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Creatine and methylation


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#1 pSimonKey

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Posted 11 August 2005 - 08:34 AM


The Creatine Secret - Part 1
by Alfredo Franco-Obregón, PhD



Background

Setting the Stage for Muscle Growth

It is a safe bet that most athletes never stop and think about their “methylation status”. Ironically, most athletes do spend huge amounts of mental energy scheming of ways of peaking their “anabolic status” in hopes of stimulating muscle growth. In truth, however, methylation and anabolism are inextricably linked processes. Figuratively speaking, methylation sets the stage on which anabolism is played out.



What is Methylation?

Without a doubt, methylation is one of the most commonly employed forms of cellular regulation. Estimates are that the body performs this indispensable process billions of times each second just to maintain life. Without going into too much detail, methylation is the attachment of a methyl group (CH3) to a biomolecule. And, although seemingly insignificant in complexity, this process can profoundly influence your ability to build new muscle tissue as well as to offset the decline in physical and mental capacities that typically accompany aging. The scope of this biochemical process is (in all honesty) all encompassing. Methylation is applied at the levels of our genes as well as is responsible for functionalizing many known growth factors, hormones, neurotransmitters, metabolic mediators and structural components of the cell. Indeed, life itself would not be possible without methylation, much less muscl e growth. For an athlete there is no room for compromises in methylation capacity.



How does Creatine Influence Methylation?

A small sampling of the important molecules activated by a methylation reaction include adrenaline, carnitine, DNA, the polyamine growth regulators (putrescine, spermidine and spermine) and, of course, creatine. In fact, the synthesis of creatine is the single greatest drain of the body’s methyl reserves, consuming over 70% of the body's entire supply. Furthermore, given that the body’s methyl reserves are limited in size, creatine synthesis alone could potentially create a state of methyl-deficiency. In a physiological sense, we have three principal options: (1) increase the size of the body’s methyl reserves; (2) increase the recycling rate of the body’s methyl reserves; or (3) create a scenario where the body no longer needs to synthesize creatine; that is, provide all the creatine the body needs through the diet. In this respect, athletes who supplement with creatine monohydrate are in fact, putting this third scenario into play, essentially sparring their methyl reserves and making more methyl groups available for the activation and synthesis other extremely important cellular targets.



Authors Note: It is my personal belief that many of the “mysterious benefits” often attributed to creatine supplementation, but lacking full explanations, have to do with its ability to increase the body’s capacity to methylate important cellular targets, including our genes and essential anabolic modulators.




Simply Increasing Methyl Intake is the Wrong Approach

The body stores methyl groups in the form of a molecule known as S-AdenosylMethionine, or SAM. SAM is a derivative of the essential amino acid, methionine. The problem is, however, that the byproduct of SAM utilization utilization (de-methylation) is a new molecule known as homocysteine. And, homocyteine is bad real news for our overall h ealth and emotional well-being. Elevated homocysteine levels have been implicated in the development of Down’s syndrome, Parkinson’s disease, Alzheimer's disease, stroke, dementia, coronary heart disease, vascular disease, anemias, renal disease and hepatic disease. Therefore, simply increasing our methionine intake (creating a surplus of SAM to be potentially converted into homocysteine), without taking into consideration the process of reconverting homocysteine into SAM, is a very dangerous physiological scenario. Therefore, although methionine intake is imperative in sustaining the methylation reactions that are necessary for life, not disposing of the homocysteine created from methionine consumption is counterproductive to health.



Homocysteine & Sex!

The elevated levels of homocysteine in the blood stream are highly indicative of the chances of developing several human disorders. For instance, serum homocysteine levels are typically 1.5 microMolar higher in men than women, ultimately translating into a 15% greater risk of cardiovascular disease in males. The source of this disparity is the significantly larger amounts of muscle mass in men, necessitating greater amounts of endogenous creatine synthesis to meet muscular requirements; remember, creatine synthesis produces homocysteine. Creatine supplementation may hence represent an effective strategy to reduce serum homocysteine levels in males (or anyone) at high risk of developing cardiovascular disease.




