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marylin monroe
Showing posts with label immune health. Show all posts
Showing posts with label immune health. Show all posts

Ursolic Acid, Leucine or Placebo for mTOR, IGF-1, Irisin, Size & Strength Gains & Fat Loss? Plus: Tart Cherry Powder as Anti-Oxidant Immune Protector for Athletes

Weights are better than pills, but in some cases, they can also work synergistically.
A new month, a new exercise & supplementation research overview for the "SuppVersity Short News". In today's installment I am going to highlight the latest evidence for the beneficial anti-oxidant & immuno-protective effects of tart cherry powder in endurance athletes. I am going to discuss the disappointing results of a comparison between leucine and ursolic acid as mTOR-elevating, IGF-1 receptor modulators in the post-workout window. And I am going to contrast these findings to the results of a non-sponsored chronic resistance training + ursolic acid intervention from a group of Korean scientists.
Read more short news here at the SuppVersity

Obesity Research Upd. Nov. '14

Exercise Res. Upd. Nov '12(1)

Exercise Res. Upd. Nov '12(2)

Nutrition Res. Update Nov. '14

Weight Loss Tricks & More

Reductive Stress, Iron & the Military
  • Tart cherry powder as anti-oxidant immuno-protector - Scientists from the Texas A&M University reported at the Eleventh International Society of Sports Nutrition (ISSN) Conference and Expo that the provision of tart cherries, not as whole fruits, but in 480 mg capsules that contained a freeze dried powder (one capsule daily), for 10 days leading up to a half-marathon, the 27 endurance trained or triathlete (21.8±3.9 yr, 15.0±6.0% body fat, 67.4±11.8 kg) men (n=18) and women (n=9) completed in less than one hour lead to a significant reduction of the immune response to exercise. In particular, the statistical analyses of the data revealed a...
    "[...] significant group x time quadratic effect [...] for WBC [white blood cell count] (p=0.034) [and] a trend toward a significant delta value based on group assignment for WBC (p=0.09)" (Goodenough. 2014).
    In spite of the fact that the mitigated immune response following exercise did, as Goodenough et al. point out "correlate with the decreased catabolic response indicated by BUN/Cr ratio and cortisol levels reported in a companion abstract", and notwithstanding the results of a similar study which found that
    "acute supplementation with powdered tart cherries over the 7 days leading up to, during, and 2 days after intense resistance exercise helps to minimize post-training perceptions of pain in the most biomechanically loaded regions of the quadriceps muscle group associated with the back squat compared to a placebo" (Levers. 2014),
    the overall benefits are probably negligible for normal trainees. For training junkies and professional athletes, though, the ameliorated stress and immune response, as well as a minor decrease in pain may yet be good reasons to give tart cherry supplements a try.
Homebrew blackberry "supplement" inhibits lipid oxidation.
In case you're not into tart cherries, a recent non-sponsored study that does not use a commercial supplement from the Islamic Azad University (Niloofari. 2014) shows that you can also boil 100g blackberries with some water for 10 minutes, then cool them and place them in a sealed containers in order consume 100ml of the black- berry "soup" daily. In said study the consumption of this extract lead to a significant reduction in the producton of lipid oxidation products in obese subjects during a standar- dized resistance training program. Accordingly, we can assume that this "homebrew" supplement will have similar protective effects on the cell membranes as the capped tart cherry extract from the perviously discussed study.
  • Ursolic acid or leucine, what's more anabolic on paper? Yes, there is a good reason I underlined the words "on paper". Why? Well, the experiment David Church, Neil Schwarz, Mike Spillane, Sarah McKinley, Tom Andre and Darryn S Willoughby conducted may employ a randomized, cross-over design, but still investigated only the acute effects of 3g leucine (LEU), ursolic acid (UA) or placebo on IGF-1 (a serum regulator of MPS) and the Akt/mTOR pathway.

    The 9 apparently healthy, resistance-trained [regular, consistent resistance training (i.e. thrice weekly) for at least 1 year prior to the onset of the study] men between the ages of 18-30 who had volunteered to participate in this study consumed the supplements immediately afer a lower-body resistance exercise that involved 4 sets of 8-10 repetitions at 75-80% 1-RM on the angled leg press and knee extension exercises. A venous blood sample was obtained before, and 0.5, 2, and 6 hr post-exercise, whereas a vastus lateralis muscle biopsy was obtained before and 2 and 6 hr post-exercise. 
    Figure 1: the results of the ursolic acid vs. leucine comparison are not exactly exciting (Church. 2014).
    The analysis of these blood and muscle samples revealed that there were no differences  observed among the three "supplements" (one of them being the placebo) for serum IGF-1 (p > 0.05), the expression of IGF-receptors or the phosphorilation of Akt, and p70S6K (p > 0.05).

    The only significant difference the researchers observed was a significant increase in phosphorylated mTOR in response to the 3g of leucine compared to UA and PLC (p = 0.001).
     
  • Ursolic acid: Different study different outcome - In the defense of ursolic acid it should yet be mentioned that Hyun Seok Bang et al. recently found that the chronic supplementation with 3x450mg/day of ursolic acid lead to concomittant increases in serum irisin and muscle strength, as well as impressive reductions in bod fat in twenty-four Korean men with over 3 years of resistance training experience.
    Figure 2: Changes in body composition (left) and IGF-1 & irisin levels (right) in response to 8 weeks of resistance training + placebo or resistance training + 3x450mg/day of ursolic acid (Bang. 2014).
    As you can see in Figure 2, significant increases in IGF-1 weren't observed in this study either. Accordingly, Church et al. may simply have been betting on the "wrong anabolic horse" and the chronic effects like the strength gain and fat loss Bang et al. observed in their trained subjects alluded them due to the nature of study, i.e. an acute vs. chronic exercise supplementation regimen.
BCAAs Don't Build Muscle, Study Says | Learn more
Bottom line: In view of the fact that the ursolic acid studies teach us not to judge a supplement by an acute / short-term study I refuse to make a commendation for or against tart cherries - no matter, whether they're fresh or powdered.

What I am willing to admit, though, is that the study by Bang et al. (2014) yielded pretty impressive results. Results that are not yet enough to fully convince me that all the hilarious claims you will find on ursolic acid supplements are true, but results that will have me keep an eye on future studies investigating the effect of chronic ursolic acid supplementation on body composition and physical performance | Comment on Facebook!
References:
  • Bang, Hyun Seok, et al. "Ursolic Acid-Induced Elevation of Serum Irisin Augments Muscle Strength During Resistance Training in Men." The Korean Journal of Physiology & Pharmacology 18.5 (2014): 441-446.
  • Church, David, et al. "A comparison of the effects of ursolic acid and l-leucine supplementation on IGF-1 receptor and AKT-mTOR signaling in response to resistance exercise in trained men." Journal of the International Society of Sports Nutrition 11.Suppl 1 (2014): P19.
  • Goodenough, C., et al. "Powdered tart cherry supplementation mitigates the post-exercise immune response with reduction in total antioxidant status and serum triglyceride levels following an acute bout of intense endurance exercise." Journal of the International Society of Sports Nutrition 11.Suppl 1 (2014): P34. 
  • Levers, K., et al. "Powdered tart cherry supplementation demonstrates benefit on markers of catabolism and muscle soreness following an acute bout of intense lower body resistance exercise." Journal of the International Society of Sports Nutrition 11.Suppl 1 (2014): P31. 
  • Niloofari, A., Et Al. "Responses Of Oxidative Stress Indices To Resistance Exercise After Blackberry Extract Supplementation." IJBPAS 3.12 (2014): 2798-2810.

