Guest guest Posted March 15, 2004 Report Share Posted March 15, 2004 http://coldcure.com/html/dep.html Rapid Recovery From Depression Using Magnesium Treatment DEPRESSION REALLY SUCKS! It needlessly sucks happiness and joy out of a person and may even suck the life out too if it can't be brought under control. I believe that curing stress- and/or diet-induced depression is extremely simple and quick using magnesium rather than drugs for many people - fortunately! Read my story and check out the facts in the links. Many links are directly to medical articles in the National Library of Medicine (PubMed) and other authoritative sources. You may find my story to be important to you. Remember my point of view that depression, and particularly stress- and/or diet-induced depression, and many other " diseases " discussed below are often symptoms of magnesium deficiency (either directly or indirectly through excess stress) and not diseases. The National Institute of Health (NIH) reports that a sign of magnesium deficiency is depression. NIH defined magnesium deficiency symptoms have three categories: Early symptoms include (one or more) irritability, anxiety (including Obsessive Compulsion Disorder (OCD) and Tourette syndrome), anorexia, fatigue, insomnia, and muscle twitching. Other symptoms include apathy, confusion, poor memory, poor attention and the reduced ability to learn. (NOTE: If this essay appears difficult to understand, consider your magnesium status.) Moderate deficiency symptoms can consist of the above and possibly rapid heartbeat, irregular heartbeat and other cardiovascular changes (some being lethal). Severe deficiency symptoms can include the one or more of the above symptoms and one or more severe symptom including full body tingling, numbness, and a sustained contraction of the muscles, along with hallucinations and delirium (including depression) and finally dementia (Alzheimer's Disease). If the NIH knows this, why don't doctors use magnesium to treat depression and other mental (and physical) disorders??? In 1989, C. Norman Shealy M.D., Ph.D. demonstrated that 99% of depressed patients have one or more neurochemical abnormalities; and that depression is a chemical disease as is diabetes, not a psychiatric disease. It seems to me that not using magnesium to treat depression is pure malpractice! We could rebuild and save lives! Magnesium ions are shown involved at the very heart of neural synaptic activity in this figure. Are you magnesium depleted or deficient? See this wonderful quick quiz by Dr. Pricilla Slagle, M.D., a magnesium expert very interested in helping people with magnesium problems. Also, visit Dr. Hertert C.Mansmann, Jr., MD at THE MAGNESIUM RESEARCH LABORATORY, another very interested magnesium expert. Magnesium deficiency is a major risk factor for heart problems and diabetes and many other heatlh issues, including sudden death. " The Magnesium Factor " by Mildred S. Seelig, MD, MPH and Andrea Rosanoff, PhD is an outstanding new book by the world's leading magnesium researcher and is highly recommended reading for learning how to prevent high blood pressure, heart disease, diabetes, and other chronic conditions. Many of today's " diseases " are actually " symptoms " of magnesium deficiency, and are not diseases. For another eye opener, see this amazing list and thorough documentation of hundreds of " diseases " that are often nothing more than magnesium deficiencies. What would happen to " medicine " , pharmaceutical company income, and public health if these " diseases " were treated with magnesium before trying side-effect laden drugs? Wouldn't this approach to improving public health be more ethical? Unfortunately, for space reasons, this essay is restricted to mental health issues reasonably related to depression, but the health risks resulting from magnesium deficiency are very broad and need much exploration. Depression Defined Depression is an extremely common condition that affects more than 1 in 20 people in any one year in Western society. It is one of several hyperemotional states. A sudden loss of interest in life combined with a feeling of worthlessness may be associated with depression. Normally joy, sadness and grief are parts of everyday life. While a short period of depression in our response to daily problems is normal, a long period of depression and sadness is abnormal and is called " clinical depression " . Depression can run in families, partly because families tend to eat the same foods and pass from one generation to the next similar eating patterns, and partly through genetics. Concerning genetics, I have found no evidence in the medical literature of a " depression " gene, but much evidence for a search for one. I suspect that the strong genetic component will be found to involve improper or inadequate magnesium metabolism. Depression may be associated with a variety of symptoms, including but not limited to: Persistent sadness and pessimism Feelings of loneliness, guilt, worthlessness, helplessness, or hopelessness Loss of interest or enjoyment in nearly every aspect of life Diminished ability to think or lack of concentration Insomnia or oversleeping Poor appetite associated with either weight gain or loss Fatigue, lack of energy Physical hyperactivity or inactivity Loss of interest in sex Physical symptoms such as headache, backaches, stomach troubles, constipation and blurred vision Anxiety, agitation, irritability Thoughts of suicide or death (90% of suicides result from depression) Slow speech; slow movements Drug or alcohol abuse A drop in school performance Most depressive episodes are triggered by stressful personal event such as loss of a loved one or change of circumstances, and depression over a short period is a normal coping mechanism. Long-term stress-induced depression often, if not always, results when magnesium levels fall to dangerously low levels in the body by biochemical stress reactions discussed below. Magnesium deficiency related depression is a fixable biochemical problem and not necessarily a physiological problem. Depression can also be due to many other factors such as underlying disease (particularly hepatitis C), brain chemical imbalances requiring antidepressant drugs of one type or another, hormonal imbalance (particularly hypothyroidism and low testosterone), low cholesterol, Wilson's Disease, food allergy (particularly gluten intolerance), and adverse reaction to medications, each of which requires professional care. Magnesium deficiency is not necessarily the only cause of depression, but it can be very useful in recovering from depression because the blood and body often become depleted of magnesium in depression, particularly stress-induced or diet-induced depression. Often, depression that does not respond to SSRI's (classical antidepressants) will respond best to treatment with magnesium. Symptoms listed for paying for magnesium serum level tests to detect hypomagnesemia (low blood levels of magnesium) by a major United States insurance carrier include depression. However, magnesium is an intracellular cation, and its only valid measurement is through Intracellular spectroscopy testing, or red blood cell (not whole blood or serum) testing. A huge list of diseases and health conditions meriting magnesium status testing is here. Not too certain what your problem is? If you are interested in knowing generally about mental health issues generally, look through the Mental health Net site. If you are interested in what life as a manic depressive (bi-polar) is like, You can test your own level of mania on the Goldberg Depression Inventory here, and depression here. MY STORY From early 2000 to summer of 2003, this essay focused upon magnesium glycinate as the preferred source of magnesium. Now, in late summer of 2003, I have shifted emphasis from magnesium glycinate to magnesium taurate, which appears superior to all other forms of magnesium in treating treatment resistant depression. Other effective magnesium compounds mentioned throughout this essay are ranked well behind magnesium taurate and are not recommended unless magnesium taurate can not be obtained. Also, I have major PRECAUTIONS at this link concerning ineffective and harmful compounds of magnesium for treating depression. After years of study, I remain truly amazed at the tremendous benefits of magnesium and other nutrients in treating and preventing depression. In particular, I see magnesium as an important research topic for survival considering its limited availability from our Western diets and its ability to inexpensively cure and prevent many expensive diseases, life threatening or not. As you will see from this essay, our dietary choices and our overconsumption of certain foods are contributing to massive illness, including depression. I know how bad depression can be, because I spent September of 1999 through April of 2000, in a clinical depression that worsened from the beginning. By Christmas the depression suddenly became much worse, nearly suicidal in intensity, and remained that way for four more months. I had always thought that I was a mild hypo manic-depressive, not a suicidal idiot. In my highs I was capable of deep, insightful thought and amplified abilities in general which I considered to be an advantage. Never did I think that things could go so wrong with my biochemistry that it would cause me to have suicidal thoughts and tendencies. How wrong I was. I had been taking Zoloft (an antidepressant) since 1987 which seemed to take care of my depression. I lived on Zoloft, but by September of 1999, it stopped working, - and I knew that something was really wrong. My depression was preceded by many years and accompanied by major stress from over-work, treatment responsive depression, anxiety, hypomania, fibromyalgia, infrequent panic attacks, anger, stress, poor diet, overwhelming emotional feelings, night time muscle spasms, paranoia, asthma, prickly sensations in hands, arms, chest and lips. I wanted to sleep all day and had trouble getting up in mornings. Occasionally my lips felt