Your Body Is Hoarding Your Testosterone. Here's How to Get It Back. Prime Choice

Your Body Is Hoarding Your Testosterone. Here's How to Get It Back.

Total testosterone is only part of the story. If it's bound to SHBG or being converted to estrogen, your body can't use it. Here's how to fix both problems at once.

By Amanda, BSc Exercise Science | Prime Choice Club

In Part 1 of this series we covered the foundational science of testosterone: why it matters for muscle, energy, mood, cognitive function, and metabolic health in both men and women, and how chronic blood sugar instability and the cortisol cascade actively suppress it through the pregnenolone steal mechanism.

If you haven't read Part 1 I'd encourage you to start there. But for those who have, this is the part of the conversation that most testosterone content never gets to, and it's often the reason people try testosterone support supplements and get disappointing results.

Here's the thing most single-product testosterone formulas miss: optimizing testosterone is a two-problem equation. The first problem is production: are you making enough? The second problem is bioavailability: is the testosterone you're making actually free and available to receptors, or is it bound up in a protein that renders it useless, or being converted to estrogen by an enzyme that's running too hot?

Both problems are real. Both are common, especially after 35. And they require different interventions. This is why Test Ultra and Alpha Drive work best as a stack rather than individually: one addresses production, the other addresses availability and protection. Together they cover the full equation.

Total testosterone is what gets measured. Free testosterone is what actually works. If your SHBG is high or your aromatase activity is elevated, the gap between those two numbers is where your results are disappearing.

 

THE TWO-PROBLEM FRAMEWORK

Think of your testosterone system as a pipeline with two potential failure points.
Failure point one is upstream: not enough testosterone is being produced. This is the LH signaling problem. Luteinizing hormone from the pituitary gland tells the Leydig cells in the testes (in men) and the theca cells in the ovaries (in women) to produce testosterone. When that signal is suppressed, whether by chronic cortisol from the pregnenolone steal, by nutrient deficiencies in the minerals required for steroidogenesis, or by simple age-related decline in HPG axis sensitivity, production falls. This is what most testosterone supplements address.

Failure point two is downstream: testosterone is being produced but isn't reaching its receptors in a usable form. This happens through two mechanisms. First, sex hormone-binding globulin (SHBG): a protein produced by the liver that binds tightly to testosterone and renders it biologically inactive. Testosterone bound to SHBG cannot interact with androgen receptors. Only free testosterone and loosely albumin-bound testosterone are bioavailable. When SHBG is elevated, which chronic stress, excess estrogen, thyroid dysfunction, and aging all promote, total testosterone can look normal on a lab test while free testosterone is critically low. Second, aromatase: the enzyme that converts testosterone (and androstenedione) to estrogens. Elevated aromatase activity, which occurs with increased body fat (particularly abdominal fat), chronic inflammation, and high cortisol, continuously converts the testosterone being produced into estrogen, compounding the hormonal imbalance in both men and women.

A formula that only addresses production without addressing SHBG binding and aromatase activity is solving half the problem. The Test Ultra and Alpha Drive stack addresses both halves with ingredients specifically chosen for each mechanism.

TEST ULTRA: THE PRODUCTION LAYER

Test Ultra is the upstream formula. Its job is to support the production of testosterone through the HPG axis, provide the essential mineral foundation that steroidogenesis requires, and deliver botanicals that support LH signaling and the hormonal environment that allows the testes and ovaries to produce testosterone efficiently.

Three capsules per day provides:

Magnesium (as Magnesium Oxide, 200mg | 48% DV)
Magnesium is one of the most important minerals for testosterone production and one of the most common deficiencies in active adults. Research published in Biological Trace Element Research found that magnesium supplementation significantly increased both free and total testosterone in athletes and sedentary subjects after four weeks. Magnesium's role is mechanistic: it is required for the enzymatic reactions that convert cholesterol to pregnenolone (the first step in steroid hormone synthesis), and it modulates SHBG's binding affinity for testosterone, effectively reducing how tightly SHBG holds onto testosterone when magnesium levels are adequate. The 200mg dose here works in concert with Alpha Drive's downstream SHBG-targeting ingredients for a complete approach.

