Glaxon Specimen Max: High-Stim Pre-Workout Made with PEZ Power

Published on October 17, 2023 by PricePlow Staff | No Comments

Glaxon Specimen Max

Glaxon is one of the supplement industry’s hottest brands. While there are several reasons for this, one stands out above the rest: Glaxon’s science team is top notch. Its innovative, rigorous approach to supplement formulation constantly sets new industry trends and standards.

Earlier in the summer we covered Glaxon’s now-famous collaboration with the PEZ candy company. Readers have been blowing us up for months about how much they love these flavors.

One of the six products Glaxon included is a special edition of Specimen pre-workout series in Specimen MAX. Glaxon is also known for constantly revising and re-releasing Specimen – we’ve seen several iterations of this formula just in the last three years, with the latest and most popular being the ketone-powered Specimen Genesis. However, sometimes you want MAX power – and that’s where Specimen Max comes in.

We’ve updated our Specimen Max coverage to celebrate the new PEZ version, because this one’s bigger and badder than ever. Let’s get into how the massively stimmed pre-workout works, but first, check the PricePlow news and deals:

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Glaxon Specimen Max Ingredients

In a single 2-scoop (15 gram) serving of PEZ Specimen Max from Glaxon, you get the following:

Glaxon Specimen Max Ingredients

  • Beta-Alanine – 3,200 mg

    Beta-alanine is an ergogenic aid that can enhance athletic performance by serving as a precursor to carnosine, a dipeptide molecule.[1] Carnosine plays a vital role in eliminating lactic acid from muscles, a process crucial for preventing muscular fatigue. By increasing carnosine levels, beta-alanine effectively delays the onset of fatigue, thereby enhancing endurance during physical activities.[1,2]

    Supplementation with beta-alanine is preferred over carnosine due to the latter’s poor oral bioavailability. By comparison, beta-alanine supplements possess excellent oral bioavailability, making them an effective strategy for increasing carnosine levels. Because the other carnosine precursor, histidine, naturally occurs at high levels in ubiquitous foods, histidine intake is very unlikely to limit carnosine synthesis. Therefore, beta-alanine becomes the limiting factor,[3,4] making it a strategic choice for supplementation.

    Meta-analyses of over 40 published studies show that beta-alanine is particularly effective for enhancing endurance during exercises lasting between 30 seconds to 10 minutes.[2,5]

    Don’t worry about the tingles

    Users commonly report experiencing a tingling sensation in their face or upper body after consuming beta-alanine. If you experience this sensation, rest assured – a comprehensive analysis of beta-alanine safety confirmed that these tingles are benign.[6]

  • Betaine Anhydrous – 2,500 mg

    Betaine, also known as trimethylglycine (TMG), serves as another ergogenic aid. However, it works by a different mechanism than beta alanine.

    Methyl donor

    Glaxon Specimen Max PEZ

    One of ergogenic aids’ essential shared traits is their capacity to augment adenosine triphosphate (ATP) production, the body’s usable energy currency that’s indispensable for all cellular tasks. If your body were an engine, ATP would be the gas – without it, nothing runs. Because of its crucial role in cellular functioning, upregulating ATP can lead to superior athletic and cognitive performance.

    Betaine’s key mechanism of action is serving as a potent methyl donor.[7] In fact, betaine is one of the most powerful methyl donors currently known.[8] Among other things, increasing your body’s systemic availability of methyl groups through betaine supplementation can increase endogenous synthesis of ATP,[9] which can potentially increase your muscle cells’ capacity for physical work.

    Improves hormonal response to exercise

    Betaine also upregulates key metabolic hormones like AMP-activated protein kinase (AMPK), which control your cells’ rate of energy generation.[10]

    Homocysteine regulation

    Betaine’s role as a methyl donor is also pivotal in regulating homocysteine, an amino acid byproduct of methionine metabolism. Elevated homocysteine levels significantly increase one’s risk of developing cardiovascular disease (CVD), and betaine supplementation has demonstrated effectiveness in lowering homocysteine levels,[11,12] making it a potentially impactful investment in long-term cardiovascular health and athletic performance.

    Osmolyte

    Another contributing factor to betaine’s significant ergogenic effect is its status as an osmolyte, meaning it can influence the behavior of biological fluids. By manipulating osmotic pressure around cells, betaine facilitates the influx of extra water into cells, inducing a state of cellular hyperhydration. This enhanced hydration can improve performance by augmenting cellular nutrient access and rendering cells more resilient to heat stress.[7,13-19]

  • Astrolyte Electrolyte Blend (Fructooligosaccharides, Magnesium Citrate, Sodium Chloride, Potassium Citrate) – 1,000 mg

    Astrolyte is Glaxon’s proprietary electrolyte blend, a vital component in several of their premier supplements, including Specimen, Specimen GFY, their nitric oxide booster Plasm Surge, and even their sleep aid, Tranquility.

    Glaxon Specimen Max PEZ

    This is a pretty awesome ingredient, and we’re glad to see it making an appearance in Glaxon’s PEZ formula.

    This specialized blend consists of:

    • Sodium chloride (salt) – essential for muscle contractions and peak athletic performance[20,21]
    • Potassium – known for promoting cardiovascular health [22-25] and maintaining optimal bone density[26]
    • Magnesium – beneficial for enhancing insulin sensitivity,[27-29] regulating glycemic levels,[27-29] and managing blood pressure.[28,30-32]

    These electrolyte minerals are invaluable additions to any pre-workout formula because they are lost through sweat during intense exercise, which necessitates electrolyte replenishment for optimal performance and swift recovery.

    However, the standout feature of this ingredient isn’t a mineral – it’s the inclusion of fructooligosaccharides (FOS). These FOS are a unique type of carbohydrate that can actually enhance mineral absorption, particularly sodium, potassium, and magnesium [33-36]. By combining FOS with electrolytes, Glaxon ensures maximum effectiveness for your investment.

    Additionally, FOS exert a prebiotic effect,[37] nurturing the beneficial bacteria vital for a healthy gut.

    Notably, Astrolyte carries a natural sweetness, approximately 0.3 to 0.6 times as sweet as sugar [38,39], enhancing the overall taste of Glaxon Specimen Genesis.

    If you want a comprehensive treatment of this ingredient, we wrote an article dedicated to Astrolyte, highlighting its multifaceted hydration properties. To delve deeper into the topic, check out Glaxon Astrolyte: Hydrating Electrolytes That Do More.

  • Electro-Nitrate Blend (Sodium Nitrate as NO3-T, Potassium Nitrate as NO3-T) – 500 mg

    Nitrates are a direct precursor to nitric oxide (NO) – nitrates form the nitric part of NO. They upregulate NO by interacting with your body’s salivary glands, which incorporate nitrates into the NO molecule.[40-42]

    Glaxon Specimen Max PEZ

    The primary benefit of NO is that it triggers vasodilation, a process in which arteries relax, reducing cardiovascular resistance and easing the burden on your heart. This expanded arterial diameter not only lowers blood pressure and heart rate but can also, by improving circulation, enhance athletic performance and recovery.[43,44] In the long run, regular vasodilation can even lower the risk of cardiovascular diseases and hypertension, stroke, and heart attack.[45]

    Research shows that nitrates can:

    • Improve circulation[46]
    • Enhance aerobic efficiency[46-49]
    • Increase strength[50,51]
    • Augment cellular energy production[51-53]

    This last one may come as a surprise to regular PricePlow Blog readers, since NO’s impact on mitochondrial function isn’t discussed very often – but a preliminary yet growing body of research indicates that NO can improve mitochondrial function by stimulating mitochondrial biogenesis![54,55]

  • Caffeine Anhydrous – 400 mg

    Caffeine is a methylxanthine stimulant that has been shown to cross the body’s blood-brain barrier.[56] This property enables caffeine to exert great influence over the workings of your central nervous system.

    Caffeine’s capacity for boosting mood and focus are legendary, but the reason we see it in so many pre-workout formulas is that it can improve athletic performance as well.[57] In other words, caffeine can give us more physical energy. Broadly speaking, we can divide caffeine’s effects into two fundamental categories:

    Glaxon Logo

    1. Anti-fatigue – Caffeine blocks neuronal receptors for adenosine, a nucleotide byproduct of ATP hydrolysis that naturally builds up in brain tissue while we’re awake. As adenosine accumulates, it causes progressively intensifying feelings of mental and physical weariness. But by preventing adenosine from interacting with its cellular receptor, caffeine can also prevent the onset of fatigue.[58,59]
    2. Pro-metabolic – Caffeine also gives us energy in a more literal sense, by cranking up cellular metabolism. The mechanism of action here is caffeine’s inhibition of phosphodiesterase, an enzyme that breaks down cyclic adenosine monophosphate (cAMP). The second-order effect of this is that cAMP levels rise, leading to a boost in cellular-metabolic rate and increase in caloric expenditure.[57-61]

    Fat oxidation and body composition

    Caffeine Molecule

    Caffeine molecular diagram – a fitness blog classic

    If being lean is important to you, it’s vital to note that caffeine can actually increase the body’s rate of fat burning.[62] The effect size here can be pretty big – one study actually found that caffeine can cause the body to burn fat 50% faster than baseline.[63] According to a comprehensive 2020 meta-analysis on this subject, this effect shows up with doses as small as 3 milligrams of caffeine per kilogram of bodyweight.[64]

    Ergogenic effects

    Research indicates that caffeine can enhance various aspects of physical performance, including strength, speed, power, and endurance.[57,58,60,62,63] Due to its affordability and proven safety, caffeine stands as one of the most widely used ergogenic aids in the supplement industry.