Complete Reliance on Creatine Synthesis Also Elevates Serum Homocysteine Levels

Oddly, just as over-consumption of methionine-rich food sources might elevate serum homocysteine levels, so does their under-consumption. This seeming paradox stems from the fact that meat and fish, as well as being good sources of methionine, are also rich sources of creatine. Therefore, under-consuming sources of dietary creatine, increases the need for creatine synthesis and consequently, increases the production of homocysteine.



Essential B-Vitamins Reduce Serum Homocysteine Levels

The principal mechanism whereby the body rids itself of homocysteine involves two B-vitamins, folate and B12 (shown in red in figure). Originally, folate received its name from folium, the Latin word for leaf. Nearly 70 years ago (1941) an American scientist named Esmond Snell isolated a "growth factor" from spinach (leafs) that promoted cell division and growth. In truth, however, the life-sustaining properties of folate had been unwittingly demonstrated a few years before Snell's isolation. In 1938 Robert Stokstad identified a component from yeast that was effective at treating megaloblastic anemia. Stokstad named his healthful agent "Factor U". Subsequently, exact chemical characterization demonstrated Snell's folate and Stokstad's mysterious Factor U to be one in the same.

Nearly four tons of spinach leafs were required by Snell to isolate enough folate for initial biochemical characterization, indicating that plants contain only scant amounts of folate. The richest natural sources of folate are in fact, of animal origin, in particular, the liver. B12 (cobalamin) is the other B-vitamin used to neutralize homocysteine and is similarly enriched in animal products, especially milk and cheese.

It is now known that folate and B12 act collectively by re-methylating homocysteine, thereby recreating methionine, which is then quickly converted into SAM by the cell. Therefore, supplementing with these important B vitamins has two important consequences: (1) it replenishes the body's SAM reserves; and (2) it removals potentially dangerous homocysteine from the blood stream. In essence, folate and vitamin B12 are the body’s most important methionine recyclers.




Creatine synthesis produces homocysteine that needs to be removed from the blood stream (before harm is done to the organism) with the assistance of the B vitamins, folate and B12. Importantly, creatine supplementation, by circumventing the need for creatine synthesis, effectively spars the body's methyl reserves and diminishes the production of homocysteine.

Take a closer look at the creatine synthesis here: http://www.creatinem.../synthesis.html




In this unique sense, vegans represent a worst-case scenario. First, animal proteins are the richest natural sources of creatine. And, as mentioned previously, dietary creatine deficiency results in creatine synthesis presiding over all else. Complete reliance on creatine synthesis, in turn, results in homocysteine levels rising dangerously. Secondly, animal proteins are also very good sources of folate and vitamin B12. These B vitamin are needed to re-create methionine (SAM) from homocysteine, effectively completing the methylation cycle. Therefore, the dual absence of creatine and essential B vitamins from the diet creates a potentially very dangerous scenario that would completely undermine muscle growth and recovery.



Maximizing Methylation Status for Optimal Anabolism

Frankly, a suboptimal methylation status will put the brakes on muscle growth! In this respect, combining creatine supplementation with targeted vitamin B intervention will doubly amplify muscle anabolics by maximizing the body’s methyl reserves while simultaneously providing a greater training stimulus for muscle growth.

Essential B vitamins will also assist in the final stage of creatine synthesis by increasing the availability of SAM. This effect of B vitamins, in turn, means that lower doses of creatine can be taken to produce the same benefits. This strategy (see guide, below) is highly recommended for the elderly, persons wishing to alleviate the symptoms associated with taking large amounts of creatine as well as anyone predisposed to renal dysfunction.



Doses of Folic Acid & Vitamin B12

Surprisingly, the folate found within natural sources is not readily available to the body, as it exists in large conglomerations of many folates bound by glutamate residues (polyglutamates). These polyglutamates must first be enzymatically cleaved into individual folates (monoglutamates) before they can be absorbed into the blood stream. This process is inefficient, however, reducing the bioavailability of natural folates by as much as 25% to 50%. Here in lies the major advantage of synthetically derived folate, or folic acid; folic acid is more easily absorbed by the body.

Based on scientific studies, to maintain optimal methylation levels an average person in relatively good health should consume between 500-1000 micrograms of folic acid and 100-500 micrograms of vitamin B12 each day. The requirements for an athlete, on the other hand, will be substantially greater, possibly several-fold. Strenuous exercise severely damages muscle, which then needs to be repaired and rebuilt (to a greater degree) during periods of rest; this is the basic paradigm of strength training. It is thus essential that methylation capacity be sufficiently high during moments of recovery from exercise as to support tissue growth and prevent the loss of existing muscle.

