence the same cycle. I add that, taken as a whole and in its details, the THEORY HAS BEEN CONFIRMED, VERIFIED, CORROBORATED by a great number of other facts of general anatomy and of pathological anatomy and of physiology.1
1. See particularly the notes and publications following:A. Bechamp: Facts useful for the history of the origin of the bacteria. Natural development of these little plants in the frozen parts of certain plants. C. R.. Vol. LXVTII. p. 466(1869).A Estor: Note for use in the history of the microzymas contained in animal cellules. C. R.. Vol. LXVIII. p. 519. It relates to the microzymas in bacterian evolution in a cyst which had just been removed.Bechamp and Estor: On the microzymas of pulmonary tubercle in the cretacious state. C. R., Vol. LXVII, p. 960 (1868). It relates to the discovery of microzymas in a condition of evolution within the tubercle, regarded as the remains of the destroyed epithelium of the pulmonary alveoli.Bechamp and Estor: Facts useful for the history of the microzymas and bacteria. Physiological transformation of bacteria into microzymas and of microzymas into bacteria in the digestive tube of the same animal. C. R., Vol. LXXVI, p. 1143 (1873).Bechamp: Facts useful for the history of the histological construction of the glairine of Molitg. C.R., Vol. LXXVI. p. 1485 (1873).Bechamp: The diseases of the silk worm. C. R.. various notes from 1866 to 1374. They relate to the pebrine, a parasitic disease, and to the flacherie, a microzymian disease, not parasitic.J. Grasset: On the histological phenomena of inflammation. Treatise regarding a new theory, based upon the consideration of the molecular granulations (microzymas). Gazette Med. de Paris, year 1873.E. Baltus: Theory of the Microzyma, a theoretic and practical study of pyogenesis (the formation of pus). Theses of the Faculty of Montpellier, year. 1874, No. 41.J. Bechamp: The microzymas and their functions at the different ages of the same being. Theses of the Faculty of Montpellier, 1875, No. 63.A Bechamp: Microzymas and disease; in "Les Microzymas," etc., p. 744. (Chamalet, 60, Passage Choiseul.)A Bechamp: Puerperal septicaemia, pleurisy, the albuminuria and the preface to Microzymas et Microbes. (Chainalct, 60, Passage Choiseul, Paris.)A. Tripier: Electricity and Cholera. Genesis, prophylaxy and treatment. (Georges Carre, pub. 1884). In this memoir there will be found a comparison of the microbian system and the microzymian theory, highly original and at the same time the conception of what the eminent author terms the individual coefficient.
When by the attentive study of these facts one has become convinced that the microzymian theory is their pure and simple expression, it will be at once recognized that the cellule is already an organ in which, by nutrition, the conditions of the preservation of the microzymas with the constancy and regularity of their chemical and physiological functions are unceasingly realized. And it will thus be understood that the microzymian molecular granulations, whether of certain cellules, of the vitellus, or of the blood, also realize after their manner the conditions of this constancy and regularity. When these conditions are no longer realized they may undergo vibrionian evolution.
The most prominent fact in the history of the microzymas, that which has been the most disputed, precisely because of their capacity to undergo vibrionian evolution, is the fact of their anatomical autonomy. Now this faculty, which is only manifested when the normal conditions of existence of the microzymas, functioning as anatomical elements, are no longer fulfilled, is the best proof which could be given of the change which has happened in their condition, causing their irregular and changed functioning.
In fact, in their various anatomical situations, the microzymas remain morphologically similar to themselves. They function in each cellule, in each organ, in each anatomical system, naturally, chemically and physiologically for themselves while preserving their individuality; at the same time that by coordination, according to the happy and thoroughly scientific expression of Dr. Antoine Cros, they function for the benefit of the microzymian molecular granulations of the cellules, of the organs and of the various anatomical systems taken altogether, whose physiological condition of health is preserved by them.
But if from some etiological cause certain changes happen in an organ, changes such as auscultation or percussion can precisely ascertain, as, for instance, an increase in the volume of the spleen, M. Cross tells us that there is a decoordination, a functional perturbation in the entire organism and disease. It is worth mentioning that from the time Dr. Cros became acquainted with the microzymian theory, he did not hesitate to recognize the microzymas as the anatomical agents of the decoordination; how does it happen?
Among the causes which produce disease, a sudden chill in summer is the one most frequently indicated or invoked. The chill is at the same time an influence and a lowering of temperature. I do not insist on the fact that it is only something living which is painfully affected, so as to confine myself to the physical phenomenon.
But the microzymas are very sensitive to variations of temperature; so much so that even the geological microzymas act regularly only at temperatures near 40° to 42 °C. (= 104° to 107° F.); in fact, the microzymas of the chalk of Sens do not act so as to cause fecula to ferment in a temperature below 38° C. (= 100°.4 F.). Further a very slight lowering of the temperature is sufficient for the egg which should produce a bird not to produce one, and to putrefy or to produce the monsters of Dareste when the heat is not uniformly applied. In fact, the influences of the medium (as if it should become neutral or acid), which modify the activity of the microzymas acting alone, are various.
That which happens to the isolated microzymas happens also to those of the egg and for those of the organism. Suppress the air and the egg does not become a fowl, but undergoes another kind of change.
If from any cause whatever the air does not have access or has an insufficient access to the pulmonary alveolae, and their epithelium becomes the pulmonary tubercle, the cellules become reduced to their microzymas, which are then found in vibrionian evolution in the tubercle in the cretatious state. If the decoordination resulting from an irregular functioning of a part of an anatomical system is sufficient to bring on a malaise which is not removed, there will arise a diseased condition because of a sharp change of the conditions of existence of the microzymian anatomical elements, and the change in the medium sufficient to cause the decoordination will manifest itself by the vibrionian and bacterian evolution of the microzymas of such or such part of the system.
It is thus that in the disease called "Sand de rate" (Anthrax), so thoroughly studied by Davaine, the diseased microzymas end by evolving into what that learned physician called bacteridiae, the blood globules undergoing the changes which are so characteristic. The bacteridiae were not the cause of the diseased condition, but were one of its effects; proceeding from the morbid microzymas they were capable of inducing this diseased condition in the animal whose microzymas were in a condition to receive it. Hence it is seen that the alteration of natural animal matters is spontaneous, and justifies the old aphorism so concisely expressed by Pidoux: "Diseases are born of us and in us."
On the other hand, the disregard of this law of nature, the firm establishment whereof is completed by the present work, necessarily led M. Pasteur to deny the truth of the aphorism, and to imagine a pathogenic panspermy, as he had before conceived, a priori, that there was a panspermy of fermentations. That M. Pasteur after having been a sponteparist should reach such a conclusion was natural enough; he was neither physiologist nor physician, but only a chemist without any knowledge of comparative science.
What is astonishing is, that he should have succeeded in procuring the triumph of a preconceived system among physicians and in academies, and to procure the rejection of the microzymian theory [without examination. Trans.]. For instance, an enlightened physician thus summed up the fundamental proposition of M. Pasteur: "The microbes always come from without; they constitute species which remount from generation to generation up to the origin of the world."1
An eminent surgeon, M. Verneuil, ended by admitting as a demonstrated theorem that there is no spontaneous tetanus, that there is no spontaneous small pox, syphilis, glanders, hydrophobia, tuberculosis, charbon or malignant pustule; declaring that the pathogenic problem consisted solely in discovering how and when the microbe, also called virus, come from without, penetrates into the organism; declaring that the question is thus stated between old medicine and the microbina medicine "with extreme simplicity and without the least ambiguity.2a
1. Gazette medical, Paris, 6th Series. Vol. V, p. 218. This is precisely what M. Chamberland said of micro-organisms in general: "Recherches sur I'origine el le developpement des organismes microscopiques." Theses de la Faculte des Sciences. Parais, 1879. See also "Microzymas et Microbes," p. 25, 2d Ed.
2. C. R_,Vol. CV, p. 552.
[a. There is an implication to be found in the statement of Surgeon Verneuil, though probably not meant by him, to which assent must be given when understood. It is TRUE that there is no such THING as tetanus, small pox. syphilis, etc., as is implied by the general use of nosological terms. Disease is not a thing, an entity: it is a condition, and the error of regarding the condition of disease as an entity has confirmed, where it has not originated, much of the prevailing erroneous treatment of the sick. Nosological terms have a use; it is that of bringing to the mind of the physician a group of pathological symptoms, which may or may not be present in the case of the patient under consideration; from them, when present, the diseased condition of the patient can be recognized and treated.
Unfortunately, through not understanding this truth, attempts are frequently made to treat, not the patient, but the name, which has been given to a collection of morbid symptoms. A broken limb is a thing; the inflammation which results from it is a condition, and if gangrene ensues the gangrene is not a thing, but a condition to be taken into consideration with all the other symptoms in the treatment of the patient. The surgeon, Verneuil, had probably a glimmering perception of this truth, but he misapplied it, for his theory and practice, as a physician, and the theory and practice of nearly all modern medicine assume that the condition to be treated is a thing having a name and this name is treated instead of the patient.—Trans.]
But these assertions (of Surgeon Verneuil) are reduced to nothing, when we call to mind that the pretended germs of the air are only the microzymas of organisms which have disappeared, which had become bacteria by evolution; that even at the Academy of Medicine I said—and no one ventured to contradict me—that no one had ever been able to reproduce a disease on the nosological roll by taking the pretended pathogenic microbe in normal air, but only in the diseased animal. And I add, that just as with time the fibrin-ous microzymas lose the property of decomposing oxygenated water so, as proved long ago by Davaine, after a short time the blood of an animal which had died of anthrax [sang de rate] no longer communicated that diseased condition; and the same is true in all cases.
THUS NORMAL AIR NOT ONLY DOES NOT, BUT CANNOT, CONTAIN THE PRETENDED PATHOGENIC MICROBES, AND THE VERY PRINCIPLE OF MICROBIAN MEDICINE CONSTITUTES A FUNDAMENTAL ERROR.
But no attention was paid to this. Abandoning the famous dogma of the closure of the body to germs from without, it was admitted "that the human organism carries constantly a large number of microbes of many different species" which only await the moment when "the organism being disturbed in its physiological functioning will be given over to the activity of its own microbes; whose presence it had theretofore borne without being affected." M. Jaccond wrote the above [nonsense] with reference to two cases of acute pneumonia following a chill.1
1. "Journal des societes scientifiques," 4 May, 1887, p. 156.
In M. Pasteur's set, M. Jaccond's opinion was accepted; and although their master had declared that the cellules were not living, his disciples imagined that the leukocytes (under the name of phagocytes) were living like amoeba and able to perform movements called amaeboid. And it was imagined that these phagocytes formed themselves into troops to pursue and devour the microbes. There was thus a phagocytosis,a- which was trumpeted forth as providential. The precise knowledge of the blood reduces to its just value this latest form of the struggle against the microzymian theory. Of all the suppositions and fancies of M. Pasteur, there remains only, even for his disciples, that which consists in admitting a sole cause, the germs or microbes of the air, to explain the phenomena of fermentations and disease.
Nevertheless all physicians did not think as did Verneuil or as did M. Jaccond. Before 1866, while the triumph of the microbian medicine was in full swing, Dr. A. Tripier did not admit that there was a microbe come from without to be considered. His attention had been drawn to the new opinions by considering how frequently in the classical books of medicine a sudden chill led to everything. Here is the masterly way in which he explained it:
[These words must be erased from the language of science. Trans.]
"It is not at the time when the consideration of the individual coefficient tends to take a larger and larger place in nosological speculations that we must return to a simple etiology which has been rightly questioned. I am far from pretending that the savants to whom we are indebted for such interesting researches in the direction of specific causes design to bring everything within it, but those who do not exhibit that much prudence must be reminded that to constitute a morbid state the concurrence of many conditions are indispensable, that however specific it may be, a single cause is no cause at all."
It was thus that M. Tripier placed in parallel lines etiology according to the ancient medicine and the microbian medicine. I will state later the profound meaning of the expression, drawn from algebra,a or "individual coefficient". Let us say, at first, that it has been supposed that maladies resulting from specific causes are poisonings by living matters capable of reproducing themselves in the organism. The mechanism of these poisonings, says M. Tripier, "has been explained in many ways without being permitted to reject one on account of another."
