Acupuncture & Chinese Medicine ● Longevity Nutrition

histamine

 

This article is not intended to diagnose or treat any diseases.

Due diligence is a necessary part of the healing process.  If you believe you are worth the effort, then seek the knowledge you need to reveal the truth.

 

IMG_1919In the world of functional medicine and nutrition we use a large array of herbs, vitamins, minerals, amino acids and other biological substances to restore function and support healing. Most of the supplements we use are fairly safe. Even when the diagnosis is incorrect or if a side effect occurs, most reactions will resolve quickly with no permanent harm.  However, there is a handful of supplements that can cause, at best, a setback and, on occasion, significant side effects. Betaine hydrochloride (HCl) is one of them. When used appropriately and under the correct diagnosis, Betaine HCl can have seemingly magical effects on conditions like acne, eczema, asthma, idiopathic malnutrition, GERD and other digestive issues. However, a visit to most mainstream medical websites will advise you, “Do not take Betaine HCL”. This is with good reason. Betaine HCL can exacerbate several underlying health conditions and, in rare instances, can cause life-threatening health issues.

Betaine HCL is used to treat a condition called hypochlorhydria (insufficiently strong stomach acid).  Although it hasn’t been subject to rigorous clinical trials, here is the simplified hypothesis; when acid is the stomach is not strong enough (pH between 1.5 and 3.5) animal protein cannot be effectively digested into amino acids and smaller protein fragments. As a result, the stomach somehow detects this problem and continues to produce weak acid. The weak acid fills up past the stomach and into the esophagus. Unlike the iron-clad lining of the stomach, the esophagus is easily damaged by acid. The thinking is that Betaine HCl works by restoring the correct pH (increasing the acidity) of stomach acid. When the correct dosage achieved, the excess production of weak acid stops and normal digestion of protein and minerals resumes. If the correct dose is not achieved, supplementing with Betaine HCl has little value. Practitioners, here is a link to a method that was originally presented by Jonathan Wright M.D. on how to figure out the correct dose of Betaine HCl. As the author describes, most cases require no more than 2500mg for reestablishing adequate acid levels. I have seen a few cases where the replacement dose was over 6000mg per meal.

 

Accurate Diagnosis is Crucial

There are many downstream health issues that can arise from inadequate digestion of protein. These include IBS, excessive flatulence, leaky gut syndrome, asthma, acne, allergies, eczema, acid reflux, idiopathic malnutrition, premature osteoporosis etc. There are scientifically sound explanations for each of these that we will discuss another time. However, any of these conditions can be caused by other factors and, none of them is a defining symptom of low stomach acid (hypochlorhydria).

Most importantly, acid reflux, often diagnosed as GERD, is NOT a pathognomonic symptom of hypochlorhydria. The exact same symptoms can be caused by overgrowth of bacteria and in small intestine, excess production of acid, stagnation of the motor migrating complex and, more commonly, by excess histamine. This is why decades of research produced two classes of drugs to treat GERD. These are the proton pump inhibitors (PPI’s) and H2 blockers (Histamine receptor blockers). It can be implied that the effectiveness of these two categories of drugs in treating symptoms can shed some clarity on the root of the problem. In more complex cases, hypochlorhydria and excess histamine will occur simultaneously.

The Big Cautions With Betaine HCl

Esophageal Damage and Strictures

Pills of Betaine HCl can get lodged in areas where the esophagus has narrowed from scar tissue or has shrunk from old age. This usually causes a strong, sharp pain. If the pill remains for more than a couple of minutes, it can literally burn the area. If this happens, the irritation can last several days and it is best to discontinue the course of Betaine HCl therapy until it is completely healed. To prevent damage to the esophagus in cases like these, it is crucial to flush the area until the pill is small enough to move on. This can be done by sipping a weak solution of baking soda in warm water (1/4 tsp per 12 oz of water) OR by diluting a full dose of a liquid antacid in warm water. DO NOT use baking soda if the patient has high blood pressure. This scenario is more common in elderly patients and it is better to break up the Betaine HCl capsules before swallowing them. As a general rule, if this happens, don’t hesitate to seek medical attention.

 

Exacerbation of Gastritis

Gastritis is inflammation of the stomach lining. It has many causes but ultimately occurs because the cells lining the stomach cannot replace themselves quickly enough to maintain the integrity of the tissue. When this happens, any small amount of acid can quickly damage the lining. This is a potentially dangerous situation as ulcers can form. Possible causes include excessive alcohol consumption, use of corticosteroids and NSAIDS, stress, excess acid production, nutritional deficiencies, excess levels of histamine and infection.