    Nootropic

    Besides just make us feel better mentally, caffeine can also improve certain dimensions of cognitive performance, like attentiveness, psychomotor vigilance, reaction time, and working memory.[65-67]

    Dose warning

    400 milligrams of caffeine is a huge dose! If you aren’t sure whether you can handle a dose this big, talk to your doctor before taking Glaxon Specimen Max PEZ! Please!

  • Yerba santa (Eriodyctyon californicum) [Aerial Parts] Extract (as SantEnergy Nu) – 400 mg

    Yerba santa is an evergreen aromatic shrub that’s found in California and Oregon.

    It goes by many informal names in English, including mountain balm, bear’s weed, gum bush, gum plant, and consumptive weed. Yerba santa was of such significance to early Native Americans and settlers that Spanish and French have multiple colloquial names for it as well.

    SantEnergyNu

    For millennia, the tribes native to Southern California and Northern Mexico employed yerba santa for the purpose of improving breathing and mitigating the symptoms of respiratory inflammation.[68] Scientific studies have found some efficacy in the use of yerba santa for bronchial congestion, asthma, and hayfever.[69]

    Decreasing the effort required to breathe is an obvious benefit in a pre-workout formula, but yerba santa can be beneficial for body composition as well. It’s been shown to improve certain aspects of cellular metabolism[70] and trigger thermogenesis,[71] the process by which cells burn calories off as heat. That translates into a slightly bigger deficit on your next cut.

    Taste benefit

    Yerba santa has the ability to conceal the bitter taste of certain ingredients (caffeine is one example).[72] This means it can potentially improve the flavor of a product like Glaxon Specimen PEZ. The precise mechanism of action has yet to be elucidated, but it probably has something to do with bioactive constituents like homoeriodictyol, eriodictyol, and sterubin.[73]

  • Cholinace (VitaCholine as Choline L+Bitartrate), Alpha-GPC (L-Alpha Glycerylphosphorylcholine), CDP – Choline (Cytidine 5′-Diphosphocholine) – 300 mg

    Cholinace is an awesome focus-enhancing ingredient developed in-house by Glaxon. It contains various forms of choline, an essential B vitamin that’s indispensable for good organ health[74] and the synthesis of cellular phospholipid bilayer membranes.[75] This makes choline absolutely crucial for overall health and well-being.

    Glaxon Specimen Max PEZ

    Choline can also be particularly important in certain kinds of exercise. For example, prolonged endurance exercise (e.g., running a marathon) has been shown to significantly delete choline levels, and this depletion has been proposed as an explanation for the infamous “hitting the wall” phenomenon that has prevented many endurance athletes from finishing their races.[76,77]

    However, choline shows up in pre-workout formulas for a different reason – it’s also a precursor to acetylcholine, a neurotransmitter that’s centrally implicated in learning and memory consolidation. For this reason, acetylcholine upregulation has long been a popular nootropic strategy. For example, early biohackers touted acetylcholine agonists like huperzine A as the key to learning languages more efficiently.

    As it turns out, acetylcholine is also found at high concentrations within neuromuscular junctions,[78] where it helps actuate muscle contractions and can improve neuromotor skills like coordination and balance.[79,80]

    Cholinace consists of three different choline forms:

    • Vitacholine, which consists of the highly bioavailable L-isomer form (choline L-bitartrate)
    • Alpha-GPC, which is unique in its ability to cross the blood-brain barrier, making it especially good at upregulating acetylcholine synthesis.[81] Alpha-GPC has also recently been shown to have significant ergogenic properties, which lead to improvements in strength, power, and even growth hormone and thyroid secretion.[82,83]
    • Citicoline is especially good for upregulating norepinephrine and dopamine, while also increasing dopamine receptor density.[84]

    These are all highly effective forms of supplemental choline, so it’s not surprising to see that Glaxon has used their Cholinace brand in so many products as of late.

  • Rhodiola (Rhodiola crenulata) [Root] Extract (Std. to 6% Salidrosides as RhodioPrime 6x) – 250 mg

    There are basically two species of Rhodiola widely used in nutritional supplement design – Rhodiola rosea and Rhodiola crenulata. While these plants are essentially similar in their effects, each species has a different bioactive emphasis.

    NNB Nutrition RhodioPrime

    At 6% salidroside, NNB Nutrition’s RhodioPrime is the best way to feel the serious power of this wonderful herb!

    Rhodiola plants naturally contain rosavins and salidroside, the two bioactive constituents that account for most of the benefits from rhodiola supplementation. Although supplement science has traditionally focused on rosavins, it actually turns out that salidroside may be the more beneficial compound.[85,86] And, as it turns out, Rhodiola crenulata, despite being less popular than the rosea species, actually contains more salidroside.[87,88]

    That’s why Glaxon is using NNB’s trademarked RhodioPrime, which has the highest concentration of salidroside of any Rhodiola extract currently on the market, with an unprecedented 6% standardization. Generic extracts typically contain only 1% salidroside by weight.

    How salidroside works

    Research studies show that salidroside can:

    • Enhance long-term potentiation (LTP) in the hippocampus[88]
    • Increase autophagy through the mTOR pathway[89]
    • Enhance oxygen utilization via hypoxia-inducible factor-1 (HIF-1)[90]
    • Increase levels of neurotransmitters, such as dopamine, norepinephrine, epinephrine, histamine, and serotonin[91]

      • RhodioPrime NNB Nutrition

    • Inhibit the monoamine oxidase (MOA) enzyme responsible for neurotransmitter breakdown[92]
    • Upregulate neuropeptide Y, a hormone with anti-cortisol effects[93]

    Putting this all together, we can see that salidroside-rich extracts can be expected to have powerful adaptogenic and anti-stress effects.

    Through these mechanisms, salidroside supplementation has been shown to:

    • Improve cognitive performance[94]
    • Decrease felt stress and anxiety[95]
    • Enhance mood[95]
    • Mitigate depressive symptoms[96]

    In general, Rhodiola extracts can fight physical and mental fatigue,[97,98] improve athletic performance,[99] decrease appetite,[100] and positively alter glucose metabolism.[101]

  • Velvet Bean (Mucuna pruriens) [Seed] Extract – 250 mg

    Mucuna pruriens, also known by its colloquial name velvet bean, is loaded with potent antioxidants and is recognized for its capacity to upregulate dopamine.[102] Mucuna extracts are usually standardized for the amino acid L-DOPA,[103] which is the direct precursor to dopamine.[104]

    Since dopamine is the neurotransmitter most responsible for focus, motivation, and reward, increasing dopamine synthesis through L-DOPA supplementation can definitely help you power through tough workouts.

    Glaxon Specimen Max PEZ

    But wait, there’s more! Besides augmenting dopamine production, L-DOPA has significant anti-stress effects, thanks to its cortisol-lowering ability.[105-107] This makes L-DOPA a great ingredient to combine with stimulants like rauwolfia and caffeine, which are both present and generously dosed in Glaxon Specimen PEZ.

    Cortisol rises during exercise,[108,109] which isn’t necessarily bad, but we definitely don’t want it to stay elevated, and we may wish to blunt the cortisol response if possible. The reason is that chronically elevated cortisol can tank testosterone production.[110,111] It can also, in the long run, have a significant catabolic effect.[112]

    L-DOPA also regulates prolactin,[106] (which could be considered a stress hormone,) that rises during and after exercise.[113]

    Fortunately for us, Mucuna doesn’t just support testosterone production indirectly – it can also directly increase testosterone synthesis[114] and actually improve sperm count and quality.[115]

    Mucuna’s pro-testosterone, anti-cortisol effect is enough for us to call this an anabolic supplement, but as if that weren’t enough, Mucuna and L-DOPA have been shown to increase the production of growth hormone (GH).[116-118]

  • English Ivy (Hedera helix) [Leaf] Extract – 200 mg

    Glaxon Specimen Max

    English ivy is a great source of saponins and flavonoids,[119] which are known for improving cellular fatty acid metabolism[120] and, potentially, body composition.[121]

    Rat studies have shown that Hedera extracts can exert anti-diabetic effects by decreasing HbA1c and increasing insulin sensitivity.[122] This effect size was large enough for the study authors to see histological differences between the organ tissue of Hedera rats compared to placebo rats.

    Hedera can also help mitigate respiratory symptoms by acting as a natural bronchodilator.[123-125] This has the potential to make breathing— and hence workouts— just a little easier.

