Formulator’s Corner #08: Mitochondria-Boosting Pre-Workout RTD

Published on July 20, 2022 by Mike Roberto | No Comments

There’s a trend going around the sports nutrition segment of the supplement industry lately: fully-dosed RTD pre-workout drinks! Shortened from “Ready to Drink”, RTDs are useful for their convenience, and can be sold and consumed on-site at a gym or store without needing water and a shaker cup.

Formulator's Corner #08 - Mitochondria-Boosting Pre-Workout RTD

Tired of pre-workout drinks with too much caffeine? Using NNB Nutrition’s novel ingredients, we formulated a hypothetical mitochondrial health boosting pre workout RTD in Formulator’s Corner #08!

RTDs have been around for decades, but over the past year, brands are dosing them far better, thanks to improvements in bottling technology and ingredient solubility. This gives us an opportunity to give our two cents and showcase something a bit different for today’s Formulator’s Corner profile.

In this article, we create a theoretical RTD pre-workout supplement that focuses on feel-good, clean energy with mitochondrial support ingredients. It’s an RTD-friendly twist on our previous Mitochondria-Enhancing Formulator’s Corner Pre-Workout, with non-soluble ingredients removed and replaced with ingredients that will stay blended and stable in water.

Re-igniting The Power of Mito…

While many RTD pre-workouts are roughly the same, we’re leaning on novel ingredient developer NNB Nutrition(news), a company that focuses on metabolic health and “clean energy”, to provide us with a powerful formula that doesn’t need too much caffeine.

You can read our article titled The Power of Mito to understand the importance of mitochondrial health, which is the driving force behind this ideation. The mitochondria are our cell powerhouses, and are pivotal to healthy energy. This formula includes added ingredients to support the mitochondria, letting us keep the caffeine at a reasonable 250 milligrams per bottle.

Below is how we’d make an RTD pre-workout without tons of stimulants that leaves the customer feeling better than they started – and it’s one that will differentiate well from the competition. First, check out our NNB Nutrition news alerts, as we have more news on these ingredients coming soon:

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Our Hypothetical Mito-Friendly Pre-Workout RTD Ingredients

Our goal here is to provide a feel-good pre-workout that’s strong, effective, and supportive of the mitochondria – but with a reasonable 250 milligrams of caffeine that will work better than energy drinks that use even more. The following would come in a 12oz bottle:

  • HydroPrime Glycerol – 5g

    Formulator's Corner Mito Pre-Workout RTD Ingredients

    Our theoretical mito-boosting pre-workout RTD. This one’s made to feel good!

    We start our formula with an ingredient that’s in our Formulator’s Corner Mito-Friendly Pre-Workout Powder, only in a much larger dose! HydroPrime Glycerol is NNB Nutrition’s powerful osmolyte ingredient that helps the body elevate osmotic pressure and increase its total water volume in the body.[1] This leads to better hydration, and with enough glycerol and water (you’d want to keep drinking more than what’s in the 12 ounce bottle), leads to a “hyperhydration” effect.[2]

    We have an article titled Glycerol: The Ultimate Guide for Hydration, Heat Protection, and Pumps that gives the main details, but the main benefits found by researchers are that glycerol can:

    • Improve power[1]
    • Increase endurance[3]
    • Provide better heat protection[4]

    But most of all, glycerol’s hyperhydration effect often leads to better pumps, thanks to improved cell volumization.

    Glycerol is the main backbone in many fatty acids and can also be used as an energy substrate – this is why you’ll see our label providing some calories. Beyond that, there aren’t too many mitochondrial benefits, but we have plenty of other ingredients to provide support. Here, we’re synergizing with betaine, taurine, and some electrolytes to improve hydration.

    How much to use? Depends on texture and flavor profile

    NNB Hydroprime

    A better form of glycerol

    HydroPrime is recognized as the industry’s most stable form of glycerol that consistently passes lab tests. The question is, how much to add here?

    Anyone who’s ever used a lot of glycerol will notice that it’s thicker – this may be useful if your flavor system supports it (such as a “gummy” flavor), but it may be too thick for others (like a lemon lime or fruit punch). We’re starting with a solid 5 gram dose, but if it’s too thick, we may need to tone it down. If we can add more, we will!

  • L-Citrulline – 4g

    Before finishing our hydration pump blend, we have to get into nitric oxide production! With RTDs, the de-facto NO booster is L-citrulline, the amino acid that helps the body produce more L-arginine, which subsequently converts to nitric oxide (NO).[5]

    Glycerol

    When it comes to hydration, endurance, cell volumization, and heat tolerance, water is king. And this simple ingredient — glycerol — enables you to hold more water for better performance!

    While arginine is known to be beneficial to the mitochondria in neurotransmitters,[6] the issue is that it isn’t very orally bioavailable[7,8] — but L-citrulline works better than arginine itself in terms of increasing plasma arginine and total nitric oxide levels![9] This is why you see it in so many pre-workouts.

    With greater nitric oxide production, the blood vessels widen in an effect known as vasodilation, leading to improved blood flow and muscle pumps! This leads to a mitochondrial benefit of better ATP production,[10,11] but also greater work output, recovery, lower perceived exertion, and reduced soreness.[12-15]

    As a bonus, arginine, which is the resulting amino acid from much of our L-citrulline consumption, has been shown to improve health in synaptic mitochondria in the brain.[16]

    Additionally, L-citrulline has been shown to prevent heat-induced mitochondrial dysfunction,[17] a nice added bonus that pairs incredibly well with the effects of glycerol (above) and betaine (below):

  • Betaine Anhydrous – 2.5g

    We often see betaine in pre-workout supplements due to its multifactored health benefits.[18] Also known as trimethylglycine, betaine pairs incredibly well with glycerol thanks to its ability to:

    Betaine Muscle

    A landmark 2013 study showed that 2.5 grams of betaine every day can have profound effects on body mass and strength[19,20]

    • Improve hydration and water balance as an osmolyte[21,22]
    • Boost endurance and sports performance[23,24]
    • Help weightlifters increase muscle mass[19,20]
    • Reduce fat mass in dieters[25]

    We cover the above points frequently since betaine is deservedly in so many pre-workouts. Mechanistically, much of this happens beyond its function as an osmolyte because betaine is also a methyl donor,[21,26] leading to tremendous benefits for the mitochondria. For instance, it promotes more mitochondrial content while inhibiting the creation of liver fat.[26]

    Betaine also improves mitochondrial respiration.[27] Synergizing with another mitochondria-boosting ingredient below (MitoBurn), betaine boosts the browning of white adipose tissue thanks to its stimulation of mitochondrial biogenesis.[28] These effects combined, it increases overall mitochondrial activity, which supports our goal of better cellular energy.