Combine a stomach that is severely irritated by excess histamine and add Betaine HCl and you have yourself a new condition that can take several weeks to fully heal.

Symptoms of gastritis can easily go unnoticed. This is especially true for people who are busy, overwhelmed and/or highly driven. I meet people all the time in my practice who have had low to mid-grade symptoms of gastritis for years without giving it a single consideration that something could be wrong. This can also happen because some people have an altered perception of pain in their digestive tract. Nerve blocks and cauterizations as well as medications, like antidepressants, narcotics and opioids, can reduce pain sensations. Practitioners! Confirm your diagnosis before prescribing Betaine HCl and proceed cautiously with the dose. DO NOT assume that patients will notice side effects immediately.

 

A True Story of a Gastritis Nightmare

More than a decade ago, I had a nutrition consultation with a gentleman who had clear signs of gastritis. Although he didn’t think so, his lifestyle was extremely stressful. He was founder and CEO of a very successful chain of stores. He worked long hours and traveled frequently. Drinking too much alcohol was one way he compensated for the stress. His symptoms manifested as a dull ache (fairly mild) above his naval that was worse on an empty stomach, with water, with spicy food and about 20 minutes after eating (food usually absorbs acid for a few minutes before the stomach makes more). He denied any sign of dark, tarry pieces in his stool (a sign of bleeding in the digestive system). At the time of our meeting, he was preparing to leave for a big game hunting trip in east Africa. I insisted that he consult a physician before departing. His first week in the African bush he developed anemia as a result of a bleeding ulcer. It took several days for him to reach a facility with adequate medical care. He ended up having to have surgery and, more unfortunately, a blood transfusion that left him with a lifelong disease.

 

 

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Deeper examination of the scientific literature reveals new concerns that the food additive, azodicarbonamide, not only carries potential risks but also demonstrates that it is time for an overhaul of the FDA’s policies.  This article represents scores of hours of research and triple-checking all calculations.  I dedicate this to “The Food Babe”, a very courageous lady who is helping to bring awareness of the chemicals that are needlessly added into what would otherwise be considered “food”. This post demonstrates that it is time to stop this madness and allow science and logic to prevail.

I recently listened to an interview on NPR presenting the varying perspectives on a recent petition initiated by Vani, The Food Babe, asking Subway to discontinue using the chemical azodicarbonamide in their bread.  I was a disappointed that no one could provide more definitive, in-depth information other to regurgitate than was already available on the PubChem or the FDA’s website.  Always up for a challenge in biochemistry, I thought I would do a little research about how this stuff behaved once it entered the body.  Other than its ability to act as an immunosuppressant, and being a carcinogen and irritant at unrealistically high doses, I discovered that very little was known about azodicarbonamide.  After doing some calculations based on the very limited data available, I was ready to surrender any concerns I had about consuming commercial bread when I came across several articles discussing how a known carcinogen, semicarbazide, was formed during dry heating of azodicarbonamide.  This was demonstrated in several separate studies by heating both commercial flours[1] and plastic seals in many twist off lids[2] to temperatures between 150−200 °C (302-422 F).  The average cooking temperatures for bread are 350-375 F for home baking and 400-450 F for commercial baking. The amounts detected in the lids ranged from approximately 2.0-8.5mg per Kg (a kilogram is 2.2 pounds).  Yikes, 8.5 mg/Kg is a lot!  It’s a good thing we don’t eat plastic seals on lids. I wonder if any of this leeches into the contents of the jar.  The amounts detected in the bread were much lower, around 0.2mg per Kg.  Granted this is not a huge amount.  After all, the average American “only” consumes about 1.75 pounds of bread per week.  But out of curiosity, I went to Toxnet to find out the safe level of consumption for humans of semicarbazide.  As of March 17th 2014 it said, “No data are available in humans. Limited evidence of carcinogenicity in animals.”  Don’t confuse “limited evidence” with “the evidence suggests limited carcinogenicity”.  After doing a little more digging, I discovered that the reason for this statement was two fold.  First, there simply aren’t many studies investigating the “toxigenicity” or “carcinogenicity” of this known carcinogen.  Second, it was difficult to assign a “safe” value because certain ethnic groups, like the Japanese, are really good at eliminating semicarbazide from their cells.  Caucasians on the other hand eliminate it about half as fast as the Japanese[3].  What’s really amazing is that they have information on the exact biochemical mechanism by which it causes DNA damage but they have no information on what levels an animal or human can consume before it becomes “unsafe”.