On Short Notice: Nucleotide Supplementation Increases Performance & Fortifies Immune Response. Plus: Oleic Acid Increases, SFA Lowers E2, Testosterone & DHT Binding

Are nucleotides a useful supplements for intensity maniacs and can olive oil reduce your free testosterone levels?
If you have been visiting the SuppVersity for a while now, you were probably surprised to see that the "Short News" (aka "On Short Notice") are back. The reason, I changed my mind and reintroduced this assembly of short news items is that I realized that there is an intemediate category of news and infos between the very short Facebook news that (a) disappear in the oblivion of the SuppVersity Facebook Wall, (b) don't allow me to post graphics that would illustrate the study results and (c) still take some time to write and the detailed analysis in the "original" SuppVersity articles.

So, if you disagree and can give me a good reason why I should not post news compilations like the one at hand more regularly, speak now or forever hold your peace ;-)

Nucliotide supplementation counters immune suppressive effects of exercise

(Ostojic. 2013) - I think I mentioned a similar study a couple of weeks ago in the SuppVersity Facebook News, but since this most recent investigation into the ergogenic effects of the small organic nitrogen-based combinations of a five-carbon sugar and a phosphate group that
  • form the building blocks of nucleic acids, such as DNA and RNA, and 
  • participate in cellular signaling and metabolism
deals with in young, healthy, fit men and their response to the provision of a supplement that looks similar to something you are probably goint to see on the market pretty soon, I thought it may be interesting enough to make it into this "news" article-format.
Figure 1: Illustration of the molecular structure of nuleotides (Sadava. 2000)
The supplement we are talking about is a combination of different nucleotides, i.e. cytidine 5′-monophosphate, uridine 5′-monophosphate, guanosine 5′-mono-phosphate and adenosine 5′-mono-phosphate from partially purified (90%) germinated barley seeds extracted during sporulation and the reason it's worth knowing what was in it, because it was able to ...
  • Want a quick performance fix? Use sodium bicarbonate | learn more
    significantly increase time to exhaustion (+7%)
  • ramp up serum levels of immunoglobulin A and
  • elevate the NKC cytotoxic activity
in the blood of the 14 recreationally active participants (age 22; BMI 24kg/m²; body fat 11%) who participated in a standardized incremental exercise test on the treadmill ("Run till you drop") after taking 50mg/day of this product for 2 weeks.

Oleic Acid Increases E2, Testosterone & DHT Binding

Not from Greece, the land of olive oil and eve's cheese, but from Spain comes a study that links Oleic acid, the mono-unsaturated fat from Olive oil to increases in SHBG. The researchers from the Universitat Autònoma de Barcelona analyzed the lab reports and nutrition data of a total of 315 men and observed that
"SHBG serum levels were significantly higher in subjects using olive oil for cooking in comparison with subjects using sunflower oil. The SHBG levels correlated positively with MUFA (p < 0.001) and negatively with saturated fatty acids (p = 0.003)." (Sáez-López. 2013)
Based on multiple regression analysis of the data, the scientists calculated that the amount of MUFA in the subjects' diets accounted for 20.4% of SHBG variance. Despite the fact that this means that your MUFA intake determines "only" 20% your SHBG levels, the data in Figure 1 (left), clearly indicates that these 20% show pretty significant correlations with important health markers.
Figure 2: Correlation between SHBG levels and BMI, MUFA intake (in % total fat) and fasting blood glucose - left; correlation between phospholipid MUFA and SFA content and SHBG - right (Sáez-López. 2013)
In order to elucidate the underlying mechanisms, the scientists conduced an additional in-vitro study, in the course of which Sáez-López were able to confirm that oleoyl-CoA, a metabolite that's produced, when oleic acid is metabolized, downregulates PPAR-γ in the liver (HepG2 cells).

As a SuppVersity veteran, you'll know that any reduction in PPAR-gamma in the adipose tissue will result in a decreased propensity of fat storage (read up on it). In the liver, PPAR-gamma is  responsible for the production of SHBG, as well. In view of the fact that SHBG binds and deactivates* androgens and estrogens (*this is not essentially correct for all tissues!), your MUFA intake could thus be one of the set-screws that determine the level of unbound sex-steroids in your blood.
With 60-80% olive oil is one of the best sources of oleic acid and this is not a reason to stop consuming it - irrespective of T-binding (read more)
Bottom Line: Based on the currently available evidence it appears as if nucleotide supplements could have a future as immune and performance booster for intense training athletes.

Despite the fact that it is unlikely that there will be any side effects, (a) the increased immune activity, which could be a problem for people with auto-immune disease and (b) the non-existence of scientific evidence to support their long-time efficacy (and safety), I would wait and see how things develop before investing significant amounts of money in supplemental RNA / DNA precursor.

Something very similar is true for results of the Sáez-López study that investigated the "SHBG raising" effects of oleic acid. In view of the negative association between SHBG levels BMI and fasting blood glucose, which have, by the way, been observed in previous studies: Phillips & Gerald, for example, observed a significant negative correlation between SHBG and the waist / hip ratio in 55 obese men aged 21 to 70 (Philips. 1993). And while SHBG binds testosterone the small change will not render all your testosterone useless, so that you don't have to be afraid of sudden olive oil induced anti-virility effects ;-)

References:
  • Ostojic, Sergej M., Kemal Idrizovic, and Marko D. Stojanovic. "Sublingual Nucleotides Prolong Run Time to Exhaustion in Young Physically Active Men." Nutrients 5.11 (2013): 4776-4785.
  • Phillips, Gerald B. "Relationship between serum sex hormones and the glucose-insulin-lipid defect in men with obesity." Metabolism 42.1 (1993): 116-120.
  • Sadava, D. et al. Life: The Science of Biology, 9th ed. 2009
  • Sáez‐López, Cristina, et al. "Oleic acid increases hepatic sex hormone binding globulin production in men." Molecular nutrition & food research (2013).

Baking Soda For Stressed White Blood Cells: 0.3g/kg NaCO3 90min Before an Anaerobic Workout Protect Your Immune Cells From "Stress" and Oxidative Damage

Image 1: Pure baking soda is not (yet?) a staple of the supplemental arsenal of many athletes. The scientific evidence with regard to its immediate ergogenic effects is ambigious and the mere presence of the word "sodium" in "sodium bicarbonate" scares the hack out of those athletes (bodybuilders and figure competitors) who may benefit most from a few grams of this potent alkalizer.
"Sodium"! This word alone is usually enough to scare bodybuilders and fitness athletes to death. "Sodium!? Isn't that the stuff that makes me look bloated?" The answer is easy: No! While sodium will help you retain enough water in your body to perform in the gym, the amount of sodium you ingest usually has little impact on the amount of water you will be holding, only when you start modulating your sodium intake, your body will react with changes in the renin-andiotensin-aldosterone system and you will be fluctuating "nicely" back and forth from super-bloated to weak and dehydrated... this is yet commonly ignored within the fitness community and thus it is no wonder that most supplement producers are anxious not to include any ingredients in their products that would show up on the label as "sodium" - after all, there are still costumers out there who have not enrolled at the SuppVersity and will thusly run away screaming as soon as they take a closer look on the label of a product they were just about to buy.