Zinc (as Zinc Oxide, 30mg | 273% DV)
Zinc at 273% of the daily value is a genuinely therapeutic dose targeted at one of the most well-documented mineral-hormone relationships in sports science. Zinc is required for the activity of the LH receptor in Leydig cells and for the enzyme 5-alpha reductase that produces DHT. Research by Prasad et al. published in Nutrition found that zinc-restricted men experienced dramatic reductions in testosterone, and that zinc supplementation restored levels. Zinc also inhibits aromatase, the enzyme that converts testosterone to estrogen, providing an additional layer of estrogen control from the mineral foundation. For anyone training hard and sweating regularly, zinc losses through sweat are significant and daily replenishment is not optional.

Tribulus terrestris fruit (750mg)
At 750mg this is the highest-dosed botanical in the Test Ultra formula and the one with the longest documented history of use for male vitality. Tribulus's primary proposed mechanism is increasing the concentration of luteinizing hormone (LH), the pituitary signal that tells the gonads to produce testosterone. Research published in the Journal of Alternative and Complementary Medicine found significant effects on LH levels and sexual function. The fruit extract specifically, rather than the root or aerial parts, contains the highest concentration of protodioscin, the primary active saponin associated with LH stimulation. At 750mg this formula is delivering a dose consistent with the research showing the most meaningful hormonal effects.

Chrysin (Oroxylum indicum seed, 75mg)
Chrysin is a flavone with documented aromatase-inhibiting activity. Research published in Science by Kellis and Vickery confirmed chrysin's ability to inhibit human estrogen synthetase (aromatase) in vitro. By reducing aromatase activity, chrysin helps prevent the conversion of testosterone to estrogen, keeping more of the testosterone being produced in its active androgenic form. Notably, chrysin appears in both Test Ultra and Alpha Drive's EstroControl Blend, reinforcing the aromatase inhibition mechanism from both products in the stack. The combined chrysin dose across both formulas strengthens this protective effect.

Epimedium (Horny Goat Weed, Epimedium sagittatum aerial, 50mg)
Epimedium's primary active compound, icariin, is a potent PDE5 inhibitor, the same mechanism targeted by pharmaceutical erectile dysfunction medications. Beyond vascular effects, icariin has documented effects on testosterone and has been shown in research to support androgen receptor expression. Research published in Urology documented epimedium's effects on testosterone signaling and sexual function. For women, epimedium supports androgen activity relevant to libido, bone density, and the muscular and cognitive benefits of adequate testosterone.

Tongkat Ali (Eurycoma longifolia root, 50mg)
Tongkat Ali is the most well-studied natural testosterone support botanical in Southeast Asian medicine. A randomized controlled trial published in Andrologia found that standardized Tongkat Ali extract significantly improved testosterone levels and quality of life scores in men with late-onset hypogonadism. A separate study published in the Journal of the International Society of Sports Nutrition found that Tongkat Ali reduced cortisol by 16% and increased testosterone by 37% in moderately stressed subjects over four weeks. Both effects are relevant: direct testosterone support and cortisol reduction address the pregnenolone steal mechanism we covered in Part 3 of the blood sugar series. Tongkat Ali appears in both Test Ultra and Alpha Drive's TestSupport Blend, making the combined dose across the stack more meaningful.

Saw Palmetto Berries (Serenoa repens, 50mg)
Saw palmetto inhibits 5-alpha reductase, the enzyme that converts testosterone to DHT. This has two relevant effects. First, it modulates DHT levels, which is relevant for men concerned about androgenic side effects of elevated testosterone. Second, saw palmetto has documented effects on estrogen signaling, supporting a favorable testosterone-to-estrogen ratio. Its inclusion alongside chrysin creates a complementary protective layer: chrysin addresses aromatase (testosterone-to-estrogen conversion), saw palmetto addresses 5-alpha reductase (testosterone-to-DHT conversion), allowing more testosterone to remain in its free, bioavailable form.