    Additionally, betaine offers cell protection: It preserves mitochondrial function by defending the liver from stress in animal models[29] and limits reactive oxygen species that harm mitochondrial respiration.[30]

  • Taurine – 1g

    The last major piece of our hydration ingredients (aside from the electrolytes added), we have taurine, which serves a mountain of roles in the body just like betaine does.[31] It’s yet another osmolyte that assists in water storage and transfer,[31] and is in several other pre-workout supplements.

    The primary athletic effect from a gram dose of taurine is its efficacy in boosting endurance,[32] but there are also potential focus and nitric oxide improvements.[33,34]

    The entire breadth of taurine’s mechanisms of action aren’t fully understood, but researchers are beginning to believe that a lot of it is mitochondria-related. An article recently published in Molecules named “The Role of Taurine in Mitochondria Health: More Than Just an Antioxidant” makes a very strong argument that this conditionally-essential ingredient has a pivotal role in mitochondrial health, and they use 250 studies to back up their claim.[35]

  • L-Carnitine L-Tartrate – 1g

    In our powdered formulator’s corner pre-workout, we used acetyl L-carnitine to support fatty acid transport to the mitochondria for ATP (energy) production.[36] However, that form of the ingredient is not very stable in liquid RTD form. The solution, if you wish to have carnitine in an RTD beverage, is to switch to L-Carnitine L-Tartrate, also known as LCLT.

    Taurine Endurance

    Taurine’s effect on endurance, with success in doses anywhere from 1 gram to 6 grams.[32]

    We like L-carnitine in athletic supplements because ATP is the energy currency in our cells, and carnitine provides a delivery mechanism to help us produce more. Citing over 200 articles, a huge review of its athletic benefits was published in 2018, concluding that carnitine boosts oxygen uptake, reduces soreness, and improves workout recovery.[37]

    L-carnitine has also repeatedly been shown to help with weight loss / BMI reduction[38] and blood sugar regulation.[39] It’s especially useful for those who are carnitine-deficient,[37,40-45] which is generally those who don’t eat red meat. We can’t put red meat into an RTD (can we?) so this is the next best option, on top of suggesting a healthy, meat-heavy diet for athletes.

    It’s worth noting that the most successful studies use 2 or more grams of carnitine, but it may be difficult to get this much into an RTD. If it can be achieved, it is definitely worth considering.

    L-Carnitine Function

    “L-carnitine function. l-carnitine shuttles long-chain fatty acids inside the mitochondria by forming a long chain acetylcarnitine ester. The complex is then transported into the mitochondrial matrix by carnitine palmitoyltransferase I (CPT I) and carnitine palmitoyltransferase II (CPT II). The fatty acids are then broken down through the process of β-oxidation to deliver the 2-carbon molecules to the Krebs cycle, leading to the generation of energy under the form of adenosine triphosphate (ATP). In addition, by binding an acetyl group, l-carnitine can maintain the levels of Acetyl-CoA and coenzyme A, playing its buffering role.”[37]

    Now that we’ve got delivery and hydration covered, it’s time to get to the novel ingredients that would set our RTD apart from the rest:

  • BioNMN – 500mg

    NMN Supplement

    Need more clean energy? Then there’s a good chance you need more NAD+ — and an incredible way to generate more is with NMN Supplementation.

    In our opinions, it takes more than caffeine and some hydration to truly improve energy. We have some ATP-supporting ingredients, but how can we catalyze even more ATP production?

    The answer is with a potent NAD+ (nicotinamide dinucleotide) booster to better regulate mitochondrial function — and the best way to do that is to provide its most powerful precursor, nicotinamide mononucleotide, also known as NMN. We do that with NNB Nutrition’s highly-bioavailable NMN ingredient named BioNMN.

    Driving ATP production with NAD+

    NAD+ is critical for countless biochemical reactions, one of its most important being a catalyst for ATP production.[46] NAD+ levels drop as we age, and low NAD+ levels are correlated with many diseases[47-49] — these disease may even be caused by low NAD+ levels. This is why it’s so important we work to keep levels high.[50]

    BioNMN: Boost NAD+ the right way

    We can’t simply supplement NAD+ though — especially not in an RTD.

    NMN Insulin Sensitivity

    See how NMN improves insulin sensitivity in overweight / insulin resistant women, and it’s dramatic for a few individuals.[51]

    It’d make great sense to simply supplement NAD+, but it’s not orally bioavailable. Supplement companies originally tried using niacin (which we’ve added below) as well as “NR” (nicotinamide riboside) to increase NAD+, but it turns out that NR is converted to NMN anyway,[46,52] making it costly and more wasteful.

    But once NNB Nutrition was able to stabilize NMN with BioNMN, it became a far better option. It gets into cells quickly (around 10 minutes), and researchers believe it has its own transporter.[53] Once taken up, researchers have found many benefits:

    • Cardioprotection[54-57]
    • Neuroprotection[58,59]
    • Insulin sensitivity improvements[51,60-62]
    • Additional anti-obesity properties[63,64]

    It’s also been found to be very safe in humans.[65]

    NNB Nutrition’s BioNMN takes NMN bioavailability to a new level, and is backed by an incredibly innovative novel ingredient development team

    From our perspective, BioNMN provides a profound “clean energy” that allows us to keep caffeine down – especially alongside the RhodioPrime Rhodiola added below. It’s not in many pre-workouts, but it is soluble in water – and we would love to have it in any pick-me-up drink.

    You can learn more about BioNMN in our article NMN Supplements (Nicotinamide Mononucleotide): The NAD+ Energy Precursor.

  • MitoBurn – 500mg

    Next up with our mito-boosting ingredients is MitoBurn, another incredible novel ingredient from NNB Nutrition. MitoBurn is L-BAIBA, the bioactive form of the non-protein amino acid BAIBA (β-aminoisobutyric acid) that serves as a myokine (“muscle messenger”). L-BAIBA is a metabolite of the BCAA valine,[66] and it functions as a signal to the rest of the body that muscle contractions and exercise are occurring.[67]

    BAIBA Results

    Beta-aminoisobutyric acid (BAIBA), induces beneficial effects on lipid homeostasis in mice.[68]

    When other organs see increases in L-BAIBA, it initiates numerous “exercise programs” that include fat oxidation, bone preservation, and glucose transfer. This occurs naturally in the body with exercise, but researchers have investigated what happens when more is supplemented – and the effects have been incredible:

    The benefits of L-BAIBA

    Numerous L-BAIBA benefits have been discovered in research:

    MitoBurn PricePlow

    MitoBurn (L-BAIBA) has flipped the fat burner niche on its head by supplying more of this exercise-based signaling molecule to dieters

    • Improved fat breakdown and oxidation[66,69,70]
    • Ketone body production[71]
    • White adipose tissue conversion to “beige” fat that’s more metabolically active[72,73]
    • Lower insulin resistance and better blood glucose tolerance[66,70]
    • Reduced inflammation[70]
    • Better lipid profiles[66]
    • Increased bone health[74]
    • Improved kidney health[75]

    MitoBurn is used in a lot of fat burners because of these effects, but for our pre-workout supplement, we’re really focusing on its ability to activate the PPAR alpha and PGC-1 alpha pathways[76,77] because PGC-1 can increase the number of mitochondria in cells![78]

    MitoBurn Logo

    MitoBurn from NNB Nutrition has been tested out to be a pure form of L-BAIBA, and has completely disrupted the supplement market!