It is thusly no wonder that (at least to my knowledge) KreAlkalyn, where NACO3 is the working ingredient of the highly advertised buffering system, is the only product using sodium bicarbonate, or soda ash, as it is also called, as one of its main constituents (more on this topic in the SuppVersity Creatine Special). In medical settings NACO3 was and, in parts, still is still the "drug" of choice to combat acute acidosis. It is thus no wonder that Daniel J. Peart and his colleagues from the University of Hull in the United Kingdom, as well as the Bond University in Queensland, Australia are not the first scientists who speculated that athletes, especially those competing in (primarily) anaerobic sports, could benefit from the alkalizing effects of their grandmothers' secret weapon in the war against fungi and bacteria on her kitchen furnishings (Peart. 2011).
Image 2: "Cholesterol is the devil and sodium is his little brother!" Everyone who still believes everything the medical orthodoxy says, please raise your hands!
A note on the dangers of "salt": Firstly, baking soda is "only" ~28% sodium, which means that for every 4 grams you ingest you get roughly 1 g of sodium. Secondly, it is arguable how much of the sodium is effectively taken up and will be floating around in your blood. As T. Lakhanisky points out in his dossier for the Belgian government: "The uptake of sodium, via exposure to sodium carbonate, is much less than the uptake of sodium via food. Therefore, sodium carbonate is not expected to be systemically available in the body." (Lakhanisky. 2002) And thirdly, there is more and more evidence that suggests that the chloride rather than the sodium content of common table salt (NaCl = NatriumChloride) is the root cause of "sodium induced hypertension" in "sodium sensitive" individuals / animal models. Only recently, a study by Schmidlin et al. showed that chloride loading induced hypertension in the stroke-prone spontaneously hypertensive rat despite profound sodium depletion (Schmidlin. 2010). So, if you asked me, rather than pointing at salt as the #2 on the list of greatest evils (obviously cholesterol is still #1, here) the medical orthodoxy would be better advised to address the imbalances between sodium and potassium, which are so characteristic of the western diet, instead of painting yet another black and white picture where sodium is the bad guy and potassium the dangerous mineral that cannot be sold OTC in dosages >80mg.... but hey, this would be the topic for a whole new blogpost and as gross as it may sound, the chance that you get diarrhea from the baking soda is probably 1000x higher than the remote possibility of increases in blood pressure. A 1990 study by Luft et al. even found that the blood pressure of 10 mildly hypertensive and normal subjects decreased by 5mmHg after 7 days in the course of which they drank 3 liters of sodium bicarbonate containing water per day (Luft. 1990)
In their study, Peart et al. had a group of seven recreationally active men (age 22.3 ± 2.9 years,
height 181.6 ± 4.5 cm, body mass 78.1 ± 8.1 kg, and physical activity 4.2 ± 0.6 h/week) "with no history of supplementing their diet with ergogenic agents" perform a 4-min bout of all-out exercise on an air-brake cycle ergometer on three different occasions (spaced exactly 1 week apart). While the first was an acclimatization session the second and third bout were performed after the ingestion of either 0.3g/kg sodium bicarbonate (trial 2) or plain table salt (trial 3) in "low-energy flavored water" 90 minutes prior to exercise.
Figure 1: Blood ph levels after ingestion of placebo or 0.3g/kg sodium bicarbonate (data adapted from Peart. 2011)
As you can see in figure 1, the ingestion of ~23.4g of baking soda produced a rather slight but significant shift towards a more alkaline blood ph level (compared to placebo), which became much more pronounced after the exercise bout (p<0.003). Interestingly, there was yet no significant difference (p>0.26) in exercise performance as measured by average and peak power (means ± SD; average power 292 ± 43 W vs. 291 ± 50 W; peak power 770 ± 218 W vs. 775 ± 211 W; work completed 71 ± 10 kJ vs. 68 ± 10 kJ) between the groups.

Baking soda: A non-ergogenic ergogenic?

The latter observation, i.e. no or statistically non-significant increases in acute exercise performance upon sodium bicarbonate ingestion, stands in line with ~75% of the previous findings, a recent meta-analysis by Carr et al. summarizes as follows:
The remaining 38 studies and 137 estimates for sodium bicarbonate produced a possibly moderate performance enhancement of 1.7% (90% CL ± 2.0%) with a typical dose of 3.5 mmoL/kg/BM (∼0.3 g/kg/BM) in a single 1-minute sprint, following blinded consumption by male athletes. In the 16 studies and 45 estimates for sodium citrate, a typical dose of 1.5 mmoL/kg/BM (∼0.5 g/kg/BM) had an unclear effect on performance of 0.0% (±1.3%), [...] Study and subject characteristics had the following modifying small effects on the enhancement of performance with sodium bicarbonate: an increase of 0.5% (±0.6%) with a 1 mmoL/kg/BM increase in dose; an increase of 0.6% (±0.4%) with five extra sprint bouts; a reduction of 0.6% (±0.9%) for each 10-fold increase in test duration (e.g. 1-10 minutes); reductions of 1.1% (±1.1%) with nonathletes and 0.7% (±1.4%) with females. Unexplained variation in effects between research settings was typically ±1.2%.
Despite these rather mediocre immediate effects of bicarbonate pre-loading, the main finding of the study at hand hints at hitherto overlooked long(er)-term immune benefits the consumption of sodium bicarbonate might have.
Figure 2: HSP-72 expression in mono- and lymphocytes in response to anaerobic exercise after ingestion of placebo or 0.3g/kg sodium bicarbonate (data adapted from Peart. 2011)
As you can see in figure 2 the stress-induced HSP-72 expression in white blood cells (lymphocytes and monocytes) in response to the HIT exercise was almost completely abolished. Along with the nullification of the already low amount of oxidative stress (cf. T-BARs in figure 3), these results suggest that bicarbonate supplementation has a stress-protective effect on immune cells during anaerobic exercise.
Figure 3: Oxidative stress due to anaerobic exercise as measured by TBAR expression after ingestion of placebo or 0.3g/kg sodium bicarbonate (data adapted from Peart. 2011)
It is yet important to note that the scientists point out that it "is unclear at this stage whether the attenuation was due to a reduced state of acidosis, reduced oxidative stress or a combination of both." Moreover, it is difficult to say which consequences this would have on future bouts of exercise and whether and to which degree athletes would actually benefit - or, if we think of the hormesis hypothesis and the ongoing debate concerning the effects of antioxidants on exercise induced adaptations - maybe even compromise their performance, would yet need further investigations.

We may yet assume that, just as it is the case with antioxidants, the dosage will have to be matched to the individual workload to see optimal results. With people exercising just enough to see any adaptations seeing no and people who do crossfit 2x a day seeing the most beneficial results from (partially) blocking the exercise induced oxidative stress.

480mg/day Polypodium Leucotomos Reduce Infection Rates in High Performance Athletes by 75%! Plus: Extract Protects Against UV Radiation, Cancer, Trauma & Could Be Ergogenic

Don't worry if you have not heard of Polypodium leucotomos before. After all, that's why you're here! To get your daily dose of SuppVersity news and learn, right?
It's starting to get cold and wet outside and aside from my always healthy self, everyone around is getting sick... sounds familiar? Or are you one of those ailing people who always wonder how the others beard the common cold and did not have a single flu in their whole life? I can assure you, it's not just zinc + vitamin C ;-)

That said, I honestly don't believe that the supplement today's news is about will get the job done, if you don't have your diet and workout regimen in check, but if it reduces the incidence of infections in high performance athletes by 75% it can hardly be useless when it comes to protecting yourself from the sniffers and nose blowers all around, can it?

Dear SuppVersity reader, meet Polypodium leucotomos your immune systems best friend!?

Assuming that I've now gotten your attention, let's get right to the facts. The said supplement is an extract from Polypodium leucotomos a fern that is native to the tropical and subtropical regions of the Americas and has a long history as a folk remedy in Honduras, where it is used for a wide variety of ailments. Interestingly, respective extracts have been sold under the label "anapsos" ever since the 1970s. Nevertheless, I am not sure if anybody who does not know the LEF product catalog by heart has ever heard of Polypodim (if you did, probably in relation to skin health) -- specifically not in the context of infectious diseases in high performance athletes, which was what Bartolomé Marí Solivellas and Teo Cabanes Martín were interested in, when they conducted their 3 months study on the effects 480 mg/day Polypodium leucotomos extract (Armaya fuerte; Centrum laboratories, Alicante, Spain / researchers report no conflict of interest) on the onset of infectious processes and relapses during an 8-month follow up from June 2010 to January 2011 (Solivellas. 2011).