that they were going to vibrate or tingle off my face. I even saw a spider disappear into my arm once. About 10 years ago, I had a very painful bout with calcium oxalate kidney stones, a recognized sign of magnesium deficiency. A few weeks before I was hospitalized in January of 2000, I had very low energy, mental fogginess, depression with strange suicidal thoughts and I was under enormous stress. Now, I can recognize these " mental " symptoms as symptoms of magnesium deficiency and/or calcium toxicity. I won't bother you with the details of my hospitalized depressive episode, except to say that I was put on nearly every antidepressant drug known and had severe side effects to all of them and felt sicker and sicker. None worked. I lost a lot of weight, and I was extremely constipated. I also had a cardiac arrhythmia. Being disgusted with the treatment provided, I went home. I couldn't work and about all I did was sleep, eat cheese, hard candy, fatty foods, bread, ice cream, tapioca pudding, drink a lot of milk, consume other bad-for-you high-calcium delicacies, watch TV and read. Maybe I secretly figured that if I didn't die slowly and agonizingly from depression, maybe I would die quickly with a heart killing diet. My reading preferences are in the biomedical field. At home, I researched medical journals, books and everything medical that I could find on depression and manic depression. I learned nothing of usefulness, at least nothing that my doctor had not already told me. I did find that certain foods like wheat and high carbohydrate diets can trigger dysphoric rage and depression, so it seemed to me that correcting nutritional problems should be beneficial, and that nutritional research would be worthwhile. On April 12, 2000, I looked like I was dying to several people important in my life. My psychiatrist agreed and took me off all antidepressant medications and put me on a tiny amount of lithium carbonate (150 mg twice a day). NOTE: At the end of each following section of this essay, I have placed a link concerning my rules for success, and the affirmation that " Depression is not a psychosis. " . I apologize ahead of time for being terribly redundant. My rules and my understanding of mood disorders as a magnesium deficiency are so commonly ignored, that I decided they were too important not to heavily emphasize. Cured with Lithium or Magnesium? Shortly later, I picked up a 1975 copy of Nutrition Almanac, McGraw-Hill Book Company, New York, and happened to open it to the magnesium section. I was interested to find that magnesium was low in the serum of people who were suicidally depressed and others who were seriously depressed. The article indicated that magnesium dietary supplements had been effective in treating depression. Also, a person with a magnesium deficiency is apt to be uncooperative, withdrawn, apathetic, nervous, have tremors... essentially lots of neurological symptoms associated with depression. I was fascinated to notice that cardiac arrhythmias, heart attacks and kidney stones were also mentioned as magnesium deficiency related. Ah-ha! These looked like good clues, but definitely not convincing. That same day, I found the next clue in my library. It was in a 1995 textbook in which I had a published article about zinc lozenges and the common cold. In Handbook of Metal-Ligand Interactions in Biological Fluids - Bioinorganic Medicine, volume 2, Marcel Dekker, Inc., New York, there is a chapter by Durlach et al, entitled " Diverse Applications of Magnesium Therapy " . Its authors assert that in their clinical and open trials they found symptoms of chronic magnesium deficiency in neuroses to include anxiety, hyper-emotionality (could this be crying, grieving or other forms of depression?), fatigue, headaches, insomnia, light-headedness, dizziness, nervous fits, lump in throat, blocked breathing and respiration, cramps, strong tingling, pricking, creeping feeling on the skin having no real cause, chest pain (either of a cardiac nature or not), palpitations, dysrhysthmias, Raynaud's syndrome, and more including latent tetany, constipation, and myocardial infarction. Some of these symptoms were stated as occurring as part of panic attacks, sometimes with the feeling of imminent death. In a paper by the same group, Durlach showed that aging was a risk factor for magnesium deficiency. In another Durlach article, magnesium deficiency and dementia were equated as being one and the same. In another paper, Singh et al. showed that magnesium status was inversely associated with prevalence of coronary artery disease. I had a calcium oxalate kidney stone a few years ago and was told that I needed to increase my dietary intake of magnesium. I didn't but now wish that I had because it is established that magnesium prevents calcium oxalate kidney stones. Of significant interest was Durlach's statement that chronic primary magnesium deficit affects about 15 to 20 percent of the Western population, while other sources more recently place the deficit much higher at nearly 70 percent. One reason given for the deficit is that magnesium-rich foods are rich in energy (fattening), and they are being avoided in an effort to maintain weight, and because we are eating more junk food void of magnesium. Wow! This magnesium/depression hypothesis is coming together! Just a few months previous to the onset of my depression, I had been hospitalized for chest pain, cardiac dysrhysthmia and an inability to take in more than about 1/5 my normal breath. The hospital found no cardiac problems, and the internist gave me an IV drip of magnesium sulfate solution. A few hours later all of those symptoms vanished as rapidly as they had come. What I was beginning to see was that nearly all illnesses in my adult life were magnesium deficit related. From which foods do we get magnesium? According to my Nutrition Almanac, a cup of peanuts or almonds would satisfy the RDA for magnesium, while only 1/4 cup of kelp (Warning! very high in glutamate) would be needed. Soy flour, bran flakes, whole wheat, raw brown rice, avocado, wheat bran, shrimp, tuna, Brazil nuts, cashew nuts, sesame seeds, walnuts and collard greens also supply significant dietary magnesium. In the audio Bible, Genesis 1:29 - " God said, Behold, I have given you every herb bearing seed, which is upon the face of all the earth, and every tree, in the which is the fruit of a tree yielding seed; to you it shall be for meat. " I marvel at the similarity of Biblical teaching to the above list of foods containing large amounts of magnesium. Succeed! Depression is not a psychosis! NIH Table of Food Sources of Magnesium The National Institute of Health has prepared the following food table showing the best sources of magnesium in the U.S. diet. Look at it! They are nearly all highly fattening foods. I would rather not get fat and just take my magnesium supplements to handle my depression problems. The very idea of loading up on these fattening foods should make anyone depressed. The government is a robot saying over and over " cut down on fattening foods " for your health! BS! For us manic depressives and depressives, following the NIH dietary guidelines suggested in the NIH link on keeping magnesium intake low is suicidal, not just because they limit our intake of magnesium, but of other extremely critical nutrients including taurine, boron and Essential Fatty Acids (EFA) such as the Omega-3 EFAs. Even so, the NIH admits that a sign of magnesium deficiency is depression. Even though the NIH list appears accurate, it may be misleading for us because many of these foods have much more calcium than magnesium. Excess calcium over magnesium inhibits absorption of magnesium from the diet. A list of foods in this web page having more magnesium than calcium is here. Food Milligrams %DV Kelp 100 grams (Warning! very high in glutamate)760 190 Alfalfa 100 grams230 58 Avocado, Florida, 1/2 med103 26 Wheat germ, toasted, 1 oz90 22 Almonds, dry roasted, 1 oz86 21 Cereal, shredded wheat, 2 rectangular biscuits80 20 Seeds, pumpkin, 1/2 oz75 19 Cashews, dry roasted, 1 oz73 18 Nuts, mixed, dry roasted, 1 oz66 17 Spinach, cooked, 1/2 c65 16 Bran flakes, 1/2 c60 15 Cereal, oats, instant/fortified, cooked w/ water, 1 c56 14 Potato, baked w/ skin, 1 med55 14 Soybeans, cooked, 1/2 c54 14 Peanuts, dry roasted, 1 oz50 13 Peanut butter, 2 Tbs.50 13 Chocolate bar, 1.45 oz45 11 Bran (pure), 2 Tbs44 11 Vegetarian baked beans, 1/2 c40 10 Potato, baked w/out skin, 1 med40 10 Avocado, California, 1/2 med35 9 Lentils, cooked, 1/2 c35 9 Banana, raw, 1 medium34 9 Shrimp, mixed species, raw, 3 oz (12 large)29 7 Tahini (from sesame seed), 2 Tbs28 7 Raisins, golden seedless, 1/2 c packed28 7 Cocoa powder, unsweetened, 1 Tbs27 7 Bread, whole wheat, 1 slice24 6 Spinach, raw, 1 c24 6 Kiwi fruit, raw, 1 med23 6 Hummus, 2 Tbs20 5 Broccoli, chopped, boiled, 1/2 c19 5 *DV = Daily Value. DVs are reference numbers based on the Recommended Dietary Allowance (RDA). They were developed to help consumers determine if a food contains very much of a specific nutrient. The DV for magnesium is 400 milligrams (mg). The percent DV (%DV) listed on the nutrition facts panel of food labels tells adults what percentage of the DV is provided by one serving. Even foods that provide lower percentages of the DV will contribute to a healthful diet. Wow! I am lucky to be alive! My diet had excluded all magnesium rich foods for months. I wonder if people who go on diets delete these critical foods from their diet, start to feel a bit low, and rightfully decide to forget dieting. It is well known that some people must eat fattening foods simply to feel well. Is magnesium demand from fattening foods the link between fat people and depression avoidance? I know that I am not as hungry using magnesium supplements. Actually, I think the cure for hunger is magnesium, because the foods (mainly wheat) that used to be our main source of magnesium and other nutrients are no longer good sources for them. A few days after digesting what I had learned, I checked MedLine for some backup. I looked