  • Theobromine – 150 mg

    Theobromine has stimulant, vasodilating, and bronchodilating effects.[126] It can also help increase NO production by downregulating arginase, the enzyme responsible for breaking down the NO precursor arginine.[127] This adds to the NO-related benefits we discussed in the sodium and potassium nitrate (NO3-T) section.

    Much like caffeine, theobromine upregulates cyclic adenosine monophosphate (cAMP) by downregulating the enzyme phosphodiesterase.[128] Again, this can increase cellular-metabolic rate,[129,130] causing ergogenic effects.

    Compared to caffeine, theobromine is a more potent vasodilator. It triggers significant relaxation of arterial smooth muscle tissue, which can decrease blood pressure and heart rate even though theobromine is technically a stimulant![131] Caffeine and theobromine are often stacked together precisely to mitigate caffeine’s effect on blood pressure.[132]

    Theobromine also has a longer half-life than caffeine, meaning its initial effects aren’t as jarring and the taper-off causes less intense withdrawal symptoms.[133]

  • Glaxon x PEZ

    Read more about the Glaxon X PEZ Collab on PricePlow

    Astragin (Astragalus membranaceus [Root] and Panax notoginseng [Root]) Extract – 25 mg

    AstraGin is a great ingredient for increasing the bioavailability of other ingredients.[134-138] AstraGin upregulates intestinal cells’ production of adenosine triphosphate (ATP), which increases their ability to perform the essential work of absorbing ingested food and supplements from the digestive tract. By increasing the effectiveness of other ingredients, AstraGin gives you the more bang for the buck you drop on Glaxon Specimen PEZ.

    Taking AstraGin regularly can potentially make intestinal tissue healthier, too.[139]

  • Rauwolfia (Rauwolfia vomitoria) [Root Bark] Extract – 3 mg

    As if 400 milligrams of caffeine wasn’t enough stimulant action, we’re now getting an impressive 3 milligram dose of rauwolfia. This extract of the shrub Rauwolfia vomitoria is standardized for rauwolscine, an alkaloid that’s often referred to as alpha yohimbine or alpha yo.

    Rauwolscine is basically a stronger form of yohimbine (the ingredient we’ll discuss in the next section). Both alkaloids block alpha-2 receptors,[140,141] which helps prevent fat storage while cranking up cellular metabolism.[141]

  • Yohimbe (Pausinystalia johimbe) [Root Bark] Extract – 2 mg

    Glaxon Specimen Max

    Finally, we’ve got 2 milligrams of yohimbe extract, which is almost certainly standardized for yohimbine HCl. As we discussed in the rauwolscine section, yohimbine is an alpha-2 antagonist, and can help increase energy while preventing fat gain.

  • Vitamins and minerals

    Besides the botanical bioactives, Glaxon Specimen PEZ also offers some important complementary vitamin and mineral support:

    • Vitamin C (as Ascorbic Acid) – 250 mg (278% DV)

      Vitamin C and nitrates have synergistic effects on NO production,[142] and vitamin C can also help prevent nitrate tolerance from developing during regular nitrate supplementation.[143] It can also help manage stress by helping keep adrenal glands healthy.[144,145]

      • Vitamin B2 (as Riboflavin) – 10 mg (769% DV)

      Riboflavin is needed for your body to produce flavoprotein enzymes, which are crucial for vital physiological functions like electron transport, cell signaling, protein folding, and metabolizing fatty acids and various substances, including pharmaceutical drugs.[146] Its role in the electron transport chain is particularly significant for adenosine triphosphate (ATP) production.[146]

    • Vitamin B3 (as Nicotinic Acid) – 50 mg (313% DV)

      Niacin (Vitamin B3) can upregulate your body’s synthesis of NAD+, which is crucial for the electron transport chain that produces all your ATP.[147-149] Your body uses NAD+ for a vast array of metabolic functions, including cellular energy, as well as liver function and DNA repair.[150-153]

      • Nicotinic Acid was first discovered through the oxidation of nicotine

    • Vitamin B6 (as Pyridoxal-5′-Phosphate) – 5 mg (294% DV)

      Vitamin B6 is crucial for protein metabolism, homocysteine regulation, and neurotransmitter production.[154]

    • Vitamin B12 (as Methylcobalamin) – 200 mcg (8333% DV)

      The methylcobalamin form of vitamin B12 is a powerful methyl donor.[155] B12 is important for red blood cell production[156,157] and homocysteine regulation.[158]

    • Choline (as Choline L-Bitartrate) – 92 mg (17% DV)

    • Magnesium (as Magnesium Citrate) – 31 mg (7% DV)

    • Chloride (as Sodium Chloride) – 120 mg (5% DV)

    • Sodium (from Sodium Chloride and Sodium NItrate) – 170 mg (7% DV)

    • Potassium (From Potassium Citrate and Potassium Nitrate) – 144 mg (3% DV)

All Available Specimen Max Flavors

Glaxon Specimen Max

    Conclusion

    Specimen Max is truly a jam-packed pre-workout formula – not only are there a ton of ingredients, but the stimulant doses used are truly epic. We have absolutely no doubt that this is a formula that will get you powerful results, if you can tolerate it. More specifically, if you’re not sure whether you can handle 400 milligrams of caffeine at once, or the famous “yoyo” blend of rauwolscine AND yohimbine, you must talk to your doctor before using Glaxon Specimen PEZ.

    Glaxon Specimen MAX – Deals and Price Drop Alerts

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    About the Author: PricePlow Staff

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    The team's collective experiences and research target athletic performance and body composition goals, relying on low-toxicity meat-based diets.

