Fresh Supps Pre-Workout: Great Flavors, Effective Formula, Amazing Artwork

Published on October 12, 2023 by PricePlow Staff | No Comments

Fresh Supps Pre

Fresh Supps founder and CEO Greg Helton has an impressive resume, even by the standards of the most seasoned supplement veteran. With a decade of industry experience under his belt, including 7 years as chief marketing officer of Musclesport and 1 year as VP of Ryse, not to mention an ISSA personal training certification, Greg was perfectly positioned to start his own premium supplement brand, and the results have been amazing.

Fresh Supps Pre-Workout

Earlier this year, the Fresh team released the Fresh Supps Pre-Workout formula, a strong and affordable formula that boasts 6 grams L-citrulline and a total of 360 milligrams caffeine from two caffeine sources. This is a milestone for any new supplement company – a pre-workout is the traditional initial offering and plays a big role in establishing a company’s reputation.

Well, we’re pleased to report that Fresh put together a great product. Let’s get into the details, but first, check the PricePlow news and deals:

Fresh Supps Preworkout – Deals and Price Drop Alerts

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Ingredients

In a single 2-scoop (16 gram) serving of Fresh Pre, you get the following:

Fresh Supps Pre Ingredients

  • L-Citrulline – 6,000 mg

    Citrulline is a conditionally essential amino acid known for its ability to enhance nitric oxide (NO) production.[1]

    When we say “conditionally essential,” we mean that your body’s natural production of citrulline might be limited under specific pathophysiological conditions, such as illness, stress, or injury. These situations increase your citrulline requirements beyond the norm, making the amino acid essential. At these times, it’s crucial to consume an adequate amount of the amino acid to bridge the gap between your body’s demand and its production capacity.

    In the conversion pathway from citrulline to NO, the process looks like this:

    Citrulline → arginine → NO

    As you can see, there’s an intermediate step between citrulline ingestion and NO synthesis: the conversion of citrulline to arginine.

    Given that arginine is the most direct precursor to NO, you might wonder why we wouldn’t rather supplement with arginine directly. The reason is that arginine’s oral bioavailability is relatively low. Citrulline, on the other hand, is better absorbed, leading to higher arginine levels in the bloodstream than could be achieved by ingesting arginine itself.[2,3] Then the elevated arginine level drives NO synthesis.

    Having more NO in your blood can be beneficial for athletes, gym enthusiasts, or anyone looking to optimize their cardiovascular health. That’s because NO induces vasodilation, a process where blood vessels expand, which increases blood flow. This leads to improved tissue perfusion and reduces the workload on the heart. Enhanced NO production can also result in lowered heart rate and, importantly, reduced blood pressure.[4-6]

    The potential advantages of vasodilation include better tissue oxygenation, enhanced nutrient delivery, and more efficient removal of metabolic waste. All of these factors can contribute to improved gym performance and quicker post-exercise recovery.

    Citrulline Arginine Ornithine Nitric Oxide Ammonia

    Citrulline’s participation in the nitric oxide cycle and the urea cycle. The enzyme argininosuccinate converts citrulline to arginine, and arginine stimulates the production of nitric oxide

    In terms of athletic benefits, citrulline supplementation has been linked to:

    • Enhanced power output by increasing oxygen utilization[7]
    • Increased endurance by as much as 50%[8]
    • Reduced post-workout muscle soreness[8]
    • Stimulation of growth hormone (GH) secretion[9]
    • Decreased protein breakdown[10]
    • Augmented muscle protein synthesis[11,12]

    Additionally, citrulline supplementation increases blood levels of ornithine,[13] an amino acid that eliminates ammonia from the body.[14] Ammonia, being a toxic metabolic byproduct of amino catabolism in muscle tissue during exercise, is a source of both mental and physical fatigue. Thus, reducing ammonia levels is one mechanism by which supplemental citrulline can increase endurance.

    Ornithine also has a documented ability to enhance metabolic function and improve sleep quality while reducing feelings of stress. Its impact on lowering the cortisol-to-DHEA ratio appears to play a significant role in this process.[14]

  • Beta-Alanine – 3,200 mg

    Beta-alanine is a long-standing staple in the realm of sports supplements, thanks to its low cost, excellent safety profile, and bona fides as an ergogenic aid – defined as any substance or technique amplifying athletic performance.

    Beta Alanine Total Work Done

    Beta alanine leads to more work done, which can lead to gains if you take advantage of them!

    Its endurance boosting mechanism of action is binding to L-histidine, which forms a dipeptide molecule called carnosine. Carnosine is highly concentrated in muscle tissue, where it plays a pivotal role in eliminating lactic acid (or lactate), yet another pesky metabolic byproduct of exercise that can cause muscular fatigue as it accumulates.[15]

    Beta-alanine supplementation reduces lactate accumulation in muscles, thus staving off anaerobic fatigue at moderate to high exercise intensities. This can translate into increased endurance during workouts.

    Now, again, you might wonder why not directly supplement with carnosine? The answer lies in carnosine’s poor oral bioavailability, which makes it ineffective when taken orally. Since beta-alanine’s bioavailability is much higher, it actually increases carnosine levels more effectively than a carnosine supplement can.

    Since beta-alanine (as opposed to histidine) availability is almost always the bottleneck on carnosine production,[4,5] increasing beta-alanine intake reliably boosts carnosine levels.

    Two big meta-analyses, examining over 40 peer-reviewed papers, have concluded that showcasing beta-alanine is best at increasing endurance within a particular intensity range. That range is any effort that can be sustained between 30 seconds and 10 minutes.[16,17]

    What about the tingles?