    Alongside ingredients like betaine (above) and PQQ (below), this makes for an incredible addition to a mito-boosting pre-workout supplement, and it’s one we haven’t seen in an RTD application yet!

    You can learn more about BAIBA in our article titled BAIBA: Weight Loss Ingredient Generates Exercise in a Pill?!

  • RhodioPrime 6X – 250mg

    Next to BioNMN, Rhodiola is our next favorite non-stimulant energy booster to consider in a pre-workout like this. Rhodiola is a popular mood and vitality booster,[79] and NNB Nutrition’s RhodioPrime 6X is standardized to a high-energy, high-nootropic 6% salidroside content.

    Rhodiola

    Rhodiola: The Adaptogen Powered by Salidroside. In this article, we dive deep into rhodiola, and take a different approach to the adaptogenic herb!

    We love this ingredient because we’re big on the salidroside – it’s been shown to improve cellular functioning,[80] which is the overall goal of our pre-workout. Additionally, it can boost long-term potentiation (LTP) in the brain’s hippocampus[81] while boosting feel-good catecholamine uptake / activity.[82-85]

    In fact, animal models show that salidroside is protective to the mitochondria and improves mitochondrial energy.[86-88]

    The end result? A consistent mood-boosting effect with research showing improvements to general well-being and cognition.[89,90]

    The issue is that there are way too many weak and untested Rhodiola extracts on the market, and for our mito-boosting workout purposes, we want the nootropic edge of salidroside. This is why we asked NNB Nutrition to come up with something better than anything on the market, and they got RhodioPrime 6X to 6% salidroside standardization – an industry best.

    Rhodiola Benefits

    Look at these perceived changes in as little as three days, and they only got better over time![91]

    You can read more about the epic herb in our article titled Rhodiola: The Salidroside-Powered Adaptogen of the Vikings.

  • Caffeine Anhydrous – 200mg (of 250mg caffeine total)

    We won’t go on forever talking about caffeine – most users know what it does and how it feels for them. Right now, we’re seeing a lot of dependence on the stimulant, and brands are dosing pre-workouts very high with them – as much as 400 milligrams in one bottle.

    Formulator's Corner #05 - Mitochondria Boosting Pre Workout Supplement

    We were previously tasked to make a mitochondrial health boosting pre workout supplement powder that provided clean energy. Inside is quite the formula that we’d love to try out!

    To us, huge doses like that are not necessary – with the enhancement from BioNMN, RhodioPrime 6X, MitoBurn, and PQQ, we believe that less caffeine can be used to achieve more. However, we do want some, since it’s expected in any stimulant-based pre-workout supplement and is effective for enhancing mitochondrial function in animal models.[92]

    We’ve settled on 250 milligrams total from a blend that will provide some extended release caffeine below. This is more than most popular energy drinks (which often but don’t always average around 200 milligrams), but less than a lot of the more aggressive, fully-dosed pre-workout RTDs.

    It’s open for discussion – if anything, with this kind of formula, we’d go with less caffeine, not more. So some brands may opt for 175 – 225 milligram total yield, and still have a phenomenal feeling pre-workout.

  • Dicaffeine Malate – 68mg (yields 50mg of 250mg caffeine total)

    Dicaffeine malate is a caffeine that’s bound to malic acid, which serves to prolong the caffeine “energy curve”. It’s roughly 73% caffeine by weight, so 68 milligrams yields us 50 milligrams more, bringing us to a total of 250 milligrams of caffeine.

  • AstraGin – 25mg

    Next, we look for some ingredient amplification and gut permeability enhancement. It’s done with AstraGin, a blend of Astragalus membranaceus and Panax notoginseng from NuLiv Science.

    NuLiv Science has internal data showing improved citrulline uptake, which is our key for including it:

    AstraGin Citrulline

    One of AstraGin’s most popular use-cases is its ability to enhance citrulline absorption – especially right when we’d want it: during our workout![93]

    We understand that our 4 grams of citrulline, while solid and clinically-supported, is not the highest dose on the planet. While this wouldn’t be marketed for its pumps, we still want them to be strong, so a little bit of AstraGin can go a long way in supporting our citrulline.

  • PQQ – 20mg

    Our final holdover from our powdered mito-boosting pre-workout, we’re adding a water soluble form of pyrroloquinoline quinone, better known as PQQ.

    Mitochondria

    The mitochondria are the powerhouses of our cells. But how do they work, how is our food supply damaging them so badly, and what can we do to fix the issue? Prepare to meet the Power of Mito, presented by NNB Nutrition.

    This molecule is an “REDOX agent” antioxidant[94] that’s been shown to boost oxygen metabolism and blood flow to the brain, ultimately assisting with cognition.[95] PQQ has also been shown to lessen fatigue and reduce stress.[96]

    Even better, PQQ can promote mitochondrial biogenesis,[97] leaving us with more mitochondria.[98] This allows us to keep the caffeine at sub-300 (and lower) levels, alongside the other mito-boosters inside.

  • Added Ingredients

    The main ingredients are above, but there’s more we can do to improve mitochondrial and athletic performance:

    • Iodine (as Potassium Iodide) – 300mcg (200% DV)

      It’s not a Formulator’s Corner supplement without us adding some iodine to the mix! On this blog, we consistently harp on the data suggesting a re-emergence of iodine deficiency in the west.[99] This is due to less consumption (it’s not in the fancy sea salts everyone has switched to from iodized salt) as well as competing elements like fluoride in the water supply and bromine in bread.[100,101]

      Iodine is great for thyroid function, and what we’ve found is that providing it to anyone who’s iodine deficient is like giving them rocket fuel. Sometimes, you don’t need caffeine – you need other minerals you’re low on. And this is one that we believe too many individuals are unknowingly low. So we’re putting a decent dose inside.

    • Sodium – To taste, benzoate, etc. ~5% DV

      Salt is great for athletes, who are often not getting enough in.[102] Additionally, it may be used to improve the taste, and some sodium may come from preservative ingredients like sodium benzoate. This dosage is not set in stone.

    • Potassium – Citrate, sorbate, etc. ~4% DV

      Keto Diet Sodium Potassium Balance

      It’s all about the potassium sodium BALANCE. Too many supplements are too heavy on sodium without adding potassium.

      As fans of electrolytes, we’re as big on potassium as we are on sodium. Our goal here is simply to keep potassium levels balanced (or greater) than those of sodium. This is because it’s a known “shortfall nutrient” that’s difficult to get a lot of,[103] especially in our modern food environment.

      Many studies show that the sodium-potassium ratio is more important than sodium itself when it comes to blood pressure and cardiovascular disease,[104-108] so we love to point this out. Additionally, sodium actually helps with vasodilation,[109-111] and should probably be in more pre-workout supplements – perhaps even more than we have here!