The study participants were all athletes who took part in competitive activity, trained or competed for 20 hours per week and had and still were periodically monitored in a sports medicine clinics. Overall, a total of 116 athletes (58 men and 58 women, aged 18-30 years) were included. 63 of them in the Polypodium leucotomos extract-treated group (PL) and 53 in the control group (C), with 58 males and
58 females aged 18–30 years (subjects with autoimmune or chronic disease were excluded; 14 additional athletes were excluded during the trial, either because they left or were non compliant, i.e. didn't take their supps). Most of them were competitive volleyballers, football players, track & field athletes and cyclists.

The protocol: A 2x 240mg/day preload from June to August

The participants in the active arm of the trial had to consume their daily dose of 480mg in two 240 mg servings, one in the morning and one at night, while the the control group did not take Polypodium
leucotomos extract (no question: The fact that the study was not placebo controlled is a bummer!). This means that the acute supplementation did not coincide with the aforementioned period of sniffing and nose blowing, and any effect that would be seen over the whole 8-months follow-up must be due to permanent benefits in response to the supplementation in those first three months (it also reduces the influence of the placebo effect, after all we are quite forgetful and don't really think about the pills we popped in the summer, when we are getting sick in autumn).

The results: 75%! less infections in the treatment group

Table 1: Prevalence of infectious processes in the control group and study group (Solivellas. 2012)
Even at a very cursory glance at the data in table 1 you should notice the two most important figures: "28" and "7", as in 28 infections in the control (=unsupplemented group) and only 7 infections in the treatment (=480mg/day Polypodium leucotomos extract) group - that's a pretty impressive number. Since, both study arms had been of the same size (n = 50), after a couple of athletes had been excluded from the active arm due to non-compliance, this is a 75% reduced risk of catching any type of infection (see table 1 for detailed breakdown). According to the authors, of those, ...
"[...] the cases of pharyngoamygdalitis were the most noteworthy – 12 patients (24%) in the control group compared to three patients (6%) in the Polypodium leucotomos extract"-treated group." (Solivellas. 2011)
The incidence of infections was yet not the only thing that was reduced. What's probably about as important as the number / rate of infections are the facts that
  • the "symptomatic improvement was more favorable" (Solivellas. 2011) in patients from the study and 
  • the number of relapses, i.e. a 1/7 vs. 12/28 in the active and passive arm of the study, were significantly lower (-66%)
Since the SuppVersity user stats tell me that most of you are living in the Northern Hemisphere and that it stands out of question that all of you work out (right? ;-), these results alone would be reason enough to take a closer look at Polypodium leucotomos, Calaguala, Anapsos, Heliocare, Kalawalla, Polypodiaceae or whatever other funky name the herb may go, where you are currently living.

Anapsos can do more than render athletes 'infectious disease proof', much more!

This would not be the SuppVersity, though, if I would not tell you "the whole story" about what turns out to be quite an outstanding fern species with beneficial health effects that go well beyond giving your immune system a major boost. And though I have to admit that I did not go back into the 1970s, when the first commercially available extract that goes, as I've mentioned before, by the name Anapsos hit the market. Even the research that has been done in the 21st century only did suffice to compile a pretty impressive list of scientifically backed beneficial health effects, of which I have selected only those, I thought you may be interested in:
  • Protection against skin cancer  and related pathologies - PL protects the melanocytic nevi in your skin from forming sporadic melanoma in response to UV radioation, dark eyed patients with higher UVR sensibility (lower basal minimal erythematous dose) would benefit most (dosage 1080mg of PL; Aguilera. 2012). Similar results in rodents, where 300mg/kg of PL 5 days before UVR exposure "reduced the number of proliferating cells by 13%, increased the number of p53(+) cells by 63%, enhanced the antioxidant plasma capacity (ORAC) by 30% and reinforced the network of dermal elastic fibres" (Rodríguez-Yanes. 2012). Also helps against photo aging, polymorphic light eruption, idiopathic photodermatosis, UV-B induced immuno-suppression in the skin,
  • Prevention of hyperpigmentation (and psoriasis) - Hydroquinone has been a cornerstone for the treatment of hyperpigmentation; however, concerns regarding adverse effects have prompted a search for alternative agents, one that was suggeted only recently is Polypodium leucotomos (Konda. 2012). Ameliorative effects have also been observed in psoriasis patients, although it appears that more research would be necessary to make any recommendations (Middelkamp-Hup. 2004)
  • Remission of subacute cutaneous lupus erythematosus (SCLE) - SCLE is an uncommon autoimmune disease that results in substantial photosensitivity of affected patients. Eruptions often are triggered or exacerbated by UV light (UVL) exposure and a recent case in Cutis shows that while the disease was at best "moderately controlled" with hydroxychloroquine sulfate, "near total remission of disease" was achieved after the addition of oral Polypodium leucotomos supplement (Breithaupt. 2012).
  • Amelioration of atopic dermatitis, reduction of antihistamine requirements - Scientists have only shown recently in a phase IV randomized, double-blind, placebo-controlled, multicenter trial involving 105 patients aged between 2 and 17 years who were receiving topical corticosteroids to treat moderate atopic dermatitis that PL administered for 6 months led to a statistical significant reduction in oral histamine use of  4.5% (for those interested, patients received Anapsos 120 mg manufactured by Especialidades Farmacéuticas; Ramirez-Bosca. 2012).
  • Prevention of the shift in Th1/Th2 (immune characteristics) in response to trauma - In 2007 already researchers from the University of Zaragzoa found that PL blocked the postoperative (day 1) increases in IL-6 and IL-10 in rats undergoing fracture..On postoperative day 7, "rats undergoing fracture showed an increase of IL-6 levels", the latter was not observed in the PL supplemented rats who had increased levels of the "good" inflammatory cytokine IL-12 on postoperative day 7, instead (Navarro-Zorraquino. 2007)

"Hold on, but didn't you say on SHR and in a couple of blogposts that ROS are necessary?" True, ROS (radical oxygen species) are necessary, as they are a signalling molecule and 'toxic junk', both at a time. Whenever your body is however, figuratively speaking, unable to 'read the signals for the signals' -- which happens to be the case for unfortunate majority of the sedentary Western society -- you better cut back on the forest of signs than have them accumulate in the form of toxic metabolic waste and damage (oxidize) your tissue. Always keep in mind: Whenever we are talking about physiological processes it's all about balance and simply about good or bad and black and white.
The list above did already skip a couple of skin related benefits and still: As I mentioned before, there is probably lots more you could find once you start digging deeper and going further back in the archives. What the hitherto elucidated and probably also all future benefits do have in common is that they are in one way or another related to the potent antioxidant effects of certain not exactly specified molecules the (sub-)tropical fern apparently contains.

Whatever antioxidant (I rather suppose it's a synergistic cocktail) Polypodium leucotomos may contain, it must -- contrary to many other antioxidants which fall victim to their own kamikaze tactics (aka "free radical scavenging") often way before they make it to the target tissue-- actually get to where it is needed and can thus exert its potent antioxidant effects right in the skin, the wound, the broken bone,... and maybe the strained muscle!?

If the latter was the case, and the antioxidants in this peculiar American farn had similar effects in muscle tissue as they were observed by Navarro-Zorraqino et. al. in their rodent model -- namely the induction of an increase in IL-12 and a faster decrease in IL-10 expression -- the concerns about 'too much of a good thing' I addressed in the red box to the right, would not just have been unwarranted; in view of the established pro-anabolic effect of IL-10 (cf. Argilé. 2001) they would actually be absurd (just as the common understanding that all cytokines were "bad", by the way).

Bottom line: I guess, you will agree: This stuff is interesting. However, there have been plenty of "interesting" supplements in the past, which did not deliver. So, if you are merely interested in the last mentioned ergogenic effects, which could obviously be present, you better wait for a respective trial and the corresponding SuppVersity news, before you fill your supplement rack with tons of Polypodium leucotomos. If you are supplement fanatic, got some money to spare and are interested in the immune boosting or UV protective effects, you may want to give it a try.