    Most people, upon taking beta-alanine, experience an intense tingling sensation in their face and torso. If this happens to you, don’t be alarmed – the 3,200-milligram dose of beta-alanine has been extensively researched, and found to be safe. Furthermore, a recent meta-analysis on beta-alanine safety backs up that long-standing consensus.[18]

  • Betaine Anhydrous (Trimethylglycine) – 2,000 mg

    Betaine, also referred to as trimethylglycine (TMG), is another ergogenic aid, although acting through a mechanism that’s very different from beta-alanine’s.

    Betaine Muscle

    A landmark 2013 study showed that 2.5 grams of betaine every day can have profound effects on body mass and strength

    Methyl donor

    A commonly shared trait among ergogenic aids is their capacity to upregulate adenosine triphosphate (ATP) production. ATP is the body’s energy currency— the usable form of energy that cells consume to perform all metabolic processes. Increasing cellular ATP levels can enhance cellular function, ultimately contributing to improved athletic and cognitive performance.

    This happens to be one of betaine’s most important mechanisms of action – it can increase ATP production and improve mitochondrial respiration.[19]

    Betaine does this by acting as a methyl donor. That means it carries methyl groups (chemical formula CH3) to locations in the body where they’re needed to perform cellular-metabolic processes.[20] In fact, betaine stands as one of the most potent methyl donors identified thus far.[21]

    Fresh Supps Pre Just Peachy

    Methyl groups play a key role in regulating homocysteine, an amino acid generated by the body’s metabolism of the amino acid methionine. Elevated homocysteine levels significantly increase the risk of cardiovascular disease (CVD),[22] but fortunately, betaine supplementation has been shown to decrease homocysteine levels[23] through its methyl-donating action, making it a potentially good long-term investment in cardiovascular health and athletic ability.

    Osmolyte

    Another one of betaine’s ergogenic mechanisms can be explained by its status as an osmolyte, meaning it can influence the behavior of biological fluids. Specifically, betaine can change the osmotic pressure gradient around your body’s cells, thus encouraging the influx of additional water into these cells. This state of cellular hyperhydration can enhance performance by granting cells increased access to nutrients[24,25] and fortifying their resistance to heat stress.[26]

    Effects of Betaine Supplementation

    Research has revealed that betaine supplementation can lead to improvements in:

    • Strength[27,28]
    • Endurance[29,30]
    • Power[26-28,31]
    • Body composition[32,33]

    One particularly notable study from 2013 had participants take 2,500 milligrams of betaine daily, which is close to the dose used in Fresh Pre. Over six weeks, the volunteers achieved over 5 pounds of muscle gain and 6 pounds of fat loss, translating to a 3% reduction in body fat.[25,34]

  • Pink Himalayan Salt – 500 mg

    Pink Himalayan salt is included in the Fresh Pre formula to provide electrolyte support. During intense workouts, we lose essential electrolytes through sweat, with sodium being the most significant loss. Therefore, supplementing with additional salt is generally advisable for anyone who’s breaking a sweat in the gym.

    Fresh Supps Pre Lemon Italian Ice and Mother Pucker

    While pink Himalayan salt also contains trace amounts of minerals, its primary component is sodium. Despite sodium often being criticized for its putative role in hypertension, it’s a crucial electrolyte mineral necessary for optimal muscle function, peak performance, and efficient recovery.[35] Inadequate sodium levels can impair all of these functions.[36]

    A 100-milligram dose of pink Himalayan salt equates to about 200 milligrams of sodium. That’s not a huge amount of sodium, but it can make a difference if you’re monitoring your sodium intake.

    It’s worth mentioning, in any case, that a 2015 research review found a J-shaped association between sodium intake and cardiovascular mortality, with the lowest risk found at intakes between 3,000 and 5,000 milligrams per day.[37] That’s 3 to 5 grams of sodium — not salt!

  • S7 (Green Coffee Bean Extract, Green Tea Extract, Turmeric Extract, Tart Cherry, Blueberry, Broccoli, Kale) – 50 mg

    S7 is a specialized nitric-oxide-boosting blend of seven botanical extracts chosen for their rich polyphenol antioxidant content. Comprising 3% curcumin, 30% catechins, and 60% polyphenols by mass, S7 has performed exceptionally well, including a 270% increase in serum nitric oxide (NO) in clinical studies.[38]

    Here’s a detailed breakdown of how each ingredient in S7 works:

    • Green Coffee Bean Extract – sourced from green (unroasted) coffee beans, which naturally have a higher concentration of chlorogenic acid (CGA) compared to roasted beans.[39] This is desirable as CGA possesses significant antioxidant,[40] anti-inflammatory,[40] and anti-hypertensive[41] properties. Research suggests that CGA can enhance vascular tissue’s response to exercise,[42] potentially maximizing the benefits of your cardio sessions.
      • FutureCeuticals S7 Nitric Oxide

      These seven constituents can help you boost nitric oxide levels – and at a low dose so it fits in a capsule form factor!