up " magnesium " AND " depression " . Sure enough it was there. Calcium/magnesium imbalances with magnesium being low were found in depressed patients that had attempted suicide. Other articles supported the concept too. For example, high serum and cerebrospinal fluid calcium / magnesium ratios were found in recently hospitalized acutely depressed patients. The further I looked on the web, the more exciting and proliferate the became - which, hopefully, is reflected in this page. Another book in my library, The Dictionary of Minerals, Thorsons Publishing Group, New York, point-blank read, " Therapy with magnesium has been used to treat ...mental depression... " . Magnesium has recently been medically demonstrated to reduce severe therapy resistant mania. That was enough evidence for me. That same day I purchased magnesium glycinate, a non-toxic dietary supplement found in a local health food store. How much should I take each day? Was it safe? I really didn't know and didn't much care. I made a decision to start out with about 3 times the 400 mg/day RDA for magnesium, with 400 mg in the morning, 400 mg mid afternoon and 400 mg at bedtime. I used Carlson's chelated magnesium glycinate (200 mg magnesium elemental) product. I was an optimist by this time so I bought 3 bottles. What did it taste like? To me the first few times I used magnesium glycinate it tasted strangely metallic. But taking it with milk it didn't taste metallic at all. This is an important observation that merits explanation. There are chemicals in milk fats and other food fats that bind magnesium and other bioactive minerals to biologically inactive state. That may be a reason why fatty foods are bad for the heart. One might consume enough magnesium to fulfill the RDA, but if the magnesium is bound so tightly to a stearate or oleate that it is non soluble and is excreted through the feces without being absorbed into the blood, what good is it? What happens to the heart? Heart attack! I think this is why some in the FDA think the RDA for magnesium should be raised to about 900 mg per day. Other people using magnesium glycinate have not noticed any strange metallic taste. Within a few days to a short week, I felt remarkably better, my depression lifted noticeably, but I was getting a bit of diarrhea. Yeah! I didn't need that damned lithium corkscrew anymore!! (just kidding). Oh, the taste of those tablets! I needed some coated magnesium glycinate tablets. Actually, the taste was bad during the first few weeks only, after that the taste was not noticeable. Who knows what that means. Within a week to 10 days of starting magnesium, I felt close to being well. I looked so well, that my psychiatrist thought I looked better than he had ever seen me. One interesting fact from The Dictionary of Minerals is that lithium intake is associated with an increase in magnesium, calcium and phosphate blood serum concentrations. A possible explanation for these findings is that Li+ displaces Mg2+ from intracellular binding sites. As I improved, I lowered my dosage of magnesium to find the best dosage for me. I lowered it too much and symptoms rapidly came back. Eventually, I stabilized the dosage at four 200-mg elemental magnesium (as magnesium glycinate) tablets a day. Four hundred mg is the RDA for magnesium for men. Succeed! Depression is not a psychosis! June 7, 2000 My depression is completely, totally, absolutely gone, gone, gone! I am active and can function mentally, emotionally, and physically at my best again. No more cardiac arrhythmia! Not only that, my vision and bowels have also returned to normal - finally. I consider myself to be back to my good old normal self - although my critics will never admit that I am normal and have never been normal. Whatever normal is. Yet, a strange anxiety that the depression would return remained unabated. What caused my rapid recovery after being a treatment resistant, non-responder for many months? Did going off those antidepressant meds cause it? Was it my imagination? Would I have gotten well anyway? Was it just the lithium? I seriously doubt it. My bet is on repletion of magnesium, both by dietary supplementation and action by lithium in increasing blood serum levels of magnesium. I can now see that my diet has been deficient in magnesium for years. My diet did not include high-in-magnesium foods listed above. Worse, I had been on a magnesium depleting diet from eating fatty foods and ingesting too much calcium. If I hadn't realized my magnesium problem, I probably would have died of a heart attack, like these guys warn. I repleted my body with magnesium, but did not use a great excess of magnesium as such might be toxic. If you have time, search the above link's depression links, and do a search or two for " depression " , " suicide " and " serotonin " . When I conducted a mini search, I was overwhelmed with relating magnesium deficiency with mental illness. Succeed! Depression is not a psychosis! Stress as Ultimate Cause of Depression If you are a medical or science type you might like to read Mechanisms of Action on the Nervous System in Magnesium Deficiency and Dementia. One paragraph in this link is so important that I quoted it here: " Although a neurosis pattern due to magnesium deficiency is frequently observed and simply cured through oral physiological supplementation, neuroses are preeminently conditioning factors for stress (thus increasing demand for magnesium). Neuroses may therefore very frequently produce secondary magnesium depletion. They require their own specific anti neurotic treatment and not mere oral magnesium physiological supplementation, but both genuine forms of neurosis due to primary neural magnesium deficiency and magnesium depletion secondary to a neurosis may exist. These two conditions may be concomitant and reinforce each other. In these stressful patients it may be difficult to establish the primacy of one or the other. In practice, physiological oral magnesium supplements may be added to psychiatric treatments, at least at the start. " I interpret this to mean that magnesium alone can prevent stress from resulting in neuroses. Stress intensifies release of two major classes of " stress hormones " , the catecholamines and corticosteroids, which normally greatly increase survival of well animals when their lives are threatened. Catecholamines are chemically similar small molecules derived from the amino acid tyrosine. The major catecholamines are dopamine, norepinephrine, and epinephrine (old name: adrenalin). Dopamine is a neurotransmitter (a chemical used to transmit impulses between nerve cells) found mainly in the brain. Norepinephrine is the primary neurotransmitter in the sympathetic nervous system (controls the " fight or flight " reaction) and is also found in the brain. Epinephrine is not only a brain neurotransmitter, but also a major hormone in the body. Epinephrine is secreted from the adrenal medulla in response to low blood glucose, exercise, and various forms of acute stress (in the latter case, the brain stimulates release of the hormone). Epinephrine causes a breakdown of glycogen to glucose in liver and muscle, the release of fatty acids from adipose tissue, vasodilation of small arteries within muscle tissue, and increases the rate and strength of the heartbeat. All of the catecholamines are metabolized by their target tissues or by the liver to become inactive substances that appear in the urine: For example, dopamine becomes HVA, norepinephrine becomes normetanephrine and VMA, and epinephrine becomes metanephrine and VMA. Consequently, a urine test for elevated catecholamines is both simple and available. Corticosteroids are group of natural and synthetic analogues of the hormones secreted by the hypothalamic-anterior pituitary-adrenocortical (HPA) axis, more commonly referred to as the pituitary gland. These include glucocorticoids, which are anti-inflammatory agents with a large number of other functions; mineralocorticoids, which control salt and water balance primarily through action on the kidneys; and corticotropins, which control secretion of hormones by the pituitary gland. They have been thorougly researched and developed as drugs in the treatment of many diseases. Corticosteroids are used to provide relief for inflamed areas of the body. They are extremely strong drugs. They lessen swelling, redness, itching, and allergic reactions. They are often used as part of the treatment for a number of different diseases, such as severe allergies or skin problems, asthma, arthritis and certain cancers and leukemias. They have many well-known side effects. When magnesium deficiency exists, stress paradoxically increases risk of cardiovascular damage including hypertension, cerebrovascular and coronary constriction and occlusion, arrhythmias, sudden cardiac death (SCD), asthma, anxiety and depression. Dietary imbalances such as high intakes of fat and/or calcium (Ca) can intensify inadequacy of magnesium, especially under conditions of stress. Thus, stress, whether physical (i.e. exertion, heat, cold, trauma - accidental or surgical, burns), or emotional (i.e. pain, anxiety, excitement or depression) and dyspnea (difficulty in breathing) as in asthma increases need for magnesium. Magnesium deficiency intensifies adverse reactions to stress that can be life threatening. Such reactions are mediated by excess release of the stress hormones, catecholamines and corticosteroids, which are increased by low magnesium and high calcium levels, and which further lower tissue magnesium in a feed back fashion, and suppress testosterone production. More on the consequences of magnesium deficiency on the enhancement of stress reactions; preventive and therapeutic implications is here and in the following figure. Genetic differences in magnesium utilization may account for differences in vulnerability to magnesium deficiency and differences in body responses to stress. There are so many stressors in our active lives that adversely affect magnesium reserves; it is a miracle that we can live on our puny magnesium