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    References

    1. Trexler, E.T., Smith-Ryan, A.E., Stout, J.R. et al.; “International society of sports nutrition position stand: Beta-Alanine.”; J Int Soc Sports Nutr 12, 30 (2015); https://jissn.biomedcentral.com/articles/10.1186/s12970-015-0090-y
    2. Hobson, R M, et al; “Effects of β-Alanine Supplementation on Exercise Performance: a Meta-Analysis.”; Amino Acids; Springer Vienna; July 2012; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374095/
    3. Harris, R. C., et al. “The Absorption of Orally Supplied β-Alanine and Its Effect on Muscle Carnosine Synthesis in Human Vastus Lateralis.” Amino Acids, vol. 30, no. 3, 24 Mar. 2006, pp. 279–289, 10.1007/s00726-006-0299-9; https://pubmed.ncbi.nlm.nih.gov/16554972/
    4. Dunnett, M., and R. C. Harris. “Influence of Oral ß-Alanine and L-Histidine Supplementation on the Carnosine Content of Thegluteus Medius.” Equine Veterinary Journal, vol. 31, no. S30, July 1999, pp. 499–504, 10.1111/j.2042-3306.1999.tb05273.x; https://pubmed.ncbi.nlm.nih.gov/10659307/
    5. Saunders, Bryan, et al. “β-Alanine Supplementation to Improve Exercise Capacity and Performance: A Systematic Review and Meta-Analysis.” British Journal of Sports Medicine, vol. 51, no. 8, 18 Oct. 2016, pp. 658–669; https://bjsm.bmj.com/content/51/8/658.long
    6. Dolan, Eimear, et al. “A Systematic Risk Assessment and Meta-Analysis on the Use of Oral β-Alanine Supplementation.” Advances in Nutrition, vol. 10, no. 3, 13 Apr. 2019, pp. 452–463, 10.1093/advances/nmy115; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520041/
    7. Lee I. Betaine is a positive regulator of mitochondrial respiration. Biochem Biophys Res Commun. 2015 Jan 9;456(2):621-5. doi: 10.1016/j.bbrc.2014.12.005; https://pubmed.ncbi.nlm.nih.gov/25498545/
    8. Craig, Stuart AS. “Betaine in Human Nutrition.” The American Journal of Clinical Nutrition, vol. 80, no. 3, 1 Sept. 2004, pp. 539–549, 10.1093/ajcn/80.3.539; https://www.sciencedirect.com/science/article/pii/S0002916522035602
    9. Deminice R, Vannucchi H, Simões-Ambrosio LM, Jordao AA. Creatine supplementation reduces increased homocysteine concentration induced by acute exercise in rats. Eur J Appl Physiol. 2011 Nov;111(11):2663-70. doi: 10.1007/s00421-011-1891-6. Epub 2011 Mar 11. PMID: 21394640. https://link.springer.com/article/10.1007/s00421-011-1891-6
    10. Apicella JM, Lee EC, Bailey BL, Saenz C, Anderson JM, Craig SA, Kraemer WJ, Volek JS, Maresh CM. Betaine supplementation enhances anabolic endocrine and Akt signaling in response to acute bouts of exercise. Eur J Appl Physiol. 2013 Mar;113(3):793-802. doi: 10.1007/s00421-012-2492-8. Epub 2012 Sep 14. PMID: 22976217. https://link.springer.com/article/10.1007/s00421-012-2492-8
    11. Olthof, M. R., & Verhoef, P. (2005). Effects of betaine intake on plasma homocysteine concentrations and consequences for health. Current drug metabolism, 6(1), 15-22; https://pubmed.ncbi.nlm.nih.gov/15720203
    12. Ganguly, Paul, and Sreyoshi Fatima Alam. “Role of homocysteine in the development of cardiovascular disease.” Nutrition journal vol. 14 6. 10 Jan. 2015, doi:10.1186/1475-2891-14-6; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326479/
    13. Boel De Paepe; “Osmolytes as Mediators of the Muscle Tissue’s Responses to Inflammation: Emerging Regulators of Myositis with Therapeutic Potential”; EMJ Rheumatol. 2017;4undefined:83-89; https://www.emjreviews.com/rheumatology/article/osmolytes-as-mediators-of-the-muscle-tissues-responses-to-inflammation-emerging-regulators-of-myositis-with-therapeutic-potential/
    14. Caldas, Teresa, et al. “Thermoprotection by Glycine Betaine and Choline.” Microbiology, vol. 145, no. 9, 1 Sept. 1999, pp. 2543–2548, 10.1099/00221287-145-9-2543; https://pubmed.ncbi.nlm.nih.gov/10517607/
    15. Roti, M; “Homocysteine, Lipid and Glucose Responses to Betaine Supplementation During Running in the Heat”; Medicine & Science in Sports & Exercise: May 2003 – Volume 35 – Issue 5 – p S271; https://journals.lww.com/acsm-msse/Fulltext/2003/05001/HOMOCYSTEINE,_LIPID_AND_GLUCOSE_RESPONSES_TO.1501.aspx
    16. Armstrong, Lawrence E, et al. “Influence of Betaine Consumption on Strenuous Running and Sprinting in a Hot Environment.” Journal of Strength and Conditioning Research, vol. 22, no. 3, May 2008, pp. 851–860, 10.1519/jsc.0b013e31816a6efb; https://pubmed.ncbi.nlm.nih.gov/18438230
    17. Lee, Elaine C, et al. “Ergogenic Effects of Betaine Supplementation on Strength and Power Performance.” Journal of the International Society of Sports Nutrition, vol. 7, no. 1, 2010, p. 27, 10.1186/1550-2783-7-27; https://jissn.biomedcentral.com/articles/10.1186/1550-2783-7-27
    18. Cholewa, Jason M et al. “Effects of betaine on body composition, performance, and homocysteine thiolactone.” Journal of the International Society of Sports Nutrition vol. 10,1 39. 22 Aug. 2013, doi:10.1186/1550-2783-10-39; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844502/
    19. Zhao, Guangfu et al. “Betaine in Inflammation: Mechanistic Aspects and Applications.” Frontiers in immunology vol. 9 1070. 24 May. 2018, doi:10.3389/fimmu.2018.01070 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976740/
    20. Strazzullo P., Leclercq C.; “Sodium.” Advanced Nutrition; March 2014; 5(2) 188-190; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951800/
    21. Valentine, V. 2007. “The Importance of Salt in the Athlete’s Diet.” Current Sports Medicine Reports vol. 6,4 (2007): 237-40. https://pubmed.ncbi.nlm.nih.gov/17617999/
    22. Weaver, Connie M. “Potassium and Health.” Advances in Nutrition, vol. 4, no. 3, 1 May 2013, pp. 368S377S, 10.3945/an.112.003533; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3650509/
    23. Fulgoni, Victor L., et al. “Foods, Fortificants, and Supplements: Where Do Americans Get Their Nutrients?” The Journal of Nutrition, vol. 141, no. 10, 24 Aug. 2011, pp. 1847–1854, 10.3945/jn.111.142257; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3174857/
    24. Cook, Nancy R. “Joint Effects of Sodium and Potassium Intake on Subsequent Cardiovascular Disease.” Archives of Internal Medicine, vol. 169, no. 1, 12 Jan. 2009, p. 32, 10.1001/archinternmed.2008.523; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC2629129/
    25. Lemann, Jacob, et al. “Potassium Administration Increases and Potassium Deprivation Reduces Urinary Calcium Excretion in Healthy Adults.” Kidney International, vol. 39, no. 5, May 1991, pp. 973–983, 10.1038/ki.1991.123; https://pubmed.ncbi.nlm.nih.gov/1648646/
    26. Gregory, Naina Sinha, et al. “Potassium Citrate Decreases Bone Resorption in Postmenopausal Women with Osteopenia: A Randomized, Double-Blind Clinical Trial” Endocrine Practice, vol. 21, no. 12, Dec. 2015, pp. 1380–1386, 10.4158/ep15738.or; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC5558825/
    27. Rodriguez-Moran, M., and F. Guerrero-Romero. “Oral Magnesium Supplementation Improves Insulin Sensitivity and Metabolic Control in Type 2 Diabetic Subjects: A Randomized Double-Blind Controlled Trial.” Diabetes Care, vol. 26, no. 4, 1 Apr. 2003, pp. 1147–1152, 10.2337/diacare.26.4.1147; https://care.diabetesjournals.org/content/26/4/1147.long
    28. Guerrero-Romero, Fernando, and Martha Rodríguez-Morán. “Magnesium Improves the Beta-Cell Function to Compensate Variation of Insulin Sensitivity: Double-Blind, Randomized Clinical Trial.” European Journal of Clinical Investigation, vol. 41, no. 4, 17 Jan. 2011, pp. 405–410, 10.1111/j.1365-2362.2010.02422.x; https://pubmed.ncbi.nlm.nih.gov/21241290/
    29. Mooren, F. C., et al. “Oral Magnesium Supplementation Reduces Insulin Resistance in Non-Diabetic Subjects – a Double-Blind, Placebo-Controlled, Randomized Trial.” Diabetes, Obesity and Metabolism, vol. 13, no. 3, 24 Jan. 2011, pp. 281–284, 10.1111/j.1463-1326.2010.01332.x; https://pubmed.ncbi.nlm.nih.gov/21205110/
    30. Hatzistavri, L. S., et al. “Oral Magnesium Supplementation Reduces Ambulatory Blood Pressure in Patients with Mild Hypertension.” American Journal of Hypertension, vol. 22, no. 10, 1 Oct. 2009, pp. 1070–1075, 10.1038/ajh.2009.126; https://pubmed.ncbi.nlm.nih.gov/19617879/
    31. Kawano, Yuhei, et al. “Effects of Magnesium Supplementation in Hypertensive Patients.” Hypertension, vol. 32, no. 2, Aug. 1998, pp. 260–265, 10.1161/01.hyp.32.2.260; https://www.ahajournals.org/doi/10.1161/01.hyp.32.2.260