    • Green Tea Extract – naturally contains large amounts of polyphenol and catechin antioxidants,[43] most notably epigallocatechin gallate (EGCG). High EGCG intake has been associated with increased lipolysis,[44,45] the process through which the body breaks down stored fat for energy. Several studies suggest that EGCG can reduce the absorption of dietary carbohydrates,[46] potentially mitigating weight gain or even promoting weight loss.
    • Turmeric Extract – contains high amounts of curcumin, a yellow-orange bioactive constituent that’s the primary determinant of turmeric’s characteristic color. Curcumin is a hugely anti-inflammatory compound, and has been identified as a great potential adjunct therapy for a wide range of ailments implicating chronic inflammation,[47] including depression.[48] Curcumin can also help support exercise by augmenting the body’s antioxidant capacity.[49]
    • Tart Cherry – a recovery superstar, know for its ability to mitigate post-workout muscle soreness while improving biochemical measures of recovery like creatine kinase, lactate dehydrogenase, interleukin-6 (IL-6), and C-reactive protein (CRP).[50]
    • Blueberry – another great food for accelerating muscle recovery after a workout.[51] It’s also loaded with powerful antioxidants and anti-inflammatory compounds.[52]
    • Broccoli – high in sulforaphane, a sulfurous compound that can help improve arterial and venous health by downregulating inflammatory processes.[53]
    • Kale – chock full of relatively uncommon antioxidants and polyphenols like quercetin and kaempferol.[54] Both of these have a documented ability to reduce blood pressure,[55] and can offer some therapeutic benefit in a wide range of medical conditions.[56]

  • Taurine – 1,000 mg

    Taurine is very much in vogue these days, as more and more supplement manufacturers are catching on to this jack-of-all-trades ingredient. Taurine has the ability to increase athletic endurance, improve cellular hydration, facilitate mitochondrial respiration, upregulate dopamine, fight oxidative stress, and more.

    Taurine Browning of Fat

    Taurine can induce the browning of fat, which is important because brown fat is more mitochondrial-dense and metabolically active!

    Osmolyte

    Like betaine, taurine is an osmolyte that can improve the hydration status of your cells by influencing cellular osmotic pressure.[57] Again, cellular hyperhydration is a desirable state for exercising performance because it improves cellular nutrient access, the removal of metabolic waste, and resistance to heat stress.[58]

    According to a 2018 meta-analysis, a single 1,000-milligram dose of taurine can substantially increase athletic endurance when taken immediately before an exercise session.[59]

    Taurine is also a potent antioxidant,[60,61] and can help optimize intracellular calcium signaling in muscle tissue.[62]

    Taurine-GABA connection

    Taurine imitates a neurotransmitter called gamma-aminobutyric acid (GABA), which has inhibitory effects on neurons[63] by downregulating the excitatory action of glutamate and calcium. Taurine can also trigger brain cells to produce new mitochondria, which can be great for cognitive health and function since mitochondria play a crucial role in neuronal energy production.[63,64]

    Taurine can help protect brain cells from stress, as well as upregulate dopamine production and signaling.[65] This can help you stay motivated and focused during your workouts.

  • L-Tyrosine – 500 mg

    L-tyrosine stands out as a pre-workout ingredient for several reasons.

    Eddie Hall Myprotein THE Pre-workout Supplement Tyrosine

    Tyrosine has a big impact on neurotransmitters!

    Firstly, it plays a crucial role in supporting your thyroid gland. This gland produces the vital hormones triiodothyronine (T3) and thyroxine (T4), which are indispensable for athletic performance, fat loss, and muscle building. To produce these hormones, the thyroid requires an ample supply of tyrosine.[66,67]

    For people in the pre-workout target market, thyroid support can be especially important – intense workouts and calorie restriction, common practices among gym enthusiasts, can suppress thyroid function by elevating cortisol levels.[68-70] Increased cortisol, resulting from vigorous exercise and calorie reduction, can heighten the risk of low thyroid function. Supplementing with tyrosine in such scenarios can help maintain optimal thyroid function.

    Secondly, tyrosine serves as a precursor for the synthesis of important neurotransmitters like dopamine, adrenaline, and noradrenaline.[71-73] These catecholamine neurotransmitters play a pivotal role in creating focus, motivation, and mental energy. Adrenaline and noradrenaline are instrumental in initiating and regulating the body’s stress response and crucial for achieving peak performance in the gym – but they also help improve body composition by reducing appetite and increasing the body’s fat-burning rate.[74]

    Lastly, tyrosine has been extensively studied by militaries all over the globe for its anti-stress and wakefulness-promoting effects, especially during sleep deprivation. A meta-analysis on studies conducted by the United States military concluded that tyrosine outperforms caffeine in increasing alertness in sleep-deprived individuals, making it a valuable asset for maintaining cognitive performance under challenging conditions.[75,76]

  • Caffeine Anhydrous – 300 mg (of 360mg total yield)

    Caffeine is a methylxanthine stimulant that’s able to cross the blood-brain barrier.[77] This allows caffeine to have a high degree of influence over the way the central nervous system functions.

    Fresh Supps Pre

    As most of us know from personal experience, caffeine has the ability to improve mood, enhance focus, and even increase athletic performance.[78] In a word, caffeine can give us more energy. The drug does this by two mechanisms of action.

    Anti-fatigue

    First, it inhibits the action of adenosine, a nucleotide byproduct of ATP hydrolysis that accumulates in the brain while we’re awake and causes feelings of mental and physical fatigue.[79,80] You can understand this as more of a fatigue-decreasing effect than an energy increasing effect, helping restore alertness to baseline.