      As researchers have noted quite simply, “Adult Americans consume too much sodium and not enough potassium,”[112] so if we’re adding sodium, we’re finding a way to add potassium too.

    • Niacin – 150% DV

      Alongside BioNMN, niacin (vitamin B3) can also help with NAD+ production.[113] We’re including niacinamide, but aren’t using a huge dose like some pre-workouts because it could cause annoying flushing. 30 milligrams (150% DV) may provide these benefits without much annoyance – but it’s really the BioNMN that we’re leaning on most for NAD+ support.

A pre-workout RTD that’d feel good

When looking at pre-workout supplements on the market, many of them are insanely high-energy, or have epic pumps, but not all of them provide the type of clean energy we’d often like to feel.

Formulator's Corner: A Better Healthy Coffee

Alternative to pre-workout is coffee! We made a unique coffee blend in Formulator’s Corner #03.

Although we had to ditch a few ingredients that wouldn’t be stable in RTD form from our mito-boosting powder (like creatine pyruvate, apigenin, and the acetyl version of carnitine), this still has the cornerstone mito-boosters like BioNMN, RhodioPrime 6X, MitoPrime, and PQQ to get the job done. The question is how much glycerol we can pack in here alongside betaine and taurine, and what flavor system we’d use to make it work.

Make this into a Burn supplement with CaloriBurn GP grains of paradise extract

Finally, one may wish to formulate a fat burning “Burn” pre-workout supplement with a base formula like this. If that’s the case, consider adding CaloriBurn GP grains of paradise extract to the mix. That will add some spice, but also provide additional thermogenic support. In that case, we’d likely reduce HydroPrime glycerol (to reduce just a few calories) and consider adding extra fat burning ingredients like a low dose of synephrine.

We need more mitochondria-minded pre-workouts

Back to our formula, we truly believe more pre-workout supplements need mitochondria-boosting support – users are far too often using caffeine when it’s not exactly what’s always needed. The energy issue could be as simple as low iodine levels, or as complex as low NAD+ levels. Either way, we tried to support numerous types of athletes with a powerful yet reasonable mito-friendly formula that works in liquid.

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About the Author: Mike Roberto

Mike Roberto

Mike Roberto is a research scientist and water sports athlete who founded PricePlow. He is an n=1 diet experimenter with extensive experience in supplementation and dietary modification, whose personal expertise stems from several experiments done on himself while sharing lab tests.

Mike's goal is to bridge the gap between nutritional research scientists and non-academics who seek to better their health in a system that has catastrophically failed the public.