Chinese Hawthorn Berries (Crataegus pinnatifida, 50mg)
Hawthorn provides cardiovascular and circulatory support that complements the testosterone optimization goal directly. Adequate testosterone depends on robust blood flow to the gonads and adequate oxygen and nutrient delivery to Leydig cells. Hawthorn's vasodilatory and heart rate variability-improving effects also support the parasympathetic nervous system tone that allows the HPG axis to operate without being suppressed by the sympathetic stress response.

Winged Treebine (Cissus quadrangularis stem, 50mg)
Cissus quadrangularis contains phytosterols including beta-ecdysterone, compounds with documented anabolic effects on muscle protein synthesis. Research has shown Cissus to improve recovery from resistance training and support lean mass maintenance. It appears in both Test Ultra and Alpha Drive's TestSupport Blend, reinforcing the anabolic support layer across the stack. Its anti-inflammatory properties also reduce the chronic low-grade inflammation that suppresses HPG axis function.

ALPHA DRIVE: THE BIOAVAILABILITY AND PROTECTION LAYER

Alpha Drive is the downstream formula. Its three blends work synergistically to address the second failure point: making the testosterone that Test Ultra supports more bioavailable, protecting it from conversion to estrogen, and supporting the liver function that hormone clearance depends on.

Two capsules per day across three targeted blends:

EstroControl Blend  105mg  |  Aromatase inhibition and estrogen metabolism
Indole-3-Carbinol (I3C)
I3C is one of the most researched natural estrogen metabolism modulators available. Found naturally in cruciferous vegetables, I3C promotes the conversion of estrogen to its weaker, more easily cleared metabolite 2-hydroxyestrone rather than the more potent and potentially proliferative 16-alpha-hydroxyestrone. Research published in the Annals of the New York Academy of Sciences confirmed I3C's ability to shift the 2-OH to 16-OH estrogen ratio in a favorable direction. For men this reduces tissue estrogen load, improving the testosterone-to-estrogen ratio. For women navigating estrogen dominance from the progesterone depletion that chronic cortisol produces, I3C helps clear excess estrogen through the liver's Phase II detoxification pathway, supporting the hormonal balance that adequate testosterone and progesterone require.

Chrysin (Oroxylum indicum seed)
The second appearance of chrysin in the stack reinforces the aromatase inhibition layer that Test Ultra initiated. With chrysin in both formulas, the combined dose creates a more sustained aromatase-inhibiting environment throughout the day. Research originally published in Science documented chrysin's direct inhibition of aromatase activity, making it one of the most mechanistically well-supported natural aromatase inhibitors available.

Resveratrol (Japanese knotweed, Polygonum cuspidatum root)
Resveratrol is a polyphenol with well-documented effects on hormonal health, cellular energy, and inflammation. Its role in this blend is as an estrogen receptor modulator: resveratrol binds to estrogen receptors but activates them more weakly than endogenous estrogen, effectively reducing the overall estrogenic signal without eliminating it. Research published in PNAS confirmed resveratrol's estrogen receptor binding activity. It also activates SIRT1 and AMPK, supporting the cellular energy and insulin sensitivity that underlie the metabolic environment where healthy testosterone production is maintained. Its anti-inflammatory effects reduce the aromatase upregulation that chronic inflammation drives.

TestSupport Blend  507mg  |  Free testosterone optimization and HPG axis support

Fenugreek Extract (Trigonella foenum-graecum seed, contains saponins)
Fenugreek is one of the most studied natural SHBG-modulating ingredients available. Its steroidal saponins, particularly protodioscin and diosgenin, compete with testosterone for SHBG binding sites, effectively displacing bound testosterone and increasing the free testosterone fraction. A study published in the International Journal of Sport Nutrition and Exercise Metabolism found that fenugreek extract significantly increased free testosterone and improved body composition in resistance-trained men compared to placebo. The SHBG mechanism is distinct from the LH stimulation that Test Ultra's Tribulus and Tongkat Ali provide, making fenugreek a genuinely additive ingredient in the stack rather than a redundant one.