"According to M. Pasteur," said he, "the multiplication of microbes would be the consequence of the introduction of germs introduced from without. For M. Bechamp the microbe a1 might proceed from a special mode of evolution of living molecular granulations which he named microzymas, granulations which exist in all protoplasm, the vicious evolution whereof might be regarded as causes independent of the introduction of leaven of foreign origin."
The radical difference between the principle of the microbian medicine and that of the microzymian theory of disease is thus clearly expressed. The microzymas are not then the cause of disease, but by their defective or morbid functional evolution under the various influences whereof I have spoken, their evolution may become vibrionian. It was only through the ambiguity that M. Pasteur succeeded in creating, that M. Tripier was able to say that I had admitted that the microbe proceeded from the microzyma, and that later M. Jaccond thought that the microzymas are the special microbes of the human organism.1
[a. The term "individual coefficient" was first introduced to indicate the amount and direction of errors which each individual astronomer was prone to commit.—Trans.]
[a. The term microbe, introduced for the sole purpose of drowning the grand discoveries of Bechamp, is, as presently shown, an etymological solecism.—Trans.]
1. This is how the ambiguity was created. The surgeon, Sedillot, thoughtlessly invented the word microbe as a name for the vibrioniens, which eventually Davaine regarded as the living agents of disease. M, Pasteur, heedless of the inacurracy, even from an etymological point of view of this word applied to a microscopic being of immense longevity, adopted it to designate the micro-organized ferments; thus beer yeast was a microbe, as also the bacteridia of Davaine.
He went further, and in a book published under his auspices he permitted the following definition to appear: "Under the name of microscopic beings or microbes are meant all living beings too small to be seen by the naked eye, all those which can only be seen with the aid of instruments which can enlarge them a great number of times, such as the small worm called trichina, which produces trichinosis, and an acarus, which produces the itch..." The work from which the above is quoted appeared in 1833 with a preface by M. Pasteur. Here we perceive how all diseases are regarded as parasitic on the same ground as the itch, and how the microzymas have become to be miscalled microbes!
To appreciate the antinomy between the microbian system and the microzymian theory, and to give to this work its practical utility by showing that the theory explains what the system is powerless to make clear, it will be sufficient to recall the two fundamental facts upon which rest the fabric of the demonstration that the blood is a flowing tissue, and, like all tissues, is spontaneously alterable.
The first is that a mixture of proximate principles, under the specified conditions, is naturally unalterable; but on contact with a limited or unlimited quantity of common air the same mixture always changes, owing to the various ferments which develop in it from the germs carried in this air. This mixture then does not alter spontaneously.
The second, that a natural animal matter, tissue, or humor, withdrawn from a living animal in perfect health, and under the same conditions, inevitably alters, even when absolutely protected from the air and its germs. Natural animal matter then is spontaneously alterable.
It is also desirable to recall: First, that the differences in the nature of the two orders of substances is such, that in the alteration of the former the micro-organisms consist of several categories of different species; while in the alteration of the latter only one category is to be found, viz., the microzymas, and afterwards, most frequently, the vibrioniens, products of their evolution; second, that, corroborating the facts, creosote in adequate quantity hinders the alteration of the former in contact with a limited volume of air, preventing the appearance of ferments; while the same quantity does not hinder the alteration of the latter, nor, in suitable cases, the vibrionian evolution of the microzymas.
Of these two facts M. Pasteur has only regarded the first and has denied the second, and it is because he and savants who have trusted to his word have looked upon the animal body only as organs constituted of a mixture of immediate principles—protoplasm—where nothing exists capable of becoming a vibrionien, that they have thought that the microbe coming from without is the sole cause of the alteration of this mixture and of disease. Now if the organism were what they think, and the sole cause of disease were what they say, a mixture of immediate principles necessarily altering an exposure to the air, every one would, of equal necessity, become diseased; but even in times of epidemics the majority are not attacked! An explanation of this fact has been sought in the microbe itself and in other considerations of the like order; but they are all worthless, for if the air contains that which changes the mixture, it does not contain that which causes disease.
The old medicine explained the immunity of the living by the receptivity, the predisposition, which those who are not attacked do not possess. M. Tripier, more precise, invokes the individual coefficient. But a mixture of proximate principles which, when exposed to the air, is always ready to be altered enjoys no immunity!
In exact language one can only speak of receptivity of the individual coefficient, of that which is regarded as a living body. But what is a living body? What is life?
Life, say some, is a special force, manifesting itself in ponderable matter. J. R. Mayer denies this. However it may be, they, the former, speak of a physical theory of life. We have seen that, according to Pasteur, life is that which elaborates the proximate principles, the natural substances of which the organism is composed.
Bichat said: "Life is the totality of the functions which resist death." But what is life? What is death? And what is the individual coefficient in the microzymian theory? For there is no longer any question of protoplasm!
Bichat said that life was a property of tissue because he regarded elementary tissues as the living elements of organized beings, which, in his view, possessed in themselves a permanent principle of reaction which enabled them to resist the causes of destruction which surround them.
The microzymian theory verifies the conception of Bichat even on this point; in fact:
The microzyma is the fundamental anatomical element, autonomically living, proliferating, while remaining morphologically similar to itself. It is in reality an apparatus whose functions manifest themselves, in a medium which realizes the conditions of its existence, by chemical reactions which cause it to produce the special zymases depending upon its special nature and the various proximate principles varying according to the place and the medium where it functions in the organism. Isolated from the organism and consequently in new conditions, as in the case of fibrin, there are some which act like lactic ferment with regard to fecula, etc.
In short, the microzymas resist so well the ordinary causes of destruction that, in the calcareous and other rocks, geological microzymas are to be found, now living, which functioned as anatomical elements of the animals of the epoch of those rocks. Here then we have the organized being, living per se, physiologically imperishable, unsuspected until I described it.a It is in it alone, functioning as an anatomical element, wherein resides the permanent principle of reaction which enables the organisms, whereof it composes the cellules, the tissues, the organs, to preserve themselves by nutrition and resist the athmotelluric (Tripier) conditions which
[a. Literally "of which I spoke," but the real meaning is as given above in my translation.—Trans.]
unceasingly tend to destroy them. And as there is no anatomical element simpler than the microzyma, and none other like it, resistant to total destruction, if we call life the totality of the anatomical properties which render the microzymas constructors of cellules by synthesis, and capable of becoming bacteria or vibrios by evolution; and the aggregate of the physiological and chemical energies which enable them to produce the zymases and to nourish themselves by transforming for their own use the materials of the medium in the anatomical systems wherein they function, eliminating at the same time that which they disassimilate after having used it, it must surely be admitted that LIFE is, in them allied, it is true, to matter, but to the matter in the structured organization, morphologically defined, and not simply to ponderable matter. So much for the general statement.
We now know that the microzymas are functionally different in the various anatomical systems of the same animal, and that they may be functionally different also in the same organs of the same structure in man and animals. It thence results that it is not always permissible in experimenting to draw conclusions from one animal to another and least of all to man. So that if we could admit with Bichat that life is a property of tissue, this property is not the same in all the tissues of the same structure and in their microzymas.
I will endeavour to explain my opinion upon the cause which leads to one kind of zymas being produced by one microzyma and another kind by another microzyma.
If there is the life of a microzyma, the life of a cellule and that of the organs of an anatomical system, there is also the life of the organized WHOLE. This necessarily results from the coordinated entirety of the particular lives of the organs and I hence of the individual lives of the microzymas which function in it. It is this view of the functions which Bichat called I he entirety of the functions which resist death.
But if the microzyma is physiologically imperishable, what is the death of the living whole? It is the opposite of that which constitutes its life, viz.: the absolute decoordination of the functions of the microzymas.
It is thus that in a part abstracted from a living animal, muscle or blood, etc., nothing is dead; but the microzymas, the only things antonomically living, being in decoordination, are no longer in their normal condition of existence; they now function only for themselves, determining the changes which attend the disorganizations of the tissues and the destruction of the cellules."
Now what is the meaning of the happy expression, "individual coefficient," introduced into medical language by M. Tripier? As in algebra a quantity is said to be a function of another upon which it depends, so in the microzymian theory it may be said that an organism, a cellule, are quantities which are functions of the microzymas which compose it and upon which it depends. Thus the expression of coefficient applied to the number which multiplies these quantities can be readily understood.
The individual coefficient is the factor which increases or diminishes in the microzymas the sum of the energy which enables them to resist the various causes which, by disturbing their functioning, determine morbidity in them, and thence disease and death.
The factor, whatever it may be, being the same, the variable, that is to say, the microzyma, differing, the result will necessarily vary. Now it is a proven fact, the microzymas are functionally different in the species, in the races and even in the individual, according to sex and age, in the different anatomical systems; the individual coefficient then is relative to the functional differences of the microzymas of the individual.
The state of perfect health results from the constancy and regularity of the coordinated functioning of all the organs the microzymas whereof are anatomically and physiologically healthy; for even, in the state of coordination, it is necessary to take into account heredity, diatheses, atavism, which may in some way have affected the particular microzymas of the individual.
The individual coefficient then is a complex constant dependent upon the particular coefficients of such or such functional systems of the individual.
To return to the blood, here is a typical example which justifies the above considerations.
I said that in anthrax (sang de rate) the bacteridia, regarded as specific cause, were the result of the vicious evolution of the microzymas of the blood, become morbid as the consequence of a decoordination, M. Jaccond would say, of some disturbance in the physiological functioning of the organism.
But it is evident that if the interior medium were inert or passive, this decoordination, in such a mixture of proximate principles, would be an effect without a cause, nothing leading it to become disturbed in its supposed functioning; for such a mixture has been shown to be unalterable of itself; while on the contrary it would immediately, infallibly, be placed in a condition of alteration determined by the agent, microbe, or specific ferment come from without. In short, on the hypothesis of a pure interior medium, a mixture of proximate principles, for a soil of culture, as it is called, for the microbe whose multiplication is poisonous, all the sheep would be equally susceptible, especially in times of epidemic, to contract anthrax (sang de rate) under identical circumstances, by contagion, and in all cases by inoculation.
Well, this does not happen. The adult sheep of the race called the African sheep is refractory to anthrax; it does not contract the disease by contagion, and generally not even by inoculation. The individual coefficient is not the same under identical circumstances, for the French sheep and for that of Africa. And as proof that the coefficient differs according to age, it is enough to state that the African lamb is not refractory, while the adult sheep of the same race is. Let us then say that the microzymas in the blood of the African adult sheep are among those which, even when ill treated, do not undergo that vicious alteration which would make them become carbuncular; with the lambs of the same race it is otherwise.
If the internal medium were the mixture imagined by microbian medicine, the foregoing facts would be incapable of explanation. For the medium would be inert and passive; since it has been proved that such a mixture is always disposed to allow the multiplication of the microzyma or of another like specific ferment able to alter it for its (the ferment's) own nourishment, and which medium without the ferment would be unalterable under other ordinary athmotelluric influences, cold, etc. It is the individual coefficient in relation to the functional differences of the microzymas of the subjects which alone explains the immunity of some, the susceptibility of others, since it has been demonstrated that in the interior medium there is nothing autonomically living, acting and physiologically impressionable except the microzymas.
In the language of the old medicine, immunity, susceptibility, is the capacity of the living organism to resist an impression, not to undergo, or to undergo the influence of external or internal agents. The microzymian theory adopts this thoroughly physiological language since it is only the microzymas of the living organism which can receive impressions and suffer or not suffer their influence; that is to say, resist or not resist the perturbing causes of their functioning according as the individual coefficient is abnormal or normal.
But what proof have we of this resistance, and of the mechanism of the harmlessness of the microzymas from without? The following is one I have given of it.
The isolated microzyma of beer yeast performs the function of a lactic ferment, producing little alcohol; in its function of anatomic element in the globule of beeryeast it never produces lactic acid. The young yeast, vigorous, acting strongly on cane sugar, even in contact with the air and with the addition of the chalk whose microzymas always effect lactic fermentation, still does not produce lactic acid; it resists, and microzymas of the chalk when added also fail to produce it.
But if the beer yeast be old, in some respect altered,a and even protected from the air, it will produce lactic acid, and the more, if calcareous rock or even pure carbonate of lime has been added. There we have the immunity of the beeryeast organism and its acquired susceptibility; the immunity which enabled it to resist the influence of the microzymas of the air and of the chalk, annihilating their influence; the susceptibility which enabled these microzymas to produce lactic acid without hindering those of the chalk in performing their work. Here we have the picture of the immunity and of the susceptibility of the microzymas of the cellules and of the tissues of the internal medium of an animal organism."a1
[a. The French text is aleree, which, I believe, to be a press error fur alteree.—Trans.)