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References

  1. Patlar, Suleyman et al; “The effect of glycerol supplements on aerobic and anaerobic performance of athletes and sedentary subjects.”; Journal of human kinetics; vol. 34; 2012; 69-79; doi:10.2478/v10078-012-0065-x; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590833/
  2. Nelson, Jeff L, and Robert A Robergs. “Exploring the Potential Ergogenic Effects of Glycerol Hyperhydration.” Sports Medicine, vol. 37, no. 11, 2007, pp. 981–1000, 10.2165/00007256-200737110-00005. https://www.ncbi.nlm.nih.gov/pubmed/17953468
  3. Montner, P., et al. “Pre-Exercise Glycerol Hydration Improves Cycling Endurance Time.” International Journal of Sports Medicine, vol. 17, no. 1, 1 Jan. 1996, pp. 27–33, 10.1055/s-2007-972804. https://pubmed.ncbi.nlm.nih.gov/8775573/
  4. Anderson, M. J., et al. “Effect of Glycerol-Induced Hyperhydration on Thermoregulation and Metabolism during Exercise in the Heat.” International Journal of Sport Nutrition, vol. 11, no. 3, 29 Sept. 2001, pp. 315–333. https://research.monash.edu/en/publications/effect-of-glycerol-induced-hyperhydration-on-thermoregulation-and
  5. Bailey, SJ et al.; “l-Citrulline supplementation improves O2 uptake kinetics and high-intensity exercise performance in humans.”; Journal of Applied Physiology; 119(4) pp. 385-395; 2015; https://journals.physiology.org/doi/full/10.1152/japplphysiol.00192.2014
  6. Hirata, Koji, et al. “Effect of L-Arginine on Synaptosomal Mitochondrial Function.” Brain & Development, vol. 30, no. 4, 1 Apr. 2008, pp. 238–245, pubmed.ncbi.nlm.nih.gov/17889473/, 10.1016/j.braindev.2007.08.007; https://pubmed.ncbi.nlm.nih.gov/17889473/
  7. Castillo, L, et al. “Splanchnic Metabolism of Dietary Arginine in Relation to Nitric Oxide Synthesis in Normal Adult Man.” Proceedings of the National Academy of Sciences of the United States of America, vol. 90, no. 1, 1 Jan. 1993, pp. 193–197; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC45626/
  8. Wu, Guoyao. “Intestinal Mucosal Amino Acid Catabolism.” The Journal of Nutrition, vol. 128, no. 8, 1 Aug. 1998, pp. 1249–1252, 10.1093/jn/128.8.1249; https://academic.oup.com/jn/article/128/8/1249/4722724
  9. Schwedhelm, Edzard et al.; “Pharmacokinetic and pharmacodynamic properties of oral L-citrulline and L-arginine: impact on nitric oxide metabolism.”; British journal of clinical pharmacology vol. 65,1 (2008): 51-9.; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291275/
  10. Bendahan, D. “Citrulline/Malate Promotes Aerobic Energy Production in Human Exercising Muscle.” British Journal of Sports Medicine, vol. 36, no. 4, 1 Aug. 2002, pp. 282–289, 10.1136/bjsm.36.4.282; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1724533/
  11. Giannesini B., et. al.; European Journal of Pharmacology; “Citrulline malate supplementation increases muscle efficiency in rat skeletal muscle;” September 2011; https://pubmed.ncbi.nlm.nih.gov/21664351/
  12. Perez-Guisado J, Jakeman PM; Journal of Strength and Conditioning; “Citrulline malate enhances athletic anaerobic performance and relieves muscle soreness;” May 2010; http://www.ncbi.nlm.nih.gov/pubmed/20386132
  13. Hickner RC. et. al.; Medicine and Science in Sports and Exercise; “L-citrulline reduces time to exhaustion and insulin response to a graded exercise test;” 2006; http://www.ncbi.nlm.nih.gov/pubmed/16679980
  14. Sureda, Antoni, et al. “L-Citrulline-Malate Influence over Branched Chain Amino Acid Utilization during Exercise.” European Journal of Applied Physiology, vol. 110, no. 2, 25 May 2010, pp. 341–351, 10.1007/s00421-010-1509-4; https://pubmed.ncbi.nlm.nih.gov/20499249/
  15. Rhim, Hye Chang, et al. “Effect of Citrulline on Post-Exercise Rating of Perceived Exertion, Muscle Soreness, and Blood Lactate Levels: A Systematic Review and Meta-Analysis.” Journal of Sport and Health Science, Feb. 2020, 10.1016/j.jshs.2020.02.003. https://www.sciencedirect.com/science/article/pii/S2095254620300168
  16. Hirata, Koji, et al. “Effect of L-Arginine on Synaptosomal Mitochondrial Function.” Brain & Development, vol. 30, no. 4, 1 Apr. 2008, pp. 238–245, pubmed.ncbi.nlm.nih.gov/17889473/, 10.1016/j.braindev.2007.08.007; https://pubmed.ncbi.nlm.nih.gov/17889473/
  17. https://pubmed.ncbi.nlm.nih.gov/35791786/
  18. Arumugam, Madan Kumar, et al. “Beneficial Effects of Betaine: A Comprehensive Review.” Biology, vol. 10, no. 6, 22 May 2021, p. 456, 10.3390/biology10060456; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC8224793/
  19. 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/
  20. 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/
  21. Craig, S. The American Journal of Clinical Nutrition; “Betaine in human nutrition.” 2004; https://pubmed.ncbi.nlm.nih.gov/15321791/
  22. 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/
  23. Trepanowski, J., Farney, T., et al. Journal of Strength and Conditioning Research; “The effects of chronic betaine supplementation on exercise performance, skeletal muscle oxygen saturation and associated biochemical parameters in resistance trained men.” 2011; https://pubmed.ncbi.nlm.nih.gov/22080324/
  24. Lee, E., Maresh, C., et al. Journal of the International Society of Sports Nutrition; “Ergogenic effects of betaine supplementation on strength and power performance.” 2010; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915951/
  25. Cholewa, Jason M., 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
  26. Zhang, Lifang, et al. “Betaine Increases Mitochondrial Content and Improves Hepatic Lipid Metabolism.” Food & Function, vol. 10, no. 1, 2019, pp. 216–223, 10.1039/c8fo02004c; https://pubmed.ncbi.nlm.nih.gov/30534761/
  27. Lee, Icksoo. “Betaine Is a Positive Regulator of Mitochondrial Respiration.” Biochemical and Biophysical Research Communications, vol. 456, no. 2, 9 Jan. 2015, pp. 621–625, pubmed.ncbi.nlm.nih.gov/25498545/, 10.1016/j.bbrc.2014.12.005; https://pubmed.ncbi.nlm.nih.gov/25498545/
  28. Du, Jingjing, et al. “Betaine Supplementation Enhances Lipid Metabolism and Improves Insulin Resistance in Mice Fed a High-Fat Diet.” Nutrients, vol. 10, no. 2, 26 Jan. 2018, p. 131, 10.3390/nu10020131; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC5852707/
  29. Kharbanda, Kusum K., et al. “Betaine Treatment Attenuates Chronic Ethanol-Induced Hepatic Steatosis and Alterations to the Mitochondrial Respiratory Chain Proteome.” International Journal of Hepatology, vol. 2012, 2012, 10.1155/2012/962183; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3235488/
  30. Kwon, Do Y., et al. “Impaired Sulfur-Amino Acid Metabolism and Oxidative Stress in Nonalcoholic Fatty Liver Are Alleviated by Betaine Supplementation in Rats.” The Journal of Nutrition, vol. 139, no. 1, 3 Dec. 2008, pp. 63–68, 10.3945/jn.108.094771; https://pubmed.ncbi.nlm.nih.gov/19056644/