deficient diets without vastly more cardiac and psychiatric problems. Magnesium is a required nutrient for people to handle stress in general and stress in neuropsychiatric disorders. Not getting sufficient dietary or supplemental magnesium during medical treatment for stress related disorders such as anxiety and depression is bound to fail. A short and easy to read summary of magnesium and its stress relief action is presented here by Dr. Leo Galland. He points out that stress depletion of magnesium is often so intense that dietary sources are insufficient, and supplementation is required. Measure your level of stress here. These effects and aggressive behavior are easily observed in the mouse model. Magnesium is now marketed as an anti stress mineral. Stress, diuretics, fluoride, refined flour, chemotherapy, too much sugar, antibiotics, large amounts of protein, and high fat foods decrease absorption of magnesium, as do foods high in oxalic acid (mainly fresh spinach and possibly tea in excess) which deplete magnesium in the body, which in turns lowers one's resistance to stress and depression (a feedback loop). Overweight and obese people are usually low in magnesium, a mineral necessary to metabolize (burn) fat. People working outside in high temperatures and high humidity often become magnesium deficient and have stress related problems. What blows my mind is that there has already been an extraordinary amount of work collecting data that shows magnesium to be a profoundly important nutrient in preventing and treating hundreds of illnesses and conditions, particularly those illnesses related to stress. It seems that magnesium deficiency in our diet is responsible for many forms of bad health and early death. Don't take my word for it, rather visit Paul Mason's site and see his huge list of magnesium treatable disorders. Also, the Health-World web site has a growing but still incomplete list of magnesium deficiency symptoms, which include (alphabetically) acute heart attacks, agoraphobia, anxiety, angina pectoris, asthma, back aches, breast tenderness, cardiac arrhythmias, chronic fatigue syndrome, can't take a deep breath, carbohydrate craving (especially of chocolate) and carbohydrate intolerance, chest tightness, chronic cardiovascular disease, chronic fatigue syndrome, coronary artery disease, cramps, depression, diabetes, difficulty swallowing, eclampsia of pregnancy, feeling uptight, frequent sighing, epilepsy, headaches, high blood pressure, hyperactivity, insomnia, jaw joint (TMJ) dysfunction, lump in the throat-especially provoked by eating sugar, menstrual cramps, muscle soreness, muscle tension, mitral valve prolapse, musculoskeletal disorders, neck pain, numbness, palpitations, panic disorder, pre-eclampsia, premenstrual irritability, photophobia, panic attacks, restlessness with constant movement, salt craving, tingling, twitches, urinary spasms, zips, zaps and vibratory sensations. I remain amazed and perplexed that magnesium deficiency remains, for the most part, ignored, neglected, and forgotten. There is one medical journal Magnesium Research that reports the subject very well, but it is a very difficult journal to find in nearly all medical libraries. It is the official organ of the International Society for the Development of Research on Magnesium. Their first publication date was July, 1988, which makes it a johnny-come-lately among medical journals. The publisher is John Libbey and Company in London. Typically, magnesium researchers find that their work finds no interest by other journal editors, and they end up submitting their work to Magnesium Research simply to get it published, where it is totally ignored by establishment medical doctors and, until recently, remained the subject of academic curiosity. Fortunately, independent-minded physicians and citizens can research the National Library of Medicine's PubMed index and find these precious life-sustaining journal articles. Paul mason is trying to bring much original research on magnesium and health to the Internet. The full text of many vital magnesium and health articles can be directly viewed at this vital link. It seems to me that by ignoring these magnesium deficiency disorders, that medicine has a guaranteed retirement fund. What do I mean? Look at the above list, and other similar lists carefully and you will see that much of medicine is dedicated to developing medications for, and treating these specific symptoms and not treating the underling cause (magnesium deficiency). Consequently, patients remain ill and return to doctors' offices for more expensive drugs. Folks, billions of dollars of pharmaceutical drug company income and physician income is at stake! Be warned! Can I be so obtuse as to say that magnesium supplementation had nothing to do with my recovery? Can I be so callous as to not recommend magnesium to others who are suffering from depression, bi-polar disorder, or any of the anxiety related symptoms listed above? Or any of the symptoms of magnesium deficiency listed here? Duh!!! I am positive that all suffering from clinical depression want relief - NOW! No waiting for a med to kick in 4 to 8 weeks! You want it now!!! However, without sufficient magnesium, recovery will most likely be very difficult and prolonged. Succeed! Depression is not a psychosis! January 19, 2001 Update and Miscellaneous Musings Looking back over the last year, I now realize that the increases in lithium that I was prescribed (a gradual increase from 300 to 1050 mg lithium carbonate per day) was associated with progressive reductions in feeling of well being (sort of a placid zombie-like feeling) and pending damage to thyroid function (excess lithium causes hypothyroidism). On December 5, 2000, I decided that it was imperative for me to stop lithium because I did not want to have to be dependent upon thyroid extract for the rest of my life due to the toxicity of lithium. Even though lithium is a mineral element, it is not found in the human diet except in trace amounts (which are related to even temperament). However, magnesium is a vital to life essential human nutrient. I.E. there is no RDA for lithium (or any drug), but there is for magnesium! Actually, lithium is a drug that is being used to sustitute for a nutrient, magnesium! How tricky of those docs! What a way to drum up business! Surprisingly, I began to feel better, even better than I felt in June when I first started taking low-dose lithium and high-dose magnesium. After several months off of lithium, people say I look ten years younger. I feel much sharper and my mental capabilities have returned to what is normal for me. I hope that I will never again take lithium. I now strongly suspect that the main biochemical function of lithium is to raise magnesium levels in the blood as mentioned above, with the mental benefit coming not from lithium but from lithium induced increased magnesium blood levels. This idea could account for the 40 percent failure rate of lithium in preventing future depressive episodes. That is to say, if dietary magnesium intake is so low that not even lithium can return it to normal levels, then one succumbs to depression or other magnesium deficiency disorders. I remember meeting people (in group therapy classes and elsewhere) that looking backward seem likely to have been magnesium deficient. I remember a bright young lady that was terribly suicidal. She was totally resistant to all known antidepressants. She was so thin that she was nearly skin and bones and obviously was malnourished. She wanted to commit suicide so badly that she was under constant supervision. I can't help but wonder if she was misdiagnosed, meaning that she was severely, gravely magnesium depleted. I remember meeting many other people who were depressed; one was a single female registered nurse, who was overwhelmed by her stressful hospital duties and her desperate family child care situation. I remember a lovely young suicidal woman whose favorite tune was the theme from M*A*S*H. Apparently, she had no idea of the lyrics to the song " Suicide is Painless " . She had been pounding out that song on piano for years. I wonder if she would have been there had her favorite song been something else. A 40ish man who could no longer accept that he was, in his opinion, a failure in his business. A lawyer who couldn't handle further domestic abuse. An internationally acclaimed scientist and editor who was overwhelmed by his time-line oriented job. Young children who were sad all of the time for no apparent reason, even if they were given all the toys they wanted. There was a young gay who desperately didn't want to be gay. Each of these people, and I suspect most depressives, share one thing common in their lives. STRESS! Magnesium deficiency can be brought on by diet too. I know a wonderful young lady who felt that she was too fat for her husband and went on a 1-month starvation diet. She lost enough weight, but became extremely magnesium deficient; and developed very difficult to treat multiple cardiac and depression symptoms causing enormous stress in her life. The strange part about stress is that magnesium deficiency and stress reinforce and build upon each other, resulting in a difficult to manage, unstable downward spiral. Succeed! Depression is not a psychosis! FURTHER RESEARCH When I purchased my first bottle of magnesium glycinate, it was not from intelligence that I chose that particular compound of magnesium. It was just what was available on the shelf at the store I visited. After considerable research, I found that the store provided the second best form of magnesium that I could have chosen to treat depression. Only magnesium taurate (a form of magnesium that decreases chances of diarrhea) is superior to all other forms of magnesium. Both glycine and taurine have been used to effectively treat depression. Also taurine (the ligand in magnesium taurate) has been shown to be low or absent in 100 percent of people with depression and chronic pain according to Shealy. I quit taking and quit recommending magnesium glycinate