Most animal studies performed with semicarbazide use large doses between 50 and 150 mg/kg/day.  These doses are big enough that the average human is likely to never have anything close to this kind of exposure.  Side effects using these big doses ranged from severe birth defects, liver hemorrhages and kidney failure[4].  In grasshoppers it was shown to have a mutagenic effect on the sperm of grasshoppers[5].  OK, fair enough!  It was a grasshopper.  There are no studies examining this on humans.

However, another peer-reviewed study using much smaller doses demonstrated “the incidence of lung tumors rose from 21-50% in the females and from 23-30% in the males, while the incidence of blood vessel tumors increased from 5-18% in females, but not in males” when compared to untreated controls[6].  These doses ranged from 2.2-4.0 mg/day delivered in drinking water.  This is still a lot when you consider that the maximum ever found in bread was about .1 mg per pound.  Nonetheless, since this is a ‘known carcinogen” I thought I would see if there was any evidence of bioaccumulation.  Bioaccumulation studies are performed on many toxic chemicals to make sure that they can’t accumulate over time to levels that are toxic.  Hmmmm…no bioaccumulation studies for semicarbazide (or azodicarbonamide).   However, we do have one study dating all the way back to 1963 showing that .3-1.4% of hydrazine (a close relative of semicarbazide which is metabolized through the same biochemical pathways) remained in a mouse carcass 48 hours after administering doses[7].  Since the research hasn’t been performed we have to make a couple of assumptions here but let’s pretend that the clearance rate of hydrazine is similar to semicarbazide.

Here is simplified version of the calculation:  (It’s really boring and nerdy.  If you prefer to skip the math, the answer is at the bottom of the paragraph.  For other biochemists out there…yes, enzyme kinetics is slightly more complicated but this is completely within the realm of possibility)

From earlier, the average American could conceivably consume about .175 mg per week of semicarbazide by eating 1.75 pounds of bread per week that contains azodicarbonamide.  We can break this down to 0.025 mg per day or 0.050mg every 48 hours.  The mean average of hydrazine retention (and presumably semicarbazide retention) is .85% every 48 hours SO 0.05mg consumed every 48 hours times .85% (.0085) leaves .0015mg remaining somewhere in the body every week.  In order to accumulate the lowest dose that can potentially cause health problems 2.2mg, the average American would have to eat 1.75 pounds of bread per week for 28 years and 73 days.  If they were the type of person who eats bagels for breakfast, a Subway sandwich for lunch and pizza for dinner, they might accumulate these levels in under 5 years.

The average lifespan of a laboratory mouse is three years and they are kept in a sterile environment where they are not exposed to any other chemicals that might interfere with the experiment.  Humans, by contrast, are messy to study.  We are exposed to small amounts of thousands of chemicals everyday that could interfere with any well-intentioned lab experiment.  This brings me to my next point.  As I mention above, both semicarbazide and azodicarbonamde are part of a larger family of chemicals called hydrazines.  This whole family of chemicals is metabolized (broken down) by enzymes in the digestive system and liver using a process called acetylation.  Think of acetylation like a toilet that flushes these chemicals out of the body.  As long as there is enough room in the toilet and enough water to eliminate these chemicals, then everything is hunky dory.  But what happens if there are more chemicals than the toilet can effectively eliminate?   Other chemicals that are also eliminated through this pathway include many weed killers, acetopminphen (aka Tylenol™), brain chemicals like seretonin and dopamine, the allergy chemical histamine and carcinogenic heterocyclic amines that are produced by cooking meat at high temperature.  The body can produce more enzymes as it needs to keep up with these demands but, like all things in Nature, there is a point at which the system becomes overwhelmed.  In other words, the toilet begins to back up.

