Formulator’s Corner #04: An Elite Women’s Health Supplement in TWO Caps
Women have a lot to deal with, especially in today’s society. In the middle of everything running in and around women’s lives, health remains core to it all. But with a culture of ultra-processed foods and diminished nutrition, it has become increasingly difficult to avoid various deficiencies and their consequences.
A multi-faceted women’s supplement in two capsules
Several companies have developed “women’s health supplements”, but NNB Nutrition tasked us to do one better, targeting more pitfalls that commonly trap women. We took it upon ourselves to pack as many beneficial ingredients as possible into two capsules, knowing that we all have limits to the number of capsules we’re willing to take every day.

How many women’s health ingredients can we theoretically pack into just two capsules? Thanks to NNB Nutrition, the answer is… a lot!
Below, we’ve formulated our “dream women’s supplement” with ten ingredients, with various beneficial components:
- Mood and energy (stimulant-free)
- Hormonal health
- PMS and Menopause relief
- Metabolic wellness
- Inflammation
- Immunity
- Better Sleep
Made possible by NNB Nutrition
It’s only possible thanks to NNB Nutrition’s novel ingredients, which give us powerful effects without taking up too much space. This supplement includes what your general women’s multivitamin doesn’t – and with only two capsules, it’d be no major deal to add to your stack, but the results would be impossible to miss.
It’s all below, but first, sign up for our NNB Nutrition news alerts so that you don’t miss new science-driven content and their future ingredient releases:
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Our Women’s Health Formula Ingredients
Consider this a thought experiment of how we’d maximize space and effects in just two capsules to give women some sensational benefits. While this isn’t an actual supplement, it’s one we’d love to see created (especially for our significant others), addressing numerous issues that women deal with from day to day, month to month, and even during menopause.
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RhodioPrime 6X (Rhodiola crenulata extract [6% salidroside] [root]) – 200 mg
If we could pack this into two capsules, women would get a lift in so many ways – from mood and energy to PMS / menopause relief to inflammation to immunity and more!
We start our formula off with a “mood-boosting bang” in the best way we know how – with NNB Nutrition’s RhodioPrime 6X, the industry’s premier high-salidroside Rhodiola extract.
Rhodiola is a fascinating and incredibly well-researched adaptogen that helps the brain and body adjust to stress and regulate various neurotransmitter levels. We’re primarily interested in its ability to improve serotonin production,[1] which serves as a key mood and emotion regulator amongst other effects.
This leads to several incredible benefits:
The numerous benefits of Rhodiola
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Stress and anxiety relief – In as little as 14 days, Rhodiola has been shown to significantly reduce anxiety, stress, anger, confusion, and depression.[2] Another study, using 200 milligrams like we have here, showed improvements in all stress measurements, and the effects began in three days![3]
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Mood enhancement – The study cited above touches upon improved mood through a reduction of depression,[2] and further research has verified that Rhodiola can significantly boost mood in users with clinical mood disorders.[4]
When compared to popular pharmaceutical drugs, Rhodiola held its own, leading to modest improvements but with far fewer side effects.[5]
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Menopause relief – In 2015, researchers published a paper reviewing the connections between estrogen decline, menopause-related health risks, and how Rhodiola can protect against them.[6]
The paper has relevant sections on:
- Neuroprotection,
- Psychological stress, anxiety, depression, and fatigue,
- Cardiovascular protection,
- Osteoporosis prevention,
- Anticarcinogenic and chemoprotective,
- Hormonal effects, and
- Clinical case studies[6]
After analyzing the mechanisms and research available, they went so far to title their paper “Pause menopause with Rhodiola rosea”, concluding the following:”Numerous lines of evidence indicate that Rhodiola should be investigated as a potential selective estrogen receptor modulator (SERM) to prevent, delay or mitigate menopause-related cognitive, psychological, cardiovascular and osteoporotic conditions.”[6]
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Mental Fatigue and Tiredness Reduction – A study on a low (100 milligram) dose of Rhodiola found improved general well-being, including better cognition, mental clarity, physical fitness.[7] Reductions in mental fatigue have been noted and replicated in several studies across several dosages and extracts.[2,3,8-14]
In addition, one of these studies also documented improved sleep quality and reduced the consequences of sleep deprivation,[2] benefits nearly all of us can enjoy.
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Physical Fatigue Reduction – With some overlap from the above studies, athletes have experienced clinically reduced physical fatigue,[9,15,16] improving endurance and enabling them to train with more vigor.
Notably, athletes have less muscular damage when using Rhodiola, as measured by creatine kinase levels.[17-19]
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Improved Cognition and Attention – Rhodiola also serves as an incredible nootropic, or cognition-enhancing supplement, with several studies demonstrating improved overall cognition[3,7,8,20] and attention.[10,16]
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Potential Appetite Regulation – We’ve seen animal studies demonstrate reduced binge eating with Rhodiola,[21] potentially due to the serotonin support it provides.
There are so many great reasons to take this adaptogen, it’s questionable not to include a powerful extract in a health supplement.
Focus on salidroside with RhodioPrime 6X
Rhodiola: The Adaptogen Powered by Salidroside. In this article, we dive deep into rhodiola, and take a different approach to the adaptogenic herb!
Over time, researchers have begun to realize that the salidroside portion of Rhodiola extracts are what drive the most impressive feel-good effects that we seek.[22,23] Many supplements are extracted for rosavins, but they alone are not targeting the energetic pathways as heavily as salidroside (such as AMPK and mTOR).[24] The researchers targeting menopause specifically call out salidroside’s mechanisms in improving women’s health.[6]
For this reason, we asked NNB Nutrition to develop a high-salidroside Rhodiola extract, and its name is RhodioPrime 6X. This is a mood-boosting, energetic, and extremely experiential ingredient that has an industry-leading 6% salidroside extract. It feels great, and is exactly what we hoped for NNB to create.
Rhodiola used right
Rhodiola extracts aren’t just for women, but women are too often neglected in supplements that use the potent adaptogen. We’re too used to seeing this ingredient in high-stimulant workout supplements and aggressive nootropic (cognitive-boosting) supplements — two categories that are rather male-dominated. While Rhodiola is incredible in those formulas, they’re often dosed in a way that prevents women from getting a full dosage.
At 6% salidroside, NNB Nutrition’s RhodioPrime is the best way to feel the serious power of this wonderful herb!
With this formula, that changes right here. Rhodiola alone makes this a women’s supplement worth considering, but we’ve only gotten started. Next we’ll focus on some women-specific issues, hormonal improvements, then get to inflammation and metabolic enhancement.
You can learn more in our articles titled “Rhodiola: The Salidroside-Powered Adaptogen of the Vikings” and “NNB RhodioPrime 6X: The Strongest Rhodiola Extract (6% Salidroside)“.
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Chaste Tree Extract (Vitex Agnus-Castus) – 200mg
Now getting to women’s health, Chaste Tree Extract is a plant with many incredible benefits, especially with regards to menopause, PMS, infertility, and other reproductive issues.[25-27] Also known as Vitex agnus-castus, the plant can help combat many of the changes of menopause, including hot flashes, fatigue, dizziness, bone loss, weight gain, and poor mood.[25]
Chaste Tree Extracts have been studied well enough to have a systematic review of eight randomized controlled trials, finding that the ingredient is safe and beneficial in dealing with bloating, anxiety, migraines, cramps, fatigue, insomnia, and general irritability.[26,27]
The exact mechanism is being explored, and scientists believe that chaste tree extract is able to activate various dopamine pathways in the brain,[25] which is an incredible effect to pair with the serotonin boost from RhodioPrime 6X above!