[a1. We are here presented with a forcible illustration of the reckless ignorance of those physicians who practice the inoculation of organic poisons, such as the products of diseased conditions known as vaccines, anti-toxines, etc., upon man and other animals, whether as preventives or as remedies. Even the changes mentioned in the text, as some of the results of the learnedly devised experiments of Prof. Behamp, are unknown to these gentlemen; and, absolutely ignorant of what effect such inoculations may have upon the life forces, i.e., the microzymas of their victims, they arrogantly insist that their ignorance is learning, and induce a degeneration among those races who, recognizing their ignorance, place their faith in men as ignorant as themselves!—Trans.]
In microbian medicine the language of the old medicine is without meaning, since the former admits that one sole cause produces the disease and the alteration by fermentation of organic matter in general, making no distinction between the internal medium and a mixture of proximate principles.
The insuperable contradiction which exists between the microbian doctrines and the microzymian theory of the living organization brings into strong relief the justice of the aphorism of M. Tripier. A single cause for the disease and for the alteration or fermentation of proximate principles, however specific it may be, is no cause at all (est une cause nulle).
Yes, "the sole cause" is no cause, for I have demonstrated beyond dispute that there do not exist (I do not say germs, the word now is unsuitable) pre-existing microzymas, pathogenic or not; but there do exist microzymas, the living remains of bacteria derived by evolution from the anatomical microzymas of organisms which have disappeared or are disappearing beneath our eyes.
I limit here these considerations, referring the reader to my earlier publications for developments, which the present work completes and corroborates.1
1. For general pathology, see the three last conferences of "Les Microzymas,"etc. For special pathology, the communications, "Sur la septicaemic puerperale," "Sur la Pleuresie" and "Sur les albuminuries," in "Microzymas et Microbes." And for the physiological theory of fermentation, as well as for the true theory of nutrition, various chapters of the same works. (Chamalet, publisher, 60, Passage Choiseul, Paris.)
And now I hope it will be confessed that the error, common to all contemporary experimenters who have sought to discover the cause of the phenomenon of the spontaneous coagulation of the blood, also that of other equally spontaneous alterations, or who, like M. Pasteur, maintain the natural inalterability alike of the blood, as of all natural organic matters, is that they have regarded protoplasm as a mixture of pure proximate principles, and have held as dogma that this mixture was living and organized, although not morphologically constituted. At last I hope that it will be recognized that the discovery of the microzymas verifies the time-honored conception of Bichat, according to which, that only is living in any organism whatever, which is structured, morphologically determinate.
It is the agreement of the microzymian theory of the living organism with the brilliant conception of Bichat which gives to the theory of the blood as a flowing tissue and to the physiological and anatomical theory of its coagulation and other spontaneous alterations their highest degree of certainty.
Under the form of conclusions is here given a succinct summary of the totality of the fundamental facts, the discovery whereof has led to that of the true anatomical and chemical constitution of the blood and to the explanation of its spontaneous alterations.
(1) Ordinary air, near the earth, contains living microscopical objects called germs, and these germs are essentially microzymas.
(2) Proximate principles, and any mixture of such principles are unalterable in the presence of water, of a limited volume of air at ordinary temperature when a little creosote has been first added; and such proximate principles under such conditions do not permit any organized being to appear.
(3) Natural organic matters, vegetable or animal, tissues and humors, under like experimental conditions, always change of themselves, by a phenomenon of fermentation, and at the same time the microzymas, give birth to vibrioniens by evolution.
(4) The fibrin of the blood is not a proximate principle; it is a false membrane containing microzymas, whereof the intermicrozymian gangue is a specialized albuminoid substance.
(5) It is owing to its microzymas that fibrin decomposes oxygenated water, that it liquifies starch of amidon and that it can be dissolved, undergoing chemical change, in very dilute hydrochloric acid.
(6) The microzymas of fibrin in liquified starch undergo vibrionian evolution notwithstanding the presence of creosote.
(7) Fibrin liquifies spontaneously in carbolized water without the microzymas undergoing vibrionian evolution.
(8) The fibrinous microzymas are special; they can produce lactic and butyric fermentation in liquified starch.
(9) Natural albuminoid matters are mixtures, reducible by direct analysis into exactly defined proximate principles.
(10) The albuminoid matters reduced to proximate principles are very complex molecules composed of less complex ones, amides and their derivatives of the fatty and aromatic series. There exist of such less complex molecules, constituting an albuminoid molecule, quaternaries like urea, quinaries like taurine, which is sulphuretted; like hematosine, which is ferruginous; casein, in addition to the sulphuretted molecule, contains one which is phosphuretted; it has then six elements.
(11) There are several fibrins constituted as are those of the blood.
(12) There are a great number of different specific albumens which coagulation does not differentiate.
(13) The zymas are special albuminoid matters, likewise definable as proximate principles; they are always a functional product of the microzymas.
(14) The yellow liquid of the blood, besides its albumen, contains a haemozymas.
(15) The haemoglobin of the red corpuscle, reduced to a
definite proximate principle, decomposes oxygenated water by its noncomplex feruginous molecule, haematosine, and becomes colorless.
(16) The red corpuscle of the blood is a true cellule, having a cell-wall and its proper content. This content is constituted especially of haemoglobin and micro-zymian-molecular-granulations, the microzymas whereof decompose oxygenated water as do those of the fibrin.
(17) The blood contains a third anatomical element, the haematic-microzymian-molecular-granularions. It is the albumenoid atmosphere of these granulations which form, by allotropic transformation, the intermicrozymian gangue of the false membrane called fibrin.
(18) The flowing tissue is a content, whereof the vessels, arteries, veins and their appendages form the container.
(19) The three orders of anatomical elements of the flowing tissue only find their conditions of existence complete in their containers during life.
(20) After issuing from the vessels these conditions of existence being no longer fulfilled, the alteration of the flowing tissue commences.
(21) The microzymas of the different parts of the circulatory system possess alike the property of decomposing oxygenated water without being absolutely characteristic of them, for the microzymas of almonds and of other parts of plants and of beer yeast also possess this property. But there are animal tissues whose microzymas do not disengagethe oxygen of oxygenated water.
(22) The microzymas, anatomical elements, are living beings of a special order without analogue.
(23) The spontaneous changes of natural animal matters, whether the microzymas have or have not undergone vibrionian evolution, thanks to free access of air, lead always under certain conditions to the complete destruction by oxydation of the product of those changes; that is to say, reduce them to the mineral condition, carbonic acid, water, nitrogen. But the microzymas under whose influence the oxydation is effected are not attacked; in such wise that all which is purely proximate principle in a tissue, in a cellule and in the bacterium, having undergone total destruction, the microzymas remain, and bear testimony to the existence of the vanished organization.
(24) The geological microzymas of certain calcareous rocks and of chalk, those of the dust of the streets and of the air also bear testimony to the microzymas which functioned as anatomical elements in the tissues of organisms of geological epochs even as they function in those of the present time.
(25) That which in the air have been called germs are essentially the microzymas of the entire destruction of a living organism.
(26) Normal air contains neither pre-existing germs nor the things which have been improperly termed microbes, supposed to ascend from age to age to parents resembling them.
(27) The air contains normally no pathogenic microzymas. The carbon bacteridium of Davaine is the product of the evolution of diseased microzymas, either of haematic-microzymian-molecular-granulations, or those of the blood globules.
(28) There is no living matter which is not morphologically defined; that which has been called protoplasm in the cellule always contains microzymas as anatomical elements.
Here, for persons whom it may interest, follows a list of memoirs and articles wherein may be found the historical succession of the ideas which have enabled the resume contained in the postface to be written:
On the influence which pure water or water charged with various salts exercise at a low temperature (a froid) upon cane sugar (moulds and spontaneous generations). Annales de chimie et de physique. 3e serie, Vol. XLVIII (1855 and 1856). C. R., Vol. XL, p. 436. and Vol. XLVI, p. 44, and Annales de chimie et de Physique, 3e serie. Vol. LIV, p. 28 (1858).
Memoir upon generations called spontaneous and upon ferments. Annales de la Societe Linne de Maine et Loire, Vol. VI (1863), and see C. R.. Vol. LVII. p. 958.
Note upon alcoholic fermentation. C. R,, de 1'Academic des Sciences, Vol. LVIII, page 601 (1864), and Montpellier Medical, Vol. XII.
Upon alcoholic fermentation. Reply to M. Berthelot C. R., Vol. LVIII, p. 1116 (1864).
On some new soluble ferments (Anthozymas). C. R.. Vol. LIX. p. 496 (1864).
On the origin of the ferments of wine. C. R,, Vol. LIX p. 626 (1864).
On the escape of heat as a product of alcoholic fermentation. C. R., Vol. LX, p. 241 (1865).
Memoir upon nefrozymase. Montp. Med.. Vols. XIV and XV.
On the cause which matures wines. C. R.. Vol. LXI. p. 408 (1865), and Vol. LXIX. p. 892 (1869).
On physiological exhaustion and on the vitality of beer-yeast. C. R., Vol. LXI, p. 689 (1865).
On the harmlessness of the vapors of creosote in the breeding of the silkworm. C. R. Vol LXII p 1341 (1866).
On the parasitic disease of the silk worm. C. R., Vol. LXIII. pp. 311, 341, 391, 425, 552, 693, 1 147 ( 1866), Vol. LXIV, pp. 231, 873,980, 1042, 1043. 1185 (1867); Vol. LXV, p. 42; Vol. LXVI, p. 1 160 (1868)-Vol I .XVII. pp. 102. 443 (1868); Vol. LXLX, p. 159 (1869).
(On the role of the calcareous earths in butyric and lactic fermentations, and of the living organisms which they contain (microzymas). C. R., Vol. LXIII, p. 451 (1866).
Microzymas in the waters of Vergeze. C.R.,Vol.LXIII, p.559, and Bull.Soc.Ch.,Vol.VI,p.9,and Vol. VII, p. 159 (1866).
On the role of the microscopic organisms of the mouth in digestion, and especially in the formation of the salivary diastase: in common with Prof. Estor and Saintpierre. Mont. Med., Vol. XIX
On the molecular granulations of fermentations and of the tissues of animals (microzymas). C. R., Vol I, XVI. pp. 366. 1382(1868).
On the nature and function of the microzymas of the liver; jointly with Prof. Estor. C. R,. Vol. UCVI, i I, 'I (IHftS).
On the origin and development of the bacteria; jointly with Prof. Estor. C. R.. Vol. LXVI, p. 859 (IHftH)
On the reduction of nitrates and sulphates in cenain fermentations. C. R., Vol. LXVI, p. 547 IIIU.H)
On the spontaneous alcoholic and acetic fermentation of eggs. C. R.. Vol. LXVII. p. 523 (1868).
On the microzymas of pulmonary tubercle in the cretacious state; jointly with Prof. Estor. C. R., Vol. LXVII. p 9600 (1868)
Facts to serve for the history of the origin of bacteria; natural development of these little plants in the frozen parts of several plants. C. R., Vol. LXVIII. p. 466; Mont Med., Vol. XXII, p. 320 (1869).
Conclusions relating to the nature of the mother of vinegar and the microzymas in general. C. R., Vol I XVIII, p, 877; Gazette Medicale de Paris, 8 May, 1869.
On the alcoholic fermentation by the microzymas of the liver. C. R., Vol. LXVIII, p. 1567 (1869).
Researches relating to the microzymas of the blood and the nature of fibrin; jointly with Prof. Estor. C.R Vol. LXIXp 713 (1869).
Note for use in the history of the microzymas contained in animal cellules; by Prof. Estor. C. R., Vol. LXVII, p 529
On the nature and origin of the blood globules; jointly with Prof. Estor. C. R, Vol. LXX, p. 265 (1870)
On the geological microzymas of divers sources. C. R., Vol LXX p. 914 (1870).
On the carbonic and alcoholic fermentations of sodic acetate and of ammonium oxalate. C. R., Vol. LXX. p 69 (1870).
See also:
On the circulation of carbon in nature and the instruments of this circulation; exposition of a chemical theory of the life of the organized cellule; by A. Bechamp, Paris, Asselin; Montpellier, Seguin.
Of the microzymas of the higher organisms; by Messrs. A. Bechamp and A. Estor. Mont. M ed., Vol. XXIV, p. 32.