Another BIG concern I have is that we study the doses of these things that kill us or give us cancer (sometimes) but we don’t study the doses in which they start to negatively affect the body.  We know that semicarbazide potently inhibits the function of an enzyme called SSAO that is used to break down histamine (the allergy chemical) in vascular tissue[8].  (Hmmm, that’s a strange coincidence. The studies performed on mice produced tumors in vascular tissues.)  Would small but ongoing inhibition of SSAO cause a net overall rise in histamine levels?  OR would chronic exposure to semicarbazide cause chronically elevated levels of SSAO leading to damage to vascular tissues.  According the theory of enzyme kinetics, maybe both.  Excess activity of SSAO has been associated with diseases like neuropathy and Multiple Sclerosis[9].  If we ignore the fact that some unknown chemical might be triggering the increased activity of SSAO, we are currently looking at using semicarbazide as a drug to help these conditions[10].  Perhaps we will find that people with these diseases can benefit from increasing their consumption of azodicarbonamide-containing bread.

Using science and logic, the only possible conclusion that we can draw about the safety of adding azodicarbonamide to bread is that we have no idea what amount is safe, especially over the long term.  The data is not available because the studies haven’t been performed.  Granted, the studies cited on the FDA’s website are “peer-reviewed” but 95% of them were performed before 1986 on mice.   The average laboratory mouse lives 1.3-3 years.  This is no way is representative of a human lifespan or the daily barrage of chemical challenges posed by “living” in an age where simply breathing the air is its own science experiment.  Since the 1980’s science has evolved so quickly that it has practically broken Moore’s Law.  It is time that the recommendations made by the FDA are brought up to date to reflect the science of the new millennium and to include studies that more accurately reflect human lifespan and real-world scenarios.  At the very least all man-made chemicals that are included in our food should have bioaccumulation data.  There is no doubt that the FDA serves and has served as a vital part of human health and survival in the United States.  However, it is time for the administration that has persisted in cloaking parts of itself and of the chemical industry in antiquated dogma to either step into the new millennia and perform its duties for “the people” or to step aside and allow science and logic to prevail.

Constructive comments that contribute to the advancement of knowledge are gratefully accepted.

 


[1] Becalski A., Lau B.P.Y., Lewis D., Seaman S.W.Semicarbazide Formation in Azodicarbonamide-Treated Flour:  A Model Studylski A., Lau B.P.Y., Lewis D., Seaman S.W.  J. Agric. Food Chem., 2004, 52 (18), pp 5730–5734

[2] Stadler H., Mottier P., Phillippe G., Gremaud E., Varga, N., Laljie S., Whitaker., Kintscher J., Dudler, V., Read W.A., Castle L., Semicarbazide is a minor thermal decomposition product of azodicarbonamide used in the gaskets of certain food jars  Analyst, 2004,129, 276-281   DOI: 10.1039/B314206J

[3]  Koizumi A1, Nomiyama T, Tsukada M, Wada Y, Omae K, Tanaka S, Miyauchi H, Imamiya S, Sakurai H.  Evidence on N-acetyltransferase allele-associated metabolism of hydrazine in Japanese workers. J Occup Environ Med. 1998 Mar;40(3):217-22.

[4] Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Man. Geneva: World Health Organization, International Agency for Research on Cancer, 1972-PRESENT. (Multivolume work). Available at: http://monographs.iarc.fr/index.php p. S7 71 (1987)] **PEER REVIEWED**

[5] Bhattacharya, K. Chromosome damage induce by semicarazid in spermatocytes of a grasshopper.  Mutat Res. 1976 Jul;40(3):237-42.

[6] . Toth B., Shumizu H., Erickson J.  Carbamylhydrazine hydrochloride as a lung and blood vessel tumous inducer in Swiss Mice.  Eur J Cancer. 1975 Jan;11(1):17-22.

[7] Thomas Dambrauskas and Herbert Cornish  The Distribution, Metaboism and Excretion of Hydrazine in Rat and Mouse.   Toxicology and Applied Pharmacology 6, 653-663 (1964)

[9] Wang E. Y., Gao H. , Slater-Cid L., Zhang J, Huang L., Podar E.M., Miller A., Zhao J., O’Rourke A., Linnick M. D.  Design, Synthesis, and Biological Evaluation of Semicarbazide-Sensitive Amine Oxidase (SSAO) Inhibitors with Anti-inflammatory Activity  J. Med. Chem., 2006, 49 (7), pp 2166–2173  DOI: 10.1021/jm050538l

[10]  Kinemuchi H, Sugimoto H, Obata T, Satoh N, Ueda S.  Selective inhibitors of membrane-bound semicarbazide-sensitive amine oxidase (SSAO) activity in mammalian tissues. Neurotoxicology 2004 Jan;25(1-2):325-35.

 

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