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CurcuPrime (Tetrahydrocurcumin) – 200mg
CurcuPrime: Curcumin’s better half for diet and cardio support on top of the anti-inflammatory properties
Turmeric and its potent pigment, curcumin, are well-known for their numerous anti-inflammatory benefits[28-30] that extend to pain reduction,[31-33] metabolic improvements,[34-36] better mood / reduced anxiety,[29,37,38] and improved blood flow.[39]
PMS and Menopause hot flash protection
One study even found notably reduced PMS symptoms,[40] and another triple-blind randomized study on 93 post-menopausal women found that both curcumin and vitamin E significantly reduced hot flashes in eight weeks, with curcumin outperforming both vitamin E and placebo.[41]
The issue is that curcumin has notoriously awful bioavailability,[42] requiring us to either dose it very high or find new preparations (which still require doses higher than what we can fit into our women’s health supplement).
Tetrahydrocurcumin: a metabolite with the benefits but better bioavailability
The solution to curcumin’s bioavailability problem? NNB Nutrition’s CurcuPrime, which is a pure tetrahydrocurcumin ingredient. Discovered in 1978, tetrahydrocurcumin was quickly found to be a key bioactive metabolite of curcumin,[43] and is a strong contributor to curcumin’s potent bioactivity compared to its other metabolites.[44]
Researchers have found that tetrahydrocurcumin has superior bioavailability to curcumin,[44] enabling us to use less to get similar effects. This is due to the compound’s inclusion of four hydrogen atoms, which enable greater antioxidant activity.[45] This also makes the compound more water-soluble[46] and whiter in color, a major plus for formulators and manufacturers who loathe the staining deep yellow-orange color of curcumin.
Animal studies have shown tetrahydrocurcumin outperforming standard curcumin in metabolic tests (blood sugar response and protection from lipid oxidation).[47-49] Finally, to add to the nootropic effects we get from RhodioPrime 6X, tetrahydrocurcumin has been shown to protect acetylcholine,[44,50] keeping our “learning neurotransmitters” around longer for improved cognition.
Best of all, with better bioavailability, we can get a rather potent dose at 200 milligrams, which is what’s needed to fit so many powerful ingredients into our supplement here. When space is at a premium, CurcuPrime is a clear choice for the inclusion of a curcumin compound.
Women who are dealing with serious joint pain issues may wish to include a separate supplement stack to address that, but CurcuPrime’s powerful anti-inflammatory action at a relatively low dose makes it a wise choice for general protection. Unless women actively seek out a quality curcumin supplement, they may not get these benefits, and they’re well worth getting to everyone.
You can learn more in our articles titled “Tetrahydrocurcumin: A More Potent Alternative to Curcumin?” and “NNB Nutrition CurcuPrime: Curcumin’s Better Half for Dieters“.
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3,3′-Diindolylmethane – 200 mg
It’s unsurprising to see DIM (scientifically known as 3,3′ diindolylmethane) in a women’s health supplement, given its benefits for hormonal balance. DIM has a unique ability to lower excess estrogen levels, balancing the “good” and “bad” estrogens.
The ingredient works by inhibiting aromatase and 5a-reductase, two enzymes involved in estrogen production.[51] It doesn’t completely shut down estrogen, though, but ends up boosting levels of estradiol 2-hydroxylase (the “good estrogen”) while reducing levels of 16-alpha-hydroxy estrone (the “bad estrogen”).[52] As with anything, it’s all about equilibrium and balance.
Targets of Curcumin vs. Tetrahydrocurcumin: Curcumin is effective in modulating some, but tetrahydrocurcumin is more effective in others.
With a better estrogen balance, we can help combat the negative effects of too much estrogen, which includes (but is not limited to) headaches, irregular menstruation, swelling, fatigue, more pronounced PMS symptoms, anxiety, weight gain, and more.
Later, we’ll touch on thyroid protection with the added iodine, but research also shows that DIM DIM is an anti-estrogenic agent that can lower the risk of certain thyroid diseases and breast cancer.[53,54]
In 2016, researchers published a systematic review regarding DIM’s anti-cancer effects, stating that it can alter estrogen metabolism and apoptosis for the better while improving the response to oxidative stress.[54]
Vitex and DIM take up nearly half of our formula, but make a wonderful duo in terms of protecting women. This leaves us room to further fight inflammation:
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GlucoVantage Dihydroberberine – 100mg
CurcuPrime promotes some metabolic improvements, but nothing like what’s here in GlucoVantage, NNB Nutrition’s dihydroberberine ingredient, known as the “Super Berberine”.
How does the best glucose disposal ingredient in berberine get any better? It’s known as dihydroberberine, and sold as NNB Nutrition’s GlucoVantage, and if there’s one anti-aging ingredient we suggest, it’s this one!
Berberine is a metabolic-boosting ingredient that lowers blood sugar and drastically improves metabolic markers (such as insulin, HbA1c, and lipid levels), helping to improve insulin sensitivity.[55] It has outperformed very popular pharmaceutical drugs with fewer side effects.[56]
Assisting with the menopausal transition
Before getting into the metabolic benefits that everyone can enjoy with GlucoVantage dihydroberberine, it’s important to call out a paper published in 2015 that analyzed berberine with respect to menopausal women. Inside, the researchers noted that berberine’s mechanisms (discussed below) “suggest that this molecule could be an effective natural supplement to ensure a smooth peri- and postmenopausal transition”.[57]
The study discusses research that demonstrates berberine’s little-known ability to boost mood through MAO-A enzyme inhibition,[58] which will help keep dopamine levels elevated longer.
Undoing metabolic damage and getting nutrients where they need to go
Berberine primarily works by increasing the release of our “energy metabolism enzyme”, AMPK,[59,60] which helps drive glucose uptake into muscle cells as opposed to fat cells.[61] It also boosts insulin sensitivity by promoting adiponectin release from fat tissue,[55] further undoing metabolic damage done to the body.
This leads to numerous health benefits seen in berberine users:
The effective Dihydroberberine Dosage is 30% the dose of standard berberine, giving it far more applications and less GI discomfort!
- Improved glucose uptake,[56,62] especially into muscle cells[60,63]
- Better insulin sensitivity and insulin levels[64]
- Body recomposition (build muscle while losing fat)[56,64]
- Metabolic marker improvements[56]
Meanwhile, there are even antiviral effects, where berberine once again outperformed pharmaceutical drugs.[65]
But there’s a catch… bioavailability
Like curcumin, the issue with berberine is that it has awful bioavailability.[66-68] To get it efficaciously dosed would require large doses that won’t fit into a multi-ingredient supplement like this one, and large doses can lead to GI distress.
Thanks to NNB Nutrition, we can do far better, with GlucoVantage.
GlucoVantage Dihydroberberine: 5x more effective than berberine!
NNB Nutrition has pioneered a better berberine, once again based upon a metabolite. It turns out that what little berberine is absorbed by the gut gets turned into its metabolite dihydroberberine first, and then turns back into berberine in the intestine![69]
There’s no better GDA ingredient than berberine, and there’s no better form of berberine than dihydroberberine in NNB’s GlucoVantage!
The solution is simple: simply take dihydroberberine in the first place — and research has shown that dihydroberberine has far greater bioavailability and longer lasting effects – all at a lower dosage required![70,71]
NNB Nutrition named this ingredient GlucoVantage, and it’s a pure dihydroberberine ingredient that’s created from berberis aristata. It brings the potent metabolic benefits of berberine but without the need for high dosages and GI distress.
By adding GlucoVantage to our formula, women can get back to burning fat as opposed to sugar, and that brings numerous health benefits that will span all across the body.
You can read more in our articles titled Berberine: The Best Glucose Disposal Ingredient Just Got Better and GlucoVantage: Dihydroberberine for Superior Insulin Sensitivity. We’ve included it because anyone can benefit from it, and it’s generally only found in dietary supplements, which leaves too many people out.
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CaloriBurn GP (Grains of Paradise extract) – 40mg
Our second metabolic-enhancing ingredient, Grains of Paradise extract brings a unique boost of energy expenditure in a small serving size. Also known as Aframomum melegueta, this member of the ginger family is often used as a delicious spice that serves as a great black pepper alternative, but we like it even more for its metabolic properties.