Winged Treebine Extract (Cissus quadrangularis stem)
The second Cissus inclusion in the stack, in extracted rather than powder form, provides a more concentrated dose of the anabolic phytosterols and anti-inflammatory compounds that support lean mass maintenance and the recovery environment where testosterone's muscle-building effects are realized. The dual Cissus inclusion across both formulas ensures a consistent and meaningful dose of one of the stack's most important anabolic support ingredients.

Longjack (Eurycoma longifolia root)
The second Tongkat Ali inclusion in the stack reinforces its dual mechanism of cortisol reduction and testosterone support. Where the Test Ultra dose provides the baseline HPG axis stimulation, the Alpha Drive inclusion extends the cortisol-modulating and testosterone-preserving effects throughout the day. Research consistently shows that Tongkat Ali's effects on both cortisol and testosterone are dose-dependent, and the combined dose across both formulas ensures meaningful plasma concentrations are maintained.

3,4-Divanillyltetrahydrofuran (Urtica fissa root)
This is the most sophisticated ingredient in the stack and the one that makes Alpha Drive genuinely unique among testosterone support formulas. 3,4-Divanillyltetrahydrofuran (3,4-DVTHF) is a lignan from stinging nettle root with one very specific and well-researched mechanism: it binds to SHBG directly, competing with testosterone for the protein's binding site. Research published in Planta Medica by Schottner et al. confirmed that 3,4-DVTHF and related stinging nettle lignans bind to human SHBG with significant affinity, preventing SHBG from binding to testosterone and thereby increasing the free testosterone fraction. A separate study by Hryb et al. confirmed that stinging nettle root extracts containing these lignans block SHBG binding to its receptors in prostatic tissue. This SHBG displacement mechanism works synergistically with fenugreek's saponin approach: both compete with testosterone for SHBG binding but through different chemical structures and binding affinities, making the combined SHBG-freeing effect more robust than either alone. This is the ingredient most people have never heard of that makes the biggest difference in the bioavailability half of the testosterone equation.

LivSupport Blend  150mg  |  Liver function and hormone clearance

Milk Thistle (Silybum marianum seed, 80% Silymarin)
The inclusion of milk thistle in a testosterone optimization formula is one of the most thoughtful formulation decisions in Alpha Drive, and it's one that most people don't immediately understand until you explain the liver's role in hormonal health. Your liver is responsible for clearing excess estrogen and stress hormones from circulation. It does this through Phase I and Phase II detoxification pathways that convert hormones into water-soluble metabolites that can be excreted. When the liver is burdened by chronic inflammation, toxin accumulation, or metabolic stress, its hormone-clearing capacity is impaired. Excess estrogen recirculates. The testosterone-to-estrogen ratio worsens. And the hormonal environment that testosterone optimization depends on becomes harder to establish and maintain. Silymarin, the active compound in milk thistle at 80% standardization in this formula, has been shown in multiple clinical trials to protect liver cells from inflammatory damage, support hepatic regeneration, and improve liver enzyme markers in adults with liver stress. Research in Phytotherapy Research and the World Journal of Hepatology confirmed silymarin's hepatoprotective effects. A healthier liver clears estrogen more efficiently, supports the glucuronidation and sulfation pathways that process hormones for excretion, and maintains the metabolic health that testosterone production depends on. In Ray Peat's framework, liver health is central to hormone regulation: a healthy liver maintains appropriate hormone ratios, glycogen stores, and the metabolic environment that thyroid and sex hormone function requires. Milk thistle protects that function.

WHY THE STACK OUTPERFORMS EITHER FORMULA ALONE

This is the most important section for anyone trying to decide whether to take one or both products.

Test Ultra addresses: Are you producing enough testosterone? Through Tribulus at 750mg stimulating LH, Tongkat Ali reducing cortisol and supporting HPG axis signaling, Zinc providing the enzymatic foundation for steroidogenesis, and Epimedium supporting androgen receptor expression, Test Ultra optimizes the upstream production side of the equation.

