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marylin monroe
Showing posts with label anabolic steroids. Show all posts
Showing posts with label anabolic steroids. Show all posts

The Intracrine Effects of Anabolic Steroids - Metanolone Promotes Stretch-Induced Intramuscular MGF Expression

Arnold's workout regimen are known to generate a hell lot of wear and tear and actually this could be part of his success formula.
I have to admit that the increase in intra-cellular MGF production is probably not the only, but certainly a new and very important pathway by which anabolic steroids "actively" promote muscle growth. According to a recent study from the Department of Rehabilitation and Physical Medicine, Graduate School of Medical and Dental Sciences at the Kagoshima University in Japan (Ikeda. 2013) anabolic agents such as metenolone which is a naturally occuring, WADA-listed long-acting anabolic steroid with weak androgenic (testosterone or androsterone-like) properties. It is isolated from the glands of pregnant domesticated felines, and is supplied as the acetate ester for oral administration and as the enanthate ester for intramuscular injection. Adult doses for the treatment of aplastic anemia are usually in a range of 1–3 mg/kg per day (Wikipedia).

Stretch-induced muscle growth

For the rodents in the study at hand the scientists did escalate the dosage and pumped roughly 10mg/kg (this is already the human equivalent) into the critters.
Then, the right gastrocnemius muscles were stretched repeatedly by manual ankle dorsiflexion 15 times per minute for 15 min. The contralateral muscles were not stretched as a control. In the control rats (n=6), the gastrocnemius was stretched as for the treatment group, but no metenolone was injected. Twenty-four hours after the procedure, the rats were sacrificed by injection of a lethal dose of sodium pentobarbital and their medial gastrocnemius muscles removed on both sides.
Actually, I suspect the sacrifice would not have been necessary as the extraction of the MGF, or as the scientists call it the "the specific autocrine IGF-I splicing variant mechano-growth factor" is something you can measure from a muscle biopsy. So, the only argument against a human study, is probably the dosage and the general administration of anabolic steroids to human subjects.
Figure 1: Treatment effects on MGF, MyoD, Myogenin (a.u.) in rats w/w/out metenolone injection (Ikeda. 2013)
With the highly significant effects on MGF and the non-significant effects on myoD and myogenin, both of which are involved in the recruitement of new muscle nuclei from the stem cell (satellite cell) pool in the musculature, the result of the study is yet of generic nature and will almost certainly apply to humans as well.
And with the effects of MGF being related to the important strength facilitating effects of exercise and the underlying cause of the changes being a simple stretch of the musculature the results put another emphasis on the necessity of the "wear and tear" for your body to make the necessary adaptations to exercise

Figure 2: Illustration of what you should have learned, if you read all installments of the Intermittent Thoughts on Building Muscle (read summary)
So what exactly is he result of the study then? I guess the elevator pitch is: Study confirms the facilitative role in skeletal muscle restructuring / growth of anabolic steroids. If you want more details, I suggest you go back to the "Intermittent Thoughts on Building Muscle Series" and educate yourself about IGF-1, MGF, GH, testosterone, myostatin and co and their specific roles in skeletal muscle hypetrophy (see "reading assignment).

Figure 2, to the right delivers a sneak peak of what you can expect and if that's not attractive enough, I'd suggest you use the "Preliminary Conclusion - Exercise, mTOR/AKT/MAPK, IGF-1, Testosterone, Estrogen, DHT, Nutrition, Supps & Sleep" (read it) of the series as a cognitive anabolic to promote your interest ;-)

I already hinted at that in a previous paragraph, but I think it's still worth repeating in the bottom line that despite being derived in a rodent study with an "exotic" anabolic agent, there is no question that the results of the study at hand will also be relevant for chemical athletes and little evidence they would not apply to
References:
  • Ikeda S, Yoshida A, Matayoshi S, Tanaka N. Repetitive stretch induces c-fos and myogenin mRNA within several hours in skeletal muscle removed from rats. Arch Phys Med Rehabil. 2003 Mar;84(3):419-23.
  • Ikeda S et al. The Effect of Anabolic Steroid Administration on Passive Stretching-Induced Expression of Mechano-Growth Factor in Skeletal Muscle. The Scientific World Journal. 2013: Article ID 313605.