References:
  • Aguilera P, Carrera C, Puig-Butille JA, Badenas C, Lecha M, González S, Malvehy J, Puig S. Benefits of oral Polypodium Leucotomos extract in MM high-risk patients. J Eur Acad Dermatol Venereol. 2012 Jul 31.
  • Argilés JM, Meijsing SH, Pallarés-Trujillo J, Guirao X, López-Soriano FJ. Cancer cachexia: a therapeutic approach. Med Res Rev. 2001 Jan;21(1):83-101.
  • Breithaupt AD, Jacob SE. Subacute cutaneous lupus erythematosus: a case report of Polypodium leucotomos as an adjuvant therapy. Cutis. 2012 Apr;89(4):183-4.
  • Konda S, Geria AN, Halder RM. New horizons in treating disorders of hyperpigmentation in skin of color. Semin Cutan Med Surg. 2012 Jun;31(2):133-9.
  • Middelkamp-Hup MA, Pathak MA, Parrado C, Garcia-Caballero T, Rius-Díaz F, Fitzpatrick TB, González S. Orally administered Polypodium leucotomos extract decreases psoralen-UVA-induced phototoxicity, pigmentation, and damage of human skin. J Am Acad Dermatol. 2004 Jan;50(1):41-9.
  • Navarro-Zorraquino M, García-Alvarez F, Martínez-Fernández AR, Pastor C, Larrad L, Salinas JC, Lozano R. Pharmacological immunomodulation of surgical trauma. J Invest Surg. 2007 Sep-Oct;20(5):283-9. 
  • Ramírez-Bosca A, Zapater P, Betlloch I, Albero F, Martínez A, Díaz-Alperi J, Horga JF; Grupo de Anapsos en Dermatitis Atópica y centros de realización del estudio. Polypodium leucotomos extract in atopic dermatitis: a randomized, double-blind, placebo-controlled, multicenter trial. Actas Dermosifiliogr. 2012 Sep;103(7):599-607. Epub 2012 May 3.
  • Rodríguez-Yanes E, Juarranz Á, Cuevas J, Gonzalez S, Mallol J. Polypodium leucotomos decreases UV-induced epidermal cell proliferation and enhances p53 expression and plasma antioxidant capacity in hairless mice. Exp Dermatol. 2012 Aug;21(8):638-40.
  • Solivellas B, Martin TC. Polypodium leucotomos Extract use to prevent and reduce the risk of infectious diseases in high performance athlete. Infection and Drug Resistance. 2012 Oct 15.

Glutamine or BCAA, Which is the Better Fatique Buffer? 18g GLU Suprisingly Effective, 9.5g BCAAs (Un-)Surprisingly Useless as Blood Fatigue Factors & Cytokine Buffers

Rowing is an excellent cardio exercise for wanna be bodyuilders, by the way!
I am not really a fan of glutamine, but unlike BCAAs that are still hyped all over the Internet, the conditionally essential amino acid which is the most abundant of all amino acids in human blood is at least not falsely heralded as a potent catabolic, anabolic, weight loss adjuvant and what not, any longer.

Against that background I have to admit that I am not exactly unhappy to tell you that Ga Hee Koo, Jin Hee Woo, Sung Whun Kang, and Ki Ok Sjin who work at the Dong-A University and the Republic of Korea Airforce Academy, have recently observed that BCAAs have absolutely no, glutamine at least a minimal impact on the blood fatigue factor response of juvenile athletes in response to a 2,000 m all out rowing challenge w/ placebo, BCAA or glutamine supps.
Learn more about glutamine and BCAAs at the SuppVersity

Glutamine Helps W/ Diabetes

Whey + Casein Beat GLU + BCAA

Alanyl-Glutamine is it any good?

GLU for Glycogen Repletion?

GLU as Intra-Workout BV?

BCAAs deplete neurotransmitters
In the corresponding experiment, the scientists from the College of Sports Science at the Dong-A University had five male juvenile elite rowing athletes perform the same 2,000m rowing test at maximal intensity after having received a placebo, BCAA, or glutamine for 7 days before
the test. The specific supplementation regimen included:
  • BCAA (Spomax, Seoul, Republic of Korea) was given three times a day (25% valine, 50% leucine, 25% isoleucine, 3.15 g/day).
  • L-glutamine (Optimum Nutrition, Aurora, IL, USA, 6 g/day) was given three times a day.
Blood samples were collected from the antecubital vein on the day of testing while resting before the test, immediately at the end of test, and 30 min after the test. All tests were conducted with a 1-week interval to eliminate the potential effects from potentially longer-lasting effects of the previously administered supplement.
Which parameters did the researchers test and why? Koo et al. tested lactate, the accumulation of which will eventually impair ATP synthesis and lead to muscular fatigue. They tested the accumulation and clearance of ammonia, which can trigger central fatigue, when the levels increase rapidly during high intensity exercise. And they tested creatine kinase (CK) which is a classic marker of muscle damage and IL-8 and IL-15, two cytokines that will be elevated, when the activity of the immune system is not sufficient to deal with exercise induced stressors.
The actual test was conducted with an indoor rowing machine (Concept², Morrisville, VT, USA) two times each for supplementation with the placebo, BCAA, and glutamine. All the subjects performed a 2,000 m (Olympic single scull race) race at their own individual maximum paces (42–45 pace for 0m~250m, 40 pace for 250m~500m, 36–38 pace for 500m~1,500 m, and over 42 pace for 1,500 m~2,000 m)
Figure 1: Serum markers of fatigue and muscle damage, expressed relative to placebo (Koo. 2014)
There were no significant differences in lactate levels; a significant phopshorus-sparing effect from BCAAs (small effect size) and glutamine (large effect size) of which the scientists believe that it was mediated by the use of the amino acids to maintain adequate muscular ATP levels; and there was a non-significantly elevated level of ammonia in the glutamine group (some arginine could help clear those | learn more) that returned to normal 30 min after the test.
The dosages are not the same! That's unfair! No, it's not necessarily unfair, but it would still have been better to test 18g of glutamine vs. 18g of BCAAs. There is after all one thing both have in common: They both can be used as workout fuel in the muscle, so the advantage of glutamine may have become smaller (maybe even non-significant), if both had been administered at the same amounts.
The creatine kinase levels (a marker of muscle damage) and the levels of interleukin-8 and interleukin-15, however, were significantly lower in the glutamine than they were in either the BCAA or placebo group. This is a result of which the authors of the study believe that, it may...
"[...]represent the effects of energy supplementation from glutamine supply, which activated as a fuel in the muscle and as a nitrogen precursor for nucleotide synthesis" (Koo. 2014). 
An alternative explanation would be that glutamine (probably via its connection to glutathione; see Roth. 2002) had a direct protive effect on the skeletal muscle tissue during the workouts.
Figure 2: Serum levels of inflammatory cytokines expressed relative to placebo (Koo. 2014)
This hypothesis would also be supported by the changes in interleukin expression. i.e. the blunted increase of interleukin-8. IL-8 is an inflammatory cytokine that serves as a chemical signal which attracts neutrophils at the site of inflammation. The corresponding increase in IL-15, which was likewise reduced in response to sub-chronic glutamine supplementation, on the other hand, indicates a reduced production (not activity!) of natural killer cells.

Table 1: Intense exercise is not the only condition / disease that's associated  with low blood glutamine levels (Roth. 2002)
In that, it is crucial to understand that the authors (imho reasonably) believe that the increase in IL-8 & IL-15 is a compensatory mechanism which is initiated to counter the reduced immune function that occurs, when the amount of glutamine in the blood and skeletal tissue drops. We do after all know for sure that the this will result in a significant decrease in the cell proliferation rate of lymphocytes, the amount of antioxidants, peptides, amino sugars related to cell resistance against apoptotic processes, purines, as well as the synthesis of key molecules such as pyrimidines which are all involved in redox reactions (Roth. 2002).