    32. Guerrero-Romero, F, and M Rodríguez-Morán. “The Effect of Lowering Blood Pressure by Magnesium Supplementation in Diabetic Hypertensive Adults with Low Serum Magnesium Levels: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial.” Journal of Human Hypertension, vol. 23, no. 4, 20 Nov. 2008, pp. 245–251, 10.1038/jhh.2008.129; https://www.nature.com/articles/jhh2008129
    33. Nzeusseu, A; “Inulin and fructo-oligosaccharides differ in their ability to enhance the density of cancellous and cortical bone in the axial and peripheral skeleton of growing rats”; Bone; 38(3):394-9; 2006 Mar; https://www.ncbi.nlm.nih.gov/pubmed/16249132
    34. Ohta, A., et al. “Calcium and Magnesium Absorption from the Colon and Rectum Are Increased in Rats Fed Fructooligosaccharides.” The Journal of Nutrition, vol. 125, no. 9, 1 Sept. 1995, pp. 2417–2424, 10.1093/jn/125.9.2417; https://pubmed.ncbi.nlm.nih.gov/7666261/
    35. Delzenne, N., et al. “Effect of Fermentable Fructo-Oligosaccharides on Mineral, Nitrogen and Energy Digestive Balance in the Rat.” Life Sciences, vol. 57, no. 17, Sept. 1995, pp. 1579–1587, 10.1016/0024-3205(95)02133-4; https://pubmed.ncbi.nlm.nih.gov/7564905/
    36. Sakai, Kensuke, et al. “The Effect of Short Chain Fructooligosaccharides in Promoting Recovery from Post-Gastrectomy Anemia Is Stronger than that of Inulin.” Nutrition Research, vol. 20, no. 3, Mar. 2000, pp. 403–412, 10.1016/s0271-5317(00)00133-0; https://www.sciencedirect.com/science/article/abs/pii/S0271531700001330
    37. Sabater-Molina, M, et al. “Dietary Fructooligosaccharides and Potential Benefits on Health.” Journal of Physiology and Biochemistry, vol. 65, no. 3, 2009, pp. 315–28, 10.1007/BF03180584; https://pubmed.ncbi.nlm.nih.gov/20119826/
    38. Crittenden, R.G., and M.J. Playne. “Production, Properties and Applications of Food-Grade Oligosaccharides.” Trends in Food Science & Technology, vol. 7, no. 11, Nov. 1996, pp. 353–361, 10.1016/s0924-2244(96)10038-8; https://www.sciencedirect.com/science/article/abs/pii/S0924224496100388
    39. Yun, Jong Won. “Fructooligosaccharides—Occurrence, Preparation, and Application.” Enzyme and Microbial Technology, vol. 19, no. 2, Aug. 1996, pp. 107–117, 10.1016/0141-0229(95)00188-3; https://www.sciencedirect.com/science/article/abs/pii/0141022995001883
    40. Lundberg, Jon O., and Mirco Govoni. “Inorganic Nitrate Is a Possible Source for Systemic Generation of Nitric Oxide.” Free Radical Biology & Medicine, vol. 37, no. 3, 1 Aug. 2004, pp. 395–400, 10.1016/j.freeradbiomed.2004.04.027. https://pubmed.ncbi.nlm.nih.gov/15223073/
    41. Qu, X. M., et al. “From Nitrate to Nitric Oxide: The Role of Salivary Glands and Oral Bacteria.” Journal of Dental Research, vol. 95, no. 13, 1 Dec. 2016, pp. 1452–1456, 10.1177/0022034516673019; https://pubmed.ncbi.nlm.nih.gov/27872324/
    42. Eisenbrand, G., et al. “Nitrate and Nitrite in Saliva.” Oncology, vol. 37, no. 4, 1980, pp. 227–231, 10.1159/000225441; https://pubmed.ncbi.nlm.nih.gov/7443155/
    43. Bescós, Raúl et al. “The effect of nitric-oxide-related supplements on human performance.” Sports medicine (Auckland, N.Z.) vol. 42,2 (2012): 99-117. doi:10.2165/11596860-000000000-00000 https://dx.doi.org/10.2165/11596860-000000000-00000
    44. Le Roux-Mallouf, T., Pelen, F., et al. Aging; “Effect of chronic nitrate and citrulline supplementation on vascular function and exercise performance in older individuals.” 2019; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555465/
    45. Naseem, Khalid M. “The role of nitric oxide in cardiovascular diseases.” Molecular aspects of medicine vol. 26,1-2 (2005): 33-65. doi:10.1016/j.mam.2004.09.003 https://linkinghub.elsevier.com/retrieve/pii/S0098-2997(04)00075-5
    46. Larsen, F; “Effects of dietary nitrate on oxygen cost during exercise”; Department of Physiology and Pharmacology, Karolinska Institutet; 2007; https://pubmed.ncbi.nlm.nih.gov/17635415/
    47. Lansley, K; “Dietary nitrate supplementation reduces the O2 cost of walking and running: a placebo-controlled study”; School of Sport and Health Sciences, Univ. of Exeter; 2011; https://journals.physiology.org/doi/full/10.1152/japplphysiol.01070.2010
    48. Bailey, S; “Dietary nitrate supplementation reduces the O2 cost of low-intensity exercise and enhances tolerance to high-intensity exercise in humans”; School of Sport and Health Sciences, Univ. of Exeter; 2009; https://journals.physiology.org/doi/full/10.1152/japplphysiol.00722.2009
    49. Bescos, R; “Acute administration of inorganic nitrate reduces VO(2peak) in endurance athletes”; National Institute of Physical Education-Barcelona, University of Barcelona; 2011; https://pubmed.ncbi.nlm.nih.gov/21407132/
    50. Fulford, J; “Influence of dietary nitrate supplementation on human skeletal muscle metabolism and force production during maximum voluntary contractions”; NIHR Exeter Clinical Research Facility, University of Exeter Medical School; 2013; https://pubmed.ncbi.nlm.nih.gov/23354414/
    51. Bailey, S; “Dietary nitrate supplementation enhances muscle contractile efficiency during knee-extensor exercise in humans”; School of Sport and Health Sciences, University of Exeter; 2010; https://journals.physiology.org/doi/full/10.1152/japplphysiol.00046.2010
    52. Lundberg, J; “The nitrate-nitrite-nitric oxide pathway in physiology and therapeutics”; Department of Physiology and Pharmacology, Karolinska Institute; 2008; https://www.nature.com/articles/nrd2466
    53. Larsen, F; “Dietary inorganic nitrate improves mitochondrial efficiency in humans”; Department of Physiology and Pharmacology, Karolinska Institutet; 2011; https://www.cell.com/cell-metabolism/fulltext/S1550-4131(11)00005-2
    54. Ramírez-Sánchez I, Rodríguez A, Moreno-Ulloa A, Ceballos G, Villarreal F. (-)-Epicatechin-induced recovery of mitochondria from simulated diabetes: Potential role of endothelial nitric oxide synthase. Diab Vasc Dis Res. 2016 May;13(3):201-10. doi: 10.1177/1479164115620982; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107246/
    55. Nisoli E, Carruba MO. Nitric oxide and mitochondrial biogenesis. J Cell Sci. 2006 Jul 15;119(Pt 14):2855-62. doi: 10.1242/jcs.03062. PMID: 16825426. https://journals.biologists.com/jcs/article/119/14/2855/28995/Nitric-oxide-and-mitochondrial-biogenesis
    56. Ikeda-Murakami K, Tani N, Ikeda T, Aoki Y, Ishikawa T. Central Nervous System Stimulants Limit Caffeine Transport at the Blood-Cerebrospinal Fluid Barrier. Int J Mol Sci. 2022 Feb 7;23(3):1862. doi: 10.3390/ijms23031862. PMID: 35163784; PMCID: PMC8836437. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836437/
    57. Goldstein, E.R., Ziegenfuss, T., Kalman, D. et al.; “International society of sports nutrition position stand: caffeine and performance”; J Int Soc Sports Nutr 7, 5 (2010); https://link.springer.com/article/10.1186/1550-2783-7-5
    58. Cappelletti, Simone et al. “Caffeine: cognitive and physical performance enhancer or psychoactive drug?.” Current neuropharmacology vol. 13,1 (2015): 71-88. doi:10.2174/1570159X13666141210215655; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462044/
    59. Nehlig A, Daval JL, Debry G.; “Caffeine and the central nervous system: mechanisms of action, biochemical, metabolic and psychostimulant effects”; Brain Res Rev. 1992;17(2):139-170; https://www.sciencedirect.com/science/article/abs/pii/016501739290012B
    60. Goldstein, E.R., Ziegenfuss, T., Kalman, D. et al.; “International society of sports nutrition position stand: caffeine and performance.”; J Int Soc Sports Nutr 7, 5 (2010); https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777221/
    61. Diepvens, K et al; “Obesity and thermogenesis related to the consumption of caffeine, ephedrine, capsaicin, and green tea;” American Journal of Physiology; 2007; https://journals.physiology.org/doi/full/10.1152/ajpregu.00832.2005
    62. Burke LM. Caffeine and sports performance. Appl Physiol Nutr Metab. 2008 Dec;33(6):1319-34. doi: 10.1139/H08-130; https://cdnsciencepub.com/doi/10.1139/H08-130
    63. Norager, C B, et al; “Metabolic Effects of Caffeine Ingestion and Physical Work in 75-Year Old Citizens. A Randomized, Double-Blind, Placebo-Controlled, Cross-over Study.”; Clinical Endocrinology; U.S. National Library of Medicine; Aug. 2006; https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2265.2006.02579.x