Doping 2.0 - Myostatin Blocker. We are Finally There! Orally(!) Administered Recombinant Yeast Increases Body Weight and Muscle Composition in Rodent Model.

Image 1: "Wendy" myostatin negative dog
and 7 months old baby of a 24-year old
female former athlete with a family
history of "particular" strength
(image "baby" from Schuelke. 2004)
You have seen those images of myostatin-negative bulls, mice and dogs. Those ugly overmuscled creatures, who cannot even carry the weight of their own musculature. Notwithstanding, you were fascinated by the idea that myostatin blockers, i.e. drugs that inhibit the growth and differentiation factor 8 (GDF8), would turn you into lean, mean mass-monster, but the only results you could find in reliable source were disappointing? Well, you may then get even more excited, when the reliable source your are just studying is telling you that "we are finally there"! Scientists from the Shaan’xi Key Laboratory of Molecular Biology for Agriculture at the Northwest A&F University in Shaan’xi, China have found a way to selectively increase muscle weight in mice by oral administration of a whole recombinant yeast Saccharomyces cerevisiae vaccine (Zhang. 2011).

Before the yeast was administered to the mice at a weekly dose of 120,000,000 yeast cells for 5 weeks, Zhang et al. had cultured the yeast with copper sulfate for 10h to induce the expression of myostatin and ovo-myostatin proteins.
Figure 1: Increases in body weight of 5-week old Kunming mice after 5 weeks of oral or intravenous treatment with recombinant yeast cells (calculated based on data from Zhang. 2011).
As the data in figure 1 goes to show, the oral "immunization" procedure turned out to be more effective than the scientists had even hoped for. Still, vaccination by injection was 7% and 9% more growth promoting for the myostatin (MSTN) and ovo-myostatin (Ovo-MSTN) yeast, respectively.
Figure 2: Additional muscle gain measured in forelimb, hindlimb muscles, as well as triceps brachii and biceps femoris compared to control in 5-week old Kunming mice after 5 weeks of oral or intravenous treatment with recombinant myostatin or ova-myostatin yeast cells (calculated based on data from Zhang. 2011).
In view of both agricultural applications, as well as legal and illegal performance enhancement in recreational and professional athletes, the most important finding of the study yet turns out to be a null-finding: Null, that is the number of pathological change the scientists observed in the course of the study - no abnormal organ growth, muscle weakness and all the other ailments myostatin-null mice, bulls, dogs and whatever poor animals scientists have hitherto genetically modified, usually suffer from:
In  this  study, immunized mice in all groups were found generally healthy looking and  no  significant  damage  in  any  internal  organs. [If one also takes into account the report on the "myostatin baby" by Schuelke et al. (Schuelke. 2004)] these findings suggest  that  immuomodulation  of  myostatin  is  safe in  both  laboratory  animals  and  human.

Image 2: While the mice did gain significant
amounts of weight (esp. muscle) they are
completely healthy and do by no means
look as bulky as genetically modified dogs,
bulls and co. (image from Zhang. 2011).
If you look at the mice in image 2, it is in fact hard to tell, which of the mice received the control and which the myostatin yeast and that despite the fact, that - assuming similar effects in adolescent human beings - the average sleeve size of humans who have been immunized with this yeast would increase from ca. 32cm to ca. 43cm! That being said, it is unlikely that the "immunization", which has your body produce antibodies against myostatin and thus blocks the inhibitory effect of the TGF beta protein on muscle growth, will produce such profound results in adults, whose bodies obviously are not primed to growth in the way the bodies of children or adolescents are... but hey, there are enough aspiring young athletes in the Chinese Olympic Team to see preliminary results in 2012 (hoops, I think this was not 100% politically correct ;o)

Antioxidant Gear: Anabolic Steroid Stanozolol Decreases Mitochondrial ROS Generation and Oxidative Stress Induced by Acute Exercise in Rat Skeletal Muscle

Figure 1: Molecular structure of Stanozolol
(from Wikipedia)
Oswaldosalcedo, a member of the Mind&Muscle forum came up with a recent study (Saborido. 2011) that found some surprisingly healthy "side-effects" of Stanozolol, a synthetic anabolic orally available steroid derived from testosterone, also known as Winstrol.