    Pro-metabolic

    But caffeine also gives us more energy in a much more literal, mechanistic sense – it can upregulate cellular metabolism by inhibiting an enzyme called phosphodiesterase. Since phosphodiesterase deactivates cyclic adenosine monophosphate (cAMP), a secondary messenger that increases cellular-metabolic rate, caffeine can actually increase cAMP levels and thus crank up whole-body metabolism.[78-82]

    Fat burning and body composition

    If your fitness goals include maintaining a lean body composition, take note – caffeine can also help your body burn fat.[83] In fact, some research has indicated that caffeine can increase the body’s rate of fat burning by as much as 50%,[84] and a 2020 meta-analysis showed that elevated fat oxidation occurs with caffeine doses as small as 3 milligrams per kilogram of bodyweight.[85]

    Ergogenic aid

    Studies show that caffeine can also increase physical work capacity in several dimensions, including strength, speed, power, and endurance.[78,79,81,83,84] Because of its low cost and excellent safety profile, caffeine is one of the most popular ergogenic aids in the supplement industry.

    Cognitive benefits

    Caffeine can also improve key aspects of cognition, like attention, vigilance, reaction time, and working memory.[86-88]

    Note: There’s 60 milligrams more caffeine coming!

  • CognatiQ Coffee Fruit Extract – 100 mg

    CognatiQ, formerly called NeuroFactor, should be familiar to supplement veterans. It has a long history of use in the supplement industry. It consists of a coffee fruit extract standardized for bioactives that have been shown to increase the expression of brain-derived neurotrophic factor (BDNF).[89] BDNF is crucial for a process called neurogenesis, the creation, growth, and differentiation of new neurons.[90,91]

    CognatiQ Logo

    Elevated BDNF comes with greater neuroplasticity, which means your brain is better able to physically change itself in response to learning. In adults, neurogenesis is confined mostly to the hippocampus, a region of the brain that handles long-term potentiation,[92] the conversion of short-term memories to long-term ones.

    Studies show that BDNF is neuroprotective, and increasing BDNF production can significantly decrease the risk of developing various neurological diseases.[90,91,93,94] Conversely, decreasing BDNF can raise the risk of the same diseases.[94]

    Among lifestyle interventions, exercise is perhaps best at increasing BDNF production,[95] so putting BDNF boosters into a pre could be a good strategy for amplifying the pro-BDNF effect of your workouts.

    The 100-milligram dose used in Fresh Pre was shown in one study to increase BDNF production by a stunning 150%.[89]

  • Vitashure Caffeine SR (60% Caffeine) – 100 mg (yielding 60mg of 360mg total)

    Fresh Supps Pre

    Vitashure caffeine is a slow-release form of caffeine. It delivers all the benefits typically associated with caffeine supplementation, but with a smoother energy curve. This means that the caffeine in Vitashure is absorbed into the bloodstream more slowly, with a lower and later blood concentration peak compared to ordinary caffeine anhydrous. The initial effect is also less jarring, while the taper off is more gradual.

    Combining slow-release caffeine with caffeine anhydrous is a good strategy for giving consumers the best of both worlds – fast-acting energy from the anhydrous and a gentler withdrawal, thanks to the extended release.

    Reminder: Since Vitashure yields 60% caffeine by weight, this makes the total caffeine content of Fresh Pre 360 milligrams per serving. This is definitely a lot – use with care and ask your doctor if you aren’t sure whether you should take this much caffeine.

  • AstraGin (Astragalus membranaceus & Panax notoginseng) extract (roots) – 50 mg

    AstraGin, from NuLiv Science, is a patented bioavailability enhancer.[96-100] This means that By supporting the production of adenosine triphosphate in intestinal cells, AstraGin can increase those cells’ capacity to perform the crucial task of absorbing ingested food and nutrients from the digestive tract. Thus, AstraGin makes all other ingredients it’s taken with more effective, giving you the most bang for your hard-earned buck.

    AstraGin

    Using AstraGin on a regular basis may actually improve long-term intestinal health.[101]

All Available Fresh Pre Flavors

    Fresh Supps Pre

    Conclusion

    This is a solid first entry – not a lot of risks taken, but that’s not a bad thing, especially at this price point. We’re pleased to see the inclusion of taurine, an ingredient that we believe should be in basically all pre-workout formulas, as well as S7, an amazing nitric oxide booster that deserves a lot more attention than it’s gotten.

    The 360-milligram dose of caffeine per 2-scoop serving is nothing to sneeze at. It can definitely help with tough workouts. But, again, with a dose this big, exercising caution is warranted.

    Fresh Supps Preworkout – Deals and Price Drop Alerts

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    About the Author: PricePlow Staff

    PricePlow Staff

    PricePlow is a team of supplement industry veterans that include medical students, competitive strength athletes, and scientific researchers who all became involved with dieting and supplements out of personal need.