Whether supplementation is warranted with low(er) intensity exercise, as well, is however questionable. Previous research by Ostrowski et al. (2001), who had their subjects exercise at significantly lower intensities, did not find comparable increases in IL-8. This difference is probably due to a comparably lower amount of exercise induced stress that corresponds to the reduced intensity. In this context it's also worth mentioning that Fischer et al. (2006) report that the blood chemokine concentrations would increase little or remain stagnant unless a sufficient muscle mass is mobilized and maintained at a certain level of intensity sufficiently... now, everyone who has ever done an all-out rowing time trial will confirm: This is (a) intense and will (b) involve almost every muscle in your body.
If maximal muscle hypertrophy, not performance increases in all-out (aerobic) exercise and protecting your immune function is your goal, buy some whey + casein and stay away from glutamine & BCAAs unless you insist on wasting money on hitherto unproven promises of strength & size gains | learn more
Bottom line: In contrast to BCAAs which will "only" blunt the increase in debilitating phosphorus in the blood,  "glutamine supplementation could be helpful for enhancement of immune function and the defensive inflammatory reaction after exercise." (Koo. 2014)

The results of the study at hand do thus confirm an older piece of broscience, i.e. the importance and efficiency of adequate amounts of glutamine (15g or more per day!) for recovery and immune function. They do yet also put another question mark behind the ergogenic potential of brach-chained amino acids about which I have written repeatedly in previous articles here at the SuppVersity (in other contexts, BCAAs may well be superior to glutamine, but long-term studies to prove any of the claimed benefits are missing, as well).

Whether the results from the study at hand warrant the consumption of 18g of glutamine per day for all of us, is still questionable. If you are in a phase of your training that requires a lot of all-out exercise and already feel that your immune defenses are dwindling, it probably won't hurt to buy a cheap 500g bag of glutamine from the bulk supplier you trust. Don't expect instant results of illusive tingles as you'll get them with certain other supplements. If there are benefits they will only be visible over time and will include faster / more complete recovery, reduced rates of infection and overall fatigue. Eventually, these would help you to make faster gains in strength and size, though | Comment on Facebook.
References:
  • Fischer, Christian P. "Interleukin-6 in acute exercise and training: what is the biological relevance." Exerc Immunol Rev 12.6-33 (2006): 41.
  • Koo, Ga Hee, et al. "Effects of Supplementation with BCAA and L-glutamine on Blood Fatigue Factors and Cytokines in Juvenile Athletes Submitted to Maximal Intensity Rowing Performance." Journal of Physical Therapy Science 26.8 (2014): 1241-1246.
  • Ostrowski, Kenneth, et al. "Chemokines are elevated in plasma after strenuous exercise in humans." European journal of applied physiology 84.3 (2001): 244-245.
  • Roth, Erich, et al. "Regulative potential of glutamine—relation to glutathione metabolism." Nutrition 18.3 (2002): 217-221.

Amino Acids for Super Humans, Part IV - Purported Ergogenics (3/3): Glutamine, the Anabolic Immune Booster?

Image 1: Still one of the top-
sellers in almost all supplement
shops - l-glutamine; tip: buying
bulk powder will save money
Although glutamine is one of the non-essential amino acids, even the fact that your body continuously 'sacrifices' truly essential amino acids to synthesize glutamine in your muscle tissue, should go to tell you that, after all, glutamine, the most abundant amino acid in human muscle and plasma, cannot be so non-essential as its classification would suggest.

Under normal conditions it forms 50% of the whole body amino acid pool. In cells, esp. muscles, where glutamine makes up 66% of the amino acid pool. Within the cellular space, the purported cell-volumizer can reach concentrations that are up to 33 times higher than on the outside of the cell.

In times of acute stress, severe burns or surgical trauma, on the other hand, tissue glutamine levels have been observed to decline by up to -50% - an observation, which gave and still gives rise to the hypothesis that glutamine repletion / supplementation could ameliorate or even prevent the catabolic processes which threaten all metabolically active tissues and weaken the immune system whenever the human body is exposed to severe physiological (and even psychological) stress. In that, it is important to understand that glutamine does not reduce the amount of corticosteroids which are released in those circumstances, but may reduce the negative effects of increased cortisol and catecholamine levels on the body. In a 1995 study by Hickson et al., for example, intravenous infusion of glutamine reduced muscle mass losses subjects who had previously received a glucocorticoid infusion by -70% and ameliorated the cortisol-induced decline in untra-muscular myosin heavy-chain content by -50% (Hickson. 1995). 
Did you know that 90% of the nitrogen that is derived from BCAA catabolism is released as glutamine, which is formed primarily in your muscles, but also in your lungs, your liver and your brain in a process called glutamine synthase, where glutamate, which has a side-chain hydroxyl instead of the amine group of glutamine, and ammonia are synthesized to form glutamine. During its subsequent hydrolysis, i.e. the catalysis of glutamine to glutamate + ammonia in the intestine, cells of the immune system and the liver, a substantial amount of energy is released. In that, glutamine, the 2nd major interorgan nitrogen carrier, derives a major advantage over alanine, the #1 interorgan nitrogen carrier, from its protein and amino acid derived carbon skeleton, which constitutes an energetically denser substrate for gluconeogensis (esp. in the liver) than that of alanine or aspartate, the third most abundant interorgan nitrogen carrier in the human body.

Note: This is the detailed transcript of my show notes to "Amino Acids for Super Humans Part IV"
click here to download the podcast if you want to listen before / during / after you read the rest of the notes

I. Physiological role of glutamine in the human body

Stress-protection aside, glutamine performs a whole host of other important physiological functions. Glutamine...
  • ... is required for hepatic ureagenesis and renal ammoniagenesis, is an essential contributor to detoxification processes;
  • ... is necessary to maintain and restore an optimal ph-balance;
  • ... is a substrate / precursor to peptides and proteins, amino sugars, purines and pyrimidines;
  • ... is used as cellular fuel in muscle, intestine, skin and immune system, where it's availability / non-availability directly regulates protein synthesis and degradation;
  • ... is intricately involved in the anti-oxidant defense system of the body as a precursor to glutathione (=glutamate + cysteine + glycine) production.
Glutamine and intestinal health & function

You may be surprised to see that I devote an entire chapter of this write-up to the role of glutamine in gut health; yet with the increasing public interest in and scientific awareness of pathologies beyond Crohn's, Celiac & Co, I consider the direct effects glutamine and glutamic acid exert on the health of the intestinal system of paramount importance.