because glycine, in the doses taken and while taken for a protracted period of time, will damage its delicate balance with another amino acid, taurine. Taurine is vital to mental and cardiac health and must not be disturbed, while glycine is ubiquitous and appears highly unlikely to be bothered by too much taurine. For example, diets with up to 1% as taurine had no adverse effect on thest animals. Long term high doses of glycinate will eventually cause ever worsening cardiac arrhythmias and will never allow total recovery from depression or other mood disorders, although most people will find that it works miracles for them in the short-term. Also, both magnesium and taurine have been proven to be low in depression in about 80% and 100% of cases respectively. Read Shealy's article starting here. See sentence immediately before the Discussion section. This does not mean magnesium glycinate is harmful in the short- or near-term, it just means one shouldn't use it year in and year out, and it must be IMMEDIATELY stopped if side effects, particularly cardiac arrhytmias (PVS and/or PACs) occur. Glycine (the second component of magnesium glycinate) chelates (removes) mercury from the body, and may be supeior to even magnesium taurate for people with heavy metal posioning in the short- or near-term. Citric acid and cysteine also remove mercury and appear safer for long term use than glycine. The first stability constants for glycine, cysteine and citric acid are in the log 10 to log 14 range, which are vastly stronger bindings than can be broken by any natural biology or chemistry event occuring in the body. Glycine is a non-essential amino acid, but for people with mercury poisoning, it, cysteine and citric acid may be highly important. Because of these amazing chelating, sequestering or binding powers, if they reacted with mercury in any form in the body, they should be able to bind them much more tightly, making mercury biologically unavailable in the body. Perhaps, consumption of large amounts of these amino acids from high quality protein sources, and consumption of citrus help protect from the toxic effects of mercury. Mercury is extremely toxic and can cause depression and many symptoms associated with depression. These symptoms include, insomnia, nervousness, memory loss, dizziness, anxiety, loss of self-confidence, irritability, drowsiness, weight loss, tremors, paraesthesia (numbness and tingling), hallucinations, headaches, fatigue, muscle weakness, hearing difficulties, emotional instability, skin inflammation, incoordination and kidney damage. The common areas where mercury is found are: auto exhaust emissions, used motor oils, pesticides, fertilizers, dental amalgams (silver fillings), drinking water (tap and well), leather tanning chemicals, felt, bleached flour, processed foods, fabric softeners, fish (tuna, swordfish, shark, king mackerel and tile fish), calomel (mercury chloride contaminant in talc, body powder), paint pigments and solvents, cinnabar (mercury sulfide - used in red jewelry items), inorganic mercury laxatives, mercurochrome/methiolate anti-infectives, cosmetics (mascara), floor waxes and polishes, wood preservatives, water plumbing & piping, adhesives, batteries, used air conditioner filters (better here than in the air), broken thermometers, and some electronic equipment. Consequently, supplementing several grams of these chelating agents daily is a good idea regardless of current mental health. Succeed! Depression is not a psychosis! Collected Thoughts on Dosage Now, more than 3 years after my very rapid recovery, I still ponder the correct dosage for magnesium, perhaps because this is the number one question asked by readers. What are the facts? There are some in the FDA who believe the U.S. RDA of 400 mg for men and 350 for women is too low, and that many persons need as much as 900 a day in their diet for a normal life. Canada, who pays for its citizen's health care, has a RDA of 600 mg magnesium for adults. Dosage depends on the ligand, the thing to which the magnesum is attached. In the case of magnesium taurate, the ligand is " taurate " . Absorption is largely a property of contact of the magnesium ion with the lining of the stomach and intestines. If magnesium is lightly bound to the ligand, then the acidity of the stomach can " ionize " the magnesium from its ligand and convert it to magnesium chloride (from the stomach acid hydrochloric acid) and finally into a positively charged ionic form for transfer into the blood where it is then picked up by various other ligands for transport to cells. Stomach acid can reduce the magnesium compound to the ionic form for metal complexes that have low to modest chemical stability, releasing both the magniesum ion and the ligand. The following magnesium compounds have sufficiently low stability that they offer very high absorption and are well tolerated. Magnesium acetate, chloride, citrate, gluconate, glycinate, lactate, malate, succinate, sulfate, tartrate and taurate are all very good, ionizable sources of magnesium. Intravenously, hospitals give magnesium sulfate. Magnesium chloride would be best, but it is very hygroscopic and difficult to properly package. On the other hand, magnesium oxide, magnesium hydroxide and magnesium carbonate are totally useless because they are too tightly bound together for the stomach acid to dissociate into ionic form. They will not work except in much larger doses, which greatly increase risk of diarrhea. In fact magnesium hydroxide is used to treat constipation (Milk of Magnesia). All of the useful, ionizable compounds of magnesium taste bad. On the other hand magnesium carbonate, oxide and hydroxide have no taste. These compounds are so tightly bound not even the taste buds are affected by them. Always taste-test each bottle of magnesium to detect improperly labeled products. Improperly labeled magnesium products do exist in the United States and they do cause many people to complain that " magnesium didn't work " . Obviously, neurotoxic-to-us ligands (glutamate and aspartate) must be avoided. Much of this essay relates to and asks why one needs so much supplemental magnesium to maintain mood? Normally, people don't consider magnesium as a part of their nutrition, even though magnesium is the second most prevalent mineral inside their cells (potassium is first). Have you ever seen magnesium on a food ingredient label? Not likely. I know I haven't, except for Planters® nuts. Clearly people with mood disorders leak or do not properly absorb magnesium. Consequently, without supplements of magnesium we are in desperate condition. There is an important section in this essay that explores in depth the question of why we leak magnesium and can't properly absorb it. Please read that section to see which factors might be involved in your personal situation. You will probably need to discuss these factors with your physician. Briefly, there are two main reasons, kidney (urinary) and gastrointestinal (fecal) losses. Some losses are caused by damage to these two organs by common drugs, usually prescription drugs like steroids, birth control pills, antifungals, laxatives and antibiotics. Other causes of damage include poor diet, endocrine disorders, parasites, infection and many other shown in this link. In my case, I know medicines damaged my gut by treating a yeast infection first with prescription antibiotics (improperly prescribed) and then with steroids (a potentially dangerous medicine). Did that further predispose me to depression? I think so. There are four very important dietary causes of low magnesium, which are: (1) " Leaky gut Syndrome " - inadequate intestinal bacteria, (2) insulin / sugar problems and (3) improper calcium / magnesium ratio, and (4) low bile production. During our youth, we are usually immune to each of these problems, but as we age (either in years or from toxins such as drugs or abuse of sugars and calcium), our ability to defend ourselves from these factors declines, sometimes to the point of illness. We will now discuss the main underling non-medical reasons for low intracellular magnesium, which cause depression (and many other common illnesses). " Leaky Gut Syndrome " The answer to the question, " How much should I take to cure my depression? " , closely relates to what caused the magnesium malabsorption or leakage. In nearly all cases severe stress (metabolic, psychological, environmental, physical) is involved as a predisposing factor. However, " Leaky Gut Syndrome " may be the most frequent cause of our inability to absorb magnesium. In nearly all cases, improving digestion by any means possible, such as use of stomach acidifiers (AC Vinegar), enzymes, CoQ10, soluble fiber, and correcting " Leaky Gut Syndrome " are easy and should be our highest priorities for rapid recovery. How? First, we must realize that insufficient stomach acid prevents absorption of minerals including magnesium, and that anything that irritates or damages our intestines impairs our ability to absorb magnesium. If magnesium is not absorbed through the walls of the stomach, in the large intestines magnesium ions attract vast numbers of molecules of water and promote retention of water - the usually accepted cause of its laxative effects. However, inadequate production of bile and the resultant diarrhea may be far more important in our inability to absorb sufficient magnesium. We must also realize that magnesium when present in the gut in sufficient concentration acts on our intestinal flora in the same way as an antibiotic - a definite gut irritant! This action may be because magnesium ions (especially as magnesium chloride - the form of magnesium present in our bodies as result of hydrochloric stomach acid) have strong, wide-spectrum antibiotic action. The antibiotic action of magnesium ion, using Epsom Salt, is well appreciated in veterinary medicine, and is used daily in treating topical wounds in animals, particularly abscesses in hoofs of horses. Also, Walter Last recounts its early use in humans as an antibiotic here. Why magnesium