    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. Morita, Masahiko, et al; “Oral Supplementation with a Combination of L-Citrulline and L-Arginine Rapidly Increases Plasma L-Arginine Concentration and Enhances NO Bioavailability.”; Biochemical and Biophysical Research Communications; U.S. National Library of Medicine; 7 Nov. 2014; https://www.ncbi.nlm.nih.gov/pubmed/25445598
    2. Ochiai, Masayuki, et al; “Short-Term Effects of L-Citrulline Supplementation on Arterial Stiffness in Middle-Aged Men.”; International Journal of Cardiology; U.S. National Library of Medicine; 8 Mar. 2012; https://www.ncbi.nlm.nih.gov/pubmed/21067832
    3. Agarwal, Umang et al; “Supplemental Citrulline Is More Efficient Than Arginine in Increasing Systemic Arginine Availability in Mice.”; The Journal of nutrition; vol. 147,4; 2017; 596-602; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368575/
    4. Orozco-Gutiérrez JJ, Castillo-Martínez L, Orea-Tejeda A, Vázquez-Díaz O, Valdespino-Trejo A, Narváez-David R, Keirns-Davis C, Carrasco-Ortiz O, Navarro-Navarro A, Sánchez-Santillán R. Effect of L-arginine or L-citrulline oral supplementation on blood pressure and right ventricular function in heart failure patients with preserved ejection fraction. Cardiol J. 2010;17(6):612-8. PMID: 21154265. https://journals.viamedica.pl/cardiology_journal
    5. Wong A, Alvarez-Alvarado S, Jaime SJ, Kinsey AW, Spicer MT, Madzima TA, Figueroa A. Combined whole-body vibration training and l-citrulline supplementation improves pressure wave reflection in obese postmenopausal women. Appl Physiol Nutr Metab. 2016 Mar;41(3):292-7. doi: 10.1139/apnm-2015-0465; https://cdnsciencepub.com/doi/10.1139/apnm-2015-0465
    6. Alsop P, Hauton D. Oral nitrate and citrulline decrease blood pressure and increase vascular conductance in young adults: a potential therapy for heart failure. Eur J Appl Physiol. 2016 Sep;116(9):1651-61. doi: 10.1007/s00421-016-3418-7; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983290/
    7. Bailey, Stephen J, et al; “l-Citrulline Supplementation Improves O2 Uptake Kinetics and High-Intensity Exercise Performance in Humans.”; Journal of Applied Physiology (Bethesda, Md. : 1985); U.S. National Library of Medicine; 15 Aug. 2015; https://www.ncbi.nlm.nih.gov/pubmed/26023227
    8. Pérez-Guisado, Joaquín, and Philip M Jakeman; “Citrulline Malate Enhances Athletic Anaerobic Performance and Relieves Muscle Soreness.”; Journal of Strength and Conditioning Research; U.S. National Library of Medicine; May 2010; https://www.ncbi.nlm.nih.gov/pubmed/20386132
    9. Sureda A, Córdova A, Ferrer MD, Pérez G, Tur JA, Pons A. L-citrulline-malate influence over branched chain amino acid utilization during exercise. Eur J Appl Physiol. 2010 Sep;110(2):341-51. doi: 10.1007/s00421-010-1509-4; https://link.springer.com/article/10.1007/s00421-010-1509-4
    10. Breuillard C, Cynober L, Moinard C. Citrulline and nitrogen homeostasis: an overview. Amino Acids. 2015 Apr;47(4):685-91. doi: 10.1007/s00726-015-1932-2; https://link.springer.com/article/10.1007/s00726-015-1932-2
    11. Jourdan M, Nair KS, Carter RE, Schimke J, Ford GC, Marc J, Aussel C, Cynober L. Citrulline stimulates muscle protein synthesis in the post-absorptive state in healthy people fed a low-protein diet – A pilot study. Clin Nutr. 2015 Jun;34(3):449-56. doi: 10.1016/j.clnu.2014.04.019; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309748/
    12. Bahri S, Zerrouk N, Aussel C, Moinard C, Crenn P, Curis E, Chaumeil JC, Cynober L, Sfar S. Citrulline: from metabolism to therapeutic use. Nutrition. 2013 Mar;29(3):479-84. doi: 10.1016/j.nut.2012.07.002; https://www.sciencedirect.com/science/article/abs/pii/S0899900712002584
    13. Agarwal, Umang, et al. “Supplemental Citrulline Is More Efficient than Arginine in Increasing Systemic Arginine Availability in Mice123.” The Journal of Nutrition, vol. 147, no. 4, 1 Apr. 2017, pp. 596–602; 10.3945/jn.116.240382; https://academic.oup.com/jn/article/147/4/596/4584706
    14. Miyake, Mika, et al. “Randomised Controlled Trial of the Effects of L-Ornithine on Stress Markers and Sleep Quality in Healthy Workers.” Nutrition Journal, vol. 13, no. 1, 3 June 2014, 10.1186/1475-2891-13-53; https://nutritionj.biomedcentral.com/articles/10.1186/1475-2891-13-53
    15. 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
    16. 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/
    17. 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
    18. 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/
    19. 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/
    20. 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/
    21. 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
    22. 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/
    23. 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
    24. Boel De Paepe; “Osmolytes as Mediators of the Muscle Tissue’s Responses to Inflammation: Emerging Regulators of Myositis with Therapeutic Potential”; EMJ Rheumatol. 2017;4[1]: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/
    25. 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/
    26. 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/