Inside of grains of paradise, scientists have found four main bioactive compounds that bring its biological prowess: 6-paradol, 6-gingerol, 6-shogaol, and 6-gingerdione.[72] These compounds can stimulate PPAR (peroxisome proliferator-activated receptors), helping to “beige” white fat cells (energy consumers) towards metabolically-active, mitochondrial-dense brown fat cells (which are energy producers). Further, grains of paradise then targets the fat and increases energy expenditure.[73]
Grains of paradise (GP) has been shown to increase nerve activity, boosting core temperature,[74] which could be helpful for women who get cold too easily. It kickstarts the metabolism by forcing the body to work in order to keep the temperature regular.
Brown fat activation: a metabolic boost in humans
In a 2014 study, researchers recruited 19 healthy volunteers, giving one group 30 milligrams of GP extract per day, while another received placebo. After 30 days, the GP group demonstrated significantly increased energy expenditure and decreased visceral fat.[72] The scientists concluded that grains of paradise led to 100 more calories spent per day.
Further research has shown virtually no side effects tied to grains of paradise supplementation.[75]
Little-known mood boosting effects
While we mostly espouse grains of paradise for its metabolic properties, researchers from a 2018 cited an animal study that made “Aframomum melegueta seeds a promising candidate for a menopausal product.“[76] In that study, there was a unique antidepressant-like activity in vivo from the extract.[77] While the researchers didn’t know the direct mechanism, they suspected it to be serotonergic in effect,[77] which is perfect for PMS, menopause, and good mood in general.
CaloriBurn – a standardized, trusted GP extract
Most grains of paradise extracts focus only on the 12.5% 6-paradol concentration, but NNB Nutrition has found that it’s best to keep all bioactive constituents intact. This led them to produce CaloriBurn GP, an industry-leading grains of paradise extract that has 12.5% 6-paradol but also the other three constituents for a full spectrum of metabolic potency, and lab tests to back it up. Other generic grains of paradise extracts tested have not demonstrated peaks at all four levels, making CaloriBurn GP the top shelf grains of paradise ingredient.
At a 40 milligram dosage, we get the clinically-backed effects from two studies (one which used 30 milligrams, the other used 40), and have plenty of room for our other metabolic and hormonal ingredients.
Read more in our articles titled “Grains of Paradise: Fat Fighting Spice of the Goddesses” and “CaloriBurn: NNB Takes Grains of Paradise to Hot New Heights!“.
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AstraGin – 25mg
To further boost the absorption and bioavailability of all ingredients, we’ve chosen to include AstraGin, NuLiv Science’s patented blend of panax notoginseng and astragalus membranaceus.
AstraGin works by boosting gut permeability and upregulating key transport enzymes,[78] helping to get more active ingredients through the digestive tract and into the bloodstream.
Specific to this formula, there’s evidence supporting improved folate and curcumin uptake,[78] which may help with CurcuPrime’s already-improved bioavailability.
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MitoPrime (L-Ergothioneine) – 10mg
Found in mushrooms and organ meats, ergothioneine is the oldest — and most overlooked — energy-supporting immune system booster / antioxidant on the market. Prepare to have your mind blown by this ingredient.
The most fascinating ingredient of the entire formula, we have NNB Nutrition’s MitoPrime L-Ergothioneine. Aside from GlucoVantage, if there were one ingredient we would want every single person to take, it would be this oft-neglected vitamin-like antioxidant.
We originally introduced MitoPrime in our previous Formulator’s Corner segment, where we developed a Health-Enhanced Coffee that utilized the ingredient. There, we chose to use L-ergothionine (which is found in mushrooms and organ meats[79-82]) instead of mushrooms themselves, saving on taste, texture, and dosage. The same benefits will apply here.
In general, we’re including this for immunity, anti-aging, and antioxidant effects, knowing that it’s unlikely you’re getting enough in your diet and nearly no other supplements use it because it is stable L-ergothioneine is so hard to produce and NNB’s MitoPrime is the first of its kind on the market.
An antioxidant that outperforms the others
Research has shown that ergothioneine outperforms the three most popular antioxidants sold in similar supplements — vitamin C, glutathione, and coenzyme Q10.[82-84] In fact, it’s anywhere from 3-30x more effective than them in terms of scavenging free radicals!
Immune system support and anti-aging benefits
Piggybacking on the above effects, researchers have found that ergothioneine boosts the immune system response by speeding up immune response time.[85] It can decrease inflammation, mitigate disease-induced lung damage, protect against acute respiratory distress syndrome, and much more — which is why it’s suggested as a weapon to fight novel cold viruses and respiratory diseases.[86]
Ergothioneine targets various forms of oxidative stress, preventing damage from hydrogen peroxide[87-89] and singlet oxygen.[84] It can protect the body from bromine- and chlorine-induced trauma,[82,90] reduce inflammation-based stress,[82,91-93] and curtail nitrogen-driven stress.[94,95] Through these mechanisms, ergothioneine protects the DNA,[87] making it an incredible anti-aging compound.
We can’t produce it, but we have specific transporters for it!
Even more interesting, although humans cannot synthesize the compound ourselves,[96-99] our bodies contain a unique and specific transporter inamed OCTN1 just for this ergothioneine![87,100,101] The body even bioaccumulates it,[102] pooling it and saving it for when it’s needed to fight an oncoming free radical attack.
Considered a “longevity vitamin” by many
Because of the benefits above and more, many researchers consider ergothioneine to be a “candidate vitamin”.[103,104] They believe that this should have true vitamin status, since it’s so useful and effective but can’t be made by the body — and it’s found in foods we no longer eat much of anymore. The esteemed Dr. Ames even calls it a “longevity vitamin”,[105,106] a name we do not disagree with.
With such a massive list of benefits shown from ergothioneine, why haven’t we heard more about it? This is a must-research immune system supplement ingredient that can protect numerous organ systems.[86]
There’s far more to the history of this ingredient (it has been around far longer than most living organisms, and likely enabled their survival through time) that’s covered in our main L-ergothioneine article, but the point is that this incredible multi-faceted ingredient should not be underestimated.
MitoPrime by NNB Nutrition
As mentioned in the intro, this ingredient is incredibly difficult to create and stabilize, but the “Ingredientology” experts at NNB Nutrition have figured it out, creating MitoPrime. The dosage can be anywhere from 5-10 milligrams 2-3 times per day, for a daily dosage range of 10-30 milligrams.
We’re all for higher doses (especially since the ingredient can be bioaccumulated and thus “loaded”), but 10 milligrams per day should move the needle yet keep the price reasonable.
Meet the next-generation antioxidant ingredient, which is actually the oldest generation antioxidant: MitoPrime from NNB Nutrition!
Note that while there currently haven’t been specific studies on ergothioneine and specific issues like menopause and PMS, one investigation did conclude that higher dietary antioxidant intake is associated with lower menopausal symptoms, with fewer hot flashes, less sweating sleep problems, and reduced anxiety, exhaustion, and brain fog.[107] We firmly believe that MitoPrime can greatly contribute to overall antioxidant capacity, assisting with these issues.
We’ll continue to discuss MitoPrime and ergothioneine over time. For now, we’d love to see it in a women’s formula (any formula, really) because we know it’s so helpful but not in enough women’s diets.
Read more in our article titled “Ergothioneine: The Immunity and Energy Protector“.
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Iodine (as Potassium Iodide) – 300mcg (200% DV)
Our next two inclusions are a mineral and a vitamin that get overlooked far too often, but can have massive benefits in small doses.
Have an ingredient idea? Team NNB will co-develop it with you! The process is known as Ingredientology.
First is iodine, which is critical for thyroid hormone production[108] as well as cognition and fetal development.[109] The thyroid gland is critical for an efficient metabolism,[110] but inadequate iodine intake is one of the main causes of thyroid dysfunction.[111]
We often see iodine in seaweed and used to get much of it in iodized salt and some breads. However, scientists are beginning to see a re-emergence of iodine deficiency.[112] We suspect that this is due to the use of processed foods and gourmet sea salts that are iodine-free, as well as a switch from iodine to bromine in bread as well as fluoride added to tap water, both of which compete with iodine.