    64. Collado-Mateo D, Lavín-Pérez AM, Merellano-Navarro E, Coso JD. Effect of Acute Caffeine Intake on the Fat Oxidation Rate during Exercise: A Systematic Review and Meta-Analysis. Nutrients. 2020 Nov 24;12(12):3603. doi: 10.3390/nu12123603. PMID: 33255240; PMCID: PMC7760526. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760526/
    65. Kahathuduwa CN, Dassanayake TL, Amarakoon AMT, Weerasinghe VS. Acute effects of theanine, caffeine and theanine-caffeine combination on attention. Nutr Neurosci. 2017 Jul;20(6):369-377. doi: 10.1080/1028415X.2016.1144845; https://www.tandfonline.com/doi/abs/10.1080/1028415X.2016.1144845
    66. McLellan TM, Caldwell JA, Lieberman HR. A review of caffeine’s effects on cognitive, physical and occupational performance. Neurosci Biobehav Rev. 2016 Dec;71:294-312. doi: 10.1016/j.neubiorev.2016.09.001; https://www.sciencedirect.com/science/article/pii/S0149763416300690
    67. Klaassen EB, de Groot RH, Evers EA, Snel J, Veerman EC, Ligtenberg AJ, Jolles J, Veltman DJ. The effect of caffeine on working memory load-related brain activation in middle-aged males. Neuropharmacology. 2013 Jan;64:160-7. doi: 10.1016/j.neuropharm.2012.06.026; https://www.sciencedirect.com/science/article/abs/pii/S0028390812002845
    68. Munz, P. A; “A California flora and supplement”; University of California Press: Berkeley, CA, 1973; p 547; https://www.amazon.com/dp/0520024052
    69. Hadley, W. J.; Gisvold, O. “A phytochemical study of Eriodictyon angustifolium, Nuttley”; J. Am. Pharm. Assoc. Sci. Educ. 1944, 33, 275–7; https://www.researchgate.net/publication/246846230_A_phytochemical_study_of_Eriodictyon_angustifolium_nuttley
    70. Mödinger, Yvonne, et al. “A Food Supplement with Antioxidative Santa Herba Extract Modulates Energy Metabolism and Contributes to Weight Management.” Journal of Medicinal Food, 13 July 2021, 10.1089/jmf.2021.0016. https://www.liebertpub.com/doi/10.1089/jmf.2021.0016
    71. Santos, Tanila & Miranda, Jonatan & Teixeira, Lucimara & Aiastui, Ana & Matheu, Ander & Gambero, Alessandra & Portillo, María & Ribeiro, Marcelo. (2018). Yerba Mate Stimulates Mitochondrial Biogenesis and Thermogenesis in High Fat Diet-Induced Obese Mice. Molecular Nutrition & Food Research. 62. 1800142. 10.1002/mnfr.201800142. https://www.researchgate.net/publication/325471946_Yerba_Mate_Stimulates_Mitochondrial_Biogenesis_and_Thermogenesis_in_High_Fat_Diet-Induced_Obese_Mice
    72. Lewin, L. Ueber die Geschmacksverbesserung von Medicamenten und uber Saturationen. € Berl. Klin. Wochenschr. 1894, 28, 644–645
    73. Ley, Jakob P., et al. “Evaluation of Bitter Masking Flavanones from Herba Santa (Eriodictyon Californicum(H. & A.) Torr., Hydrophyllaceae).” Journal of Agricultural and Food Chemistry, vol. 53, no. 15, July 2005, pp. 6061–6066, 10.1021/jf0505170; https://pubmed.ncbi.nlm.nih.gov/16028996/
    74. Ueland, P. M.; “Choline and betaine in health and disease;” Journal of Inherited Metabolic Disease; 2010; 34(1), 3–15; https://onlinelibrary.wiley.com/doi/abs/10.1007/s10545-010-9088-4
    75. Sanders LM, Zeisel SH; “Choline: Dietary Requirements and Role in Brain Development;” Nutrition today; 2007;42(4):181-186; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518394/
    76. Conlay LA, Sabounjian LA, Wurtman RJ. Exercise and neuromodulators: choline and acetylcholine in marathon runners. Int J Sports Med. 1992 Oct;13 Suppl 1:S141-2. doi: 10.1055/s-2007-1024619. PMID: 1483754. https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2007-1024619
    77. Penry JT, Manore MM. Choline: an important micronutrient for maximal endurance-exercise performance? Int J Sport Nutr Exerc Metab. 2008 Apr;18(2):191-203. doi: 10.1123/ijsnem.18.2.191. PMID: 18458362. https://journals.humankinetics.com/view/journals/ijsnem/18/2/article-p191.xml
    78. Purves D, Augustine GJ, Fitzpatrick D, et al.; “Neuroscience;” 2nd edition. Sunderland (MA): Sinauer Associates; 2001. Acetylcholine. https://www.ncbi.nlm.nih.gov/books/NBK11143/
    79. Hasselmo ME; “The role of acetylcholine in learning and memory;” Curr Opin Neurobiol. 2006;16(6):710–715; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2659740/
    80. Jones BE; “From waking to sleeping: neuronal and chemical substrates”. Trends Pharmacol. Sci.; 2005; 26 (11): 578–86; https://www.ncbi.nlm.nih.gov/pubmed/16183137
    81. Marcus L, et al; “Evaluation of the effects of two doses of alpha glycerylphosphorylcholine on physical and psychomotor performance;” J Int Soc Sports Nutr; 2017;14:39; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629791/
    82. Marcus L, Soileau J, Judge LW, Bellar D. Evaluation of the effects of two doses of alpha glycerylphosphorylcholine on physical and psychomotor performance. J Int Soc Sports Nutr. 2017 Oct 5;14:39. doi: 10.1186/s12970-017-0196-5; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629791/
    83. Ziegenfuss T, Landis J, Hofheins J. Acute supplementation with alpha-glycerylphosphorylcholine augments growth hormone response to, and peak force production during, resistance exercise. J Int Soc Sports Nutr. 2008 Sep 17;5(Suppl 1):P15. doi: 10.1186/1550-2783-5-S1-P15; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3313098/
    84. Secades, JJ; “Citicoline: pharmacological and clinical review, 2016 update;” Rev Neurol; 2017; https://www.researchgate.net/profile/Julio_Secades/publication/317167480_Citicoline_pharmacological_and_clinical_review_2016_update/links/59280785a6fdcc444353790e/Citicoline-pharmacological-and-clinical-review-2016-update.pdf
    85. Panossian, A. et al. June 2010. “Rosenroot (Rhodiola Rosea): Traditional Use, Chemical Composition, Pharmacology, and Clinical efficacy.” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology vol. 17,7. 481-93. https://pubmed.ncbi.nlm.nih.gov/20378318/
    86. Grech-Baran, M. et al. June 2015. “Biotechnological Approaches to Enhance Salidroside, Rosin and Its Derivatives Production in Selected Rhodiola spp. in Vitro Cultures.” Phytochemistry Reviews: Proceedings of the Phytochemical Society of Europe vol. 14,4. 657-674. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513219/
    87. Li, Y. et al. Dec. 2017. “Rhodiola Rosea L.: An Herb with Anti-stress, Anti-aging, and Immunostimulating Properties for Cancer Chemoprevention.” Current Pharmacology Reports vol. 3,6; 384-395. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208354/
    88. Dimpfel, W. et al. May 2018. “Assessing the Quality and Potential Efficacy of Commercial Extracts of Rhodiola Rosea L. by Analyzing the Salidroside and Rosavin Content and the Electrophysiological Activity in Hippocampal Long-Term Potentiation, a Synaptic Model of Memory.” Frontiers in Pharmacology vol. 9. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976749/
    89. Liu, Z. et al. Mar. 2012. “Rhodiola Rosea Extracts and Salidroside Decrease the Growth of Bladder Cancer Cell Lines via Inhibition of The mTOR Pathway and Induction of Autophagy.” Molecular Carcinogenesis vol. 51,3; 257-67. https://www.ncbi.nlm.nih.gov/pubmed/21520297/
    90. Zheng, K. et al. Mar. 2012/ “Salidroside Stimulates the Accumulation of HIF-1α Protein Resulted in the Induction of EPO Expression: A Signaling via Blocking the Degradation Pathway in Kidney and Liver Cells.” European Journal of Pharmacology vol. 679,1-3; 34-9. https://pubmed.ncbi.nlm.nih.gov/22309741/
    91. Panossian, A. et al. June 2010. “Rosenroot (Rhodiola Rosea): Traditional Use, Chemical Composition, Pharmacology, and Clinical efficacy.” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology vol. 17,7. 481-93. https://pubmed.ncbi.nlm.nih.gov/20378318/
    92. Van Diermen, D. et al. Mar. 2009. “Monoamine Oxidase Inhibition by Rhodiola Rosea L. Roots.” Journal of Ethnopharmacology vol. 122,2; 397-401. https://pubmed.ncbi.nlm.nih.gov/19168123/
    93. Panossian A, Wikman G, Kaur P, Asea A. Adaptogens stimulate neuropeptide y and hsp72 expression and release in neuroglia cells. Front Neurosci. 2012 Feb 1;6:6. doi: 10.3389/fnins.2012.00006. PMID: 22347152; PMCID: PMC3269752. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269752/