ion is not used as a broad spectrum antibiotic in people today is unclear, but probably has little to do with efficacy and much to do with economics. Regardless, if sufficient magnesium gets into the large intestines, it can and often does disrupt the normal flora of the gut causing a form of " Leaky Gut Syndrome " in the absence of adequate bile. This effect results in inadequate absorption of magnesium, calcium and many other nutrients which can cause many disorders including depression. Treating " Leaky Gut Syndrome " therefore becomes a novel way to treat depression. How is " Leaky Gut Syndrome " treated? First, identify and avoid things that irritate the gut such as food allergens, alcohol, caffeine, sugar (excesses cause intestinal yeast overgrowth) and drugs. Second, probiotics (life-sustaining bacteria normal and required in the intestines) such as acidophilus lactobacillus (available at pharmacies, health food and grocery stores) are needed to maintain and replace intestinal flora killed by excess magnesium ion. Only the strongest, fresh (refrigerated) available should be used, in a sufficient amount (6+ billion viable microorganisms per dose) and at a frequency (3 to 5 doses a day) to terminate diarrhea nearly overnight. Taking probiotics at times of the day different from magnesium only makes sense. Just like we would never take antibiotics at the same time of taking probiotics, we must not take magnesium with probiotics. There seems to be zero risk of overdosage using quality products, but mixed probiotic cultures may not be useful particularly if un refrigerated, because they have the habit of killing each other in warm environments when stored for a long time. If you want to get really serious about GI health, do what I do, use refrigerated 450 billion bacteria VSL#3 packets several times a day. Gas may be a side effect until the body adjusts. Ask the store clerk which probiotics have been shipped and maintained in a refrigerated state and which are the strongest. Third, psyllium husk fibers or bars without added sugar are very helpful in providing intestinal bulk and harborage for the intestinal flora. Some researchers say that damage to the gut repairable using probiotics takes from 3 to 6 months, even though diarrhea can usually be terminated within a few days. Consequently, we must avoid the temptation of early withdrawal from these life- and health-sustaining agents. We need to remember that diarrhea is not necessary for there to be " Leaky Gut Syndrome " . Diarrhea is only one symptom of this disorder. Also, learn more about how and why treating " Leaky Gut Syndrome " is vital to general health recovery and other related treatments of value. The amount of magnesium that we ingest is not as important as the amount we absorb. Many times magnesium tablets do not quickly dissolve in the stomach, resulting in entire tablets getting into the intestines where they always cause diarrhea. Allowing a tablet to dissolve in a glass of water or in the mouth will reveal problems with tablet dissolution rates. In cases of slow dissolution, tablets can be crushed and dissolved in a small glass of water with soluble fiber. I have an indelicate pallet, and I chew the tablets to a powder. I don't know if others can do the same. If you find a magnesium product and it does not taste bad, it probably will not work!!! What is the result of curing " Leaky Gut Syndrome " in the treatment of depression with magnesium? Perhaps most importantly, the total daily amount of magnesium required to improve mood is lowered. On occasion, repair is so complete that supplemental magnesium may be discontinued after a few months without recurrence of depression. Importantly, if we can cure " Leaky Gut Syndrome " and our mood improves to normal, we can be assured that we have fixed a serious problem using a very simple and harmless technique that allows us to rule out more complicated causes for our problems with mood. Who could say that treating depression with probiotics is not better than treating depression with Prozac®? Taurine - The Perfect-Poop Maker! Inadequate production of bile, which is made in the liver and aids in proper digestion of fats, probably is ten times more responsible for diarrhea and malabsorption of magnesium than any other single factor while taking therapeutic doses of magnesium. How can we get our bile production high enough to improve our absorption of magnesium? Cottage cheese, low in calcium and very high in taurine (1700 mg per cup), is a good food source. Taking taurine supplements along with various ionizable magnesium compounds (such as magnesium acetate, chloride, citrate, gluconate, glycinate, lactate, malate, succinate, sulfate, tartrate), or magnesium taurate (1:10 stoichiometric ratio), seems to do the trick, because both result in perfect poop. Loose stools normally attendant with daily 1200 mg magnesium dosage (split into 200 to 300 mg doses), appeared completely preventable by taking ten times the dosage of taurine with the magnesium doses (for example: for each 200 mg magnesium dosage, 2000 mg of taurine is ingested). Taurine is a conditional essential amino acid for humans, well known to be essential in human infants, but not in adults. Its other main function is in preventing cardiac arrhythmias (palpitations) and regulating cardiac rhythm generally, by supporting potassium metabolism too. Since I have had an increasingly severe problem with cardiac arrhythmias (PACs and PVCs), such is the reason I experimented with taurine. Although the arrhythmias were slowly benefited over a one month period and finally disappeared, the poop issue became immediately evident the first morning after my initial taurine dosage. I searched the Internet and PubMed for and found only that " excess taurine acts as a diuretic and laxative " . I disagree. Perhaps such is true for people not taking large amounts of magnesium, but not true for those that are taking large amounts of magnesium taurate with CoQ10. Taurine is supposed to be one of the most abundant amino acids in the body. It is found in human and animal central nervous systems, skeletal muscles and is very concentrated in brain, heart and eye tissues. It is synthesized from the amino acids methionine and cysteine, in conjunction with vitamin B6. Animal protein (particularly seafoods) is a good source of taurine, but it is not found in vegetable protein. Vegetarians with an unbalanced protein intake, and therefore deficient in methionine or cysteine will have great difficulty manufacturing taurine. Dietary intake is thought to be more important in women as the female hormone estradiol depresses the formation of taurine in the liver. Taurine functions in electrically active tissues such as the brain and heart to help stabilize cell membranes. Taurine seems to inhibit and modulate neurotransmitters (like glycine and GABA) in the brain and helps to stabilize cell membranes. It also has functions in the gallbladder, eyes, and blood vessels and appears to have some antioxidant and detoxifying activity. Taurine aids the movement of potassium, sodium, calcium, and magnesium in and out of cells and thus helps generate nerve impulses. Zinc seems to support this effect of taurine. There have been reports on the benefits of taurine supplementation for epileptics. It has also been found to control motor tics, such as uncontrollable facial twitches. In Japan, taurine therapy is used in the treatment of ischemic heart disease. Low taurine and magnesium levels have been found in patients after heart attacks. Like magnesium, taurine affects cell membrane electrical excitability by normalizing potassium flow in and out of heart muscle cells. Supplements decrease the tendency to develop potentially lethal abnormal heart arrhythmias after heart attacks. People with congestive heart failure have also responded to supplementation with improved cardiac and respiratory function. Taurine is necessary for the chemical reactions that produce normal vision, and deficiencies are associated with retinal degeneration. Besides protecting the retina, taurine may help prevent and possibly reverse age-related cataracts. Low levels of taurine and other sulphur containing amino acids are associated with high blood pressure, and taurine supplements have been shown to lower blood pressure in some studies. Other possible uses for taurine supplementation include eye disease (including scleritis and retinal disease), cirrhosis, depression and male infertility (due to low sperm motility) and hypertension, and as a supplement for newborns and new mothers. It is vital in maintaining the correct composition of bile and the solubility of cholesterol. It has been found to have an effect on blood sugar levels similar to insulin. Very interestingly, taurine and glycine exist in the presence of a time- and dose-dependent exchange mechanism. After administering glycine to rats, researchers discovered that it produced a notable suppression of hepatic taurine content in the liver. Yet, this taurine decrease was not found in other taurine-rich organs such as the brain, heart or kidney. The mechanism for hepatic concentration of these two amino acids serves to alter liver concentrations of these amino acids without adversely affecting the rest of the body. The significance of this is very high, because as glycine goes up and taurine goes down in the liver, bile production is impaired and intestinal absorption of magnesium becomes greatly impaired, helping to explain why diarrhea resulting from magnesium taurate is essentially non-existant. In some people sensitive to this reaction, magnesium glycinate would be contraindicated, while magnesium taurate would be very helpful. Further, I believe that my PAC and PVC cardiac arrhythmias were caused by too much glycine, and that by changing from magnesium glycinate to magnesium taurate they are prevented. Like all nutrients, taurine enhances or decreases the action of other nutrients. Monosodium glutamate (MSG) is the sodium salt of the amino acid glutamic acid. If glutamic acid supplementation