Altogether, we believe that this resurgence of iodine deficiency has led to low-level hypothyroidism in our society, leading to weight gain (or trouble losing weight), fatigue, mood swings, and lethargy.
However, we’ve noticed that giving an iodine-deficient individual a small bolus of extra iodine feels like rocket fuel to them, and paired with the RhodioPrime 6X inside, this formula may provide some real stimulant-free energy.
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Folate (as L-5-Methyltetrahydrofolate) – 1.7 mg yielding 1 mg folate (425% DV)
Sometimes known as Vitamin B9, folate is an essential vitamin that is critical for fetal development that has been shown to improve mood.[113,114] It’s often supplemented as folic acid, but when taking it in this form, multiple biologically-expensive steps are required in order to get it into its active form of 5-MTHF, or 5′-methyltetrahydrofolate.[115,116]
To make matters worse, many humans have a genetic predisposition that impairs their ability to generate the active form of folate (due to a downregulated methylenetetrahydrofolate reductase enzyme – thanks primarily to mutations in the MTHFR gene),[117-119] leading to deficiencies, even if supplementing “adequate” amounts of folic acid.
The solution is to simply include the active form ourselves, as L-5-Methyltetrahydrofolate (also known as L-5-methyl-THF), which demonstrates remarkably higher bioavailability.[120,121]
This is an ingredient that should be in your multivitamin, but we simply don’t see it often enough. As with iodine, we’re confident that adding more will do nothing but great things for your health – especially since too many women seem to be deficient.
All that in two capsules? Thanks to NNB and Ingredientology
The goal here is to create the ultimate women’s supplement in two capsules. This is only possible with ingredients like RhodioPrime 6X, GlucoVantage, CaloriBurn GP, MitoPrime, and CurcuPrime from NNB Nutrition, which bring potent benefits in small amounts of space. Combining them with our “standard” women’s ingredients of DIM and Chaste Tree Extract makes this a formula that we’d love to see developed.
Non-stimulatory but experiential
Further, the combination of RhodioPrime 6X, CurcuPrime, iodine, and active folate also lead us to believe that this will be an experiential supplement – even if it’s stimulant-free! If it were developed and taken, we wouldn’t be surprised if its users noticed that they needed less caffeine throughout their days.
Add a multivitamin, magnesium, and fish oil
We understand that there are limits to the number of capsules anyone wants to take. After adding in a multivitamin, minerals (we’re major proponents of high quality magnesium supplementation), and fish oil, most women should be set for the day.
Note that vitamin E (at least 200 IU or 90 milligrams) should be somewhere included in the stack, such as in the multivitamin, as it showed efficacy against post-menopausal hot flashes in the curcumin study.[41] Vitamin E wasn’t as effective as curcumin for hot flashes, but it could still add additional help.
What about gut health? Consider NewBiome next
One additional inclusion that could be considered is gut health. While AstraGin improves gut permeability, we didn’t add additional gut health ingredients because it is highly individual, and not everybody wants or needs massive amounts of probiotics or fatty acids. However, if we venture into that space, we’ll be looking at ingredients like NewBiome, a new form of tributyrin that could combine with additional gut health promoting nutrients.
The unsung hero of this supplement, however, is MitoPrime, whose evolutionary history is so fascinating that we’re wondering how more people aren’t talking about it in the anti-aging, immunity, and beauty spaces. As the saying goes, “sell them what they want, but give them what they need” — and we believe everyone should try this candidate vitamin that has long been neglected by Western diets.

NNB Nutrition is an innovative ingredient development company with an elite team of over 100 scientists from over 10 countries.
It’s all possible with NNB Nutrition, who have taken novel ingredient development to the next level with Ingredientology. As always, all feedback is welcome in the comments below or on PricePlow’s social media outlets.
You can see the rest of our homemade formulas on our Formulator’s Corner page.
References
- Mannucci, C et al. “Serotonin involvement in Rhodiola rosea attenuation of nicotine withdrawal signs in rats.” Phytomedicine : international journal of phytotherapy and phytopharmacology vol. 19,12 (2012): 1117-24. doi:10.1016/j.phymed.2012.07.001. https://pubmed.ncbi.nlm.nih.gov/22921986/
- Cropley, Mark et al. “The Effects of Rhodiola rosea L. Extract on Anxiety, Stress, Cognition and Other Mood Symptoms.” Phytotherapy research : PTR vol. 29,12 (2015): 1934-9. doi:10.1002/ptr.5486. https://pubmed.ncbi.nlm.nih.gov/26502953/
- 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/
- Darbinyan, V et al. “Clinical trial of Rhodiola rosea L. extract SHR-5 in the treatment of mild to moderate depression.” Nordic journal of psychiatry vol. 61,5 (2007): 343-8. doi:10.1080/08039480701643290. https://pubmed.ncbi.nlm.nih.gov/17990195/
- Mao, Jun J., et al. “Rhodiola Rosea versus Sertraline for Major Depressive Disorder: A Randomized Placebo-Controlled Trial.” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology, vol. 22, no. 3, 15 Mar. 2015, pp. 394–399; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4385215/
- Gerbarg, Patricia L., and Richard P. Brown. “Pause Menopause with Rhodiola Rosea, a Natural Selective Estrogen Receptor Modulator.” Phytomedicine, vol. 23, no. 7, June 2016, pp. 763–769, 10.1016/j.phymed.2015.11.013; https://pubmed.ncbi.nlm.nih.gov/26776957/
- 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 : international journal of phytotherapy and phytopharmacology vol. 7,2 (2000): 85-9. doi:10.1016/S0944-7113(00)80078-1. https://pubmed.ncbi.nlm.nih.gov/10839209/
- Darbinyan, V., et al. “Rhodiola Rosea in Stress Induced Fatigue–a Double Blind Cross-over Study of a Standardized Extract SHR-5 with a Repeated Low-Dose Regimen on the Mental Performance of Healthy Physicians during Night Duty.” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology, vol. 7, no. 5, 1 Oct. 2000, pp. 365–371, 10.1016/S0944-7113(00)80055-0; https://pubmed.ncbi.nlm.nih.gov/11081987/
- Hung, Shao Kang, et al. “The Effectiveness and Efficacy of Rhodiola Rosea L.: A Systematic Review of Randomized Clinical Trials.” Phytomedicine, vol. 18, no. 4, Feb. 2011, pp. 235–244, 10.1016/j.phymed.2010.08.014; https://pubmed.ncbi.nlm.nih.gov/21036578/
- Ross, Stephanie Maxine. “Rhodiola Rosea (SHR-5), Part I.” Holistic Nursing Practice, vol. 28, no. 2, 2014, pp. 149–154, 10.1097/hnp.0000000000000014; https://pubmed.ncbi.nlm.nih.gov/24503750/
- Punja, Salima, et al. “Rhodiola Rosea for Mental and Physical Fatigue in Nursing Students: A Randomized Controlled Trial.” PLoS ONE, vol. 9, no. 9, 30 Sept. 2014, p. e108416, 10.1371/journal.pone.0108416; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4182456/