Exposition of the physiological theory of fermentation, according to the researches of Prof. Bechamp, by M. Estor. Messager du Midi (1865).
[The student is to understand that the above list comprises but a small fraction of the scientific work of the late Professor A. Bechamp; a fuller list, though still imperfect, occupies eight of the large folio pages of the Moniteur Scientifique (Paris) for December, 1908, and these labors were spread over fifty-three years, from 1853 to 1905 inclusive. Genius, has been defined as, in one aspect at least, the "faculity for taking infinite pains," and this faculty was possessed by M. Bechamp in an almost infinite degree.
The world has yet to learn how much it owes to this remarkable genius. The acknowledgment will be resisted by all those interests which fatten upon the ignorance and trusting confidence of the people. But thanks to his researches and discoveries it cannot be long before the medical profession will recognise the dangerous errors into which it has been led by those who succeeded in establishing a "conspiracy of silence" around Bechamp and his discoveries.—Trans.]
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To place beyond dispute the autonomy of the microzymas it is necessary to bring into prominence the facts and observations which prove that the existence of the microzymas as living beings has not been suspected by those naturalists who have studied the infusoria, nor yet by the anatomists who have studied the cellules and the tissues.
Demonstration that the microzymas, autonomous anatomical elements in living organisms, are living beings, morphologically determined, belonging to a category of their own, having no analogue.
Let us first get rid of the hypotheses that the microzymas are either the bacterium termo, or the Monas crepusculum, or the Micrococcus, or the spores of bacteria.
It is to be borne in mind that I gave the name of microzyma at first to the geological figured ferment of the chalk of Sens and of another calcareous earth; that I have discovered this ferment in other calcareous rocks, always of a spherical form, very brilliant, having the brownian movement and smaller than all the vibrioniens described by authors.' Ehrenberg described (in the chalk) the remains of fossil microscopic organisms called Polythalamies and Nautilites, but makes no mention either of Monas crepusculum nor of Bacterium punctum. In fact, none of the microzymas can be confounded with those described by Ehrenberg under those names. The microzymas are even smaller than the Bacterium termo, the smallest of the known infusoria, the first term of the animal kingdom, according to Felix Dujardin.
Nevertheless the microzymas had been seen in cloudy infusions of vegetable and animal matters, but they were taken for "the active molecules of Robert Brown"; that is to say, for molecules having the staggering or scintillating movement without change of place, called "brownian movement," and no further attention was paid to them.
In fact, the microzymas are neither the Bacterium punctum, nor the Monas crepusculum, nor even the Bacterium termo, which is much smaller than they. It will be sufficient to establish this fact by referring to the description of these monas, etc., given by F. Dujardin, in his "Historie Naturelle des Zoophytes," Infusoria, pp. 215 and 279.
On the other hand, if these bacteria, these monads, these micrococci, belong to determined species, it is contrary to the data of natural history to regard them as capable of being transformed into other genera and species of vibrioniens, as we see the microzymas produce them by evolution; the suggestion that the microzymas are the spores of schizomycetes is also untenable for the following reasons: A spore is a seminulum, or an egg, if according to the old view, the bacteria are animals, and search has been made for the eggs of bacteria; a grain, if according to the new creed the bacteria are vegetable; egg or grain, a spore cannot multiply itself as the microzyma does, and cannot therefore be the same thing.
Take the microzymas of the ovule in the Graafian vesicle in the fowl, and the microzymas of the vitellus of the mature egg. In the ovule there are ovular microzymas, in the vitellus, vitelline microzymas. At a given moment there are, say, a milligramme of microzymas in the ovule, and there are two or three grammes dried at 100° C. (I have isolated and weighed them) in the vitellus.1
They have then multiplied prodigiously during the development of the vitellus.2
So much then for the anatomical analysis for the egg of the fowl, and the chemical analysis shows that the elementary composition of the ovular microzymas is not the same as that of the vitellin, the former, as will be seen, being less carbonized; evidently their composition changed in the process of multiplication.3
Chemical analysis has further demonstrated that the vitellin microzymas of several species of birds differ from those of the fowl in their composition and especially in the properties of their respective zymases.4 This accords exactly with the microzymian theory, for it is evident that the microzymas are what they should be specifically, in order that, by incubation, the egg should produce the proper bird, its tissues, and all that pertains to its future being. And it has been demonstrated that during the development of the being, parallel with the anatomical development by the multiplication of the microzymas, there is a functional development of these, so that in each anatomical system they become that which they successively are in the embryo, in the foetus, in the adult, etc.
1. See the Memoir on The Albuminoid Mailers, pp. 140 and following.2. For the mode of multiplication of the microzymas see "Les Microzymas," pp. 490 and following.3. The Memoir above mentioned, p. 162.4. See J. Bechamp, "Normal and pathological albumins," pp. 77 and following.
If the hypothesis that the microzymas are the spores of bacteria were true, it would be necessary that there should first have existed in the circumambient atmosphere as many species of these spores as there are species of animal and vegetable ovules; next it would be necessary for these spores to penetrate as far as, and into the ovule, and should there multiply to fill up the vitellus of the egg of the fowl.
I need go no further, for there are still otherwise enormous difficulties, when we take into consideration the microzymas of the developed being, which are so different from the embryonal and foetal microzymas! But it now lies with the opponents of the microzymian theory to demonstrate the existence of these spores and of their penetration as far as, and into, the ovules and their multiplication.
We have thus discarded the hypothesis opposed to that of autonomy. It is also discarded by the following consideration, which deserves being underscored.
Shortly before M. Pasteur's admission in 1886 of the presence of the microzymas in the altered blood of his experiment, he had, for the purpose of denying them, asserted that the microzymas were the molecular granulations "which we all know." This was to his confreres of the Academy.
Yes, histologists and anatomo-pathologists knew them and represented them by a "stippling" in their figures of special tissues.
But their name even betrayed the opinion that they were neither organized nor living; in effect, the qualification of molecular was intended to indicate that it meant only small collections of some sort of matter; thus they were described as white, gray, minerals, fats, albuminoids, etc. They were even described as possessing the brownian movement; nevertheless, before the discovery of the microzymas, no one thought of connecting them either with the bacterium punctum or the monas crepusculum.
They were connected with anatomical organisms as being the remains of tissues, of destroyed cellules, or as amorphous matter; no one dreamed of making them come from outside. No consideration of the anatomical-molecular-granulations had anything to do with the discovery of the microzymas, but, as I have shown above, purely chemical considerations.
No, the molecular granulations are not the microzymas.
And from the time of our first note, Estor and I have stated that the microzymas exist only among the anatomical objects which in histology are called molecular granulations. But we held the microzymas to be autonomous anatomical elements; a more careful anatomical analysis enabled me to demonstrate that there exist naked microzymas and microzymas in the condition which I have termed microzymian molecular granulations.
Thus is disproved another gratuitous and erroneous assertion!
I return to the microzymas. I had described them from the commencement as being chemically and physiologically figured ferments, producers of zymases, which are called soluble ferments, and were placed in the same category as me figured ferments which are insoluble. Biologically, I distinguished them as being such as by evolution could become vibrionien, a fact which we have seen to be verified in every sense.
But in the experiments on spontaneous alterations, or fermentations, wherein microzymas become bacteria, we have seen that these were destroyed and that vibrioniens more and more minute appeared in their place, so that at last there remained only of these bacteria the forms nearest to the microzymas; in the same manner consequently, that by their destruction the cellules set their microzymas free, the bacteria in their complete destruction reproduce microzymas similar to those of the chalk, and we will now see how that is.
In the experiments on the spontaneous alterations of natural animal matters, the substances, which in a chemical sense are termed organic, which result from transformations by fermentation under the influence of the microzymas, before and after their vibrionian evolution, with or without the setting free of gas, are never entirely destroyed; that is to say, they are not reduced to a mineral condition, carbonic acid, water, nitrogen, etc.; for such destruction oxygen is necessary under conditions which reproduce those realized in geological epochs.
When I had discovered the microzymas in the chalk and in other calcareous rock, and became convinced that they were not dependent on atmospheric germs, I asked myself if they were not the living remains of organized being which had disappeared in geologic times.1 This hypothesis was verified in the following manner:
A kitten was killed and buried between two beds of pure carbonate of lime, and left in a cylindrical glass vessel, covered with a small quantity of paper in such wise that the air had free access to it, but its dust was excluded. The experiment lasted seven years. Every part of the body, except some fragments of bone, had disappeared. The carbonate of lime was perfectly white, so complete had been the work of destruction. Under the microscope, nothing was to be seen in the upper layers of the carbonate except microscopic crystals of aragonite of this carbonate; but in the beds adjacent to the place, and underneath, where the kitten had been, and beneath, there were crowds of glittering motile microzymas, such as are to be seen in the chalk of Sens, etc.
And with this kind of artificial calcareous rock, containing the microzymas of an animal of the present day, I was able to repeat the experiments on fermentation which I had made with the chalk of Sens and with other calcareous rocks, both lacustrine and marine.2 Such was the first experimental verification of the hypothesis that the microzymas of the chalk and of calcareous rocks are the organized remains, still living, of the beings which lived in the geological ages of the earths to which those rocks belonged. Read the note of the Comptes Rendus which I have just cited and you will be convinced that this verification has also been its vindication.
1. C. R.. Vol. LXX p. 914 (1870).2. Conference at the Congress of the French Association for the Advancement of Science. Nantes (1875).
I have said that the microzymas of the artificial chalk were the microzymas of an animal of the present epoch, but this needs some modification in terms to be quite accurate. They were the microzymas of the bacteria which the normal microzymas of the animal had first become by evolution. By fresh experiments I have learned that the microzymas of an entire body, or of the liver, of the heart, of the lungs, of the kidneys, under the conditions of my experiment become bacteria in the first phases of the phenomenon, these then disappear, becoming again microzymas, while the rest of the mailer already transformed is, under (heir influence, and with access of air, reduced to the mineral state, carbonic acid, water, nitrogen, etc.1 And I have demonstrated that whereas in the climate of Montpellier seven years were required to accomplish this, a much longer time would be needed in a colder climate, so that in a climate such as that of the Obi valley centuries were required.
It was then a legitimate conclusion that the microzymas of the calcareous rocks, of the clays, of the marls; in short, of all the rocks which contain them, are the organized and living remains of beings which had been living, of animals and plants of the geologic epochs; that these beings were histologically constituted as are the beings of our epoch, that their microzymas, during their destruction, had become bacteia by evolution, and that the microzymas, geological ferments, of these rocks, are those of these bacteria destroyed in their turn and reduced to their microzymas.
1. See "Les Microzymas," etc., pp. 624 and following. See also note: C. R., Vol. LXX, p. 914, "Les Microzymas," etc., p. 952.
It is not surprising then that, having long pursued the anticipated consequences of the hypothesis now verified, I have demonstrated the presence of the microzymas in the earths of the garrigues of the departments of Herault and of Card, in cultivated lands generally, in moor lands, in the alluvials, in the waters, in the dust of the streets, where they are to be found in crowds; often still in the condition of bacteria, proving that, like those of the calcareous rocks, they are energetic ferments. And already, prior to 1867, I had made known their role in the soil in agriculture.
These researches led to a result of very great importance; it was the demonstration that what was and still is called germs of the air are essentially nothing other than the microzymas of beings which have lived, but have disappeared or are being destroyed before our eyes. In fact, by precise experiments, I have proved that the microzymas of the air are ferments of the same order as those of the chalk, of the rocks, and of those of my experiments with artificial chalk; only, varying with the places, the circumambient a r may, along with these microzymas, contain conides of lichens, spores of mushrooms, bacteria and everything that the wind can disperse in it.1
1. See, for details. C. R, Vol. LXXIV. p. 629; Vol. LXIII, p. 451; and "Les microzymas." etc., pp. 122, 135. 940. 952.
There is then no panspermy such as that which Charles Bonnet had invented, nor that which Spallanzani and M. Pasteur (after me) had admitted. In short, there are no pre-existing germs. At each period, as in our days, and in each place there exist in the surrounding air only the microzymas of former beings which had disappeared and are disappearing with the things which the wind scatters in it.