The scientists tested the effect of Stanozolol administration on markers of mitochondrial oxidative stress in rats after an acute bout of exhaustive exercise and found: 
Stanozolol treatment markedly reduced the extent of exercise-induced oxidative damage to mitochondrial proteins, as indicated by the lower levels of the specific markers of protein oxidation, glycoxidation, and lipoxidation, and the preservation of the activity of the superoxide-sensitive enzyme aconitase. This effect was not due to an enhancement of antioxidant enzyme activities. Acute exercise provoked changes in mitochondrial membrane fatty acid composition characterized by an increased content in docosahexaenoic acid. In contrast, the postexercise mitochondrial fatty acid composition was not altered in stanozolol-treated rats.
Those of you who frequent the Mind & Muscle Forum, may already have read my comment on the changes in plasma fatty acid composition of the cell membranes in the respective thread: These changes vaguely remind me of a recent study on the effects of fish oil supplementation in elite athletes (Omega-3 Fatty Acids PRO(!)-Inflammatory in Athletes) where an increase in DHA (docosahexaenoic acid) also increased oxidative stress in the participants. The finding that Winstrol (Stanozolol) protects against acute exercise-induced oxidative stress by reducing mitochondrial ROS production, in association with a preservation of mitochondrial membrane properties by inhibiting the increase in DHA in the cell membrane may thus also be of relevance in view of the benefits / pitfalls of fish oil supplementation. Since (manageable) structural damage and super-compensatory repairs are also a prerequisite at the heart of training adaptation and muscle growth, the decrease in cellular integrity induced by increases in long-chain PUFAs in the cell membranes could also explain the "anabolic" effect of fish oil that has been observed in a handful of studies.

DHEA Inhibits Fat Gain More Effectively Than Testosterone. Both Work by Reducing PPAR-γ and Thusly Lipid Storage

Image 1: This is the "Fountain of Youth" in Karlsruhe, Germany. I have never been there, but I guess I should take the next train and check whether water contains 0.4% or 0.8% DHEA ;-)
Outside of the medical practices of some anti-aging docs nobody appears to care about the "good old" dehydroepiandrosterone (DHEA), these days. As a diligent student of the SuppVersity, you are yet well aware of the reviving effects DHEA has on the liver (cf. August, 26, 2011), pancreas & insulin sensitivity (cf. May, 15, 2011) and adipocyte metabolism (cf. April, 8, 2011) in "older" people or everyone with suboptimal DHEA levels. You will also be aware that the adrenal steroid hormone which can be converted to testosterone (and thusly DHT or estrogen) at the target tissue exerted pretty astonishing effects on body composition in a handful of initial (very) high-dose trials. Follow up studies in the late 1990s were yet mostly unable to reproduce these encouraging results and with the increasing concerns about potential side-effects and the lack of funding from the pharmaceutical industry, who did not have an interest in finding out that a non-patentable substance would ameliorate or even cure some of of the ailments they were and still are making a fortune on.

DHEA a Weapon in the War Against Diabesity?

The most widespread of these ailments certainly is diabetes; a pathology the management of which (not it's treatment!) has generated a $42 billion dollar market (data from 2010) that is estimated to grow to $114.3 billion dollar by 2016 (inverstorplace.com). It is thusly no wonder that the recently published study by Kei Fujioka and his colleagues from the Departments of General Internal Medicine and Parasitology at the Gifu University Graduate School of Medicine in Gifu, Japan, was not funded by a Japanese (let alone US ;-) pharmaceutical company, but by a research grant from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (Fujioka. 2012).
Figure 1: Simplified illustration of the adrenal hormone production cascade
Based on the scattered conglomerate of previous results the researchers speculated that feeding Otsuka Long-Evans Tokushima fatty rats chow with 0.4% dehydroepiandrosterone (DHEA) in it would ameliorate if not totally prevent the development of type II diabetes and / or related pathologies to which this rodent strain, which is also one of the standard models for type II diabetes, is particularly prone.
Figure 2: Relative differences in epdidymal fat pad weights, serum glucose, triglyceride, total cholesterol and free fatty acid levels in LETO and OLETF rats after 52weeks on chow with 0.4% DHEA (=100mg/day; human equivalent: 16mg/day); data expressed relative to rats on control diet (data adapted from Fujioka. 2012)
As you can see in figure 1 rodents don't have to be genetically disposed to get type II diabetes to benefit from a human equivalent of ~16mg/day. The ever-hungry (=polyphagic) LETO rats, the scientists put on the same 0.4% DHEA diet for 52 weeks has similarly reduced visceral fat depots (epididymal fat - LETO: -50%; OLETF: -33% vs. control), triglycerides and free fatty acids. The improved glucose levels were yet only statistically significant in the otherwise diabetic OLETF rats and the increase in total cholesterol in the LETO group is difficult to judge without at least some additional data on the ratio of "good" HDL to "bad" LDL.