    94. Dimpfel, W. et al. May 2018. “Assessing the Quality and Potential Efficacy of Commercial Extracts of Rhodiola Rosea L. by Analyzing the Salidroside and Rosavin Content and the Electrophysiological Activity in Hippocampal Long-Term Potentiation, a Synaptic Model of Memory.” Frontiers in Pharmacology vol. 9. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976749/
    95. Cropley, M. et al. Dec. 2015. “The Effects of Rhodiola Rosea L. Extract on Anxiety, Stress, Cognition and Other Mood Symptoms.” Phytotherapy Research: PTR vol. 29,12; 1934-9. https://pubmed.ncbi.nlm.nih.gov/26502953/
    96. Darbinyan, V. et al. 2007. “Clinical Trial of Rhodiola Rosea L. Extract SHR-5 in the Treatment of Mild to Moderate Depression.” Nordic Journal of Psychiatry vol. 61,5; 343-8. https://pubmed.ncbi.nlm.nih.gov/17990195/
    97. Spasov, A. et al. April 2007. “A Double-Blind, Placebo-Controlled Pilot Study of the Stimulating and Adaptogenic Effect of Rhodiola Rosea SHR-5 Extract on the Fatigue of Students Caused by Stress During an Examination Period with a Repeated Low-Dose Regimen.” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology vol. 7,2; 85-9. https://pubmed.ncbi.nlm.nih.gov/10839209/
    98. Shevtsov, V. et al. Mar. 2003. “A Randomized Trial of Two Different Doses of a SHR-5 Rhodiola Rosea Extract Versus Placebo and Control of Capacity for Mental Work.” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology vol. 10,2-3; 95-105. https://pubmed.ncbi.nlm.nih.gov/12725561/
    99. De Bock, K. et al. June 2004. “Acute Rhodiola Rosea Intake can Improve Endurance Exercise Performance.” International Journal of Sport Nutrition and Exercise Metabolism vol. 14,3; 298-307. https://pubmed.ncbi.nlm.nih.gov/15256690/
    100. Cifani, C. et al. Dec. 2010. “Effect of Salidroside, Active Principle of Rhodiola Rosea Extract, on Binge Eating.” Physiology & Behavior vol. 101,5; 555-62. https://pubmed.ncbi.nlm.nih.gov/20837037/
    101. Mao, G. et al. Apr. 2010. “Protective Role of Salidroside Against Aging in a Mouse Model Induced by D-galactose.” Biomedical and Environmental Sciences: BES vol. 23,2; 161-6. https://pubmed.ncbi.nlm.nih.gov/20514993/
    102. Agbafor, K. N., and N. Nwachukwu. “Phytochemical Analysis and Antioxidant Property of Leaf Extracts of Vitex Doniana and Mucuna Pruriens.” Biochemistry Research International, vol. 2011, 2011, 10.1155/2011/459839. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085303/
    103. Misra, Laxminarain, and Hildebert Wagner. “Extraction of Bioactive Principles from Mucuna Pruriens Seeds.” Indian Journal of Biochemistry & Biophysics, vol. 44, no. 1, 1 Feb. 2007, pp. 56–60. https://pubmed.ncbi.nlm.nih.gov/17385342/
    104. Gandhi, Kavita R, and Abdolreza Saadabadi. “Levodopa (L-Dopa).” Nih.gov, StatPearls Publishing, 27 Oct. 2018; https://www.ncbi.nlm.nih.gov/books/NBK482140/
    105. Boden, G., et al. “Influence of Levodopa on Serum Levels of Anterior Pituitary Hormones in Man.” Neuroendocrinology, vol. 10, no. 5, 1972, pp. 309–315, 10.1159/000122100; https://pubmed.ncbi.nlm.nih.gov/4350777/
    106. Müller, T., et al. “Acute Levodopa Administration Reduces Cortisol Release in Patients with Parkinson’s Disease.” Journal of Neural Transmission, vol. 114, no. 3, 24 Aug. 2006, pp. 347–350, 10.1007/s00702-006-0552-0; https://pubmed.ncbi.nlm.nih.gov/16932991/
    107. Shukla, Kamla Kant, et al. “Mucuna PruriensReduces Stress and Improves the Quality of Semen in Infertile Men.” Evidence-Based Complementary and Alternative Medicine, vol. 7, no. 1, 2010, pp. 137–144, 10.1093/ecam/nem171; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC2816389/
    108. Budde H, Machado S, Ribeiro P, Wegner M. The cortisol response to exercise in young adults. Front Behav Neurosci. 2015 Feb 3;9:13. doi: 10.3389/fnbeh.2015.00013. PMID: 25691863; PMCID: PMC4315045. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315045/
    109. Hill EE, Zack E, Battaglini C, Viru M, Viru A, Hackney AC. Exercise and circulating cortisol levels: the intensity threshold effect. J Endocrinol Invest. 2008 Jul;31(7):587-91. doi: 10.1007/BF03345606. PMID: 18787373. https://link.springer.com/article/10.1007/BF03345606
    110. Negro-Vilar, A. “Stress and Other Environmental Factors Affecting Fertility in Men and Women: Overview.” Environmental Health Perspectives, vol. 101, no. suppl 2, July 1993, pp. 59–64, 10.1289/ehp.93101s259; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC1519933/
    111. Axelrod, J, and T. Reisine. “Stress Hormones: Their Interaction and Regulation.” Science, vol. 224, no. 4648, 4 May 1984, pp. 452–459, 10.1126/science.6143403; https://pubmed.ncbi.nlm.nih.gov/6143403/
    112. Hasselgren, P O. “Catabolic response to stress and injury: implications for regulation.” World journal of surgery vol. 24,12 (2000): 1452-9. doi:10.1007/s002680010262 https://link.springer.com/article/10.1007/s002680010262
    113. Lennartsson, Anna-Karin, and Ingibjörg H Jonsdottir. “Prolactin in response to acute psychosocial stress in healthy men and women.” Psychoneuroendocrinology vol. 36,10 (2011): 1530-9. doi:10.1016/j.psyneuen.2011.04.007 https://linkinghub.elsevier.com/retrieve/pii/S0306-4530(11)00131-4
    114. Shukla KK, Mahdi AA, Ahmad MK, Shankhwar SN, Rajender S, Jaiswar SP. Mucuna pruriens improves male fertility by its action on the hypothalamus-pituitary-gonadal axis. Fertil Steril. 2009 Dec;92(6):1934-40. doi: 10.1016/j.fertnstert.2008.09.045. Epub 2008 Oct 29. PMID: 18973898. https://linkinghub.elsevier.com/retrieve/pii/S0015-0282(08)03935-6
    115. Shukla, Kamla Kant, et al. “Mucuna Pruriens Improves Male Fertility by Its Action on the Hypothalamus-Pituitary-Gonadal Axis.” Fertility and Sterility, vol. 92, no. 6, 1 Dec. 2009, pp. 1934–1940, 10.1016/j.fertnstert.2008.09.045; https://www.fertstert.org/article/S0015-0282(08)03935-6/fulltext
    116. “Stimulation of Growth Hormone Secretion by Levodopa-Propranolol in Children and Adolescents.” Pediatrics, vol. 56, no. 2, 1 Aug. 1975, pp. 262–266; https://pubmed.ncbi.nlm.nih.gov/169508/
    117. Chihara, K., et al. “L-Dopa Stimulates Release of Hypothalamic Growth Hormone-Releasing Hormone in Humans.” The Journal of Clinical Endocrinology and Metabolism, vol. 62, no. 3, 1 Mar. 1986, pp. 466–473, 10.1210/jcem-62-3-466; https://pubmed.ncbi.nlm.nih.gov/3080462/
    118. Galea-Debono, A., et al. “Plasma DOPA Levels and Growth Hormone Response to Levodopa in Parkinsomism.” Journal of Neurology, Neurosurgery, and Psychiatry, vol. 40, no. 2, 1 Feb. 1977, p. 162, 10.1136/jnnp.40.2.162; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC492632/
    119. Yu M, Shin YJ, Kim N, Yoo G, Park S, Kim SH. Determination of saponins and flavonoids in ivy leaf extracts using HPLC-DAD. J Chromatogr Sci. 2015 Apr;53(4):478-83. doi: 10.1093/chromsci/bmu068. Epub 2014 Jun 30. PMID: 24981979. https://pubmed.ncbi.nlm.nih.gov/24981979/
    120. Marrelli, Mariangela et al. “Effects of Saponins on Lipid Metabolism: A Review of Potential Health Benefits in the Treatment of Obesity.” Molecules (Basel, Switzerland) vol. 21,10 1404. 20 Oct. 2016, doi:10.3390/molecules21101404 https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC6273086/
    121. Bertoia, Monica L et al. “Dietary flavonoid intake and weight maintenance: three prospective cohorts of 124,086 US men and women followed for up to 24 years.” BMJ (Clinical research ed.) vol. 352 i17. 28 Jan. 2016, doi:10.1136/bmj.i17 https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4730111/
    122. Saeed Khan S, Adil A, Naeem S, Jaffar N, Khatoon H, Ansar H, Shafiq Y. Evaluation of Acute and Chronic Antidiabetic Activity of Ivy (Hedera helix L.) Aqueous Leaf Extract in Rat Model. Pak J Biol Sci. 2020 Jan;23(11):1357-1368. doi: 10.3923/pjbs.2020.1357.1368. PMID: 33274862. https://pubmed.ncbi.nlm.nih.gov/33274862/
    123. Hoffman D. et al; “Efficacy of dry extract of ivy leaves in children with bronchial asthma–a review of randomized controlled trials”; Phytomedicine. 2003 Mar;10(2-3):213-20; https://www.ncbi.nlm.nih.gov/pubmed/12725580
    124. Lang C. et al; “A Valuable Option for the Treatment of Respiratory Diseases: Review on the Clinical Evidence of the Ivy Leaves Dry Extract EA 575®”; Planta Med. 2015 Aug;81(12-13):968-74; https://www.ncbi.nlm.nih.gov/pubmed/25875509
    125. Schönknecht K. et al; “Efficacy of dry extract of ivy leaves in the treatment of productive cough”; Wiad Lek. 2017;70(6 pt 1):1026-1033; https://www.ncbi.nlm.nih.gov/pubmed/29478973