But if we reflect that the species of microzymas are: first, as numerous as the species of eggs, of seeds, of spores of the various species of animals and plants; next, that there are in each animal and vegetable organism, already developed or in process of development, microzymas as specifically numerous as there are anatomical systems and organs, tissues and special cellules in these organisms, it is easy to conceive that the species of atmospheric microzymas are present in enormous numbers. One can also understand the very great number of changes which these microzymas may cause, when some one of these species fall into a fermentescible medium in which it can multiply, and either evolve in it/or build in it a cellule, or a mould.
If then, as I have demonstrated experimentally, there are besides microzymas, and as well in animals as in plants, among the micro-organisms of the circumambient air, spores, conides of fungi, of lichens, even actual cellules of ferments,1 it is easy to understand that if these micro-organisms fall into fermentescible media they will develop in it, each according to its nature, and that various productions, moulds, divers cellules, and at the same time vibrioniens, may appear in it.2
But in all the observations and in all the experiments relative to the spontaneous change of natural vegetable and animal matters, and in the fermentations of sugar or of fecula by aid of the tissues and humors of animals, when the influence of the micro-organisms of the air has been destroyed or suppressed,3 only microzymas and vibrioniens, and vibrios or bacteria, fruits of their evolution, are seen; this proves that the microzymas are autonomous anatomical elements existing in it of themselves.
1. "Sur L'origine des ferments du vin," by A. Bechamp, C. R., Vol. LIX, p. 626 (1864).2. See C. R., Vol. LXXIV. p. 115, and "Les Microzymas," etc.. p. 948.3. Here a complementary explanation is necessary to explain more clearly the mode of action of creosote in the experiments in which it has been employed to annihilate the influence of germs of the air. And first of all, in speaking of germs, it no longer relates to this vague something, which when called upon by Ch. Robin to define, M. Pasteur called "origin of life," but figured ferments, upon which creosote exercises an influence clearly determined. I must therefore recall that I have several times insisted on the fuel that creosote is efficient in annihilating the influence of the germs of a limited volume of the surrounding air, unless the air be renewed. And it is so, because a limited volume of air contains only limited number of micro-organismic ferments. But creosote, while it does not prevent the ferments from acting, hinders their multiplication. In reality the ferments of a limited volume of air, which are capable of acting upon a fermentescible medium, do act upon it, but only in proportion to their quantity, in such wise that the result is so inappreciable that it is as though it were nothing; it is thus that the quantity of sugar, inverted, in the presence of creosote, by the microzymas of a small limited volume of air can be determined neither by reagents, nor by the polariscope. But if a slow current of several hundred litres of the same air is caused to act upon a creosoted solution of sugar the microzymas and other micro-organisms retained by the liquor render this at last cloudy, and. thus accumulated, there are among them some which effect the inversion, without developing moulds, while the microzymas undergo a greater or less vibrionian evolution. Such is the exact idea to be formed of the influence of the creosote, and of the role of the atmospheric ferments. When, owing to their presence, productions such as moulds are produced, it is because die special conditions of existence of these moulds, etc., have been realized. But microzymas in their function of anatomical elements only become vibrioniens from the substance of tissues and humors, ever, in spite of the presence of creosote, provided the volume of air be limited or completely absent.
These statements and considerations may be summed up in the following propositions:
(1). The microzymas of the animal organism proceed from the vitellin microzymas, which are autonomous anatomical elements in the vitellus.
(2). The number of anatomical species of microzymas is enormous.
(3). The essential biological characters of the microzymas are to be creators of cellules by synthesis and of vibrioniens by evolution.
(4). The physiological and chemical characters of microzymas are to produce the zymases and to be themselves ferments having a determined form.
These propositions are also true for plants beginning with the ovule; but from the fact that a microzyma may become a vibrionien by evolution, it necessarily follows that the species of microzymas being innumerable the species of vibrioniens are likewise innumerable.
It is further important to remember that an anatomical element microzyma is animal in an animal, vegetable in a vegetable. Hence arises this question: To what kingdom belongs the bacterium of such or such an animal microzyma? Of such or such a vegetable microzyma? We must remember that any microzyma, before it accomplishes the evolution which produces a bacterium, passes through the evolutionary phases of microzyma slightly changed in form, of microzyma successively associated in twos, in threes, in several grains, etc. But those forms have been described under the names of Monas, of Bacterium termo and punctum, of Coccus, of Diplococcus, of Torulo, of Streptococcus, of Micrococcus, of Mesococcus, of Microbe with a point, of Microbe with a double point, etc. Nor is that all; bacteria in spontaneously destroying themselves to become microzymas similar to those of the rock-chalk or of the artificial chalk of my experiments, have passed through new forms, of which the most constant is that which has also been described as the Bacterium termo.1
1. See, on this subject, Felix Dujardin, "Les Zoophites Infusoire," p. 232.
But what are such specifications worth, based only upon the shape, on the length and thickness, upon the color, the motility or immotility of the object specified? In the order of received ideas it would be too tedious to discuss them; it suffices for me to say that Felix Dujardin, who knew the germ theory and did not allude to it in his explanations, was of opinion that the phenomena observed in these changes were favorable to the doctrine of spontaneous generation; and consequently that outside of the microzymian theory it is all incomprehensible and arbitrary. A priori one cannot tell to what kingdom a bacterium belongs, for one can only distinguish a microzyma, and consequently a bacterium, by the origin and function of the microzyma. An example will make this clear: Take the parotid gland of a man, and that of a horse, the structure and functions of which seem to be the same and of which the microzymas of the cellules are morphologically identical; well, while the parotidian microzymas of man liquify and energetically saccharify the starch of fecula, those of the horse liquify that starch but do not saccharify it And we have established by other differences of the like kind that the microzymas of the different anatomical systems of a same organism may differ one from the other; and by still greater reason those of different organisms may differ.
Plants, like animals, being anatomically constituted living by their respective microzymas, the bacteria which these microzymas can become are evidently limited to the two kingdoms; and so perhaps the question whether a vibrionien is animal, as was thought, or plant, as is now asserted, is an idle one.
But if one chooses in spite of all this to insist that the bacteria are plants and that the microzymas are their spores, a new question would arise, of which of the species of schizomycetes which the same microzyma may become before becoming a perfect bacterium (Bacterium termo, Monas crepusculum, torula, Diplococcus, Streptococcus, Micrococcus, etc.)—is it first the spore, in the organism before evolution, and then in the chalk-rock, or in the artificial chalk, after the total destruction of the organism?
According to accepted notions the reply cannot be otherwise than uncertain! According to the microzymian theory here is the answer.
An anatomical element, microzyma, in a plant or in an animal, whose conditions of existence have just changed, can become a bacterium by evolution, and the intermediate evolutionary phases, like those of the tadpole, which becomes a frog, leaves the special nature of the microzyma still existing; there are not new species. The perfect bacterium depends on the nature of the microzyma, as the perfect batrachian depends on the particular nature of its tadpole.
Every bacterium resolves itself by spontaneous destruction into a microzyma, and the microzymas thus evolved are different from the anatomical microzyma which has become a bacterium, not morphologically, nor functionally so far as regards being a figured ferment, but by a collection of properties, which assure the perennity of the form and of the function in a condition of individual separateness.
But the chief difference consists in this: The anatomical element microzyma in the vitellus is the organized commencement of all animal organization, and in the ovule of the plant it is the commencement of all plant organization. On the other hand, the microzyma resulting from the destruction of a bacterium is the organized end of all organization.
AND HERE IS SOMETHING STUPENDOUS! The geological microzymas, as well as those of the artificial chalk in my experiment, are organized and living, not only because, without change of form, they are individually figured ferments, but also because under certain conditions, such as those of the fibrin in the experiment described in the first chapter, at the same time that they act as ferments they can again become bacteria by evolution. The microzymas not only possess the sort of perennity of which I spoke; they enjoy also the stupendous duration of the geological epochs from the time the microzymian rocks have been formed down to the present time. And this duration means for us, that the microzymas have been constituted physiologically imperishable. And this last statement must convince us that the microzymas are organized living beings, of a class apart, without analogue.
And it is thus, precisely because the microzymas are, essentially and by destination, autonomous anatomical elements in each anatomical system, becoming what they ought to become in each, by substantial and functional development, parallel with the development of such system in the development of the entire organism, that they are organized living beings of a class apart as above stated.
The following is the experimental proof that this new principle of anatomy and physiology is well founded.
The vitellin microzymas of the egg of the fowl do not pre-exist in the ovule; they are the result of a substantial development, and of the proliferation of the ovular microzymas.
To prove this, it will be sufficient to make the elementary analysis of the microzymas of the vitellus of the fowl's egg, and of those of the ovules remaining in the Graafian vesicle, while these ovules are only a few millimetres in diameter. The following are these analyses:
Vitellin Microzymas Ovular MicrozymasCarbon 52.67% 50.63%Hydrogen 7.17% 7.36%Nitrogen 15.71% 15.67%Oxygen, etc.1
1. See"Memoire sur les matieres albuminoid." p. 161, and the correction in the note on p. 489.
The difference of two per cent, of carbon in the percentage composition answers to great differences in the nature of the proximate principles of these microzymas. I will add that the vitellin microzymas contain much more mineral matter than the ovular. It is thus evident that the microzymas of the ovule become vitellin microzymas by substantial development, while they multiply and the vitellus grows. In short, one may say that the ovular microzymas become vitellin microzymas by maturing.
It would take too long to dwell as long as might be desirable on this result and upon the whole of the chemical, physiological and anatomical phenomena which this ripening necessitates in order that the vitellin microzymas should become fitted to play their part, chemical, physiological and histogenic, during the embryonic development, etc. I must refer the student to what I have said elsewhere.1 What is most important to bear in mind is, that no matter how high one goes [in the scale of living beings] the microzymas are found in the ovule, and that these microzymas are not those which are to be found in the vitellus, but will become them.
1. See Les Microzymas," etc, pp. 487 and following.
All the special facts which I have made known, including the last, authorize me in erecting into a general principle the precise experimental idea; that the microzyma, the final term of the anatomical analysis, is in truth the simple anatomical element which satisfies the conception of Bichat and completely destroys that of living matter not morphologically defined.
The cellularists, it is but fair to recall, regarding the cellule as the simplest anatomical element, believed it proceeded necessarily from a former cellule, omnis cellula e cellula, holding it to be the vital unit, living per se, and regarded an entire organism as the sum of these units. But we now know that that was a deduction from incomplete and superficial observations, for the cellule, a transitory anatomical element, has the microzyma for its anatomical element. It is this which alone possesses all the characters of an anatomical element, living per se, and which must be regarded as the unit of life. It is what I have already stated in the following terms:
"The microzyma is at the beginning and at the end of every living organization. It is the fundamental anatomical element whereby the cellules, the tissues, the organs, the whole, of an organism are constituted living."
Let us devote a few words to develop this idea. Let us penetrate a little further into this notion of a fundamental anatomical element, which, as has been said, implies that the microzyma is the living atom of the organization as the physical atom is the element of the molecule of a simple body. This would be true if the microzyma were unchangeable in its simplicity. But in reality it is essentially mutable, as are all living bodies; and it is especially so, in order that it may fulfil its numerous functions. In fact, the microzymas, functionally different in the different anatomical systems of the same species, and different at all ages, beginning with the embryonal stage, have been primitively those of the vitellus, after having been those of the ovule. A microzyma then is not, properly speaking, an atom; but always anatomically simple, it becomes, by nutrition, that which it needs to become, so as to accommodate itself to each new condition of existence which the successive phases of the development of each anatomical system provide for it. It is thus that even in the embryo, in that which will be the ovary, a category of microzymas becomes again ovular microzymas to recommence the same cycle. I add that, taken as a whole and in its details, the THEORY HAS BEEN CONFIRMED, VERIFIED, CORROBORATED by a great number of other facts of general anatomy and of pathological anatomy and of physiology.1
1. See particularly the notes and publications following:A. Bechamp: Facts useful for the history of the origin of the bacteria. Natural development of these little plants in the frozen parts of certain plants. C. R.. Vol. LXVTII. p. 466(1869).A Estor: Note for use in the history of the microzymas contained in animal cellules. C. R.. Vol. LXVIII. p. 519. It relates to the microzymas in bacterian evolution in a cyst which had just been removed.Bechamp and Estor: On the microzymas of pulmonary tubercle in the cretacious state. C. R., Vol. LXVII, p. 960 (1868). It relates to the discovery of microzymas in a condition of evolution within the tubercle, regarded as the remains of the destroyed epithelium of the pulmonary alveoli.Bechamp and Estor: Facts useful for the history of the microzymas and bacteria. Physiological transformation of bacteria into microzymas and of microzymas into bacteria in the digestive tube of the same animal. C. R., Vol. LXXVI, p. 1143 (1873).Bechamp: Facts useful for the history of the histological construction of the glairine of Molitg. C.R., Vol. LXXVI. p. 1485 (1873).Bechamp: The diseases of the silk worm. C. R.. various notes from 1866 to 1374. They relate to the pebrine, a parasitic disease, and to the flacherie, a microzymian disease, not parasitic.J. Grasset: On the histological phenomena of inflammation. Treatise regarding a new theory, based upon the consideration of the molecular granulations (microzymas). Gazette Med. de Paris, year 1873.E. Baltus: Theory of the Microzyma, a theoretic and practical study of pyogenesis (the formation of pus). Theses of the Faculty of Montpellier, year. 1874, No. 41.J. Bechamp: The microzymas and their functions at the different ages of the same being. Theses of the Faculty of Montpellier, 1875, No. 63.A Bechamp: Microzymas and disease; in "Les Microzymas," etc., p. 744. (Chamalet, 60, Passage Choiseul.)A Bechamp: Puerperal septicaemia, pleurisy, the albuminuria and the preface to Microzymas et Microbes. (Chainalct, 60, Passage Choiseul, Paris.)A. Tripier: Electricity and Cholera. Genesis, prophylaxy and treatment. (Georges Carre, pub. 1884). In this memoir there will be found a comparison of the microbian system and the microzymian theory, highly original and at the same time the conception of what the eminent author terms the individual coefficient.