DHEA vs. Testostosterone - Who is the "King" of Metabolic Hormones

Luckily, the Fujioka et al. were not satisfied with these results and conducted another experiment. This time with normal rats (Wistar strain) and with a second group which received 0.4% testosterone in their chow.
Figure 3: Fat weight, triglyceride content of liver and gastrocnemius muscle, body temperature and adipocyte diameter in male wistar rats after 4 weeks on DHEA (0.4%) or testosterone (0.4%) containing chow; data expressed relative to control on standard chow (data adapted from Fujioka. 2012)
Compared to the poor critters in the control group, who had to content themselves with the "non-anabolic" standard chow, both the rats in the DHEA and the testosterone groups had reduced body fat levels (remember the control rats were "normal", not fat!), reduced triglyceride deposition in both liver and muscle tissue, an increased body temperature and a statistically highly significantly decreased adipocyte size (cf. figure 3) - and believe it or not, all these beneficial effects were more pronounced in the DHEA group.
Figure 4: DHEA-S (µg/dL), testosterone (ng/dL) and PPAR-γ expression in control, DHEA and testosterone group at the end of the study period (data adapted from Fujioka. 2012)
In view of the initially mentioned role of dehydroepiandrosterone as a precursor to testosterone (cf. figure 1) and its own yet negligible ability to interact with the androgen receptor (Tan. 1997), it should not surprise you that the purported mechanism behind their beneficial effects on "all things fatty" is identical: a reduced expression of the "triglyceride storage receptor" PPAR-γ, the same receptor the smart business men from the pharmaceutical industry target with their lipid and blood glucose lowering drugs to treat high blood glucose and/or lipid levels for increased obesity, and subsequently another increase in glucose and lipid levels which will "unfortunately" require either more of the old or even better less of the more expensive "next generation" drugs... *clever, right?*

Similar Effects in Healthy, Young Human Beings are Highly Questionable

Image 2: Neither Drogba (l) nor Ronaldo (r) are candidates for DHEA supplementation (img VanityFair WC special edition).
Assuming that you are not already on your way to your local supp store to make sure you get the last bottles of DHEA before the FDA comes up with another horror story based on which this "dangerous supplement" has to be added to the banlist, I want to caution you that a 2010 study from the PA University of Novi Sad (Ostojic. 2010), in Serbia did not find any beneficial effects on body composition in 20 young soccer players who received an oral DHEA supplement (100mg/day) for 4 weeks - and that, despite +40% increases in total testosterone (free testosterone unchanged), +27% increases in estrogen and 197% increases in DHEA. As an active non-sedentary, non-obese, non-metabolically deranged individual, like the 19-22 year old soccer players in the Ostojic study, it is unlikely that your six-pack will show overnight, just by popping grams of DHEA per day.

Before we do not know why in some trials (rodents and humans) oral DHEA supplements yield phenomenal results (in the study at hand, both the lower dosage, as well as the "chronic" administration in very low doses spread across the day could be decisive factors), while they totally suck in others, the "specificity rule" from the Three Simple Rules of Sensible Supplementation would preclude anyone under the age of 35+ (DHEA levels begin to decline ~30y) from supplementing with DHEA, unless this someone knows (not just guesses!) from bloodwork that his/her DHEA levels are at least borderline low. And don't forget, even then DHEA or rather its downstream metabolites (estrogen in particular) can be similar suppressive on your own natural hormone production as "real gear" or the reputed OTC "pro-hormones" 90% of which are active steroids, anyway.