Table 1: Effects of glutamine supple-
mentation on intestinal health
(Stehle & Fürst in ed. Cynober. 1955)
In their contribution to Pharmacological nutrition: immune nutrition (ed. Cynober, Fürst, Lawin. 1995) Stehle and Fürst compiled a list of immediate effects of glutamine supplementation on gut function (cf. table 1), many of which could be of great importance for athletes, who are not only particular reliant on optimal nutrient absorption, but also at an extraordinary risk of developing increased gut permeability, which has lately become commonly known and almost hysterically feared as "leaky gut" (syndrome). In this context, Carl V. Gisolfi writes in a review of the importance of optimal intestinal function for athletes (Gisolfi. 2000):
An increase in gut permeability may be an important link to gut-barrier impairment (Fig. 3). The hypothesis proposes that exercise stress produces biochemical changes that uncouple oxidative phosphorylation, reducing ATP produc ion and increasing Ca2+ efflux from mitochondria and endoplasmic reticulum. These events lead to increased cytosolic Ca2+ concentration, the generation of reactive oxygen species, and loss of tight junction control, producing increased intestinal permeability. [...] When the tight junctions open, their maxi-
mal channel size is too small to permit passage of endotoxin but will allow passage of luminal contents that are chemotactic for neutrophils. These agents (dietary antigens, chemotactic oligopeptides) stimulate intraepithelial lymphocytes to secrete interferon-γ. [...] Interferon-γ opens tight junctions and activates macrophages and neutrophils to release oxygen radicals and immunosuppressive peptides. Thus increasing intestinal permeability by opening tight junctions can initiate immunologic and inflammatory events that can alter gut structure and function.
Image 2: More than 50% of the
dietary glutamine are used by your
digestive system and do not even
reach systemic circulation.
Scientifically documented causative factors for increased gut permeability in athletes are ...
  • prolonged exercise (triathlon, marathon, etc.)
  • high intensity endurance exercise at 80% of VO2 max
  • (co-)ingestion of aspirin with medium intensity exercise at 60-65% of VO2 max
And desite the fact that Coeffier et al., in a recent review on the efficiacy of gutamine supplementation in patients with irritable bowel syndrome, state that previous "clinical studies with oral glutamine in CD [Crohn's disease] are until now disappointing" (Coeffier. 2010). There is substantial evidence for glutamine to exert beneficial effects on overall enterocyte health and accumulating evidence for the ability of glutamates, the carboxylate anions and salts of glutamic acid, to stabilize the gut lining and to reduce intestinal permeability (Vermeulen. 2011).
Did you know that in a 2010 study by dos Santos et al. (dos Santos. 2010), administration of glutamine at a dose of 500mg/kg/day (human equivalent ~40mg/kg or 3.2g per day for an adult weighing 80kg) to mice with experimentally induced intestinal obstruction "decreased intestinal permeability and bacterial translocation to physiologic levels in the treated animals and preserved intestinal barrier integrity".
Thus, even if the following dissertations will entail the conclusion that the ergogenic value of glutamine is largely overrated, the increase in gut permeability that has been observed after strenuous workouts (Davis. 2005) would be an argument in favor of post-workout glutamine / glutamic acid supplementation, you should remember.

    II. Glutamine and the athlete

    While intravenous glutamine infusions are a longstanding and well-established part of medical treatment strategies used in hospitalized and critically ill patients (Windle. 2006), the use(-fulness) of glutamine as a dietary supplement for athletes is still questioned by many of the practicing exercise and nutrition scientists. In the following I will try to tackle the two most frequent promises you ill hear and read about in the advertisements for respective products.

    "Glutamine supplementation saves athletes from getting sick"

    It is unquestionably true that glutamine is of paramount importance for healthy immune function (Calder. 1999).
    It is also non-debatable that intense exercise, and, in that, specifically chronic endurance exercise (cf. figure 1),  has been shown to decrease both serum as well as tissue glutamine levels.
    Figure 1: Serum glutamine and glutamate levels in ultra-marathon runners pre- and at different time-points post exercise (data adapted from Castell. 1997)
    As the data from figure 1 documents, the exercise induced decline of glutamine levels is yet far from being as dramatic as the -50% drop which has been reported for hospitalized critically ill patients. Nevertheless, the highly advertisable claims of increased incidences of upper respiratory infects due to weakened immunity secondary to exercise induced glutamine-deficiency are going on forever and I doubt that this will ever change, although the recently published position stand on dietary supplements by Walsh et al. is only the latesst in a line of reviews to conclude, based on contemporarily available evidence, that glutamine supplementation for athletes is "[n]ot recommended, [because] body stores [generally] exceed exercise-lowering effects" (Walsh. 2011).

    With reference to the purported beneficial effects of supplemental glutamine on immunity in the athletic population, Newsholm et al. (Newsholm. 2011) write in Part 18 of a 2010/11 series on purported ergogenic sport supplements in the British Journal of Sports Medicine:
    Glutamine supplementation after exercise reduced the self-reported incidence of illness in endurance athletes. However, when glutamine was given to athletes to combat exercise-induced depletion of circulating glutamine, no effects were observed on the immune parameters studied, apart from reduced neutrocytosis and increased circulating IL-6.
    But if the existing anecdotal evidence is not merely a result of placebo effects (If you spent 50 bucks on a big pot of l-glutamine you do want that stuff to work, don't you? And if each and every "pro" tells you it does, it should work, shouldn't it?) or an increased awareness of how healthy you have "become", now that you are taking supplemental glutamine (when you have in fact been healthy all along), dosing issues, the addition of other nutrients and most importantly, training type and intensity would have been taken into consideration to explain the inconsistency of respective trials.
    Did you know that moderate training, in contrast to the bodybuilding "go heavy or go home" type of training, leads to "improved glutamine availability due to a positive balance between muscle synthesis and peripheral clearance", while physical inactivity can reduce glutamine synthesis and availability!
    In this context, it is noteworthy that declining glutamine levels after / in the course of periods of increased training intensity have only lately been (re-)introduced as a potentially useful indicator of overtraining by Agostini & Biolo (Agostini. 2010). They point out that "[s]trenuous physical exercise as well as exhaustive training programs [which] lead to glutamine depletion due to lowered synthesis and enhanced uptake by liver and immune cells". Lower glutamine levels, on the other hand, have been "associated" (notice we do not have enough evidence for a causal relationship here) with compromised immunity. Immediate / continuous repletion of whole body glutamine stores (serum & tissue) via adequate dietary or supplemental intake could thus very well help to maintain immunity.

    Image 3: BCAAs are not only way
    more ergogenic, they may in fact
    also be a more versatile source of
    glutamine than l-glutamine, itself.
    Personally, I find it telling that much of the positive data on glutamine supplementation for immune health comes from studies on endurance athletes from the early and late 1990s. If you consider the poor nutritional advice those athletes were given at that time, many of them were hardly getting enough protein along with the shitloads of carbohydrates they were told to eat. Now, someone who lacks essential amino acids, and more specificically BCAAs, for glutamine production, is of course at higher risk of 'running out of fuel for his immune system', especially if he exhausts his already compromised tissue stores by chronic endurance exercise.

    Conversely, the group of athletes who consumes the largest amounts of supplemental glutamine, i.e. bodybuilders, is probably the one who will benefit least of all from additional l-glutamine in their diet. No wonder that Candow et al. who studied the effect of a standardized strength training protocol with or without a 0.9g/kg lean tissue mass glutamine supplement on strength, body composition and protein turnover in young athletes found "that glutamine supplementation during resistance training has no significant effect on muscle performance, body composition or muscle protein degradation in young healthy adults" (Candow. 2001). While this obviously does not say anything about immunity you may safely assume that the latter was not compromised in the first place and thus evidently would not have benefited from the roughly 50-60g of l-glutamine (certainly a "sufficient" dose ;-) the subjects in the Candow study consumed.

    "Glutamine increases regeneration and improves muscle and strength gains"

    My preceding remarks on the useful- respectively -lessness of glutamine supplementation in marathon runners and bodybuilders have already touched on one of the recurring themes of the Amino Acids for Super Humans series: What is essential and beneficial for athlete A in situation B may be ineffective for athlete B in situation B or even athlete A in situation A. The data (table 2) from studies, which evaluated the effects of oral glutamine supplementation on exercise-related parameters in humans ("+" indicates improvement; "#" indicates no effect; "-" indicates detrimental effect), substantiates this observation. 