  31. Ripps, H. et al. Nov. 2012. “Review: Taurine: A “Very Essential Amino Acid.” Molecular Vision vol. 18. 2673-86. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501277/
  32. 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
  33. 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/
  34. Guizoni, D. et al. Jan. 2020. “Modulation of Endothelium-Derived Nitric Oxide Production and Activity by Taurine and Taurine-Conjugated Bile Acids.” Nitric Oxide vol. 94,1; 48-53; https://www.sciencedirect.com/science/article/abs/pii/S1089860319302113
  35. 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/
  36. Sahlin, K. “Boosting Fat Burning With Carnitine: An Old Friend Comes Out from the Shadow.” Journal of Physiology vol. 589,Pt 7 (2011): 1509-10. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099008/
  37. Fielding, Roger, et al. “L-Carnitine Supplementation in Recovery after Exercise.” Nutrients, vol. 10, no. 3, 13 Mar. 2018, p. 349, 10.3390/nu10030349. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872767/
  38. Pooyandjoo, M., et al. “The Effect of (L-)Carnitine on Weight Loss in Adults: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.” Obesity Reviews, vol. 17, no. 10, 22 June 2016, pp. 970–976, 10.1111/obr.12436. https://pubmed.ncbi.nlm.nih.gov/27335245/
  39. Ruggenenti, Piero, et al. “Ameliorating Hypertension and Insulin Resistance in Subjects at Increased Cardiovascular Risk: Effects of Acetyl-L-Carnitine Therapy.” Hypertension (Dallas, Tex.: 1979), vol. 54, no. 3, 1 Sept. 2009, pp. 567–574, 10.1161/HYPERTENSIONAHA.109.132522. https://pubmed.ncbi.nlm.nih.gov/19620516/
  40. Krajcovicová-Kudlácková, M., et al. “Correlation of Carnitine Levels to Methionine and Lysine Intake.” Physiological Research, vol. 49, no. 3, 2000, pp. 399–402; https://pubmed.ncbi.nlm.nih.gov/11043928/
  41. Lombard, K A, et al. “Carnitine Status of Lactoovovegetarians and Strict Vegetarian Adults and Children.” The American Journal of Clinical Nutrition, vol. 50, no. 2, 1 Aug. 1989, pp. 301–306, 10.1093/ajcn/50.2.301; https://academic.oup.com/ajcn/article-abstract/50/2/301/4651007
  42. Krajcovicová-Kudlácková, M., et al. “Correlation of Carnitine Levels to Methionine and Lysine Intake.” Physiological Research, vol. 49, no. 3, 2000, pp. 399–402; https://pubmed.ncbi.nlm.nih.gov/11043928/
  43. Rebouche, Charles J. “Carnitine Function and Requirements during the Life Cycle.” The FASEB Journal, vol. 6, no. 15, Dec. 1992, pp. 3379–3386, 10.1096/fasebj.6.15.1464372; https://faseb.onlinelibrary.wiley.com/doi/abs/10.1096/fasebj.6.15.1464372
  44. Malaguarnera, Mariano, et al. “Serum Carnitine Levels in Centenarians.” Clinical Drug Investigation, vol. 17, no. 4, 1999, pp. 321–327, 10.2165/00044011-199917040-00008; https://link.springer.com/article/10.2165/00044011-199917040-00008
  45. Malaguarnera, Mariano, et al. “L-Carnitine Treatment Reduces Severity of Physical and Mental Fatigue and Increases Cognitive Functions in Centenarians: A Randomized and Controlled Clinical Trial.” The American Journal of Clinical Nutrition, vol. 86, no. 6, 1 Dec. 2007, pp. 1738–1744, 10.1093/ajcn/86.5.1738; https://pubmed.ncbi.nlm.nih.gov/18065594/
  46. Nikiforov, Andrey et al. “The human NAD metabolome: Functions, metabolism and compartmentalization.” Critical reviews in biochemistry and molecular biology vol. 50,4 (2015): 284-97. doi:10.3109/10409238.2015.1028612; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4673589/
  47. Fang, Evandro F., et al. “NAD + in Aging: Molecular Mechanisms and Translational Implications.” Trends in Molecular Medicine, vol. 23, no. 10, Oct. 2017, pp. 899–916, 10.1016/j.molmed.2017.08.001; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7494058/
  48. Imai, Shin-ichiro, and Leonard Guarente. “NAD+ and Sirtuins in Aging and Disease.” Trends in Cell Biology, vol. 24, no. 8, Aug. 2014, pp. 464–471, 10.1016/j.tcb.2014.04.002; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4112140/
  49. Schultz, Michael B., and David A. Sinclair. “Why NAD + Declines during Aging: It’s Destroyed.” Cell Metabolism, vol. 23, no. 6, June 2016, pp. 965–966, 10.1016/j.cmet.2016.05.022; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC5088772/
  50. Aman, Yahyah, et al. “Therapeutic Potential of Boosting NAD in Aging and Age-Related Diseases.” Translational Medicine of Aging, Elsevier, 18 Aug. 2018. https://www.sciencedirect.com/science/article/pii/S2468501118300063
  51. Yoshino, Mihoko, et al. “Nicotinamide Mononucleotide Increases Muscle Insulin Sensitivity in Prediabetic Women.” Science, 22 Apr. 2021, 10.1126/science.abe9985; https://science.sciencemag.org/content/early/2021/04/21/science.abe9985
  52. Poddar, Saikat Kumar et al. “Nicotinamide Mononucleotide: Exploration of Diverse Therapeutic Applications of a Potential Molecule.” Biomolecules vol. 9,1 34. 21 Jan. 2019, doi:10.3390/biom9010034. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359187/
  53. Grozio, Alessia, et al. “Slc12a8 Is a Nicotinamide Mononucleotide Transporter.” Nature News, Nature Publishing Group, 7 Jan. 2019. https://www.nature.com/articles/s42255-018-0009-4
  54. Yamamoto, Takanobu et al. “Nicotinamide mononucleotide, an intermediate of NAD+ synthesis, protects the heart from ischemia and reperfusion.” PloS one vol. 9,6 e98972. 6 Jun. 2014, doi:10.1371/journal.pone.0098972. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048236/
  55. Martin, Angelical S et al. “Nicotinamide mononucleotide requires SIRT3 to improve cardiac function and bioenergetics in a Friedreich’s ataxia cardiomyopathy model.” JCI insight vol. 2,14 e93885. 20 Jul. 2017, doi:10.1172/jci.insight.93885. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518566/
  56. Nadtochiy, Sergiy M et al. “Cardioprotection by nicotinamide mononucleotide (NMN): Involvement of glycolysis and acidic pH.” Journal of molecular and cellular cardiology vol. 121 (2018): 155-162. doi:10.1016/j.yjmcc.2018.06.007. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103815/
  57. Park, Ji H et al. “Nicotinamide mononucleotide inhibits post-ischemic NAD(+) degradation and dramatically ameliorates brain damage following global cerebral ischemia.” Neurobiology of disease vol. 95 (2016): 102-10. doi:10.1016/j.nbd.2016.07.018. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5580241/
  58. Wang, Xiaonan et al. “Nicotinamide mononucleotide protects against β-amyloid oligomer-induced cognitive impairment and neuronal death.” Brain research vol. 1643 (2016): 1-9. doi:10.1016/j.brainres.2016.04.060. https://pubmed.ncbi.nlm.nih.gov/27130898/
  59. Kimura, Ryoichi et al. “Beta amyloid-induced depression of hippocampal long-term potentiation is mediated through the amylin receptor.” The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 32,48 (2012): 17401-6. doi:10.1523/JNEUROSCI.3028-12.2012. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6621862/