is given, as is sometimes done with alcoholics, it tends to reduce taurine. MSG itself can also reduce taurine levels. The amino acids beta-alanine and beta-hypotaurine, as well as the B-vitamin pantothenic acid, may also interfere with taurine’s functions. Zinc, on the other hand, enhances taurine’s effects. Zinc deficiency and combined vitamin A and zinc deficiency are associated with an increased excretion of taurine in the urine and with depleted taurine levels in the tissues where it is normally found. Cysteine (found in meat) and vitamin B6 are the most critical nutrients to support the manufacture of taurine in the body of human beings or those species that are able to synthesize enough. Taurine is an important regulator of cellular ion transport and osmotic balance, aspects that are pivotal to renal function. The kidney not only regulates body taurine status, but emerging information also suggests that body taurine status is of consequence for renal function. While reduction in endogenous taurine stores can attenuate renal excretory function, exogenous taurine supplementation is kidney-protective and augments kidney function in several conditions that are associated with reduction in diuresis and natriuresis. Thus taurine treatment may be of potential benefit in conditions that are associated with impaired kidney function and the accompanying dysregulation of body fluid and electrolyte homeostasis. I say that anything that improves kidney function is vital to us. Taurine supplementation is now recommended for the prevention and treatment of diabetes. In order to determine the effects of taurine supplementation or depletion on the morphological changes of pancreatic beta-cells in streptozotocin-induced diabetic rats, rats were fed diets supplemented with 1, 2 or 3% taurine or 5% beta-alanine in their drinking water for 7 weeks. After 3 weeks, diabetes was induced by streptozotocin injection (50 mg/kg body-weight). Pancreatic morphology was observed by transmission electron microscopy. The pancreatic beta-cell of the non-diabetic (CO) group had the many secretory granules, rough endoplasmic reticulum and rod shaped mitochondria. However, the beta-cells of non taurine-supplemented diabetic (EO) group were severely damaged, showing depleted secretory granules. In the 1% taurine-supplemented diabetic group, the beta-cells were less damaged compared to the EO group and had some apparently normal secretory granules, but most of rough endoplasmic reticulum and mitochondria was destroyed. The beta-cell of 2% taurine-supplemented diabetic group had swollen rough endoplasmic reticulum, round-shaped mitochondria and some apparently normal secretory granules. The beta-cell of 3% taurine-supplemented diabetic group was little different from that of non-diabetic group. The pancreatic beta-cell of taurine-depleted diabetic group was not destroyed but had many small secretory granules which appeared immature. This was reflected in the blood glucose concentrations of this group. Therefore, taurine may prevent insulin-dependent diabetes by protection of the pancreatic beta-cell and may also preserve normal secretory granules. From these results, taurine supplementation may be recommended for prevention and treatment of diabetes. Beta-alanine worsened diabetes. Magnesium, however, plays an important role in the regulation of insulin secretion by altering the sensitivity of the beta cells of the Islets of Langerhans to glucose. The MSGTruth.org site commented that taurine was the antidote for glutamate poisoning. I questioned Carol Hoernlein, the founder of the MSGTruth.org site about her point of view and she wrote me back writing: George, The MSG toxicity - taurine deficiency link theory is my own. I developed the theory over ten years ago. At first in my research of glutamate toxicity and its effect on cardiovascular health, most of the neuroscientific data at the time linked glutamate toxicity to its effect on the amino acid cysteine. (Glutamate and cysteine compete for uptake in the body.) I then was given an article about the amino acid taurine by a colleague. That was the link. Taurine deficiency symptoms are the exact same symptoms of MSG reaction. Particularly a racing heart. (Taurine is the amino acid that regulates heart beat.) When I realized that the body manufactures taurine from cysteine, the pieces fell into place. I then tested my theory. The next MSG reaction I had, I took taurine in pill form. The headache went away, the racing heart calmed down, the blood pressure went down, and I was able to sleep. Since that time, I have used it quite often and always keep some handy as an " antidote " . It is interesting to note, that now taurine is being used in Japan to treat high blood pressure. It is also being studied to treat diabetes and epilepsy now. These are also two diseases impacted by glutamate. Glutamate triggers the pancreas to produce insulin, but too much insulin can result in insulin resistance, Type II diabetes, and obesity. Also, MSG is well known as an epilepsy trigger. All these facts point to the conclusion that ingested MSG somehow interferes with taurine formation in the body, perhaps by interfering with the uptake of the cysteine needed to make taurine. It is by no means an " official " theory, but we have had many reports of MSG sensitive persons who report relief of some MSG reaction symptoms by ingesting taurine. It is also interesting to note that the body uses Vitamin B6 to make taurine, and that Vitamin B6 deficiency makes MSG reactions worse. I will be adding a page to the website soon about taurine, as it is a fascinating amino acid. Hope this explains things a bit better. If you more questions, I'd be happy to answer them. Carol A. Hoernlein, P.E. Founder MSGTruth.org Carol's and my personal beliefs have major, scientific support. Taurine prevents glutamate excitotoxicity through regulation of calcium and mitochondrial energy metabolism according to scientists writing in the November 1999 issue of Journal of Neuroscience. They clearly and unambiguously point out that the control of intracellular calcium concentrations is a fundamental process in neuronal survival and function. This, prevention of glutamate excitotoxicity, is exactly what we need, and is a powerful reason I switched from magnesium glycinate to magnesium taurate. This importance of this point cannot be over emphasized. Further, I believe that my PAC and PVC cardiac arrhythmias were caused by too much glycine, and that by changing from magnesium glycinate to magnesium taurate they are prevented. Aspartate, glutamate, and glutamine, among other amino acids, are excitatory. They are antagonistic to the functions of taurine, alanine, GABA and glycine according to a contemporary review of taurine by Richard Smayda, D.O.. Consequently, Carol is correct, taurine does detoxify glutamates. Dr. Smayda's review is of considerable importance to all of us interested in magnesium and depression. Dr. Smayda points out that major depression is marked by alterations in serum levels of the excitatory amino acids glutamate and aspartate, accompanied by deviations in levels of taurine, serine, and glycine as well. In patients who did not respond to treatment with classical SSRI antidepressants (treatment-resistant depression - like what we are discussing in this page), characteristically lower serum levels of taurine, aspartate, asparagine, serine and threonine, with a steep increase in glutamine, were noted. Consequently, magnesium taurate is the preferred forms of magnesium for treating depression. These alterations may become valuable as diagnostic assessments to predict the response to treatment with antidepressants. I remain extremely cautious about glutamates and aspartates due to toxicity that has been previously discussed. Here is a link to an important review of taurine in biological functions and food sources, with cottage cheese being low in calcium and very high in taurine (1700 mg per cup). Who sells magnesium taurate? I like Cardiovascular Research's Magnesium Taurate product. Order a case of it from us today (click here). According to Dr. Smayda, taurine is a necessary and integral element for optimal health. Oral supplementation poses no major threat of toxicity, and its presence in foods makes it widely available to people seeking nutrition-oriented ways to improve their health. The importance of taurine cannot be overstated and its greater therapeutic application awaits only further research. It truly is part of the team of nutrients that we require for maintaining optimal health and sustaining life. However, in those individuals who develop stomach ulcers with aspirin, for instance, large doses of supplemental taurine may be contraindicated. MF MaCarty writes in Medical Hypotheses: " By a variety of mechanisms, magnesium functions both intracellularly and extracellularly to minimize the cytoplasmic free calcium level, [Ca2+]i. This may be the chief reason why correction of magnesium deficiency, or induction of hypermagnesemia by parenteral infusion, exerts antihypertensive, anti-atherosclerotic, anti-arrhythmic and antithrombotic effects. Although the amino acid taurine can increase systolic calcium transients in cardiac cells (and thus has positive inotropic activity), it has other actions which tend to reduce [Ca2+]i. Indeed, in animal or clinical studies, taurine lowers elevated blood pressure, retards cholesterol-induced atherogenesis, prevents arrhythmias and stabilizes platelets--effects parallel to those of magnesium. The complex magnesium taurate may thus have considerable potential as a vascular-protective nutritional supplement, and might also be administered parenterally, as an alternative to magnesium sulfate, in the treatment of acute myocardial infarction as well as of pre-eclampsia. The effects of magnesium taurate in diabetes deserve particular attention, since both magnesium and taurine may improve insulin sensitivity, and also may lessen risk for the micro- and macrovascular complications of diabetes. " Concerning pre-eclampsia/eclampsia, MF