    27. 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
    28. 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
    29. Hoffman, Jay R, et al. “Effect of Betaine Supplementation on Power Performance and Fatigue.” Journal of the International Society of Sports Nutrition, vol. 6, no. 1, 27 Feb. 2009, 10.1186/1550-2783-6-7; https://jissn.biomedcentral.com/articles/10.1186/1550-2783-6-7
    30. Trepanowski, John F, et al. “The Effects of Chronic Betaine Supplementation on Exercise Performance, Skeletal Muscle Oxygen Saturation and Associated Biochemical Parameters in Resistance Trained Men.” Journal of Strength and Conditioning Research, vol. 25, no. 12, Dec. 2011, pp. 3461–3471, 10.1519/jsc.0b013e318217d48d; https://pubmed.ncbi.nlm.nih.gov/22080324/
    31. Pryor, J Luke, et al. “Effect of Betaine Supplementation on Cycling Sprint Performance.” Journal of the International Society of Sports Nutrition, vol. 9, no. 1, 3 Apr. 2012, 10.1186/1550-2783-9-12; https://jissn.biomedcentral.com/articles/10.1186/1550-2783-9-12
    32. 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
    33. Jason Michael Cholewa, et al; “The Effects of Chronic Betaine Supplementation on Body Composition and Performance in Collegiate Females: a Double-Blind, Randomized, Placebo Controlled Trial”; Journal of the International Society of Sports Nutrition; BioMed Central; 31 July 2018; https://jissn.biomedcentral.com/articles/10.1186/s12970-018-0243-x
    34. Cholewa, Jason M., et al. “Effects of Betaine on Performance and Body Composition: A Review of Recent Findings and Potential Mechanisms.” Amino Acids, vol. 46, no. 8, 24 Apr. 2014, pp. 1785–1793, 10.1007/s00726-014-1748-5; https://pubmed.ncbi.nlm.nih.gov/24760587/
    35. Strazzullo P., Leclercq C.; “Sodium.” Advanced Nutrition; March 2014; 5(2) 188-190; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951800/
    36. 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/
    37. Remer, Thomas. “High Salt Intake: Detrimental Not Only for Blood Pressure, but Also for Bone Health?” Endocrine, vol. 49, no. 3, 10 May 2015, pp. 580–582, 10.1007/s12020-015-0626-6. Accessed 13 July 2021. https://link.springer.com/article/10.1007/s12020-015-0626-6
    38. Nemzer, B. V., Centner, C., Zdzieblik, D., Fink, B., Hunter, J. M., & König, D. (2017). Oxidative stress or redox signalling – new insights into the effects of a proprietary multifunctional botanical dietary supplement. Free Radical Research, 52(3), 362–372. doi:10.1080/10715762.2017.1390228 https://www.ncbi.nlm.nih.gov/pubmed/29110555
    39. Bauer D, Abreu J, Jordão N, Rosa JSD, Freitas-Silva O, Teodoro A. Effect of Roasting Levels and Drying Process of Coffea canephora on the Quality of Bioactive Compounds and Cytotoxicity. Int J Mol Sci. 2018 Oct 31;19(11):3407. doi: 10.3390/ijms19113407. PMID: 30384410; PMCID: PMC6274859. https://pubmed.ncbi.nlm.nih.gov/30384410/
    40. Farah A, Monteiro M, Donangelo CM, Lafay S. Chlorogenic acids from green coffee extract are highly bioavailable in humans. J Nutr. 2008 Dec;138(12):2309-15. doi: 10.3945/jn.108.095554. PMID: 19022950. https://pubmed.ncbi.nlm.nih.gov/19022950/
    41. Watanabe T, Arai Y, Mitsui Y, Kusaura T, Okawa W, Kajihara Y, Saito I. The blood pressure-lowering effect and safety of chlorogenic acid from green coffee bean extract in essential hypertension. Clin Exp Hypertens. 2006 Jul;28(5):439-49. doi: 10.1080/10641960600798655. PMID: 16820341. https://pubmed.ncbi.nlm.nih.gov/16820341/
    42. Ochiai R, Jokura H, Suzuki A, Tokimitsu I, Ohishi M, Komai N, Rakugi H, Ogihara T. Green coffee bean extract improves human vasoreactivity. Hypertens Res. 2004 Oct;27(10):731-7. doi: 10.1291/hypres.27.731. PMID: 15785008. https://pubmed.ncbi.nlm.nih.gov/15785008/
    43. Westerterp-Plantenga MS, Lejeune MPGM, Kovacs EMR; “Body weight loss and weight maintenance in relation to habitual caffeine intake and green tea supplementation” Obes Res 2005; 13(7):1195-1204; https://onlinelibrary.wiley.com/doi/full/10.1038/oby.2005.142
    44. Juhel C, et al; “Green tea extract (AR25) inhibits lipolysis of triglycerides in gastric and duodenal medium in vitro”; J Nutr Biochem. (2000); https://pubmed.ncbi.nlm.nih.gov/15539342/
    45. 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://pubmed.ncbi.nlm.nih.gov/1356551/
    46. 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
    47. He Y, Yue Y, Zheng X, Zhang K, Chen S, Du Z. Curcumin, inflammation, and chronic diseases: how are they linked? Molecules. 2015 May 20;20(5):9183-213. doi: 10.3390/molecules20059183. PMID: 26007179; PMCID: PMC6272784. https://pubmed.ncbi.nlm.nih.gov/26007179/
    48. Ga-Young Choi, Hyun-Bum Kim, Eun-Sang Hwang, Seok Lee, Min-Ji Kim, Ji-Young Choi, Sung-Ok Lee, Sang-Seong Kim, Ji-Ho Park, “Curcumin Alters Neural Plasticity and Viability of Intact Hippocampal Circuits and Attenuates Behavioral Despair and COX-2 Expression in Chronically Stressed Rats”, Mediators of Inflammation, vol. 2017, Article ID 6280925, 9 pages, 2017. https://doi.org/10.1155/2017/6280925 https://www.hindawi.com/journals/mi/2017/6280925/
    49. Menon VP, Sudheer AR. Antioxidant and anti-inflammatory properties of curcumin. Adv Exp Med Biol. 2007;595:105-25. doi: 10.1007/978-0-387-46401-5_3. PMID: 17569207. https://pubmed.ncbi.nlm.nih.gov/17569207/