- Kasper, Siegfried, and Angelika Dienel. “Multicenter, Open-Label, Exploratory Clinical Trial with Rhodiola Rosea Extract in Patients Suffering from Burnout Symptoms.” Neuropsychiatric Disease and Treatment, vol. 13, 2017, pp. 889–898, 10.2147/NDT.S120113; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC5370380/
- Lekomtseva, Yevgeniya, et al. “Rhodiola Rosea in Subjects with Prolonged or Chronic Fatigue Symptoms: Results of an Open-Label Clinical Trial.” Complementary Medicine Research, vol. 24, no. 1, 2017, pp. 46–52, 10.1159/000457918; https://www.karger.com/Article/FullText/457918
- Schutgens, F W G, et al. “The Influence of Adaptogens on Ultraweak Biophoton Emission: A Pilot-Experiment.” Phytotherapy Research : PTR, vol. 23, no. 8, 2009, pp. 1103–8, 10.1002/ptr.2753; https://pubmed.ncbi.nlm.nih.gov/19170145/
- De Bock, Katrien et al. “Acute Rhodiola rosea intake can improve endurance exercise performance.” International journal of sport nutrition and exercise metabolism vol. 14,3 (2004): 298-307. doi:10.1123/ijsnem.14.3.298. https://pubmed.ncbi.nlm.nih.gov/15256690/
- Noreen, Eric E., et al. “The Effects of an Acute Dose of Rhodiola Rosea on Endurance Exercise Performance.” Journal of Strength and Conditioning Research, vol. 27, no. 3, 1 Mar. 2013, pp. 839–847, 10.1519/JSC.0b013e31825d9799; https://pubmed.ncbi.nlm.nih.gov/23443221/
- Parisi, A., et al. “Effects of Chronic Rhodiola Rosea Supplementation on Sport Performance and Antioxidant Capacity in Trained Male: Preliminary Results.” The Journal of Sports Medicine and Physical Fitness, vol. 50, no. 1, 1 Mar. 2010, pp. 57–63; https://pubmed.ncbi.nlm.nih.gov/20308973/
- Abidov, M, et al. “Extract of Rhodiola Rosea Radix Reduces the Level of C-Reactive Protein and Creatinine Kinase in the Blood.” Bulletin of Experimental Biology and Medicine, vol. 138, no. 1, 2004, pp. 63–4, 10.1023/b:bebm.0000046940.45382.53; https://pubmed.ncbi.nlm.nih.gov/15514725/
- Lin, C.-H., et al. “Rhodiola Rosea Does Not Reduce in Vivo Inflammatory Activity after Continuous Endurance Exercise.” Science & Sports, vol. 34, no. 2, Apr. 2019, pp. e155–e158, 10.1016/j.scispo.2018.10.006; https://www.sciencedirect.com/science/article/abs/pii/S0765159718303204
- 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/
- Cifani, Carlo et al. “Effect of salidroside, active principle of Rhodiola rosea extract, on binge eating.” Physiology & behavior vol. 101,5 (2010): 555-62. doi:10.1016/j.physbeh.2010.09.006. https://pubmed.ncbi.nlm.nih.gov/20837037/
- 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. 9 425. 24 May. 2018, doi:10.3389/fphar.2018.00425. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976749/
- 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. 9 425. 24 May. 2018, doi:10.3389/fphar.2018.00425. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976749/
- 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. 51,3 (2012): 257-67. doi:10.1002/mc.20780. https://www.ncbi.nlm.nih.gov/pubmed/21520297/
- Naseri, Rozita et al. Nov. 2019. “Comparison of Vitex agnus-castus Extracts with Placebo in Reducing Menopausal Symptoms: A Randomized Double-Blind Study.” Korean Journal of Family Medicine vol. 40,6; 362-67. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887765/
- Rafieian-Kopaei, M. et al. Jan. 2017. “Systematic Review of Premenstrual, Postmenstrual and Infertility Disorders of Vitex Agnus Castus.” Electronic Physician vol. 9,1 3685-89. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308513/
- Cerqueira, R. et al. Oct. 2017. “Vitex Agnus Castus for Premenstrual Syndrome and Premenstrual Dysphoric Disorder: A Systematic Review.” Archives of Women’s Mental Health, vol. 20,6; 713–19. https://pubmed.ncbi.nlm.nih.gov/29063202/
- Panahi, Yunes, et al. “Antioxidant and Anti-Inflammatory Effects of Curcuminoid-Piperine Combination in Subjects with Metabolic Syndrome: A Randomized Controlled Trial and an Updated Meta-Analysis.” Clinical Nutrition, vol. 34, no. 6, Dec. 2015, pp. 1101–1108, 10.1016/j.clnu.2014.12.019; https://pubmed.ncbi.nlm.nih.gov/25618800/
- Lopresti, Adrian L, et al. “Multiple Antidepressant Potential Modes of Action of Curcumin: A Review of Its Anti-Inflammatory, Monoaminergic, Antioxidant, Immune-Modulating and Neuroprotective Effects.” Journal of Psychopharmacology, vol. 26, no. 12, 3 Oct. 2012, pp. 1512–1524, 10.1177/0269881112458732; https://pubmed.ncbi.nlm.nih.gov/23035031/
- Js, Jurenka. “Anti-Inflammatory Properties of Curcumin, a Major Constituent of Curcuma Longa: A Review of Preclinical and Clinical Research.” Alternative Medicine Review : A Journal of Clinical Therapeutic, 1 June 2009; https://pubmed.ncbi.nlm.nih.gov/19594223/
- Agarwal, Krishna Adit, et al. “Efficacy of Turmeric (Curcumin) in Pain and Postoperative Fatigue after Laparoscopic Cholecystectomy: A Double-Blind, Randomized Placebo-Controlled Study.” Surgical Endoscopy, vol. 25, no. 12, 14 June 2011, pp. 3805–3810, 10.1007/s00464-011-1793-z; https://pubmed.ncbi.nlm.nih.gov/21671126/
- Nakagawa, Yasuaki, et al. “Short-Term Effects of Highly-Bioavailable Curcumin for Treating Knee Osteoarthritis: A Randomized, Double-Blind, Placebo-Controlled Prospective Study.” Journal of Orthopaedic Science, vol. 19, no. 6, Nov. 2014, pp. 933–939, 10.1007/s00776-014-0633-0; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4244558/
- Panda, Sanjib kumar, et al. “A Randomized, Double Blind, Placebo Controlled, Parallel-Group Study to Evaluate the Safety and Efficacy of Curene versus Placebo in Reducing Symptoms of Knee OA.” BioMed Research International, vol. 2018, 25 Oct. 2018, pp. 1–8, 10.1155/2018/5291945; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC6222223/
- Tabrizi, Reza, et al. “The Effects of Curcumin on Glycemic Control and Lipid Profiles among Patients with Metabolic Syndrome and Related Disorders: A Systematic Review and Metaanalysis of Randomized Controlled Trials.” Current Pharmaceutical Design, vol. 24, no. 27, 3 Dec. 2018, pp. 3184–3199, 10.2174/1381612824666180828162053; https://pubmed.ncbi.nlm.nih.gov/30156145/
- Altobelli, Emma, et al. “Potential Therapeutic Effects of Curcumin on Glycemic and Lipid Profile in Uncomplicated Type 2 Diabetes—a Meta-Analysis of Randomized Controlled Trial.” Nutrients, vol. 13, no. 2, 27 Jan. 2021, p. 404, 10.3390/nu13020404; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7912109/
- Qin, Si, et al. “Efficacy and Safety of Turmeric and Curcumin in Lowering Blood Lipid Levels in Patients with Cardiovascular Risk Factors: A Meta-Analysis of Randomized Controlled Trials.” Nutrition Journal, vol. 16, no. 1, 11 Oct. 2017, 10.1186/s12937-017-0293-y; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC5637251/
- Fusar-Poli, Laura, et al. “Curcumin for Depression: A Meta-Analysis.” Critical Reviews in Food Science and Nutrition, 2019, pp. 1–11, 10.1080/10408398.2019.1653260; https://pubmed.ncbi.nlm.nih.gov/31423805/