When by the attentive study of these facts one has become convinced that the microzymian theory is their pure and simple expression, it will be at once recognized that the cellule is already an organ in which, by nutrition, the conditions of the preservation of the microzymas with the constancy and regularity of their chemical and physiological functions are unceasingly realized. And it will thus be understood that the microzymian molecular granulations, whether of certain cellules, of the vitellus, or of the blood, also realize after their manner the conditions of this constancy and regularity. When these conditions are no longer realized they may undergo vibrionian evolution.
The most prominent fact in the history of the microzymas, that which has been the most disputed, precisely because of their capacity to undergo vibrionian evolution, is the fact of their anatomical autonomy. Now this faculty, which is only manifested when the normal conditions of existence of the microzymas, functioning as anatomical elements, are no longer fulfilled, is the best proof which could be given of the change which has happened in their condition, causing their irregular and changed functioning.
In fact, in their various anatomical situations, the microzymas remain morphologically similar to themselves. They function in each cellule, in each organ, in each anatomical system, naturally, chemically and physiologically for themselves while preserving their individuality; at the same time that by coordination, according to the happy and thoroughly scientific expression of Dr. Antoine Cros, they function for the benefit of the microzymian molecular granulations of the cellules, of the organs and of the various anatomical systems taken altogether, whose physiological condition of health is preserved by them.
But if from some etiological cause certain changes happen in an organ, changes such as auscultation or percussion can precisely ascertain, as, for instance, an increase in the volume of the spleen, M. Cross tells us that there is a decoordination, a functional perturbation in the entire organism and disease. It is worth mentioning that from the time Dr. Cros became acquainted with the microzymian theory, he did not hesitate to recognize the microzymas as the anatomical agents of the decoordination; how does it happen?
Among the causes which produce disease, a sudden chill in summer is the one most frequently indicated or invoked. The chill is at the same time an influence and a lowering of temperature. I do not insist on the fact that it is only something living which is painfully affected, so as to confine myself to the physical phenomenon.
But the microzymas are very sensitive to variations of temperature; so much so that even the geological microzymas act regularly only at temperatures near 40° to 42 °C. (= 104° to 107° F.); in fact, the microzymas of the chalk of Sens do not act so as to cause fecula to ferment in a temperature below 38° C. (= 100°.4 F.). Further a very slight lowering of the temperature is sufficient for the egg which should produce a bird not to produce one, and to putrefy or to produce the monsters of Dareste when the heat is not uniformly applied. In fact, the influences of the medium (as if it should become neutral or acid), which modify the activity of the microzymas acting alone, are various.
That which happens to the isolated microzymas happens also to those of the egg and for those of the organism. Suppress the air and the egg does not become a fowl, but undergoes another kind of change.
If from any cause whatever the air does not have access or has an insufficient access to the pulmonary alveolae, and their epithelium becomes the pulmonary tubercle, the cellules become reduced to their microzymas, which are then found in vibrionian evolution in the tubercle in the cretatious state. If the decoordination resulting from an irregular functioning of a part of an anatomical system is sufficient to bring on a malaise which is not removed, there will arise a diseased condition because of a sharp change of the conditions of existence of the microzymian anatomical elements, and the change in the medium sufficient to cause the decoordination will manifest itself by the vibrionian and bacterian evolution of the microzymas of such or such part of the system.
It is thus that in the disease called "Sand de rate" (Anthrax), so thoroughly studied by Davaine, the diseased microzymas end by evolving into what that learned physician called bacteridiae, the blood globules undergoing the changes which are so characteristic. The bacteridiae were not the cause of the diseased condition, but were one of its effects; proceeding from the morbid microzymas they were capable of inducing this diseased condition in the animal whose microzymas were in a condition to receive it. Hence it is seen that the alteration of natural animal matters is spontaneous, and justifies the old aphorism so concisely expressed by Pidoux: "Diseases are born of us and in us."
On the other hand, the disregard of this law of nature, the firm establishment whereof is completed by the present work, necessarily led M. Pasteur to deny the truth of the aphorism, and to imagine a pathogenic panspermy, as he had before conceived, a priori, that there was a panspermy of fermentations. That M. Pasteur after having been a sponteparist should reach such a conclusion was natural enough; he was neither physiologist nor physician, but only a chemist without any knowledge of comparative science.
What is astonishing is, that he should have succeeded in procuring the triumph of a preconceived system among physicians and in academies, and to procure the rejection of the microzymian theory [without examination. Trans.]. For instance, an enlightened physician thus summed up the fundamental proposition of M. Pasteur: "The microbes always come from without; they constitute species which remount from generation to generation up to the origin of the world."1
An eminent surgeon, M. Verneuil, ended by admitting as a demonstrated theorem that there is no spontaneous tetanus, that there is no spontaneous small pox, syphilis, glanders, hydrophobia, tuberculosis, charbon or malignant pustule; declaring that the pathogenic problem consisted solely in discovering how and when the microbe, also called virus, come from without, penetrates into the organism; declaring that the question is thus stated between old medicine and the microbina medicine "with extreme simplicity and without the least ambiguity.2a
1. Gazette medical, Paris, 6th Series. Vol. V, p. 218. This is precisely what M. Chamberland said of micro-organisms in general: "Recherches sur I'origine el le developpement des organismes microscopiques." Theses de la Faculte des Sciences. Parais, 1879. See also "Microzymas et Microbes," p. 25, 2d Ed.
2. C. R_,Vol. CV, p. 552.
[a. There is an implication to be found in the statement of Surgeon Verneuil, though probably not meant by him, to which assent must be given when understood. It is TRUE that there is no such THING as tetanus, small pox. syphilis, etc., as is implied by the general use of nosological terms. Disease is not a thing, an entity: it is a condition, and the error of regarding the condition of disease as an entity has confirmed, where it has not originated, much of the prevailing erroneous treatment of the sick. Nosological terms have a use; it is that of bringing to the mind of the physician a group of pathological symptoms, which may or may not be present in the case of the patient under consideration; from them, when present, the diseased condition of the patient can be recognized and treated.
Unfortunately, through not understanding this truth, attempts are frequently made to treat, not the patient, but the name, which has been given to a collection of morbid symptoms. A broken limb is a thing; the inflammation which results from it is a condition, and if gangrene ensues the gangrene is not a thing, but a condition to be taken into consideration with all the other symptoms in the treatment of the patient. The surgeon, Verneuil, had probably a glimmering perception of this truth, but he misapplied it, for his theory and practice, as a physician, and the theory and practice of nearly all modern medicine assume that the condition to be treated is a thing having a name and this name is treated instead of the patient.—Trans.]
But these assertions (of Surgeon Verneuil) are reduced to nothing, when we call to mind that the pretended germs of the air are only the microzymas of organisms which have disappeared, which had become bacteria by evolution; that even at the Academy of Medicine I said—and no one ventured to contradict me—that no one had ever been able to reproduce a disease on the nosological roll by taking the pretended pathogenic microbe in normal air, but only in the diseased animal. And I add, that just as with time the fibrin-ous microzymas lose the property of decomposing oxygenated water so, as proved long ago by Davaine, after a short time the blood of an animal which had died of anthrax [sang de rate] no longer communicated that diseased condition; and the same is true in all cases.
THUS NORMAL AIR NOT ONLY DOES NOT, BUT CANNOT, CONTAIN THE PRETENDED PATHOGENIC MICROBES, AND THE VERY PRINCIPLE OF MICROBIAN MEDICINE CONSTITUTES A FUNDAMENTAL ERROR.
But no attention was paid to this. Abandoning the famous dogma of the closure of the body to germs from without, it was admitted "that the human organism carries constantly a large number of microbes of many different species" which only await the moment when "the organism being disturbed in its physiological functioning will be given over to the activity of its own microbes; whose presence it had theretofore borne without being affected." M. Jaccond wrote the above [nonsense] with reference to two cases of acute pneumonia following a chill.1
1. "Journal des societes scientifiques," 4 May, 1887, p. 156.
In M. Pasteur's set, M. Jaccond's opinion was accepted; and although their master had declared that the cellules were not living, his disciples imagined that the leukocytes (under the name of phagocytes) were living like amoeba and able to perform movements called amaeboid. And it was imagined that these phagocytes formed themselves into troops to pursue and devour the microbes. There was thus a phagocytosis,a- which was trumpeted forth as providential. The precise knowledge of the blood reduces to its just value this latest form of the struggle against the microzymian theory. Of all the suppositions and fancies of M. Pasteur, there remains only, even for his disciples, that which consists in admitting a sole cause, the germs or microbes of the air, to explain the phenomena of fermentations and disease.
Nevertheless all physicians did not think as did Verneuil or as did M. Jaccond. Before 1866, while the triumph of the microbian medicine was in full swing, Dr. A. Tripier did not admit that there was a microbe come from without to be considered. His attention had been drawn to the new opinions by considering how frequently in the classical books of medicine a sudden chill led to everything. Here is the masterly way in which he explained it:
[These words must be erased from the language of science. Trans.]
"It is not at the time when the consideration of the individual coefficient tends to take a larger and larger place in nosological speculations that we must return to a simple etiology which has been rightly questioned. I am far from pretending that the savants to whom we are indebted for such interesting researches in the direction of specific causes design to bring everything within it, but those who do not exhibit that much prudence must be reminded that to constitute a morbid state the concurrence of many conditions are indispensable, that however specific it may be, a single cause is no cause at all."
It was thus that M. Tripier placed in parallel lines etiology according to the ancient medicine and the microbian medicine. I will state later the profound meaning of the expression, drawn from algebra,a or "individual coefficient". Let us say, at first, that it has been supposed that maladies resulting from specific causes are poisonings by living matters capable of reproducing themselves in the organism. The mechanism of these poisonings, says M. Tripier, "has been explained in many ways without being permitted to reject one on account of another."
"According to M. Pasteur," said he, "the multiplication of microbes would be the consequence of the introduction of germs introduced from without. For M. Bechamp the microbe a1 might proceed from a special mode of evolution of living molecular granulations which he named microzymas, granulations which exist in all protoplasm, the vicious evolution whereof might be regarded as causes independent of the introduction of leaven of foreign origin."
The radical difference between the principle of the microbian medicine and that of the microzymian theory of disease is thus clearly expressed. The microzymas are not then the cause of disease, but by their defective or morbid functional evolution under the various influences whereof I have spoken, their evolution may become vibrionian. It was only through the ambiguity that M. Pasteur succeeded in creating, that M. Tripier was able to say that I had admitted that the microbe proceeded from the microzyma, and that later M. Jaccond thought that the microzymas are the special microbes of the human organism.1
[a. The term "individual coefficient" was first introduced to indicate the amount and direction of errors which each individual astronomer was prone to commit.—Trans.]
[a. The term microbe, introduced for the sole purpose of drowning the grand discoveries of Bechamp, is, as presently shown, an etymological solecism.—Trans.]