  60. Yoshino, Jun et al. “Nicotinamide mononucleotide, a key NAD(+) intermediate, treats the pathophysiology of diet- and age-induced diabetes in mice.” Cell metabolism vol. 14,4 (2011): 528-36. doi:10.1016/j.cmet.2011.08.014. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204926/
  61. Caton, Paul W. “Nicotinamide Mononucleotide Protects Against Cytokine-Mediated Islet Dysfunction.” American Diabetes Association. 2011. https://professional.diabetes.org/abstract/nicotinamide-mononucleotide-protects-against-cytokine-mediated-islet-dysfunction
  62. Irie, J et al. “Effect of oral administration of nicotinamide mononucleotide on clinical parameters and nicotinamide metabolite levels in healthy Japanese men.” Endocrine Journal. Keio University School of Medicine. Nov. 2, 2019. https://www.jstage.jst.go.jp/article/endocrj/advpub/0/advpub_EJ19-0313/_pdf
  63. Mills, Kathryn F et al. “Long-Term Administration of Nicotinamide Mononucleotide Mitigates Age-Associated Physiological Decline in Mice.” Cell metabolism vol. 24,6 (2016): 795-806. doi:10.1016/j.cmet.2016.09.013. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668137/
  64. Uddin, Golam M et al. “Head to Head Comparison of Short-Term Treatment with the NAD(+) Precursor Nicotinamide Mononucleotide (NMN) and 6 Weeks of Exercise in Obese Female Mice.” Frontiers in pharmacology vol. 7 258. 19 Aug. 2016, doi:10.3389/fphar.2016.00258. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990541/
  65. Irie, J et al. “Effect of oral administration of nicotinamide mononucleotide on clinical parameters and nicotinamide metabolite levels in healthy Japanese men.” Endocrine Journal. Keio University School of Medicine. Nov. 2, 2019. https://www.jstage.jst.go.jp/article/endocrj/advpub/0/advpub_EJ19-0313/_pdf
  66. Tanianskii, Dmitrii A et al; “Beta-Aminoisobutyric Acid as a Novel Regulator of Carbohydrate and Lipid Metabolism”; Nutrients; vol. 11,3 524; February 28, 2019; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470580/
  67. Schnyder, Svenia, Handschin, Christoph; “Skeletal muscle as an endocrine organ: PGC-1α, myokines and exercise”; Bone; Volume 80, Pages 115-125; November 2015; https://www.sciencedirect.com/science/article/abs/pii/S8756328215000459
  68. Begriche, Karima, et al. “β-Aminoisobutyric Acid Prevents Diet-Induced Obesity in Mice with Partial Leptin Deficiency.” Obesity, vol. 16, no. 9, Sept. 2008, pp. 2053–2067, 10.1038/oby.2008.337; https://onlinelibrary.wiley.com/doi/full/10.1038/oby.2008.337
  69. Maisonneuve, C, et al; “Effects of zidovudine, stavudine and beta-aminoisobutyric acid on lipid homeostasis in mice: possible role in human fat wasting”; Antiviral Therapy; 9(5):801-10; October 2004; https://pdfs.semanticscholar.org/ad85/0e69e7a66f59bd0491fbf2b39da15f6eb2cf.pdf
  70. Jung, Tae Woo, et al; “BAIBA attenuates insulin resistance and inflammation induced by palmitate or a high fat diet via an AMPK–PPARδ-dependent pathway in mice”; Diabetologia; September 2015, Volume 58, Issue 9, pp 2096–2105; https://link.springer.com/article/10.1007/s00125-015-3663-z
  71. Note, Reine et al; “Mitochondrial and metabolic effects of nucleoside reverse transcriptase inhibitors (NRTIs) in mice receiving one of five single- and three dual-NRTI treatments”; Antimicrobial agents and Chemotherapy; vol. 47,11: 3384-92; 2013; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC253807/
  72. Roberts, L, et al; “b-Aminoisobutyric Acid Induces Browning of White Fat and Hepatic b-Oxidation and Is Inversely Correlated with Cardiometabolic Risk Factors”; Cell Metabolism; Volume 19, Issue 1, pp 96-108; 2014; https://www.cell.com/cell-metabolism/fulltext/S1550-4131(13)00497-X
  73. Kammoun, HL and Febbraio, MA; “Come on BAIBA Light My Fire;” Cell Metabolism; 2014;19(1), pp 1-2; https://www.sciencedirect.com/science/article/pii/S1550413113005020
  74. Kitase, Yukiko et al; “β-aminoisobutyric Acid, l-BAIBA, Is a Muscle-Derived Osteocyte Survival Factor”; Cell Reports; vol. 22,6 (2018): 1531-1544; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832359/
  75. Wang, H, et al; “β-Aminoisobutyric acid ameliorates the renal fibrosis in mouse obstructed kidneys via inhibition of renal fibroblast activation and fibrosis”; Journal of Pharmacological Sciences; Volume 133, Issue 4; Pages 203-213; April 2017; https://www.sciencedirect.com/science/article/pii/S1347861317300038
  76. Roberts, L et al. (n.d.). b-Aminoisobutyric Acid Induces Browning of White Fat and Hepatic b-Oxidation and Is Inversely Correlated with Cardiometabolic Risk Factors. Cell metab.; 2014; https://www.cell.com/cell-metabolism/fulltext/S1550-4131(13)00497-X
  77. Bostrom, P., et al. (2012). A PGC1-a-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature, 481: 463-482; https://www.ncbi.nlm.nih.gov/pubmed/22237023
  78. Lira, V., Benton, C., Yan, Z., Bonen, A (2010); PGC-1alpha regulation by exercise training and its influences on muscle function and insulin sensitivity; Am J Physiol Endocrinol Metab, 299 (2): 145-161; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC2928513/
  79. Panossian, A., et al. “Rosenroot (Rhodiola Rosea): Traditional Use, Chemical Composition, Pharmacology and Clinical Efficacy.” Phytomedicine, vol. 17, no. 7, June 2010, pp. 481–493, 10.1016/j.phymed.2010.02.002. https://pubmed.ncbi.nlm.nih.gov/20378318/
  80. Liu, Zhongbo, et al. “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, no. 3, 22 Apr. 2011, pp. 257–267, 10.1002/mc.20780. https://www.ncbi.nlm.nih.gov/pubmed/21520297/
  81. Dimpfel, Wilfried, et al. “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, 24 May 2018, 10.3389/fphar.2018.00425. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976749/
  82. Zhong, Zhi-feng, et al. “Neuroprotective Effects of Salidroside on Cerebral Ischemia/Reperfusion-Induced Behavioral Impairment Involves the Dopaminergic System.” Frontiers in Pharmacology, vol. 10, 13 Dec. 2019, 10.3389/fphar.2019.01433. https://www.frontiersin.org/articles/10.3389/fphar.2019.01433/full
  83. Purves, Dale, et al. “The Biogenic Amines.” Nih.gov, Sinauer Associates, 2019. https://www.ncbi.nlm.nih.gov/books/NBK11035/
  84. Thangam, Elden Berla, et al. “The Role of Histamine and Histamine Receptors in Mast Cell-Mediated Allergy and Inflammation: The Hunt for New Therapeutic Targets.” Frontiers in Immunology, vol. 9, 13 Aug. 2018, 10.3389/fimmu.2018.01873. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099187/
  85. Berger, Miles, et al. “The Expanded Biology of Serotonin.” Annual Review of Medicine, vol. 60, 2009, pp. 355–66, 10.1146/annurev.med.60.042307.110802. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864293/
  86. Hu, Cai-Ying, et al. “Protective Effect of Salidroside on Mitochondrial Disturbances via Reducing Mitophagy and Preserving Mitochondrial Morphology in OGD-Induced Neuronal Injury.” Current Medical Science, vol. 41, no. 5, 1 Oct. 2021, pp. 936–943, 10.1007/s11596-021-2374-6; https://pubmed.ncbi.nlm.nih.gov/34181207/