- Ng, Qin Xiang, et al. “Clinical Use of Curcumin in Depression: A Meta-Analysis.” Journal of the American Medical Directors Association, vol. 18, no. 6, June 2017, pp. 503–508, 10.1016/j.jamda.2016.12.071; https://pubmed.ncbi.nlm.nih.gov/28236605/
- Hallajzadeh, Jamal, et al. “The Effects of Curcumin Supplementation on Endothelial Function: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.” Phytotherapy Research: PTR, vol. 33, no. 11, 1 Nov. 2019, pp. 2989–2995, 10.1002/ptr.6477; https://pubmed.ncbi.nlm.nih.gov/31423626/
- Khayat, Samira, et al. “Curcumin Attenuates Severity of Premenstrual Syndrome Symptoms: A Randomized, Double-Blind, Placebo-Controlled Trial.” Complementary Therapies in Medicine, vol. 23, no. 3, 1 June 2015, pp. 318–324, 10.1016/j.ctim.2015.04.001; https://pubmed.ncbi.nlm.nih.gov/26051565/
- Zhang, Zhiguo, et al. “Effect of Curcumin on the Diversity of Gut Microbiota in Ovariectomized Rats.” Nutrients, vol. 9, no. 10, 19 Oct. 2017, 10.3390/nu9101146; https://pubmed.ncbi.nlm.nih.gov/29048369/
- Anand, Preetha et al; “Bioavailability of curcumin: problems and promises.” Molecular pharmaceutics vol. 4,6; 2007; 807-18; https://pubmed.ncbi.nlm.nih.gov/17999464/
- Holder, G M et al; “The metabolism and excretion of curcumin (1,7-bis-(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) in the rat.”; Xenobiotica: the fate of foreign compounds in biological systems; vol. 8,12; 1978; 761-8; https://pubmed.ncbi.nlm.nih.gov/726520/
- Aggarwal, Bharat B et al; “Curcumin differs from tetrahydrocurcumin for molecular targets, signaling pathways and cellular responses.”; Molecules (Basel, Switzerland); vol. 20,1; 185-205; 24 Dec. 2014; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272158/
- Somparn, Poorichaya et al; “Comparative antioxidant activities of curcumin and its demethoxy and hydrogenated derivatives.”; Biological & pharmaceutical bulletin; vol. 30,1; 2007; 74-8; https://pubmed.ncbi.nlm.nih.gov/17202663/
- Khopde, S M et al; “Inhibition of radiation-induced lipid peroxidation by tetrahydrocurcumin: possible mechanisms by pulse radiolysis.”; Bioscience, biotechnology, and biochemistry; vol. 64,3; 2000; 503-9; https://pubmed.ncbi.nlm.nih.gov/10803946/
- Murugan, Pidaran, and Leelavinothan Pari; “Antioxidant effect of tetrahydrocurcumin in streptozotocin-nicotinamide induced diabetic rats.”; Life sciences; vol. 79,18; 2006; 1720-8; https://pubmed.ncbi.nlm.nih.gov/16806281/
- Khopde, S M et al; “Inhibition of radiation-induced lipid peroxidation by tetrahydrocurcumin: possible mechanisms by pulse radiolysis.”; Bioscience, biotechnology, and biochemistry; vol. 64,3; 2000; 503-9; https://pubmed.ncbi.nlm.nih.gov/10803946/
- Naito, Michitaka et al; “The protective effects of tetrahydrocurcumin on oxidative stress in cholesterol-fed rabbits.”; Journal of atherosclerosis and thrombosis; vol. 9,5; 2002; 243-50; https://pubmed.ncbi.nlm.nih.gov/12409634/
- Nakmareong S, et al; “Antioxidant and vascular protective effects of curcumin and tetrahydrocurcumin in rats with L-NAME-induced hypertension”; Naunyn Schmiedebergs Arch Pharmacol; 383(5):519-29; May 2011; doi: 10.1007/s00210-011-0624-z; https://pubmed.ncbi.nlm.nih.gov/21448566/
- Balunas, M. et al. Aug. 2008. “Natural Products as Aromatase Inhibitors.” Anti-cancer Agents in Medicinal Chemistry vol. 8,6; 646-82. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3074486/
- Jellinck, P. et al. Mar. 1993. “Ah Receptor Binding Properties of Indole Carbinols and Induction of Hepatic Estradiol Hydroxylation.” Biochemical Pharmacology vol. 45,5; 1129-36. https://pubmed.ncbi.nlm.nih.gov/8384853
- Rajoria, S. et al. Mar. 2011. “3,3′-Diindolylmethane Modulates Estrogen Metabolism in Patients with Thyroid Proliferative Disease: A Pilot Study.” Thyroid vol. 21,3; 299-304. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048776/
- Thomson, C. et al. July 2016. “Chemopreventive Properties of 3,3′-Diindolylmethane in Breast Cancer: Evidence From Experimental and Human Studies.” Nutrition Reviews vol. 74,7; 432-43. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059820/
- Li, Yun, et al; “Activation of AMPK by Berberine Promotes Adiponectin Multimerization in 3T3-L1 Adipocytes.”; FEBS Letters; U.S. National Library of Medicine; 23 June 2011; https://www.ncbi.nlm.nih.gov/pubmed/21536037
- Yin, Jun et al; “Efficacy of berberine in patients with type 2 diabetes mellitus.”; Metabolism: clinical and experimental; vol. 57,5; 2008; 712-7; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410097/
- Caliceti, Cristiana, et al. “Potential Benefits of Berberine in the Management of Perimenopausal Syndrome.” Oxidative Medicine and Cellular Longevity, vol. 2015, 2015, 10.1155/2015/723093; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4346702/
- Kong, L. D., et al. “Monoamine Oxidase Inhibitors from Rhizoma of Coptis Chinensis.” Planta Medica, vol. 67, no. 1, 1 Feb. 2001, pp. 74–76, 10.1055/s-2001-10874; https://pubmed.ncbi.nlm.nih.gov/11270727/
- Turner, Nigel, et al; “Berberine and Its More Biologically Available Derivative, Dihydroberberine, Inhibit Mitochondrial Respiratory Complex I: a Mechanism for the Action of Berberine to Activate AMP-Activated Protein Kinase and Improve Insulin Action.”; Diabetes; U.S. National Library of Medicine; May 2008; https://www.ncbi.nlm.nih.gov/pubmed/18285556
- Chen, Chunhua, et al; “Berberine Inhibits PTP1B Activity and Mimics Insulin Action.”; Biochemical and Biophysical Research Communications; U.S. National Library of Medicine; 2 July 2010; https://www.ncbi.nlm.nih.gov/pubmed/20515652
- Richter, Erik A, and Neil B Ruderman; “AMPK and the biochemistry of exercise: implications for human health and disease.”; The Biochemical journal; vol. 418,2; 2009; 261-75; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779044/
- Zhang, Hao, et al; “Berberine Lowers Blood Glucose in Type 2 Diabetes Mellitus Patients through Increasing Insulin Receptor Expression.”; Metabolism: Clinical and Experimental; U.S. National Library of Medicine; Feb. 2010; https://www.ncbi.nlm.nih.gov/pubmed/19800084
- Kong, Wei-Jia, et al; “Berberine Reduces Insulin Resistance through Protein Kinase C-Dependent up-Regulation of Insulin Receptor Expression.”; Metabolism: Clinical and Experimental; U.S. National Library of Medicine; Jan. 2009; https://www.ncbi.nlm.nih.gov/pubmed/19059538
- Yang, Jing et al; “Berberine improves insulin sensitivity by inhibiting fat store and adjusting adipokines profile in human preadipocytes and metabolic syndrome patients.”; Evidence-based complementary and alternative medicine : eCAM; vol. 2012; 2012; 363845; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310165/
- Cecil, Chad E., et al. “Inhibition of H1N1 Influenza a Virus Growth and Induction of Inflammatory Mediators by the Isoquinoline Alkaloid Berberine and Extracts of Goldenseal (Hydrastis Canadensis).” International Immunopharmacology, vol. 11, no. 11, 1 Nov. 2011, pp. 1706–1714, 10.1016/j.intimp.2011.06.002; https://pubmed.ncbi.nlm.nih.gov/21683808/