MaCarty writes in Medical Hypotheses: " The use of parenteral magnesium sulfate for the management of pre-eclampsia/eclampsia is well established. In striking analogy to the effects of hypermagnesemia, taurine has antivasospastic, antihypertensive, platelet-stabilizing, anticonvulsant and hypoxia-protective properties. Thus parenteral magnesium taurate can reasonably be proposed as a superior alternative to magnesium sulfate in the treatment of pre-eclampsia; administered orally as a component of prenatal supplementation, magnesium taurate might well have both preventive and therapeutic value in this syndrome. In the light of the hypoxia-protective actions of both magnesium and taurine, such supplementation might also protect fetuses experiencing temporary perinatal asphyxia, lessening the risk of cerebral palsy. " Concerning migraines, MF MaCarty writes in Medical Hypotheses: " Although the pathogenesis of migraine is still poorly understood, various clinical investigations, as well as consideration of the characteristic activities of the wide range of drugs known to reduce migraine incidence, suggest that such phenomena as neuronal hyperexcitation, cortical spreading depression, vasospasm, platelet activation and sympathetic hyperactivity often play a part in this syndrome. Increased tissue levels of taurine, as well as increased extracellular magnesium, could be expected to dampen neuronal hyperexcitation, counteract vasospasm, increase tolerance to focal hypoxia and stabilize platelets; taurine may also lessen sympathetic outflow. Thus it is reasonable to speculate that supplemental magnesium taurate will have preventive value in the treatment of migraine. Fish oil, owing to its platelet-stabilizing and antivasospastic actions, may also be useful in this regard, as suggested by a few clinical reports. Although many drugs have value for migraine prophylaxis, the two nutritional measures suggested here may have particular merit owing to the versatility of their actions, their safety and lack of side-effects and their long-term favorable impact on vascular health. " In the cat, taurine is an essential amino acid, and one of the best layman's pages on taurine on the Internet is dedicated to cats. In that page taurine is again shown to antagonize glutamates, and visa versa. Recently, it has been suggested by Chinese scientist Zhao Xi-he and co-workers that taurine may act as an antihypertensive substance through central and peripheral mechanisms in animal models and in human essential hypertension. Taurine is high in seafood and not present in plant food. Foods high in taurine are eaten by ocean-loving people in countries including Japan, Sicilie, Italy and Greece having a low incidence of cardiovascular disease and very long life spans. Taurine content of meats, poultry and aquatic products in China (mg/100 g edible portion) Food Taurine conc. Food Taurine conc. Conch 850 Hairtail fish 56 Inkfish 672 Yellow croaker 88 Blood clam 617 Eel 91 Clam 496 Chicken leg 378 Shellfish 332 Chicken breast 26 Crab 278 Pork 118 Prawn 143 Pig heart 200 Sole 256 Pig kidney 120 Crucial carp 205 Pig liver 42 Silver carp 90 Beef 64 Taurine was not detected in egg, bean, rice and other plant food. The lowest prevalence of hypertension was among people that lived in fishing areas and this may be related to the high taurine content in their diet. Fujita et al. reported that when 6 g taurine/day was given to young adult males with borderline hypertension for 7 days, their systolic and diastolic blood pressure decreased significantly to levels similar to those of the placebo-treated controls. The same effect from taurine was also found by other nutritionists in China. Zhang et al. compared the blood pressure of three populations living in fishing and farming areas in China and found that the blood pressure of populations in the fishing area was the lowest. Serum and urinary taurine content were negatively related to blood pressure. They also found that sodium excretion was positively associated with taurine excretion. American scientists attribute this amazing resistance to cardiac problems to Omega-3 essential fatty acids, but the arguement for taurine is vastly stronger, however there could easily be overlap in benefits. More on taurine in foods by H. Pasantes-Morales in " Nutrition Reports International " , Oct. 1989: Taurine is converted from methionine and cysteine, and with help from sulfur, sodium and cloride changes to taurine. The highest concentration of taurine was found in clams and octopus (41.4 micromoles/g and 31.2 micromoles/g), followed by shrimp and fish (12.4 micromoles/g and 9.1 micromoles/g). Beef, pork and lamb meat contain taurine in concentrations ranging 3.5-4.0 micromoles/g. Taurine concentration in chicken leg was 6.6 micromoles/g and in chicken breast was 1.4 micromoles/g. No taurine was found either in hen eggs (yolk or white) or in dairy products or in honey. Taurine was undetectable to trace amounts in fruits and vegetables to include rice, corn, oatmeal, pumpkin, rye, wheat, barley, sesame seed, coffee and cacao, black beans, chick peas, peanuts, walnuts, almonds, cashews, hazelnuts, pinenuts pistachios. All analysis were carried out in uncooked samples, and cooking greatly reduced taurine content of most foods. Looking at the low-taurine diseases above, one notes that they are generally diseases of aging. One may be led to ask if taurine production by the liver and retention by the kidney are impaired in aging. If yes, does supplementation of taurine make up for the losses? Eppler and Dawson found that a decrease in hepatic taurine biosynthesis may cause, in part, the observed decline in tissue taurine content in aged rats, and that taurine supplementation does restore taurine blood levels. Their study indicated that a decline in taurine content may exacerbate oxidative stress in aged rats, which can be reversed by dietary taurine supplementation. Dawson and team has done extensive research in decline in taurine in aging since 1990. They showed that age-related reduction in plasma taurine may have important consequences in respect to regulation of blood pressure, cardiovascular function, and cardioprotection, as well as possible CNS complications. Significant age-related declines in taurine content were observed in the spleen, kidney, eye, cerebellum and serum. Taurine supplementation corrected these deficits in tissue content in aged rats, and in many cases increased taurine content above that of adult controls. Urinary excretion of taurine was significantly reduced in aged rats indicating an increased need to conserve taurine. Taurine-deficient diets did not further exacerbate the age-related decline in tissue taurine content, suggesting biosynthetic adaptations to the lack of dietary taurine. Dietary taurine supplementation blunted age-related declines in serum IGF-1 and increases in serum creatinine and blood urinary nitrogen (BUN). Their studies suggest that advanced aging results in a taurine-deficient state that can be corrected by dietary supplementation. They also pointed out that taurine in the brain declined with aging, which was correlated with loss of dopamine. I add that such also appears true in humans. Consequently, to my way of reasoning, if taurine production falls off in aging, and if taurine is necessary for kidney preservation of electrolytes such as magnesium and potassium, low taurine seems to result in greatly reduced health partly by loss of magnesium through the kidneys. Therefore, my observations that my cardiac arrhythmias were caused by low magnesium (as shown by my magnesium sulfate lozenge test) can be viewed more properly as resultant from a cascade effect of low-taurine-induced magnesium, which resulted in low-magnesium-induced potassium. Life Extension Foundation magazine has a presentation of 99 scientific " taruine " abstracts. Coenzyme Q10 (CoQ10) has been reported by some people to greatly minimize the loose bowels normally found using large amounts of magnesium. Very little information concerning this effect has been found in the literature, but the effect to those that have tried 100 mg CoQ10 with each dose of magnesium has been remarkable. Here is a link to " Altered Immunity & The Leaky Gut Syndrome " by Dr. Zoltan P. Rona MD, MSc, that goes into the biochemistry of leaky gut syndrome and what can be done about it better than any other article that I have found. CoQ10 is mentioned here, but little emphasis is placed on it. Looking into the relationship between yeasts and CoQ10, one finds that ubiquinones (in the human it is CoQ10) are essential for oxidative phosphorylation in both yeasts and humans. The human coenzyme Q, CoQ10, is administered orally for the treatment of heart disease and other disorders. Some patients, however, require much higher doses than others to attain a therapeutic CoQ10 blood level. C. A. Krone et al. proposes that one possible explanation for this variability is excessive Candida colonization of the human GI tract. Many common medical treatments including antibiotics and anti-hyperchlorhydric agents increase the risk of GI tract Candida colonization. Subsequent uptake and utilization of supplemental CoQ10 by excessive yeast could diminish availability for the human subject. Data from one patient and an in vitro pilot study using two pathogenic strains of C. albicans supported Krone's hypothesis. If C. albicans in the GI tract can hinder availability and interfere with therapeutic effects of CoQ10, it could be of clinical significance for large numbers of depressed people having loose bowels from magnesium. Consequently, one can see a cause and effect relationship between ingestion of large amounts of CoQ10 and relief from loose bowels and diarrhea, thus improved recovery from depression due to improved absorption of magnesium. Consequently, the yeasts get fed their CoQ10 before we do, and sometimes we starve! Mail - More reliable, more storage, less spam Quote Link to comment Share on other sites More sharing options...
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