    50. Howatson, G., McHugh, M. P., Hill, J. A., Brouner, J., Jewell, A. P., Van Someren, K. A., … Howatson, S. A. (2009). Influence of tart cherry juice on indices of recovery following marathon running. Scandinavian Journal of Medicine & Science in Sports, 20(6), 843–852. doi:10.1111/j.1600-0838.2009.01005.x https://www.ncbi.nlm.nih.gov/pubmed/19883392
    51. McLeay, Yanita, et al. “Effect of New Zealand Blueberry Consumption on Recovery from Eccentric Exercise-Induced Muscle Damage.” Journal of the International Society of Sports Nutrition, vol. 9, no. 1, 2012, p. 19, 10.1186/1550-2783-9-19; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3583121/
    52. Riso, Patrizia, et al. “Effect of a Wild Blueberry (Vaccinium Angustifolium) Drink Intervention on Markers of Oxidative Stress, Inflammation and Endothelial Function in Humans with Cardiovascular Risk Factors.” European Journal of Nutrition, vol. 52, no. 3, 1 Apr. 2013, pp. 949–961, 10.1007/s00394-012-0402-9; https://pubmed.ncbi.nlm.nih.gov/22733001/
    53. Evans PC. The influence of sulforaphane on vascular health and its relevance to nutritional approaches to prevent cardiovascular disease. EPMA J. 2011 Mar;2(1):9-14. doi: 10.1007/s13167-011-0064-3. Epub 2011 Feb 12. PMID: 23199123; PMCID: PMC3405367. https://pubmed.ncbi.nlm.nih.gov/23199123/
    54. Olsen H, Aaby K, Borge GI. Characterization and quantification of flavonoids and hydroxycinnamic acids in curly kale (Brassica oleracea L. Convar. acephala Var. sabellica) by HPLC-DAD-ESI-MSn. J Agric Food Chem. 2009 Apr 8;57(7):2816-25. doi: 10.1021/jf803693t. PMID: 19253943. https://pubmed.ncbi.nlm.nih.gov/19253943/
    55. Larson AJ, Symons JD, Jalili T. Therapeutic potential of quercetin to decrease blood pressure: review of efficacy and mechanisms. Adv Nutr. 2012 Jan;3(1):39-46. doi: 10.3945/an.111.001271. Epub 2012 Jan 5. PMID: 22332099; PMCID: PMC3262612. https://pubmed.ncbi.nlm.nih.gov/22332099/
    56. Kiela, Pawel R., and Fayez K. Ghishan. “Physiology of Intestinal Absorption and Secretion.” Best Practice & Research Clinical Gastroenterology, vol. 30, no. 2, Apr. 2016, pp. 145–159, 10.1016/j.bpg.2016.02.007. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956471
    57. Pasantes-Morales, H., et al. “Taurine: An Osmolyte in Mammalian Tissues.” Advances in Experimental Medicine and Biology, 1998, pp. 209–217, 10.1007/978-1-4899-0117-0_27; https://link.springer.com/chapter/10.1007/978-1-4899-0117-0_27
    58. Uyanga, Victoria Anthony, et al. “Functional Roles of Taurine, L-Theanine, L-Citrulline, and Betaine during Heat Stress in Poultry.” Journal of Animal Science and Biotechnology, vol. 13, no. 1, Mar. 2022, doi: https://doi.org/10.1186/s40104-022-00675-6.
    59. Waldron, M., et al. May 2018. “The Effects of an Oral Taurine Dose and Supplementation Period on Endurance Exercise Performance in Humans: A Meta-Analysis.” Sports Medicine vol. 48,5; 1247-53; https://pubmed.ncbi.nlm.nih.gov/29546641
    60. Ibrahim, Marwan A et al. “Therapeutic role of taurine as antioxidant in reducing hypertension risks in rats.” Heliyon vol. 6,1 e03209. 17 Jan. 2020, doi:10.1016/j.heliyon.2020.e03209; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970174/
    61. Jong, Chian Ju et al. “Mechanism underlying the antioxidant activity of taurine: prevention of mitochondrial oxidant production.” Amino acids vol. 42,6 (2012): 2223-32. doi:10.1007/s00726-011-0962-7; https://pubmed.ncbi.nlm.nih.gov/21691752/
    62. Spriet, Lawrence L, and Jamie Whitfield. “Taurine and skeletal muscle function.” Current opinion in clinical nutrition and metabolic care vol. 18,1 (2015): 96-101. doi:10.1097/MCO.0000000000000135; https://pubmed.ncbi.nlm.nih.gov/25415270/
    63. Chen, C. et al. Aug. 2019. “Roles of Taurine in Cognitive Function of Physiology, Pathologies, and Toxication.” Life Sciences vol. 15, 231; https://pubmed.ncbi.nlm.nih.gov/31220527/
    64. Jong, Chian Ju, et al. “The Role of Taurine in Mitochondria Health: More than Just an Antioxidant.” Molecules, vol. 26, no. 16, 13 Aug. 2021, p. 4913, 10.3390/molecules26164913; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC8400259/
    65. Wang, Ke, et al. “Taurine Improves Neuron Injuries and Cognitive Impairment in a Mouse Parkinson’s Disease Model through Inhibition of Microglial Activation.” NeuroToxicology, vol. 83, Mar. 2021, pp. 129–136, 10.1016/j.neuro.2021.01.002; https://www.sciencedirect.com/science/article/abs/pii/S0161813X21000085
    66. Mullur, Rashmi et al. “Thyroid hormone regulation of metabolism.” Physiological reviews vol. 94,2 (2014): 355-82. doi:10.1152/physrev.00030.2013; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4044302/
    67. Rousset, Bernard. “Chapter 2 Thyroid Hormone Synthesis And Secretion.” Endotext. U.S. National Library of Medicine, 2 Sept. 2015; https://www.ncbi.nlm.nih.gov/books/NBK285550/
    68. Rousset, Bernard, et al. “Chapter 2 Thyroid Hormone Synthesis and Secretion.” Nih.gov, MDText.com, Inc., 2 Sept. 2015. https://www.ncbi.nlm.nih.gov/books/NBK285550/