Giving urgency to this caveat, a modest 10% loss in muscle mass produces a 30% loss in strength. Translating, a 70 kilogram (154 pounds) athlete who loses 0.7 kilograms (1.5 pounds) of weight because of overtraining, can expect to drop 5-7 kilograms (11-15 pounds) in the bench press, depending on his/her single repetition maximum!



Folate, Cancer & Aging

At the root of all life are nucleic acids, the DNA that comprises our genes. Our genes code for every component that the cell will ever express. That is, the selection of which genes are read will ultimately determine a muscle cell from a brain cell, an active cell from a dormant cell, a growing cell from a degenerating cell, or a young cell from an old cell. In brief, our genes decide who, and what, we are at each point in our existence.

Moreover, methylation determines which genes are read and eventually manifested in the cell. Under-methylation (hypo-methylation) switches the pattern of gene expression to one more commonly associated with cancer. For instance, hypo-methylation of the tumor suppressor gene, p53, leads to a two-fold increase in the incidence of bronchial cancer in male smokers; cigarette smoke severely compromises methylation by degrading cellular folate reserves. Folate deficiency predisposes us to cancer and has been associated with the expression of carcinomas of the colon-rectum, lungs, cervix, esophagus pancreas and breast.

DNA methylation also influences chromosome structure, the cell's ability to repair damaged DNA as well as overall genomic stability. Expectedly, hypo-methylation also results in inefficient replication of DNA, breaks in the chromosomal linear structure and inefficient repair of damaged chromosomes. Folate-based methylation thus protects our genes from spontaneous mutations and chromosome damage that could lead to cancer and cell death.

An age-related decline in methylation capacity is thought to instigate senescence and the loss of physical capacity in the elderly. Folate-deficiency, producing a premature state of hypo-methylyation, may accelerate the normal aging process.

Folate supplementation will thus slow the progressive loss in mental and physical capacities associated with aging as well as protect against many age-related diseases.




Concluding Remarks

Methylation is necessary for cellular proliferation and survival, which, in turn, are the foundations for muscle anabolism. Therefore, optimizing your body’s methylation status is an essential first step in building muscle. And, by far, the best way to maximize your methyl reserves is by combining creatine and vitamin B supplementation, a powerful duo at replenishing the body’s methyl reserves and at priming muscle growth.

Next month we will talk about another vitamin B intervention that will improve an athlete's antioxidant status. Employing this measure, in turn, will greatly augment an athlete's ability to recover from intense exercise as well as further accentuate methylation status.



Scientific References

McCarty, M. F. (2001) Supplemental creatine may decrease serum homocysteine and abolish the homocysteine 'gender gap' by suppressing endogenous creatine synthesis. Medical Hypotheses, Volume 56 (1), pages 5-7.

Stead, L. M. et al. (2001) Methylation demand and homocysteine metabolism: effects of dietary provision of creatine and guanidinoacetate. American Journal of Physiology and Endocrinological Metabolism, Volume 281, pages E1095-E1100.

Taes, Y. E. C. et al. (2003) Creatine supplementation decreases homocysteine in an animal model of uremia. Kidney International, Volume 64, pages 1331–1337.





This article was written by Dr. Alfredo Franco-Obregón, research scientist, author, and owner of Nutritional Supplements Newsletters.

Dr. Franco-Obregón is also the author of Creatine: A practical guide. This guide clearly teaches how to combine exercise, nutrition, and intelligent creatine use for explosive muscle growth, improved athletic performance, and overall good health. A MUST READ for any athlete.

Creatine: A practical guide also analyses the formulations of many of the newer creatine products currently out on the market. Learn which products are truly effective, as well as which are mainly expensive hype.
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#2 Sillewater

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Posted 24 June 2010 - 01:35 AM

I was just looking at some methylation papers and found this one:

Am J Physiol Endocrinol Metab. 2001 Nov;281(5):E1095-100.