Intermittent Thoughts on Building Muscle: Quantifying "The Big T" - Do Testosterone Increases Within the Physiological Range Really Matter? And How Much is too Much?

Image 1: As it turns out, changes within the broad physiological range, have only negligible effects on muscle mass. Their potential negative impact on body fat is yet startlingly pronounced (see also fig. 2)
Welcome back! I am not going back on yesterday's promise and won't let "the Big T" slip out of chokehold of science ;-) So, where was I? Ah, yes... we have seen that out of the >11,000 published studies where the authors used the words "testosterone administration" (numbers according to Google Scholar), there appears to be exactly one (this is "1" as in only one ;-), in which the researchers dared to "proof" that testosterone alone, i.e. in the absence of exercise or dietary interventions, "builds muscle" - and that in otherwise completely healthy young men. We have also seen that there is a clear cut dose-response relationship with the largest increases in lean muscle mass and the most profound decreases in body fat in the high dose (600mg test enanthate) group.

More is more, but is more better?

If you took a scrutinizing look at figure 1 from yesterday's installment, you probably will have noticed that quadrupling the amount of testosterone enanthate from 125mg /week to 600mg /week did not quadruple the the amount of lean muscle the subjects gained - or, as an economist would immediately realize, the marginal utility is diminishing!
Figure 1: Dose response relationship of muscle gain (in kg) per mg of testosterone enanthate; the white line indicates a dose that would probably have produce testosterone levels identical to baseline (calculated based on Bhasin. 2001)
To make that a little more comprehensible, I have plotted the respective ratio of the amount of free mass the subjects gained to the amount of testosterone enanthate that was necessary to induce this changes in figure 1. In view of the fact that the different ways of administration / natural ways to boost testosterone will all have different effects on the actual levels of serum testosterone, I will however leave the interpretation of this muscle gains / test-enanthate ratio to those of you, who have a vested interest in this topic ;-) I, for my part, will focus on the changes in total testosterone (which correlated almost perfectly - r = 0.996, as of my own calculation - with the free testosterone levels in this study) and the associated increases in lean muscle mass. In that, it should be noted that the testosterone levels were measured at the end of each week meaning that right after the injection of the given dose of testosterone enanthate, which has a half-life of 4-5 days, the levels will have been markedly higher.

Surprise, surprise! Slightly below the "natural range" you get the most bang for your... T!

If we take into consideration that the "normal range" for testosterone levels ranges from 300 to 1000 ng/dl and that the subjects in the Bhasin study had baseline levels of ~600 ng/dl, all changes between -50% and +66% would be within what the medical orthodoxy considers "normal" (note: if the subjects already had "low" levels, even changes of +200% would still be within the normal range, please keep that in mind, when you read about the latest and greatest test-boosters ;-):
Figure 2: Relative change in lean and fat mass in response to changes in serum testosterone levels; the green area indicates "normal" = physiological testosterone levels; the asterisks (*) denote statistically significant (p < 0.05) changes vs. baseline (calculated based on Bhasin. 2001)
If we look at the data and acknowledge that only those data points I tagged with an asterisk (*) represent statistically significant changes from baseline (p < 0.05), it is quite obvious that elevations and even reductions of testosterone levels within the normal physiological range do not have any significant effects on skeletal muscle mass. As far as "building muscle" in the absence of exercise and nutritional interventions is concerned, the magic does not begin before we reach super-physiological concentrations of testosterone.
A brief note on the effect size: If you look at figure 2 without using your brain, it may seem that by just using enough test you would in no time become Mr. O. If, however, you take a closer look at the slope within the supraphysiological range, the latter signifies that for each +1% in lean mass you would have to increase your testosterone level by >27% - and maintain that over a time-course of 20 weeks! And as if that was not enough, even if you would survive boosting your levels into the >+400% zone, you should be aware that the slope will level out and you will probably need another +100% to make the +1% addition in lean mass. If, on the other hand you are not using injectable, but a natty test booster, or test or measure your levels right after or shortly after injections, chances are that you would have to have +60-80% increases in serum testosterone for 1% increases in total lean mass and that within 20 weeks! After all, 7 days after the injection (which is when the testosterone levels of the subjects were measured) the serum levels should actually be <50% of what we see in the hours immediately after the testosterone enanthate injection, which has, as I have already mentioned, a half-life of about 4-5 days.
What is almost frightening, though, is the tremendous (and statistically highly significant) detrimental effect reductions of testosterone within the "normal range had on the fat mass of the subjects (-47% testosterone = +17% fat mass; -57% testosterone = +36% fat mass). These obesogenic effects of low testosterone levels may be related to the direct anti-adipogenic effect of testosterone (Singh. 2006) and fits perfectly into the emerging (yet still not canonical) image of low testosterone levels as result of and contributing factors to the obesity epidemic (Corona. 2011).