    Author(s) Protocol +/#/- Main Result(s)
    Castell. 1997 exhaustive exercise in middle-distance, marathon and ultra-marathon runners, and elite rowers, in training and competition
    2x5g glutamine vs. maltodextrin 0, 2h post exercise
    + immunity "[...] provision of oral glutamine after exercise appeared to have a beneficial effect on the level of subsequent infections [...] the ratio of T-helper/T-suppressor cells appeared to be increased in samples from those who received glutamine"
    Bishop. 2000 review of intra-workout / -competition supplementation #cortisol
    #immune
    Consuming "carbohydrate [...] but not glutamine [...] during exercise attenuates rises in stress hormones, such as cortisol, and appears to limit the degree of exercise-induced immunosuppression"
    Krzywkowski. 2001 bicycle exercise for 2 h at 75% of maximum O(2)
    5x 3.5g glutamine vs. 3.5g maltodextrin at 0, 45, 90, 135, 170min post cycling
    #immune "no effect on lymphocyte trafficking, NK and lymphokine-activated killer cell activities, T cell proliferation, catecholamines, growth hormone, insulin, or glucose [...] Neutrocytosis was less pronounced in the glutamine-supplemented group, but it is unlikely that this finding is of any clinical significance"
    Wilkinson. 2006 90 min cycling at 65% VO2max
    post-exercise oral CHO 1g/kg/h + 9.25g EAA + glutamine 0.3g/kg BW vs isoenergetic CHO-EAA w/out glutamine
    #anabolism,
    +long-term recovery
    Consuming "addition of glutamine to a CHO + EAA beverage had no effect on post-exercise muscle glycogen resynthesis or muscle protein synthesis, but may suppress a rise in whole-body proteolysis during the later stages of recovery"
    Carvalho-Peixoto. 2007 15 athletes, 120 min (approximately 34 km) outdoor running
    3 groups CHO g/kg/d + Gln 70 mg/kg/d; only CHO or only Gln in addition normal diet
    +ammonia detox "ammonia was not different for the first 60 min, but for the second hour [ammonia] was lower than in the control"
    Wilkinson. 2006 90 min cycling at 65% VO2max
    post-exercise oral CHO 1g/kg/h + 9.25g EAA + glutamine 0.3g/kg BW vs isoenergetic CHO-EAA w/out glutamine
    #anabolism,
    +long-term recovery
    Consuming "addition of glutamine to a CHO + EAA beverage had no effect on post- exercise muscle glycogen resynthesis or muscle protein synthesis, but may suppress a rise in whole-body proteolysis during the later stages of recovery"
    Favano. 2008 9 soccer players, cardiopulmonary exercise test + simulated soccer match, peptide glutamine (Gln) = 50 g of maltodextrin + 3.5 g of peptide glutamine or CHO alone 50 g of maltodextrin 30 min before test +performance "Total distance covered was 12750 [CHO] and 15571 [Gln]", i.e. +22% distance; "total duration of tolerance was 73 +/- 23 min when using CARBO and 88 +/- 24 min when using [Gln] (p<0.01)", i.e. +20% duration of tolerance"
    Bassini-Cameron. 2008 prof. football players, Gln Alanine 100mg/kg, either short-term or long-term, immediately before exercise;
    intervals (n = 18) and continuous intensity (n = 12) exercise tests
    #anabolism,
    +long-term recovery
    "[...] results suggest that chronically supplemented Gln protects against exercise-induced hyperammonemia depending on exercise intensity and supplementation duration
    Table 2: Some scientific data from human studies on oral glutamine supplementation from the last years ("+" indicates improvement; "#" indicates no effect; "-" indicates detrimental effect)
    Despite the fact that the existing human data does not support the idea that athletes in general and weight trainers or fitness fanatics in particular would benefit from the tons of glutamine supplements that are sold year by year, some of the advertisment claims are in fact based on observations in petri dishes or animal models:
    • In the petri dish, glutamine actually is the potent "cell volumizer" the advertisments would have it and its administration to isolated hepatocytes (liver cells) does in fact stimulates anabolic processes within the cells, which involve an increased synthesis of DNA, RNA, and proteins.
    • It has also been found in cell studies that glutamine-induced cell swelling activates extracellular signal-regulated kinases and p38 (mitogen-activated protein kinase, MAPK), which are involved in stress response + adaptation and could thus facilitate muscle growth.
    • Two grams of glutamine taken on an empty stomach have furthermore been shown to evoke an immediate growth hormone response, which - and this is the major caveat - is not only so minuscule that it is physiologically irrelevant; it also reduces the amount of growth hormone that is released after the sudden burst occurred, so that the overall AUC, the area under the 24h GH curve or, in other words, the overall 24h growth hormone production remains unaltered (similar effects have been observed for acetyl-l-carnitine (more on ALCAR in Part IV (2/3) of the AA for SH Series) and combinations of l-lysine and l-ornithine).
    • And even the beneficial effects of parenterally administered alanyl-l-glutamine, an alanine + glutamine dipeptide, on (unfortunately) whole body insulin sensitivity are well established (Bakalar. 2006).
    The reproduction or transfer of these effects from the respective model into real world results that would be relevant for the athletic practice have yet failed time and again and a mechanism which would explain the anecdotal evidence on the performance enhancing or muscle building effect of glutamine, which has repeatedly been confirmed by members of the bodybuilding and fitness world, could well be encapsulated within a fundamental physiological process that has acquired sort of a bad reputation lately: gluconeogenesis.
    Did you know that in a 2010 study by van Hall et al. (Hall. 2010) a glutamine/carbohydrate mixture (0.8 g x kg(-1) body weight of glucose + 0.3 g x kg(-1) glutamine) failed to increase the rate of glycogen resynthesis in muscle over glucose alone. On the other hand, an isocaloric whey hydrosolate and even a wheat hydrosolate did (whey +20%; wheat +21%). What the study by Hall et al. confirms with respect to the regenerative effects of glutamine, is confirmed in terms of its effects on immune function, muscle protein breakdown and athletic performance by findings from Basset et al. (Basset. 2000), Hole (Hole. 2001) and Lehmkuhl et al. (Lehmkuhl. 2003), where the actual immuno-modulators, anti-catabolics and ergogenics were BCAAs and creatine, and the BCAA induced elevation of glutamine levels were corollary and not causative, and the addition of supplemental glutamine to creatine monohydrate without any effect on exercise performance.
    In view of the current scare of everything carbohydrate-, god-forbid, insulin-related I hardly dare telling you that no other amino acid is so readily (ab-)used by your liver for glycogen production (=glyconeogenesis) as glutamine. This is especially true for doses that exceed the 2-5g range. They do not only provoke an accelerated glutamine clearance which is consistent with the activation of hepatic glutamine removal, but have also been shown to increase glucose formation in humans up to 7-fold (28g of glutamine infused in 4h time window; Perriello. 1997) at rest and to keep blood glucose levels up, glucose formation elevated (+24%) and glucose utilization increased (+16%) in a study, where dogs had received 12 micromol/kg/min glutamine intravenously during and after exercise (Iwashita. 2005).

    Now, even if you are a carbophobic insulin-hater, this does not mean that you should flush your glutamine supply down the toilette. In view of the fact that even the marked increase in gluconeogenesis that was observed by Perriollo et al. was not accompanied by an increase in insulin or glucogon levels, glutamine may in fact turn out to be the ideal supplement for endurance athletes or dieting body builders or figure competitors who want to maintain healthy blood glucose levels on a low carb diet. For a sedentary person on a no-carb diet, or example, even 20–40g glutamine per day would probably be enough to fuel their glycogen demands.

    Conclusion

    Image 4: You do not always need supplements.
    Oftentimes a nutritionally dense diet with a high
    amount of protein will work at least just as well
    as the latest and greatest amino acids supplement
    you read about in your favorite fitness magazine.
    The latter creative application of glutamine as a carbohydrate replacement aside, I am, based on the available data on the ergogenic effects of supplemental glutamine, inclined to subscribe to the conclusion of the authors of the BJSM Supplement Review (Newsholm. 2011) on glutamine who point out that
    [...] there is no consensus or unifying concept to explain the efficacy of exogenous provision of glutamine alone on performance in athletes, although in combination with carbohydrate or other amino acids, significant improvements have been reported. 
    Thus, notwithstanding its importance in many performance related physiological processes, an appropriately nourished human body is well able to synthesize more than enough glutamine from essential amino acids (and BCAAs in particular) to satisfy both everyday, as well as athletic demands. Consequently, athletes who wish to take advantage of the undeniably beneficial effects of adequately filled glutamine pools should give priority to the provision of adequate amounts of essential amino acids (EAAs), in general, and BCAAs, in particular. And despite the fact that the supplement industry would have you believe otherwise, most recreational athletes can easily satisfy their EAA demands by consuming a nutritionally dense high protein diet and an optional whey protein supplement.