    126. PubChem. “Theobromine.” Nih.gov, PubChem, 2019, https://www.pubchem.ncbi.nlm.nih.gov/compound/Theobromine
    127. ‌Barokah, Liberty, et al. “Protective Effect of Theobroma Cacao on Nitric Oxide and Endothelin-1 Level in Endothelial Cells Induced by Plasma from Preeclamptic Patients: In Silico and in Vitro Studies.” European Journal of Integrative Medicine, vol. 8, no. 1, 1 Feb. 2016, pp. 73–78; 10.1016/j.eujim.2015.11.023; https://www.sciencedirect.com/science/article/abs/pii/S1876382015300639
    128. Yoneda, Mitsugu et al. “Theobromine up-regulates cerebral brain-derived neurotrophic factor and facilitates motor learning in mice.” The Journal of nutritional biochemistry vol. 39 (2017): 110-116. doi:10.1016/j.jnutbio.2016.10.002 https://linkinghub.elsevier.com/retrieve/pii/S0955-2863(16)30105-X
    129. Valsecchi, Federica et al. “cAMP and mitochondria.” Physiology (Bethesda, Md.) vol. 28,3 (2013): 199-209. doi:10.1152/physiol.00004.2013 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870303/
    130. ‌Aslam, Muhammad, and Yury Ladilov. “Emerging Role of cAMP/AMPK Signaling.” Cells vol. 11,2 308. 17 Jan. 2022, doi:10.3390/cells11020308; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774420/
    131. Coleman, William F. “Chocolate: Theobromine and Caffeine.” Journal of Chemical Education, vol. 81, no. 8, Aug. 2004, p. 1232 https://pubs.acs.org/doi/abs/10.1021/ed081p1232
    132. Mitchell, E S et al. “Differential contributions of theobromine and caffeine on mood, psychomotor performance and blood pressure.” Physiology & behavior vol. 104,5 (2011): 816-22. doi:10.1016/j.physbeh.2011.07.027 https://www.sciencedirect.com/science/article/abs/pii/S0031938411003799
    133. Baggott, Matthew J et al. “Psychopharmacology of theobromine in healthy volunteers.” Psychopharmacology vol. 228,1 (2013): 109-18. doi:10.1007/s00213-013-3021-0 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672386/
    134. Lin, Hang-Ching, et al. “Method for Regulating Nutrient Absorption with Ginsenosides”; United States Patent and Trademark Office; Patent US20090181904A1; July 16, 2009; https://patents.google.com/patent/US20090181904A1/
    135. Lin, Hang-Ching, et al. “Method for Enhancing Nutrient Absorption with Astragalosides”; United States Patent and Trademark Office; Patent US20120196816A1; August 2, 2012; https://patents.google.com/patent/US20120196816A1/
    136. Lin, Hang-Ching, et al. “Method for Enhancing Nutrient Absorption with Astragalosides”; United States Patent and Trademark Office; Patent US20120196817A1; August 2, 2012; https://patents.google.com/patent/US20120196817A1/
    137. Lin, Hang-Ching, et al. “Method for Enhancing Nutrient Absorption with Astragalosides”; United States Patent and Trademark Office; Patent US8197860B2; June 12, 2012; https://patents.google.com/patent/US8197860B2/en
    138. Lin, Hang-Ching, et al. “Compound for enhancing nutrients uptake”; Taiwan Intellectual Property Office; Patent TWI271195B; 28-Dec 2004; https://patents.google.com/patent/TWI271195B/en
    139. Lee, Shih-Yu, et al. “Astragaloside II Promotes Intestinal Epithelial Repair by Enhancing L-Arginine Uptake and Activating the MTOR Pathway.” Scientific Reports, vol. 7, no. 1, 26 Sept. 2017, p. 12302, 10.1038/s41598-017-12435-y. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5614914/
    140. Perry BD, U’Prichard DC; European Journal of Pharmacology; “(3H)rauwolscine (alpha-yohimbine): a specific antagonist radioligand for brain alpha 2-adrenergic receptors;”1981; https://www.ncbi.nlm.nih.gov/pubmed/6276200
    141. Ostojic SM. Research in Sports Medicine;.”Yohimbine: the effects on body composition and exercise performance in soccer players.” 2006 Oct-Dec;14(4):289-99; https://pubmed.ncbi.nlm.nih.gov/17214405/
    142. Basaqr R, Skleres M, Jayswal R, Thomas DT. The effect of dietary nitrate and vitamin C on endothelial function, oxidative stress and blood lipids in untreated hypercholesterolemic subjects: A randomized double-blind crossover study. Clin Nutr. 2021 Apr;40(4):1851-1860. doi: 10.1016/j.clnu.2020.10.012. Epub 2020 Oct 14. PMID: 33115598. https://www.clinicalnutritionjournal.com/article/S0261-5614(20)30540-9/fulltext
    143. Daniel TA, Nawarskas JJ. Vitamin C in the prevention of nitrate tolerance. Ann Pharmacother. 2000 Oct;34(10):1193-7. doi: 10.1345/aph.19415. PMID: 11054990 . https://journals.sagepub.com/doi/10.1345/aph.19415 0pubmed
    144. Patak P, Willenberg HS, Bornstein SR. Vitamin C is an important cofactor for both adrenal cortex and adrenal medulla. Endocr Res. 2004 Nov;30(4):871-5. doi: 10.1081/erc-200044126; https://pubmed.ncbi.nlm.nih.gov/15666839/
    145. Sebastian J Padayatty, John L Doppman, Richard Chang, Yaohui Wang, John Gill, Dimitris A Papanicolaou, Mark Levine, Human adrenal glands secrete vitamin C in response to adrenocorticotrophic hormone, The American Journal of Clinical Nutrition, Volume 86, Issue 1, July 2007, Pages 145–149; https://www.sciencedirect.com/science/article/pii/S0002916523274626
    146. Pinto, JT, and Zempleni, J. “Riboflavin.” Advances in nutrition (Bethesda, Md.) vol. 7,5 973-5.15 Sep. 2016. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015041/
    147. Cantó, Carles, et al. “NAD+ Metabolism and the Control of Energy Homeostasis: A Balancing Act between Mitochondria and the Nucleus.” Cell Metabolism, vol. 22, no. 1, July 2015, pp. 31–53, 10.1016/j.cmet.2015.05.023; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487780/
    148. Chini, Claudia C.S., et al. “NAD and the Aging Process: Role in Life, Death and Everything in Between.” Molecular and Cellular Endocrinology, vol. 455, Nov. 2017, pp. 62–74, 10.1016/j.mce.2016.11.003; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419884/
    149. Yang, Yue, and Anthony A. Sauve. “NAD+ Metabolism: Bioenergetics, Signaling and Manipulation for Therapy.” Biochimica et Biophysica Acta, vol. 1864, no. 12, 1 Dec. 2016, pp. 1787–1800, 10.1016/j.bbapap.2016.06.014; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5521000/
    150. Rajman, Luis, et al. “Therapeutic Potential of NAD-Boosting Molecules: The in Vivo Evidence.” Cell Metabolism, vol. 27, no. 3, Mar. 2018, pp. 529–547, 10.1016/j.cmet.2018.02.011; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6342515/
    151. Katsyuba, Elena, et al. “NAD + Homeostasis in Health and Disease.” Nature Metabolism, vol. 2, no. 1, 1 Jan. 2020, pp. 9–31, 10.1038/s42255-019-0161-5; https://pubmed.ncbi.nlm.nih.gov/32694684/
    152. Chini, Claudia C.S., et al. “Evolving Concepts in NAD+ Metabolism.” Cell Metabolism, vol. 33, no. 6, June 2021, pp. 1076–1087, 10.1016/j.cmet.2021.04.003; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172449/
    153. Weiner, H., and X. Wang. “Aldehyde Dehydrogenase and Acetaldehyde Metabolism.” Alcohol and Alcoholism (Oxford, Oxfordshire). Supplement, vol. 2, 1994, pp. 141–145; https://pubmed.ncbi.nlm.nih.gov/8974328/
    154. National Institutes of Health. “Vitamin B6 – Fact Sheet For Health Professionals.” Office of Dietary Supplements; https://ods.od.nih.gov/factsheets/VitaminB6-HealthProfessional/
    155. Shorter KR, Felder MR, Vrana PB. Consequences of dietary methyl donor supplements: Is more always better? Prog Biophys Mol Biol. 2015 Jul;118(1-2):14-20. doi: 10.1016/j.pbiomolbio.2015.03.007. Epub 2015 Apr 2. PMID: 25841986. https://linkinghub.elsevier.com/retrieve/pii/S0079-6107(15)00043-7
    156. da Silva, Weslay Rodrigues et al. “Recognition and management of vitamin B12 deficiency: Report of four cases with oral manifestations.” Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry vol. 42,4 (2022): 410-415. doi:10.1111/scd.12685 https://onlinelibrary.wiley.com/doi/10.1111/scd.12685
    157. Langan, Robert C, and Andrew J Goodbred. “Vitamin B12 Deficiency: Recognition and Management.” American family physician vol. 96,6 (2017): 384-389. https://www.aafp.org/pubs/afp/issues/2017/0915/p384.html
    158. ‌Bala, Renu et al. “Hyperhomocysteinemia and low vitamin B12 are associated with the risk of early pregnancy loss: A clinical study and meta-analyses.” Nutrition research (New York, N.Y.) vol. 91 (2021): 57-66. doi:10.1016/j.nutres.2021.05.002 https://linkinghub.elsevier.com/retrieve/pii/S0271-5317(21)00023-3

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