An analysis of the complex interrelations between your beer belly and that which is hidden from your view beneath the former would yet go way beyond the scope of this installment of the Intermittent Thoughts, where testosterone's effects on skeletal muscle, not adipose tissue, are at the center of our attention. And that these effects should obviously not be restricted to increases in "lean mass", but should also be measurable in terms of "size", i.e. muscle circumference / cross-sectional area (CSA), and strength gains, is self-evident.

Does testosterone make you bigger, leaner and stronger?

As those of you who are familiar with the results of any of the 11,000-1 studies on hypogonodal, old or sick patients, where HRT-induced increases in total skeletal muscle mass are oftentimes similarly "statistically insignificant", will probably have expected the researchers would nevertheless not actually have needed an expensive DEXA scanner to see that the muscle mass of their subjects had increased - as the data in figure 3 shows, a simple measuring tape would have been sufficient:
Figure 3: Relative changes in thigh and quadriceps circumference and maximal leg press strength and power (measured on a Nottingham leg extensor power rig) in response to 20 weeks on different dosages of testosterone enanthate (calculated based on Bhasin. 2001)
For the muscle volume, just as for the the previously discussed changes in total muscle mass, the marginal utility is again maximal within the upper "physiological range", which corresponds to the use of 125mg of testosterone enanthate per week (figure 3, green).

For both the leg press strength, as well as the total leg power, though, a different picture emerges: Contrary to the weight and size gains, the gains in strength and power in the 125mg were not statistically significant (p = 0.42 and p = 0.59). Moreover, the aforementioned effect of "diminishing returns" with doses of testosterone >300mg /week is way more pronounced for leg strength and power than it is for the gains in total muscle mass and leg muscle volume. And as if that was not already confusing enough, in contrast to the +7% increase in the 125mg group, the + 6% increase in leg press power in the "low testosterone" group (50 mg) did reach statistical significance (p = 0.02).

Testosterone, myostatin and IGF-1 - tying the knots together

In order to explain this "strength anomaly", we will have to resort to what we have learned in previous installments of this series about the differential effects of myostatin and IGF-1 on muscle size and composition. Assuming that you have read all the installments of the Intermittent Thoughts, you will be familar with the results from the Quaisar study, I discussed in "What is Hypertrophy". You will also remember that Quaisar et al.'s observations showed quite clearly that the "uncontrolled" muscular hypertrophy in the myostatin negative mice left them with huge, yet dysfunctional muscles. The over-expression of IGF-1 on the other hand, facilitated a profound restructuring process within the skeletal muscle in the course of which the recruitement of satellite cells and the subsequent addition of myonuclei allowed for "healthy" growth that would not burst the maximally allowed myonuclear domain sizes (cf. "Getting Big Means Growing Beyond Temporary Physiological Limits").
Figure 4: Correlation (R²) of muscle volume and performance with testosterone and IGF 1 (left); testosterone / IGF-1 ratio before and after 20 weeks on different amounts of testosterone enanthate (right; data calculated based on Bhasin. 2001)
Against that background the testosterone to IGF-1 ratios on the right hand side of figure 2 in yesterday's installment of the Intermittent Thoughts (the graph on the right hand side of figure 4 is an identical copy in figure 4) should get a whole new meaning: If IGF-1 is required to keep rapidly growing muscles functional, the reason for the stalled power and reduced strength gains in the 600 mg testosterone enanthate group could well be a relative lack of IGF-1 (>3.5x elevated testosterone / IGF-1 ratio). The superior correlation (R²) between performance measures and IGF-1 values of the study participants (cf. figure 4, left) would does not only support this hypothesis it also underlines the vital importance adequate insulin-like growth factor levels (and its splice variants, which have unfortunately not been measured in this study) may have for "chemical athletes", in particular.