- Pan, Guo-yu, et al. “[Inhibitory Action of Berberine on Glucose Absorption].” Yao Xue Xue Bao = Acta Pharmaceutica Sinica, vol. 38, no. 12, 1 Dec. 2003, pp. 911–914; https://pubmed.ncbi.nlm.nih.gov/15040083/
- Maeng, Han-Joo, et al. “P-Glycoprotein-Mediated Transport of Berberine across Caco-2 Cell Monolayers.” Journal of Pharmaceutical Sciences, vol. 91, no. 12, 1 Dec. 2002, pp. 2614–2621, 10.1002/jps.10268; https://pubmed.ncbi.nlm.nih.gov/12434406/
- Chen, Wei, et al. “Bioavailability Study of Berberine and the Enhancing Effects of TPGS on Intestinal Absorption in Rats.” AAPS PharmSciTech, vol. 12, no. 2, 1 June 2011, p. 705, 10.1208/s12249-011-9632-z; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3134654/
- Feng, Ru, et al; “Transforming Berberine into Its Intestine-Absorbable Form by the Gut Microbiota.”; Nature News; Nature Publishing Group; 15 July 2015; https://www.nature.com/articles/srep12155
- Turner, Nigel, et al; “Berberine and Its More Biologically Available Derivative, Dihydroberberine, Inhibit Mitochondrial Respiratory Complex I: a Mechanism for the Action of Berberine to Activate AMP-Activated Protein Kinase and Improve Insulin Action.”; Diabetes; U.S. National Library of Medicine; May 2008; https://www.ncbi.nlm.nih.gov/pubmed/18285556
- Mohammad, Mohammad, et al; “Inhibition of pancreatic lipase by berberine and dihydroberberine: An investigation by docking simulation and experimental validation.”; Medicinal Chemistry Research; 22(5); April 2013; 2273-2278; https://www.researchgate.net/publication/255979651_Inhibition_of_pancreatic_lipase_by_berberine_and_dihydroberberine_An_investigation_by_docking_simulation_and_experimental_validation
- Sugita, Jun, et al. “Daily Ingestion of Grains of Paradise (Aframomum Melegueta) Extract Increases Whole-Body Energy Expenditure and Decreases Visceral Fat in Humans.” Journal of Nutritional Science and Vitaminology, vol. 60, no. 1, 2014, pp. 22–27, 10.3177/jnsv.60.22. https://www.jstage.jst.go.jp/article/jnsv/60/1/60_22/_pdf
- Hattori, Hiroyuki, et al. “Effect of Grains of Paradise (GP) Extract Intake on Obesity and Sympathetic Nerve Activity.” American Journal of Plant Sciences, vol. 08, no. 02, 2017, pp. 85–95, 10.4236/ajps.2017.82007. https://www.scirp.org/journal/paperinformation.aspx?paperid=73586
- Iwami, Momoe, et al. “Extract of Grains of Paradise and its Active Principle 6-Paradol Trigger Thermogenesis of Brown Adipose Tissue in Rats.” Autonomic Neuroscience: Basic & Clinical, vol. 161, no. 1-2, 26 April 2011, pp. 63-67, 10.1016/j.autneu.2010.11.012. https://www.autonomicneuroscience.com/article/S1566-0702(10)00277-8/fulltext
- Ilic, Nebojsa, et al. “Toxicological Evaluation of Grains of Paradise (Aframomum Melegueta) [Roscoe] K. Schum.” Journal of Ethnopharmacology, vol. 127, no. 2, Feb. 2010, pp. 352–356, 10.1016/j.jep.2009.10.031. https://www.ncbi.nlm.nih.gov/pubmed/19883745
- López-Ríos, Laura, et al. “Influence of a New Botanical Combination on Quality of Life in Menopausal Spanish Women: Results of a Randomized, Placebo-Controlled Pilot Study.” PLoS ONE, vol. 16, no. 7, 2021, 10.1371/journal.pone.0255015; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC8294509/
- Ojo, Esther Toluwalope, et al. “Psychopharmacological Evaluation of Antidepressant-like Activity of Ethanol Seed Extract of Grains of Paradise (Aframomum MeleguetaK. Schum.)in Mice.” Journal of Food Biochemistry, vol. 42, no. 4, 21 Feb. 2018, p. e12528, 10.1111/jfbc.12528; https://onlinelibrary.wiley.com/doi/10.1111/jfbc.12528
- NuLiv Science; AstraGin Product Dossier; https://docdro.id/rA01t9O
- Janine Ey, Edgar Schömig, and Dirk Taubert; “Dietary Sources and Antioxidant Effects of Ergothioneine.”; Dietary Sources and Antioxidant Effects of Ergothioneine; Journal of Agricultural and Food Chemistry; https://pubs.acs.org/doi/10.1021/jf071328f
- Dubost, et al; “Identification and Quantification of Ergothioneine in Cultivated Mushrooms by Liquid Chromatography-Mass Spectroscopy”; International Journal of Medicinal Mushrooms; 8(3):215-222; January 2006; https://www.researchgate.net/publication/270471344_Identification_and_Quantification_of_Ergothioneine_in_Cultivated_Mushrooms_by_Liquid_Chromatography-Mass_Spectroscopy
- Beelman, Robert; “Ergothioneine in Mushrooms-Nature’s Best Source of a New Human Vitamin?”; Penn State University; https://web.archive.org/web/20171028014650/https://plantpath.psu.edu/mushroom-industry-conference/52-mushroom-industry-conference/Bob%20Beelman.pdf
- Asahi, T, et al; “A mushroom-derived amino acid, ergothioneine, is a potential inhibitor of inflammation-related DNA halogenation”; Bioscience, Biotechnology, and Biochemistry; 80(2):313-7; 2016; https://www.tandfonline.com/doi/full/10.1080/09168451.2015.1083396
- Dong KK, Damaghi N, Kibitel J, Canning MT, Smiles KA, Yarosh DBl; “A comparison of the relative antioxidant potency of L‐ergothioneine and idebenone”; Journal of Cosmetic Dermatology; Volume 6, Issue 3, Pages 183-188; September 2007; https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1473-2165.2007.00330.x
- Rougee, M., et al; “Deactivation of Singlet Molecular Oxygen by Thiols and Related Compounds, Possible Protectors Against Skin Photosensitivity”; Photochemistry and Photobiology; Volume 47, Issue 4; April 1988; https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1751-1097.1988.tb08835.x
- Yoshida, Sumito et al. “The Anti-Oxidant Ergothioneine Augments the Immunomodulatory Function of TLR Agonists by Direct Action on Macrophages.” PloS one vol. 12,1 e0169360. 23 Jan. 2017, doi:10.1371/journal.pone.0169360; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256913/
- Cheah, Irwin K, and Barry Halliwell. “Could Ergothioneine Aid in the Treatment of Coronavirus Patients?.” Antioxidants (Basel, Switzerland) vol. 9,7 595. 7 Jul. 2020, doi:10.3390/antiox9070595; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402156/
- Paul, B D, and S H Snyder; “The unusual amino acid L-ergothioneine is a physiologic cytoprotectant.”; Cell death and differentiation; vol. 17,7; 2010; 1134-40; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885499/
- Dong, Kelly, et al; “L-ergothioneine reduces UVA340-induced hydrogen peroxide in fibroblasts more efficiently than idebenone”; Journal of American Academy of Dermatology; Volume 56, Issue 2, Supplement 2, Page AB86; February 2007; https://www.jaad.org/article/S0190-9622(06)03265-8/fulltext
- Colognato, R, et al; “Modulation of hydrogen peroxide-induced DNA damage, MAPKs activation and cell death in PC12 by ergothioneine”; Clinical Nutrition; 25(1):135-45; February 2006; https://pubmed.ncbi.nlm.nih.gov/16314005
- Akanmu, D, et al; “The antioxidant action of ergothioneine”; Archives of Biochemistry and Biophysics; 288(1):10-6; July 1991; https://pubmed.ncbi.nlm.nih.gov/1654816
- Incoronata Laurenza, et al; “Modulation of palmitic acid‐induced cell death by ergothioneine: Evidence of an anti‐inflammatory action”; BioFactors; Volume 33, Issue 4; August 19, 2009; https://iubmb.onlinelibrary.wiley.com/doi/abs/10.1002/biof.5520330401