Methylation demand and homocysteine metabolism: effects of dietary provision of creatine and guanidinoacetate.
Stead LM, Au KP, Jacobs RL, Brosnan ME, Brosnan JT.

Department of Biochemistry, Memorial University of Newfoundland, St. John's, Newfoundland, Canada A1B 3X9.


Abstract
S-adenosylmethionine, formed by the adenylation of methionine via S-adenosylmethionine synthase, is the methyl donor in virtually all known biological methylations. These methylation reactions produce a methylated substrate and S-adenosylhomocysteine, which is subsequently metabolized to homocysteine. The methylation of guanidinoacetate to form creatine consumes more methyl groups than all other methylation reactions combined. Therefore, we examined the effects of increased or decreased methyl demand by these physiological substrates on plasma homocysteine by feeding rats guanidinoacetate- or creatine-supplemented diets for 2 wk. Plasma homocysteine was significantly increased (~50%) in rats maintained on guanidinoacetate-supplemented diets, whereas rats maintained on creatine-supplemented diets exhibited a significantly lower (~25%) plasma homocysteine level. Plasma creatine and muscle total creatine were significantly increased in rats fed the creatine-supplemented or guanidinoacetate-supplemented diets. The activity of kidney L-arginine:glycine amidinotransferase, the enzyme catalyzing the synthesis of guanidinoacetate, was significantly decreased in both supplementation groups. To examine the role of the liver in mediating these changes in plasma homocysteine, isolated rat hepatocytes were incubated with methionine in the presence and absence of guanidinoacetate and creatine, and homocysteine export was measured. Homocysteine export was significantly increased in the presence of guanidinoacetate. Creatine, however, was without effect. These results suggest that homocysteine metabolism is sensitive to methylation demand imposed by physiological substrates.

PMID: 11595668 [PubMed - indexed for MEDLINE]



Which lead me to this old article. Just thought it was interesting. There's a discussion at M&M about the creatine and DHT study:

http://www.mindandmu...showtopic=42359

Edited by Sillewater, 24 June 2010 - 01:36 AM.


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#3 karoloydi

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Posted 24 June 2010 - 06:34 AM

Interesting stuff.
One question. It says that folic acid and B12 help reduce homocysteine levels.
Is the also true for the methylated versions of this vitamins? (methylfolate & methylcobalamin)

#4 Sillewater

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Posted 24 June 2010 - 06:34 PM

Maybe we shouldn't worry about homocysteine. Methylation looks like a very complicated system that we probably shouldn't mess with:

JAMA. 2010;303(24):2486-2494.
Effects of Homocysteine-Lowering With Folic Acid Plus Vitamin B12 vs Placebo on Mortality and Major Morbidity in Myocardial Infarction Survivors

#5 rephore

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Posted 26 June 2010 - 03:52 AM

Very interesting stuff. I'm going to supplement with creatine again since my muscle gains have slowed down (or stopped). This time I'm going to add some B vitamins. Hope it works.

#6 FunkOdyssey

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Posted 26 June 2010 - 06:24 AM

Creatine lowers homocysteine and improves methylation status in theory -- in practice, well not so much:

Vasc Med. 2009 Aug;14(3):239-48.
The effect of L-arginine and creatine on vascular function and homocysteine metabolism.

Jahangir E, Vita JA, Handy D, Holbrook M, Palmisano J, Beal R, Loscalzo J, Eberhardt RT.