  87. Wang, Xiaobo, et al. “Rhodiola Crenulata Attenuates Apoptosis and Mitochondrial Energy Metabolism Disorder in Rats with Hypobaric Hypoxia-Induced Brain Injury by Regulating the HIF-1α/MicroRNA 210/ISCU1/2(COX10) Signaling Pathway.” Journal of Ethnopharmacology, vol. 241, 15 Sept. 2019, p. 111801, 10.1016/j.jep.2019.03.028; https://pubmed.ncbi.nlm.nih.gov/30878546/
  88. Bai, Xiang-Li, et al. “Rhodiola and Salidroside in the Treatment of Metabolic Disorders.” Mini Reviews in Medicinal Chemistry, vol. 19, no. 19, 2019, pp. 1611–1626, 10.2174/1389557519666190903115424; https://pubmed.ncbi.nlm.nih.gov/31481002/
  89. Spasov, A. A., et al. “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, vol. 7, no. 2, 1 Apr. 2000, pp. 85–89, 10.1016/S0944-7113(00)80078-1. https://pubmed.ncbi.nlm.nih.gov/10839209/
  90. Shevtsov, V. A., et al. “A Randomized Trial of Two Different Doses of a SHR-5 Rhodiola Rosea Extract versus Placebo and Control of Capacity for Mental Work.” Phytomedicine, vol. 10, no. 2, 1 Jan. 2003, pp. 95–105, 10.1078/094471103321659780. https://pubmed.ncbi.nlm.nih.gov/12725561/
  91. Edwards, D et al. “Therapeutic effects and safety of Rhodiola rosea extract WS 1375 in subjects with life-stress symptoms–results of an open-label study.” Phytotherapy research : PTR vol. 26,8 (2012): 1220-5. doi:10.1002/ptr.3712. https://pubmed.ncbi.nlm.nih.gov/22228617/
  92. Dragicevic, Natasa, et al. “Caffeine Increases Mitochondrial Function and Blocks Melatonin Signaling to Mitochondria in Alzheimer’s Mice and Cells.” Neuropharmacology, vol. 63, no. 8, Dec. 2012, pp. 1368–1379, 10.1016/j.neuropharm.2012.08.018; https://pubmed.ncbi.nlm.nih.gov/22959965/
  93. NuLiv Science; AstraGin Product Dossier; https://docdro.id/rA01t9O
  94. Rucker, Robert, et al. “Potential Physiological Importance of Pyrroloquinoline Quinone.” Alternative Medicine Review: A Journal of Clinical Therapeutic, vol. 14, no. 3, 1 Sept. 2009, pp. 268–277; https://pubmed.ncbi.nlm.nih.gov/19803551/
  95. Nakano, Masahiko, et al; “Effects of Antioxidant Supplements (BioPQQ) on Cerebral Blood Flow and Oxygen Metabolism in the Prefrontal Cortex.”; Advances in Experimental Medicine and Biology; U.S. National Library of Medicine; 2016; https://www.ncbi.nlm.nih.gov/pubmed/27526146
  96. Nakano, M., et al; “Effect of Oral Supplementation with Pyrroloquinoline Quinone on Stress, Fatigue, and Sleep.”; Functional Foods in Health and Disease; 2012; 2(8); 307-324; https://www.functionalfoodscenter.net/files/56592277.pdf
  97. Saihara K, Kamikubo R, Ikemoto K, Uchida K, Akagawa M; “Pyrroloquinoline Quinone, a Redox-Active o‑Quinone, Stimulates Mitochondrial Biogenesis by Activating the SIRT1PGC-1α Signaling Pathway”; Biochemistry; 2017; 56; 6615−6625; https://pubs.acs.org/doi/10.1021/acs.biochem.7b01185
  98. Harris, Calliandra B, et al; “Dietary Pyrroloquinoline Quinone (PQQ) Alters Indicators of Inflammation and Mitochondrial-Related Metabolism in Human Subjects.”; The Journal of Nutritional Biochemistry; U.S. National Library of Medicine; Dec. 2013; https://www.ncbi.nlm.nih.gov/pubmed/24231099
  99. Pearce, Elizabeth N. “Is Iodine Deficiency Reemerging in the United States?” AACE Clinical Case Reports, vol. 1, no. 1, 2015, pp. e81–e82, 10.4158/ep14472.co; https://www.sciencedirect.com/science/article/pii/S2376060520303680
  100. Zava, Theodore T, and David T Zava. “Assessment of Japanese Iodine Intake Based on Seaweed Consumption in Japan: A Literature-Based Analysis.” Thyroid Research, vol. 4, no. 1, 2011, p. 14, 10.1186/1756-6614-4-14; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204293/
  101. Aggrawal, Manali, and Jeffrey Scott Rohrer. “Selective and Sensitive Determination of Bromate in Bread by Ion Chromatography-Mass Spectrometry.” Journal of Chromatography. A, vol. 1615, 29 Mar. 2020, p. 460765, 10.1016/j.chroma.2019.460765; https://pubmed.ncbi.nlm.nih.gov/31848031/
  102. 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/
  103. 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/
  104. Dyer, Alan R., et al. “Urinary Electrolyte Excretion in 24 Hours and Blood Pressure in the INTERSALT Study.” American Journal of Epidemiology, vol. 139, no. 9, 1 May 1994, pp. 940–951, 10.1093/oxfordjournals.aje.a117100; https://www.ncbi.nlm.nih.gov/pubmed/8166144
  105. Elliott, P., et al. “Intersalt Revisited: Further Analyses of 24 Hour Sodium Excretion and Blood Pressure within and across Populations.” BMJ, vol. 312, no. 7041, 18 May 1996, pp. 1249–1253, www.bmj.com/content/312/7041/1249, 10.1136/bmj.312.7041.1249; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC2351086/
  106. Cook, N. R., et al. “Effect of Change in Sodium Excretion on Change in Blood Pressure Corrected for Measurement Error. The Trials of Hypertension Prevention, Phase I.” American Journal of Epidemiology, vol. 148, no. 5, 1 Sept. 1998, pp. 431–444, 10.1093/oxfordjournals.aje.a009668; https://www.ncbi.nlm.nih.gov/pubmed/9737555
  107. Khaw, K T, and E Barrett-Connor. “The Association between Blood Pressure, Age, and Dietary Sodium and Potassium: A Population Study.” Circulation, vol. 77, no. 1, Jan. 1988, pp. 53–61, 10.1161/01.cir.77.1.53; https://www.ncbi.nlm.nih.gov/pubmed/3257173
  108. Xie, J. X., et al. “The Relationship between Urinary Cations Obtained from the INTERSALT Study and Cerebrovascular Mortality.” Journal of Human Hypertension, vol. 6, no. 1, 1 Feb. 1992, pp. 17–21; https://www.ncbi.nlm.nih.gov/pubmed/1583625
  109. Adrogué, Horacio J., and Nicolaos E. Madias. “Sodium and Potassium in the Pathogenesis of Hypertension.” New England Journal of Medicine, vol. 356, no. 19, 10 May 2007, pp. 1966–1978, 10.1056/nejmra064486; https://pubmed.ncbi.nlm.nih.gov/17494929/
  110. Haddy, Francis J., et al. “Role of Potassium in Regulating Blood Flow and Blood Pressure.” American Journal of Physiology. Regulatory, Integrative and Comparative Physiology, vol. 290, no. 3, 1 Mar. 2006, pp. R546-552, 10.1152/ajpregu.00491.2005; https://journals.physiology.org/doi/full/10.1152/ajpregu.00491.2005
  111. Amberg, Gregory C., et al. “Modulation of the Molecular Composition of Large Conductance, Ca2+ Activated K+ Channels in Vascular Smooth Muscle during Hypertension.” Journal of Clinical Investigation, vol. 112, no. 5, 1 Sept. 2003, p. 717, 10.1172/JCI18684; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC182211/
  112. Drewnowski, Adam, et al. “Reducing the Sodium-Potassium Ratio in the US Diet: A Challenge for Public Health.” The American Journal of Clinical Nutrition, vol. 96, no. 2, 3 July 2012, pp. 439–444, 10.3945/ajcn.111.025353; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3396449/
  113. Sauve, A. A. “NAD+ and Vitamin B3: From Metabolism to Therapies.” Journal of Pharmacology and Experimental Therapeutics, vol. 324, no. 3, 19 Dec. 2007, pp. 883–893, jpet.aspetjournals.org/content/324/3/883, 10.1124/jpet.107.120758; https://pubmed.ncbi.nlm.nih.gov/18165311/

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