1. This is how the ambiguity was created. The surgeon, Sedillot, thoughtlessly invented the word microbe as a name for the vibrioniens, which eventually Davaine regarded as the living agents of disease. M, Pasteur, heedless of the inacurracy, even from an etymological point of view of this word applied to a microscopic being of immense longevity, adopted it to designate the micro-organized ferments; thus beer yeast was a microbe, as also the bacteridia of Davaine.
He went further, and in a book published under his auspices he permitted the following definition to appear: "Under the name of microscopic beings or microbes are meant all living beings too small to be seen by the naked eye, all those which can only be seen with the aid of instruments which can enlarge them a great number of times, such as the small worm called trichina, which produces trichinosis, and an acarus, which produces the itch..." The work from which the above is quoted appeared in 1833 with a preface by M. Pasteur. Here we perceive how all diseases are regarded as parasitic on the same ground as the itch, and how the microzymas have become to be miscalled microbes!
To appreciate the antinomy between the microbian system and the microzymian theory, and to give to this work its practical utility by showing that the theory explains what the system is powerless to make clear, it will be sufficient to recall the two fundamental facts upon which rest the fabric of the demonstration that the blood is a flowing tissue, and, like all tissues, is spontaneously alterable.
The first is that a mixture of proximate principles, under the specified conditions, is naturally unalterable; but on contact with a limited or unlimited quantity of common air the same mixture always changes, owing to the various ferments which develop in it from the germs carried in this air. This mixture then does not alter spontaneously.
The second, that a natural animal matter, tissue, or humor, withdrawn from a living animal in perfect health, and under the same conditions, inevitably alters, even when absolutely protected from the air and its germs. Natural animal matter then is spontaneously alterable.
It is also desirable to recall: First, that the differences in the nature of the two orders of substances is such, that in the alteration of the former the micro-organisms consist of several categories of different species; while in the alteration of the latter only one category is to be found, viz., the microzymas, and afterwards, most frequently, the vibrioniens, products of their evolution; second, that, corroborating the facts, creosote in adequate quantity hinders the alteration of the former in contact with a limited volume of air, preventing the appearance of ferments; while the same quantity does not hinder the alteration of the latter, nor, in suitable cases, the vibrionian evolution of the microzymas.
Of these two facts M. Pasteur has only regarded the first and has denied the second, and it is because he and savants who have trusted to his word have looked upon the animal body only as organs constituted of a mixture of immediate principles—protoplasm—where nothing exists capable of becoming a vibrionien, that they have thought that the microbe coming from without is the sole cause of the alteration of this mixture and of disease. Now if the organism were what they think, and the sole cause of disease were what they say, a mixture of immediate principles necessarily altering an exposure to the air, every one would, of equal necessity, become diseased; but even in times of epidemics the majority are not attacked! An explanation of this fact has been sought in the microbe itself and in other considerations of the like order; but they are all worthless, for if the air contains that which changes the mixture, it does not contain that which causes disease.
The old medicine explained the immunity of the living by the receptivity, the predisposition, which those who are not attacked do not possess. M. Tripier, more precise, invokes the individual coefficient. But a mixture of proximate principles which, when exposed to the air, is always ready to be altered enjoys no immunity!
In exact language one can only speak of receptivity of the individual coefficient, of that which is regarded as a living body. But what is a living body? What is life?
Life, say some, is a special force, manifesting itself in ponderable matter. J. R. Mayer denies this. However it may be, they, the former, speak of a physical theory of life. We have seen that, according to Pasteur, life is that which elaborates the proximate principles, the natural substances of which the organism is composed.
Bichat said: "Life is the totality of the functions which resist death." But what is life? What is death? And what is the individual coefficient in the microzymian theory? For there is no longer any question of protoplasm!
Bichat said that life was a property of tissue because he regarded elementary tissues as the living elements of organized beings, which, in his view, possessed in themselves a permanent principle of reaction which enabled them to resist the causes of destruction which surround them.
The microzymian theory verifies the conception of Bichat even on this point; in fact:
The microzyma is the fundamental anatomical element, autonomically living, proliferating, while remaining morphologically similar to itself. It is in reality an apparatus whose functions manifest themselves, in a medium which realizes the conditions of its existence, by chemical reactions which cause it to produce the special zymases depending upon its special nature and the various proximate principles varying according to the place and the medium where it functions in the organism. Isolated from the organism and consequently in new conditions, as in the case of fibrin, there are some which act like lactic ferment with regard to fecula, etc.
In short, the microzymas resist so well the ordinary causes of destruction that, in the calcareous and other rocks, geological microzymas are to be found, now living, which functioned as anatomical elements of the animals of the epoch of those rocks. Here then we have the organized being, living per se, physiologically imperishable, unsuspected until I described it.a It is in it alone, functioning as an anatomical element, wherein resides the permanent principle of reaction which enables the organisms, whereof it composes the cellules, the tissues, the organs, to preserve themselves by nutrition and resist the athmotelluric (Tripier) conditions which
[a. Literally "of which I spoke," but the real meaning is as given above in my translation.—Trans.]
unceasingly tend to destroy them. And as there is no anatomical element simpler than the microzyma, and none other like it, resistant to total destruction, if we call life the totality of the anatomical properties which render the microzymas constructors of cellules by synthesis, and capable of becoming bacteria or vibrios by evolution; and the aggregate of the physiological and chemical energies which enable them to produce the zymases and to nourish themselves by transforming for their own use the materials of the medium in the anatomical systems wherein they function, eliminating at the same time that which they disassimilate after having used it, it must surely be admitted that LIFE is, in them allied, it is true, to matter, but to the matter in the structured organization, morphologically defined, and not simply to ponderable matter. So much for the general statement.
We now know that the microzymas are functionally different in the various anatomical systems of the same animal, and that they may be functionally different also in the same organs of the same structure in man and animals. It thence results that it is not always permissible in experimenting to draw conclusions from one animal to another and least of all to man. So that if we could admit with Bichat that life is a property of tissue, this property is not the same in all the tissues of the same structure and in their microzymas.
I will endeavour to explain my opinion upon the cause which leads to one kind of zymas being produced by one microzyma and another kind by another microzyma.
If there is the life of a microzyma, the life of a cellule and that of the organs of an anatomical system, there is also the life of the organized WHOLE. This necessarily results from the coordinated entirety of the particular lives of the organs and I hence of the individual lives of the microzymas which function in it. It is this view of the functions which Bichat called I he entirety of the functions which resist death.
But if the microzyma is physiologically imperishable, what is the death of the living whole? It is the opposite of that which constitutes its life, viz.: the absolute decoordination of the functions of the microzymas.
It is thus that in a part abstracted from a living animal, muscle or blood, etc., nothing is dead; but the microzymas, the only things antonomically living, being in decoordination, are no longer in their normal condition of existence; they now function only for themselves, determining the changes which attend the disorganizations of the tissues and the destruction of the cellules."
Now what is the meaning of the happy expression, "individual coefficient," introduced into medical language by M. Tripier? As in algebra a quantity is said to be a function of another upon which it depends, so in the microzymian theory it may be said that an organism, a cellule, are quantities which are functions of the microzymas which compose it and upon which it depends. Thus the expression of coefficient applied to the number which multiplies these quantities can be readily understood.
The individual coefficient is the factor which increases or diminishes in the microzymas the sum of the energy which enables them to resist the various causes which, by disturbing their functioning, determine morbidity in them, and thence disease and death.
The factor, whatever it may be, being the same, the variable, that is to say, the microzyma, differing, the result will necessarily vary. Now it is a proven fact, the microzymas are functionally different in the species, in the races and even in the individual, according to sex and age, in the different anatomical systems; the individual coefficient then is relative to the functional differences of the microzymas of the individual.
The state of perfect health results from the constancy and regularity of the coordinated functioning of all the organs the microzymas whereof are anatomically and physiologically healthy; for even, in the state of coordination, it is necessary to take into account heredity, diatheses, atavism, which may in some way have affected the particular microzymas of the individual.
The individual coefficient then is a complex constant dependent upon the particular coefficients of such or such functional systems of the individual.
To return to the blood, here is a typical example which justifies the above considerations.
I said that in anthrax (sang de rate) the bacteridia, regarded as specific cause, were the result of the vicious evolution of the microzymas of the blood, become morbid as the consequence of a decoordination, M. Jaccond would say, of some disturbance in the physiological functioning of the organism.
But it is evident that if the interior medium were inert or passive, this decoordination, in such a mixture of proximate principles, would be an effect without a cause, nothing leading it to become disturbed in its supposed functioning; for such a mixture has been shown to be unalterable of itself; while on the contrary it would immediately, infallibly, be placed in a condition of alteration determined by the agent, microbe, or specific ferment come from without. In short, on the hypothesis of a pure interior medium, a mixture of proximate principles, for a soil of culture, as it is called, for the microbe whose multiplication is poisonous, all the sheep would be equally susceptible, especially in times of epidemic, to contract anthrax (sang de rate) under identical circumstances, by contagion, and in all cases by inoculation.
Well, this does not happen. The adult sheep of the race called the African sheep is refractory to anthrax; it does not contract the disease by contagion, and generally not even by inoculation. The individual coefficient is not the same under identical circumstances, for the French sheep and for that of Africa. And as proof that the coefficient differs according to age, it is enough to state that the African lamb is not refractory, while the adult sheep of the same race is. Let us then say that the microzymas in the blood of the African adult sheep are among those which, even when ill treated, do not undergo that vicious alteration which would make them become carbuncular; with the lambs of the same race it is otherwise.
If the internal medium were the mixture imagined by microbian medicine, the foregoing facts would be incapable of explanation. For the medium would be inert and passive; since it has been proved that such a mixture is always disposed to allow the multiplication of the microzyma or of another like specific ferment able to alter it for its (the ferment's) own nourishment, and which medium without the ferment would be unalterable under other ordinary athmotelluric influences, cold, etc. It is the individual coefficient in relation to the functional differences of the microzymas of the subjects which alone explains the immunity of some, the susceptibility of others, since it has been demonstrated that in the interior medium there is nothing autonomically living, acting and physiologically impressionable except the microzymas.
In the language of the old medicine, immunity, susceptibility, is the capacity of the living organism to resist an impression, not to undergo, or to undergo the influence of external or internal agents. The microzymian theory adopts this thoroughly physiological language since it is only the microzymas of the living organism which can receive impressions and suffer or not suffer their influence; that is to say, resist or not resist the perturbing causes of their functioning according as the individual coefficient is abnormal or normal.
But what proof have we of this resistance, and of the mechanism of the harmlessness of the microzymas from without? The following is one I have given of it.
The isolated microzyma of beer yeast performs the function of a lactic ferment, producing little alcohol; in its function of anatomic element in the globule of beeryeast it never produces lactic acid. The young yeast, vigorous, acting strongly on cane sugar, even in contact with the air and with the addition of the chalk whose microzymas always effect lactic fermentation, still does not produce lactic acid; it resists, and microzymas of the chalk when added also fail to produce it.
But if the beer yeast be old, in some respect altered,a and even protected from the air, it will produce lactic acid, and the more, if calcareous rock or even pure carbonate of lime has been added. There we have the immunity of the beeryeast organism and its acquired susceptibility; the immunity which enabled it to resist the influence of the microzymas of the air and of the chalk, annihilating their influence; the susceptibility which enabled these microzymas to produce lactic acid without hindering those of the chalk in performing their work. Here we have the picture of the immunity and of the susceptibility of the microzymas of the cellules and of the tissues of the internal medium of an animal organism."a1
[a. The French text is aleree, which, I believe, to be a press error fur alteree.—Trans.)
[a1. We are here presented with a forcible illustration of the reckless ignorance of those physicians who practice the inoculation of organic poisons, such as the products of diseased conditions known as vaccines, anti-toxines, etc., upon man and other animals, whether as preventives or as remedies. Even the changes mentioned in the text, as some of the results of the learnedly devised experiments of Prof. Behamp, are unknown to these gentlemen; and, absolutely ignorant of what effect such inoculations may have upon the life forces, i.e., the microzymas of their victims, they arrogantly insist that their ignorance is learning, and induce a degeneration among those races who, recognizing their ignorance, place their faith in men as ignorant as themselves!—Trans.]
In microbian medicine the language of the old medicine is without meaning, since the former admits that one sole cause produces the disease and the alteration by fermentation of organic matter in general, making no distinction between the internal medium and a mixture of proximate principles.