- Rahman, Irfan, et al; “Ergothioneine inhibits oxidative stress- and TNF-alpha-induced NF-kappa B activation and interleukin-8 release in alveolar epithelial cells”; Biochemical and Biophysical Research Communications; Volume 302, Issue 4, Pages 860-864; 21 March 2003; https://www.sciencedirect.com/science/article/abs/pii/S0006291X03002249
- Song, Tuzz-Ying et al; “Protective Effects and Possible Mechanisms of Ergothioneine and Hispidin against Methylglyoxal-Induced Injuries in Rat Pheochromocytoma Cells”; Oxidative Medicine and Cellular Longevity; vol. 2017: 4824371; October 17, 2017; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664345/
- Aruoma, Ol, et al; “Antioxidant action of ergothioneine: assessment of its ability to scavenge peroxynitrite”; Biochemical and Biophysical Research Communications; 231(2):389-91; February 13, 1997; https://pubmed.ncbi.nlm.nih.gov/9070285
- Franzoni, F, et al; “An in vitro study on the free radical scavenging capacity of ergothioneine: comparison with reduced glutathione, uric acid and trolox”; Biomedical & Pharmacotherapy; 60(8):453-7; September 2006; https://pubmed.ncbi.nlm.nih.gov/16930933
- Eagles, Blythe Alfred, Vars, Harry M; “The Physiology of Ergothioneine”; The Journal of Biological Chemistry; 80, 615-622; December 1, 1928; https://www.jbc.org/content/80/2/615.long
- Melville, Donald, Horner, William, and Lubschez, Rose; “Tissue Ergothioneine”; The Journal of Biological Chemistry; 206, 221-228; January 1, 1954; https://www.jbc.org/content/206/1/221.long
- Melville, Donald, et al; “On the Origin of Animal Ergothioneine”; The Journal of Biological Chemistry; 216, 325-331; September 1, 1955; https://www.jbc.org/content/216/1/325.long
- Melville, Donald, et al; “The Occurrence of Ergothioneine in Plant Material”; The Journal of Biological Chemistry; 218, 647-651; February 1, 1957; https://www.jbc.org/content/218/2/647.long
- Gründemann, Dirk, et al; “Discovery of the Ergothioneine Transporter.”; PNAS; National Academy of Sciences; 5 Apr. 2005; https://www.pnas.org/content/102/14/5256
- Cheah, Irwin K, and Barry Halliwell; “Ergothioneine; Antioxidant Potential, Physiological Function and Role in Disease.”; Biochimica Et Biophysica Acta; U.S. National Library of Medicine; May 2012; https://www.sciencedirect.com/science/article/pii/S0925443911002201
- Evans, Joseph L; “Report 174-001. Foundational properties at the cellular level.”; NIS Labs; May 7, 2021; https://blog.priceplow.com/wp-content/uploads/nnb-ergothioneine-report-114-001-in_vitro_testing-20210507.pdf
- Stoffels, Christopher, et al; “Ergothioneine stands out from hercynine in the reaction with singlet oxygen: Resistance to glutathione and TRIS in the generation of specific products indicates high reactivity”; Free Radical Biology and Medicine; Volume 113, Pages 385-394; December 2017; https://www.sciencedirect.com/science/article/abs/pii/S0891584917311553
- Rice-Evans, C A, and A T Diplock; “Current Status of Antioxidant Therapy.”; Free Radical Biology & Medicine; U.S. National Library of Medicine; July 1993; https://pubmed.ncbi.nlm.nih.gov/8359712/
- Ames, Bruce N. “Prolonging healthy aging: Longevity vitamins and proteins.” Proceedings of the National Academy of Sciences of the United States of America vol. 115,43 (2018): 10836-10844. doi:10.1073/pnas.1809045115; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205492/
- Beelman, Robert B., et al. “Is Ergothioneine a ‘Longevity Vitamin’ Limited in the American Diet?” Journal of Nutritional Science, vol. 9, 2020, 10.1017/jns.2020.44; https://www.cambridge.org/core/journals/journal-of-nutritional-science/article/is-ergothioneine-a-longevity-vitamin-limited-in-the-american-diet/31B9A91CEB3A61C8F72CCFD56B85704E#
- Abshirini, Maryam, et al. “Dietary Total Antioxidant Capacity Is Inversely Related to Menopausal Symptoms: A Cross-Sectional Study among Iranian Postmenopausal Women.” Nutrition, vol. 55-56, Nov. 2018, pp. 161–167, 10.1016/j.nut.2018.04.014; https://www.sciencedirect.com/science/article/abs/pii/S089990071830371X
- Schlienger, J. L., et al. “Iodine and Thyroid Function.” La Revue de Medecine Interne, vol. 18, no. 9, 1997, pp. 709–716, 10.1016/S0248-8663(97)83750-2; https://pubmed.ncbi.nlm.nih.gov/9365722/
- Luton, Dominique, et al. “Iodine Deficiency in Northern Paris Area: Impact on Fetal Thyroid Mensuration.” PLoS ONE, vol. 6, no. 2, 2011, 10.1371/journal.pone.0014707; https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3040245/
- 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/labs/pmc/articles/PMC4044302/
- S, Zbigniew. “Role of Iodine in Metabolism.” Recent Patents on Endocrine, Metabolic & Immune Drug Discovery, 2017; https://pubmed.ncbi.nlm.nih.gov/28103777/
- 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
- Godfrey, P.S.A, et al. “Enhancement of Recovery from Psychiatric Illness by Methylfolate.” The Lancet, vol. 336, no. 8712, Aug. 1990, pp. 392–395, 10.1016/0140-6736(90)91942-4; https://pubmed.ncbi.nlm.nih.gov/1974941/
- Taylor, Matthew J, et al. “Folate for Depressive Disorders.” Cochrane Database of Systematic Reviews, 22 Apr. 2003, 10.1002/14651858.cd003390; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991158/
- Miller, Alan L. “The Methylation, Neurotransmitter, and Antioxidant Connections between Folate and Depression.” Alternative Medicine Review: A Journal of Clinical Therapeutic, vol. 13, no. 3, 1 Sept. 2008, pp. 216–226; https://pubmed.ncbi.nlm.nih.gov/18950248/
- Bhargava, Seema, and S. C. Tyagi. “Nutriepigenetic Regulation by Folate-Homocysteine-Methionine Axis: A Review.” Molecular and Cellular Biochemistry, vol. 387, no. 1-2, 1 Feb. 2014, pp. 55–61, 10.1007/s11010-013-1869-2; https://pubmed.ncbi.nlm.nih.gov/24213682/
- Gilbody, S., et al. “Methylenetetrahydrofolate Reductase (MTHFR) Genetic Polymorphisms and Psychiatric Disorders: A HuGE Review.” American Journal of Epidemiology, vol. 165, no. 1, 13 Oct. 2006, pp. 1–13, 10.1093/aje/kwj347; https://academic.oup.com/aje/article/165/1/1/232658
- Rozen, R. “Molecular Genetics of Methylenetetrahydrofolate Reductase Deficiency.” Journal of Inherited Metabolic Disease, vol. 19, no. 5, 1996, pp. 589–594, 10.1007/BF01799831; https://pubmed.ncbi.nlm.nih.gov/8892013/
- Lievers, Karin J., et al. “A Second Common Variant in the Methylenetetrahydrofolate Reductase (MTHFR) Gene and Its Relationship to MTHFR Enzyme Activity, Homocysteine, and Cardiovascular Disease Risk.” Journal of Molecular Medicine, vol. 79, no. 9, 5 July 2001, pp. 522–528, 10.1007/s001090100253; https://pubmed.ncbi.nlm.nih.gov/11692165/
- Pietrzik, Klaus, et al. “Folic Acid and L-5-Methyltetrahydrofolate.” Clinical Pharmacokinetics, vol. 49, no. 8, Aug. 2010, pp. 535–548, 10.2165/11532990-000000000-00000; https://pubmed.ncbi.nlm.nih.gov/20608755/
- Willems, Frank F, et al. “Pharmacokinetic Study on the Utilisation of 5-Methyltetrahydrofolate and Folic Acid in Patients with Coronary Artery Disease.” British Journal of Pharmacology, vol. 141, no. 5, 1 Mar. 2004, pp. 825–830, 10.1038/sj.bjp.0705446; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1574248/