Boston University School of Medicine, Boston, MA 02118, USA.
Abstract

Studies with L-arginine supplementation have shown inconsistent effects on endothelial function. The generation of guanidinoacetate (GAA) from L-arginine with subsequent formation of creatine and homocysteine and consumption of methionine may reduce the pool of L-arginine available for nitric oxide generation. Experimental studies suggest that creatine supplementation might block this pathway. We sought to determine the effects of L-arginine, creatine, or the combination on endothelium-dependent vasodilation and homocysteine metabolism in patients with coronary artery disease. Patients with coronary artery disease were randomized to L-arginine (9 g/day), creatine (21 g/day), L-arginine plus creatine, or placebo for 4 days (n = 26-29/group). Brachial artery flow-mediated dilation and plasma levels of L-arginine, creatine, homocysteine, methionine, and GAA were measured at baseline and follow-up. L-arginine and creatine supplementation had no effects on vascular function. L-arginine alone increased GAA (p < 0.01) and the ratio of homocysteine to methionine (p < 0.01), suggesting increased methylation demand. The combination of creatinine and L-arginine did not suppress GAA production or prevent the increase in homocysteine-to-methionine ratio. Unexpectedly, creatine supplementation (alone or in combination with L-arginine) was associated with an 11-20% increase in homocysteine concentration (p < 0.05), which was not attributable to worsened renal function, providing evidence against an effect of creatine on decreasing methylation demand. In conclusion, the present study provides no evidence that L-arginine supplementation improves endothelial function and suggests that l-arginine may increase methylation demand. Creatine supplementation failed to alter the actions of L-arginine on vascular function or suppress methylation demand. The unexpected increase in homocysteine levels following creatine supplementation could have adverse effects and merits further study, since creatine is a commonly used dietary supplement.

PMID: 19651674



#7 Sillewater

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Posted 26 June 2010 - 08:10 AM

Here's another example of the difference between mechanistic and outcome evidence. This also applies to the whole idea of lowering Hcy through supplementation. Does lowering Hcy actually lower risk? Doesn't look like it to me (but mechanistically it seems like it should). Thanks for the study Funk.

@rephore,

Are you aware of the raised DHT levels in the rugby players who supplemented with creatine? I can't remember the reason, was the Testosterone raised? Sure the effects for muscle/strength is good but do you really want to be bald (that is assuming DHT plays a role).
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#8 rephore

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Posted 26 June 2010 - 10:16 AM

I've been holding off using creatine for a while now. This study helped convinced me to use it again. I may forgo the B vitamins though and just use BCAAs or something similar.

Those "negative" studies are only a handful compared to the hundreds if not thousands of studies for the benefits of using creatine.

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#9 FunkOdyssey

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Posted 26 June 2010 - 03:57 PM

Also seems to raise DHT levels in men which is generally undesirable:

Clin J Sport Med. 2009 Sep;19(5):399-404.
Three weeks of creatine monohydrate supplementation affects dihydrotestosterone to testosterone ratio in college-aged rugby players.

van der Merwe J, Brooks NE, Myburgh KH.

Department of Physiological Sciences, Stellenbosch University, Stellenbosch, South Africa.

Comment in:

* Clin J Sport Med. 2010 May;20(3):220; author reply 220-2.

Abstract

OBJECTIVE: This study investigated resting concentrations of selected androgens after 3 weeks of creatine supplementation in male rugby players. It was hypothesized that the ratio of dihydrotestosterone (DHT, a biologically more active androgen) to testosterone (T) would change with creatine supplementation. DESIGN: Double-blind placebo-controlled crossover study with a 6-week washout period. SETTING: Rugby Institute in South Africa. PARTICIPANTS: College-aged rugby players (n = 20) volunteered for the study, which took place during the competitive season. INTERVENTIONS: Subjects loaded with creatine (25 g/day creatine with 25 g/day glucose) or placebo (50 g/day glucose) for 7 days followed by 14 days of maintenance (5 g/day creatine with 25 g/day glucose or 30 g/day glucose placebo). MAIN OUTCOME MEASURES: Serum T and DHT were measured and ratio calculated at baseline and after 7 days and 21 days of creatine supplementation (or placebo). Body composition measurements were taken at each time point. RESULTS: After 7 days of creatine loading, or a further 14 days of creatine maintenance dose, serum T levels did not change. However, levels of DHT increased by 56% after 7 days of creatine loading and remained 40% above baseline after 14 days maintenance (P < 0.001). The ratio of DHT:T also increased by 36% after 7 days creatine supplementation and remained elevated by 22% after the maintenance dose (P < 0.01). CONCLUSIONS: Creatine supplementation may, in part, act through an increased rate of conversion of T to DHT. Further investigation is warranted as a result of the high frequency of individuals using creatine supplementation and the long-term safety of alterations in circulating androgen composition. STATEMENT OF CLINICAL RELEVANCE: Although creatine is a widely used ergogenic aid, the mechanisms of action are incompletely understood, particularly in relation to dihydrotestosterone, and therefore the long-term clinical safety cannot be guaranteed.

PMID: 19741313






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