    69. Mullur, Rashmi, et al. “Thyroid Hormone Regulation of Metabolism.” Physiological Reviews, vol. 94, no. 2, Apr. 2014, pp. 355–382, 10.1152/physrev.00030.2013. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4044302/
    70. Wadden TA, Mason G, Foster GD, Stunkard AJ, Prange AJ. Effects of a very low calorie diet on weight, thyroid hormones and mood. Int J Obes. 1990 Mar;14(3):249-58; https://pubmed.ncbi.nlm.nih.gov/2341229/
    71. Mishra, Akanksha, et al. “Physiological and Functional Basis of Dopamine Receptors and Their Role in Neurogenesis: Possible Implication for Parkinson’s Disease.” Journal of Experimental Neuroscience, vol. 12, Jan. 2018, p. 117906951877982, 10.1177/1179069518779829. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985548/
    72. Rajeev Dalal, and Dejan Grujic. “Epinephrine.” Nih.gov, StatPearls Publishing, 2 Apr. 2019. https://www.ncbi.nlm.nih.gov/books/NBK482160/
    73. Smith, Matthew D, and Christopher V Maani. “Norepinephrine.” Nih.gov, StatPearls Publishing, 23 July 2019. https://www.ncbi.nlm.nih.gov/books/NBK537259/
    74. Ans, Armghan H, et al. “Neurohormonal Regulation of Appetite and Its Relationship with Stress: A Mini Literature Review.” Cureus, 23 July 2018, 10.7759/cureus.3032. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150743/
    75. Attipoe, Selasi, et al. “Tyrosine for Mitigating Stress and Enhancing Performance in Healthy Adult Humans, a Rapid Evidence Assessment of the Literature.” Military Medicine, vol. 180, no. 7, July 2015, pp. 754–765, 10.7205/milmed-d-14-00594; https://academic.oup.com/milmed/article/180/7/754/4160625
    76. Pomeroy, Diane E., et al. “A Systematic Review of the Effect of Dietary Supplements on Cognitive Performance in Healthy Young Adults and Military Personnel.” Nutrients, vol. 12, no. 2, 20 Feb. 2020, p. 545, 10.3390/nu12020545; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7071459/
    77. 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/
    78. 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
    79. 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/
    80. 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
    81. 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/
    82. 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
    83. 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
    84. 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
    85. 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/
    86. 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
    87. 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
    88. 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
    89. Reyes-Izquierdo, Tania, et al. “Modulatory Effect of Coffee Fruit Extract on Plasma Levels of Brain-Derived Neurotrophic Factor in Healthy Subjects.” The British Journal of Nutrition, vol. 110, no. 3, 28 Aug. 2013, pp. 420–425, 10.1017/S0007114512005338. https://www.cambridge.org/core/journals/british-journal-of-nutrition/article/modulatory-effect-of-coffee-fruit-extract-on-plasma-levels-of-brain-derived-neurotrophic-factor-in-healthy-subjects/8B291E8D053143AA5A8D33B65496B034
    90. Phillips, Cristy. “Brain-Derived Neurotrophic Factor, Depression, and Physical Activity: Making the Neuroplastic Connection.” Neural Plasticity, vol. 2017, 2017, pp. 1–17, 10.1155/2017/7260130; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591905/
    91. Miranda, Magdalena, et al. “Brain-Derived Neurotrophic Factor: A Key Molecule for Memory in the Healthy and the Pathological Brain.” Frontiers in Cellular Neuroscience, vol. 13, 7 Aug. 2019, 10.3389/fncel.2019.00363; https://www.frontiersin.org/articles/10.3389/fncel.2019.00363/full
    92. ‌Lu, B et al. “BDNF and synaptic plasticity, cognitive function, and dysfunction.” Handbook of experimental pharmacology vol. 220 (2014): 223-50. doi:10.1007/978-3-642-45106-5_9; https://link.springer.com/chapter/10.1007/978-3-642-45106-5_9
    93. Nicastri, Casey M., et al. “BDNF Mediates Improvement in Cognitive Performance after Computerized Cognitive Training in Healthy Older Adults.” Alzheimer’s & Dementia: Translational Research & Clinical Interventions, vol. 8, no. 1, Jan. 2022, 10.1002/trc2.12337; https://alz-journals.onlinelibrary.wiley.com/doi/full/10.1002/trc2.12337
    94. Zuccato, Chiara, and Elena Cattaneo. “Brain-Derived Neurotrophic Factor in Neurodegenerative Diseases.” Nature Reviews Neurology, vol. 5, no. 6, June 2009, pp. 311–322, 10.1038/nrneurol.2009.54; https://www.nature.com/articles/nrneurol.2009.54
    95. Piepmeier, Aaron T., and Jennifer L. Etnier. “Brain-Derived Neurotrophic Factor (BDNF) as a Potential Mechanism of the Effects of Acute Exercise on Cognitive Performance.” Journal of Sport and Health Science, vol. 4, no. 1, 1 Mar. 2015, pp. 14–23; 10.1016/j.jshs.2014.11.001; https://www.sciencedirect.com/science/article/pii/S2095254614001161
    96. 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/
    97. 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/
    98. 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/
    99. 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
    100. 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
    101. 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/

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