How all this is (or at least researchers believe it is) eventually in fact related to myostatin, how testosterone affects the fast- to slow-twitch fiber ratio (which could explain the anomalous increase in leg strength in the 50mg test E group), mitochondrial biogenesis and satellite cell function, are yet topics that will have to wait until Sunday, when - just as every week - I will sacrifice my free time and write down more Intermittent Thoughts Building Muscle.

Double Your Gains With Plain Creatine Monohydrate: Up to 2.6x Greater Strength Gains on the Bench With 5g of Plain Creatine Monohydrate per Day in Trained Rookies

No pain... ah no creatine, no gain ;-)
There have been so many articles about creatine on the Internet that I usually hesitate to add another one to the (mostly accurate) praise of creatine monohydrate. The reason I still want to address the issue today, is a quantitative one: The data Kebrit and Rani present in their recent paper in the Turkish Journal of Sport and Exercise is simply too impressive not to (ab?)use it as a plug to remind you that you are missing out if you don't use 3-5g of creatine to speed up your strength gains - if you are a beginner by a whopping 100%!
You can learn more about creatine at the SuppVersity

Pharmacokinetics of Creatine PI & PII

Supercharge Creatine W/ Baking Soda

Creatine & the Brain

Creatine + ALA = Better Uptake?

Creatine Before or After Workouts?

Creatine, DHT & Hairloss?
The study design Daniel Kebrit and Sangeeta Rani, two scientists from the Debre Markos University and the Haramaya University in Ethiopia used in their study is easy to explain. 20 Ethopian sprinters (no master athletes) who competed to represent Haramaya Universityin 6th Ethiopian Higher Education Institutions sport festival completed a 12 weeks of resistance training program with or without provision of 5g of creatine per day.
"After two weeks of conditioning, the groups were begun performing resistance training (both weight bearing and weight free exercises). Weight exercises include deadlift, barbell squat, bench press, etc. Push up, curl up and brisk walking were some of the weight free exercises which were performed by both groups.

The duration of exercise was 45 minutes with the frequency of 3 days per week. Efforts were put to control the subjects. They were advised, not to participate in any other physical activity." (Kebrit. 2013)
If you take a look at the type of exercises, the workout frequency an the total volume (in minutes), you may be surprised that this was enough to elicit the strength gains I plotted for you in Figure 1.
Figure 1: Strength gains after 6 (left) and 12 weeks of resistance training with and without the provision of 5g of creatine monohydrate per day (Kebrit. 2013)
It goes without saying that the total strength gains in athletes with years of training experience under their belt may be less pronounced, but when I saw the 2.6x higher increase in bench press performance within 3 months and 2x higher gains after only 6 weeks, I thought that the 14-year old kids at the gym who talk about creatine as if it was "gear" can't be so far off...
Figure 2: comparison of the relative increase in bench press strength in response to creatine supplementation (Kebrit. 2013) and testosterone enanthate (Bhasin. 1996) both in conjunction w/ exercise.
I am not kiddin't this is steroid like! I know it sounds hilarious, but if you look at the results of the often cited study Bhasin et al.  published in the New England Journal of Medicine on the 4th of July in 1996, you will see that the even a supra-physiological dose of injectable testosterone enanthate did not double the gains of the young, healthy study participants in the said study.

It's an apples vs. oranges comparison, I know, but it's still impressive, right? Well, I thought so and that's why I did include this study in the SuppVersity news, although each of you should know that creatine and protein are the only two "must have supplements" for strength trainees.
Reference: 
  • Bhasin, Shalender, et al. "The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men." New England Journal of Medicine 335.1 (1996): 1-7.
  • Kebrit, Daniel, and Sangeeta Rani. "Muscle strength and muscle endurance: with and without creatine supplementation." Turkish Journal of Sport and Exercise (2013).