The insuperable contradiction which exists between the microbian doctrines and the microzymian theory of the living organization brings into strong relief the justice of the aphorism of M. Tripier. A single cause for the disease and for the alteration or fermentation of proximate principles, however specific it may be, is no cause at all (est une cause nulle).
Yes, "the sole cause" is no cause, for I have demonstrated beyond dispute that there do not exist (I do not say germs, the word now is unsuitable) pre-existing microzymas, pathogenic or not; but there do exist microzymas, the living remains of bacteria derived by evolution from the anatomical microzymas of organisms which have disappeared or are disappearing beneath our eyes.
I limit here these considerations, referring the reader to my earlier publications for developments, which the present work completes and corroborates.1
1. For general pathology, see the three last conferences of "Les Microzymas,"etc. For special pathology, the communications, "Sur la septicaemic puerperale," "Sur la Pleuresie" and "Sur les albuminuries," in "Microzymas et Microbes." And for the physiological theory of fermentation, as well as for the true theory of nutrition, various chapters of the same works. (Chamalet, publisher, 60, Passage Choiseul, Paris.)
And now I hope it will be confessed that the error, common to all contemporary experimenters who have sought to discover the cause of the phenomenon of the spontaneous coagulation of the blood, also that of other equally spontaneous alterations, or who, like M. Pasteur, maintain the natural inalterability alike of the blood, as of all natural organic matters, is that they have regarded protoplasm as a mixture of pure proximate principles, and have held as dogma that this mixture was living and organized, although not morphologically constituted. At last I hope that it will be recognized that the discovery of the microzymas verifies the time-honored conception of Bichat, according to which, that only is living in any organism whatever, which is structured, morphologically determinate.
It is the agreement of the microzymian theory of the living organism with the brilliant conception of Bichat which gives to the theory of the blood as a flowing tissue and to the physiological and anatomical theory of its coagulation and other spontaneous alterations their highest degree of certainty.
Under the form of conclusions is here given a succinct summary of the totality of the fundamental facts, the discovery whereof has led to that of the true anatomical and chemical constitution of the blood and to the explanation of its spontaneous alterations.
(1) Ordinary air, near the earth, contains living microscopical objects called germs, and these germs are essentially microzymas.
(2) Proximate principles, and any mixture of such principles are unalterable in the presence of water, of a limited volume of air at ordinary temperature when a little creosote has been first added; and such proximate principles under such conditions do not permit any organized being to appear.
(3) Natural organic matters, vegetable or animal, tissues and humors, under like experimental conditions, always change of themselves, by a phenomenon of fermentation, and at the same time the microzymas, give birth to vibrioniens by evolution.
(4) The fibrin of the blood is not a proximate principle; it is a false membrane containing microzymas, whereof the intermicrozymian gangue is a specialized albuminoid substance.
(5) It is owing to its microzymas that fibrin decomposes oxygenated water, that it liquifies starch of amidon and that it can be dissolved, undergoing chemical change, in very dilute hydrochloric acid.
(6) The microzymas of fibrin in liquified starch undergo vibrionian evolution notwithstanding the presence of creosote.
(7) Fibrin liquifies spontaneously in carbolized water without the microzymas undergoing vibrionian evolution.
(8) The fibrinous microzymas are special; they can produce lactic and butyric fermentation in liquified starch.
(9) Natural albuminoid matters are mixtures, reducible by direct analysis into exactly defined proximate principles.
(10) The albuminoid matters reduced to proximate principles are very complex molecules composed of less complex ones, amides and their derivatives of the fatty and aromatic series. There exist of such less complex molecules, constituting an albuminoid molecule, quaternaries like urea, quinaries like taurine, which is sulphuretted; like hematosine, which is ferruginous; casein, in addition to the sulphuretted molecule, contains one which is phosphuretted; it has then six elements.
(11) There are several fibrins constituted as are those of the blood.
(12) There are a great number of different specific albumens which coagulation does not differentiate.
(13) The zymas are special albuminoid matters, likewise definable as proximate principles; they are always a functional product of the microzymas.
(14) The yellow liquid of the blood, besides its albumen, contains a haemozymas.
(15) The haemoglobin of the red corpuscle, reduced to a
definite proximate principle, decomposes oxygenated water by its noncomplex feruginous molecule, haematosine, and becomes colorless.
(16) The red corpuscle of the blood is a true cellule, having a cell-wall and its proper content. This content is constituted especially of haemoglobin and micro-zymian-molecular-granulations, the microzymas whereof decompose oxygenated water as do those of the fibrin.
(17) The blood contains a third anatomical element, the haematic-microzymian-molecular-granularions. It is the albumenoid atmosphere of these granulations which form, by allotropic transformation, the intermicrozymian gangue of the false membrane called fibrin.
(18) The flowing tissue is a content, whereof the vessels, arteries, veins and their appendages form the container.
(19) The three orders of anatomical elements of the flowing tissue only find their conditions of existence complete in their containers during life.
(20) After issuing from the vessels these conditions of existence being no longer fulfilled, the alteration of the flowing tissue commences.
(21) The microzymas of the different parts of the circulatory system possess alike the property of decomposing oxygenated water without being absolutely characteristic of them, for the microzymas of almonds and of other parts of plants and of beer yeast also possess this property. But there are animal tissues whose microzymas do not disengagethe oxygen of oxygenated water.
(22) The microzymas, anatomical elements, are living beings of a special order without analogue.
(23) The spontaneous changes of natural animal matters, whether the microzymas have or have not undergone vibrionian evolution, thanks to free access of air, lead always under certain conditions to the complete destruction by oxydation of the product of those changes; that is to say, reduce them to the mineral condition, carbonic acid, water, nitrogen. But the microzymas under whose influence the oxydation is effected are not attacked; in such wise that all which is purely proximate principle in a tissue, in a cellule and in the bacterium, having undergone total destruction, the microzymas remain, and bear testimony to the existence of the vanished organization.
(24) The geological microzymas of certain calcareous rocks and of chalk, those of the dust of the streets and of the air also bear testimony to the microzymas which functioned as anatomical elements in the tissues of organisms of geological epochs even as they function in those of the present time.
(25) That which in the air have been called germs are essentially the microzymas of the entire destruction of a living organism.
(26) Normal air contains neither pre-existing germs nor the things which have been improperly termed microbes, supposed to ascend from age to age to parents resembling them.
(27) The air contains normally no pathogenic microzymas. The carbon bacteridium of Davaine is the product of the evolution of diseased microzymas, either of haematic-microzymian-molecular-granulations, or those of the blood globules.
(28) There is no living matter which is not morphologically defined; that which has been called protoplasm in the cellule always contains microzymas as anatomical elements.
Here, for persons whom it may interest, follows a list of memoirs and articles wherein may be found the historical succession of the ideas which have enabled the resume contained in the postface to be written:
On the influence which pure water or water charged with various salts exercise at a low temperature (a froid) upon cane sugar (moulds and spontaneous generations). Annales de chimie et de physique. 3e serie, Vol. XLVIII (1855 and 1856). C. R., Vol. XL, p. 436. and Vol. XLVI, p. 44, and Annales de chimie et de Physique, 3e serie. Vol. LIV, p. 28 (1858).
Memoir upon generations called spontaneous and upon ferments. Annales de la Societe Linne de Maine et Loire, Vol. VI (1863), and see C. R.. Vol. LVII. p. 958.
Note upon alcoholic fermentation. C. R,, de 1'Academic des Sciences, Vol. LVIII, page 601 (1864), and Montpellier Medical, Vol. XII.
Upon alcoholic fermentation. Reply to M. Berthelot C. R., Vol. LVIII, p. 1116 (1864).
On some new soluble ferments (Anthozymas). C. R.. Vol. LIX. p. 496 (1864).
On the origin of the ferments of wine. C. R,, Vol. LIX p. 626 (1864).
On the escape of heat as a product of alcoholic fermentation. C. R., Vol. LX, p. 241 (1865).
Memoir upon nefrozymase. Montp. Med.. Vols. XIV and XV.
On the cause which matures wines. C. R.. Vol. LXI. p. 408 (1865), and Vol. LXIX. p. 892 (1869).
On physiological exhaustion and on the vitality of beer-yeast. C. R., Vol. LXI, p. 689 (1865).
On the harmlessness of the vapors of creosote in the breeding of the silkworm. C. R. Vol LXII p 1341 (1866).
On the parasitic disease of the silk worm. C. R., Vol. LXIII. pp. 311, 341, 391, 425, 552, 693, 1 147 ( 1866), Vol. LXIV, pp. 231, 873,980, 1042, 1043. 1185 (1867); Vol. LXV, p. 42; Vol. LXVI, p. 1 160 (1868)-Vol I .XVII. pp. 102. 443 (1868); Vol. LXLX, p. 159 (1869).
(On the role of the calcareous earths in butyric and lactic fermentations, and of the living organisms which they contain (microzymas). C. R., Vol. LXIII, p. 451 (1866).
Microzymas in the waters of Vergeze. C.R.,Vol.LXIII, p.559, and Bull.Soc.Ch.,Vol.VI,p.9,and Vol. VII, p. 159 (1866).
On the role of the microscopic organisms of the mouth in digestion, and especially in the formation of the salivary diastase: in common with Prof. Estor and Saintpierre. Mont. Med., Vol. XIX
On the molecular granulations of fermentations and of the tissues of animals (microzymas). C. R., Vol I, XVI. pp. 366. 1382(1868).
On the nature and function of the microzymas of the liver; jointly with Prof. Estor. C. R,. Vol. UCVI, i I, 'I (IHftS).
On the origin and development of the bacteria; jointly with Prof. Estor. C. R.. Vol. LXVI, p. 859 (IHftH)
On the reduction of nitrates and sulphates in cenain fermentations. C. R., Vol. LXVI, p. 547 IIIU.H)
On the spontaneous alcoholic and acetic fermentation of eggs. C. R.. Vol. LXVII. p. 523 (1868).
On the microzymas of pulmonary tubercle in the cretacious state; jointly with Prof. Estor. C. R., Vol. LXVII. p 9600 (1868)
Facts to serve for the history of the origin of bacteria; natural development of these little plants in the frozen parts of several plants. C. R., Vol. LXVIII. p. 466; Mont Med., Vol. XXII, p. 320 (1869).
Conclusions relating to the nature of the mother of vinegar and the microzymas in general. C. R., Vol I XVIII, p, 877; Gazette Medicale de Paris, 8 May, 1869.
On the alcoholic fermentation by the microzymas of the liver. C. R., Vol. LXVIII, p. 1567 (1869).
Researches relating to the microzymas of the blood and the nature of fibrin; jointly with Prof. Estor. C.R Vol. LXIXp 713 (1869).
Note for use in the history of the microzymas contained in animal cellules; by Prof. Estor. C. R., Vol. LXVII, p 529
On the nature and origin of the blood globules; jointly with Prof. Estor. C. R, Vol. LXX, p. 265 (1870)
On the geological microzymas of divers sources. C. R., Vol LXX p. 914 (1870).
On the carbonic and alcoholic fermentations of sodic acetate and of ammonium oxalate. C. R., Vol. LXX. p 69 (1870).
See also:
On the circulation of carbon in nature and the instruments of this circulation; exposition of a chemical theory of the life of the organized cellule; by A. Bechamp, Paris, Asselin; Montpellier, Seguin.
Of the microzymas of the higher organisms; by Messrs. A. Bechamp and A. Estor. Mont. M ed., Vol. XXIV, p. 32.
Exposition of the physiological theory of fermentation, according to the researches of Prof. Bechamp, by M. Estor. Messager du Midi (1865).
[The student is to understand that the above list comprises but a small fraction of the scientific work of the late Professor A. Bechamp; a fuller list, though still imperfect, occupies eight of the large folio pages of the Moniteur Scientifique (Paris) for December, 1908, and these labors were spread over fifty-three years, from 1853 to 1905 inclusive. Genius, has been defined as, in one aspect at least, the "faculity for taking infinite pains," and this faculty was possessed by M. Bechamp in an almost infinite degree.
The world has yet to learn how much it owes to this remarkable genius. The acknowledgment will be resisted by all those interests which fatten upon the ignorance and trusting confidence of the people. But thanks to his researches and discoveries it cannot be long before the medical profession will recognise the dangerous errors into which it has been led by those who succeeded in establishing a "conspiracy of silence" around Bechamp and his discoveries.—Trans.]
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