Alpha Drive addresses: Is the testosterone you're producing actually available and protected? Through fenugreek saponins and 3,4-DVTHF competing with SHBG to free bound testosterone, I3C and chrysin managing aromatase and estrogen metabolism, resveratrol modulating estrogen receptor activity and reducing inflammation-driven aromatase upregulation, and milk thistle protecting the liver function that estrogen clearance depends on, Alpha Drive optimizes the downstream bioavailability and protection side.

Taking Test Ultra alone is like increasing production at a factory while the distribution and quality control systems are still compromised. Some of the increased production reaches its destination, but much of it is lost to binding and conversion. Taking Alpha Drive alone frees and protects the testosterone you already have, but doesn't address the upstream production deficit that's common in anyone over 35.

Together they address the full pipeline. More production from Test Ultra feeding into a system where Alpha Drive ensures more of that production reaches androgen receptors in a free, bioavailable, unconverted form. The result is a meaningful improvement at both ends of the testosterone equation that neither product fully delivers alone.

Test Ultra fills the pipeline. Alpha Drive makes sure what's in the pipeline actually reaches its destination. That's what a real testosterone optimization stack looks like.

 

THE RAY PEAT FRAMEWORK REVISITED

Both formulas sit comfortably within the pro-metabolic framework we've built across this series. The central principle from Part 3 of the blood sugar series was that chronic blood sugar instability drives the pregnenolone steal: the upstream raw material that makes all steroid hormones is diverted to cortisol production, depleting testosterone, progesterone, and DHEA simultaneously.

Test Ultra and Alpha Drive work most effectively when that upstream cortisol load is being addressed through the blood sugar and lifestyle interventions covered in the earlier articles. Tongkat Ali's cortisol-reducing effect in both formulas provides additional support at the HPA axis level. But the stack cannot fully compensate for a metabolic environment where chronic blood sugar swings are continuously triggering the pregnenolone steal. The foundation matters.

Peat's emphasis on estrogen as a stress hormone is directly addressed by Alpha Drive's EstroControl Blend. I3C promoting favorable estrogen metabolism, chrysin inhibiting aromatase, and milk thistle supporting efficient estrogen clearance through the liver together create the low-estrogen, high-progesterone-to-estrogen ratio that Peat identified as protective for both sexes. Lower tissue estrogen means less interference with thyroid function, less cortisol sensitization, and a more favorable anabolic hormonal environment.

THIS WORKS FOR WOMEN TOO

I want to be explicit about this because testosterone support marketing is almost entirely directed at men, and women are significantly underserved in this space.
Women require testosterone for the same fundamental reasons men do, just at lower baseline levels: muscle protein synthesis and strength, bone density maintenance, libido and sexual function, cognitive clarity and motivation, and metabolic rate. When chronic cortisol from blood sugar instability or life stress depletes testosterone in women through the pregnenolone steal, the symptoms are often identical to what's described above for men, with the addition of worsening premenstrual symptoms, declining training responsiveness, and the gradual loss of the competitive drive and physical resilience that felt natural earlier in life.

The SHBG issue is also frequently significant in women. Elevated SHBG, which is common in women on oral contraceptives, women with thyroid dysfunction, and women with chronic inflammatory conditions, reduces free testosterone to levels that produce genuine functional deficits even when total testosterone appears adequate on lab tests.
Both Test Ultra and Alpha Drive are formulated with vegetable capsules and botanicals with documented effects in both male and female populations. The testosterone support, SHBG modulation, estrogen management, and liver support mechanisms are relevant and beneficial for women as well as men.

THE PROTOCOL

Test Ultra: three capsules daily, ideally with a meal containing dietary fat to support absorption of the fat-soluble botanical compounds.
Alpha Drive two capsules daily, also with a meal. Taking with the same meal as Test Ultra simplifies compliance and ensures the complementary mechanisms are active simultaneously.

Both formulas build over four to eight weeks of consistent use. Tongkat Ali's cortisol-reducing and testosterone-supporting effects, fenugreek's SHBG modulation, and milk thistle's hepatoprotective effects all accumulate over time rather than producing immediate acute effects. The trajectory begins within the first two weeks and becomes meaningfully apparent over the first two months.

Stack with the blood sugar and lifestyle interventions from the earlier series for the best results. The hormonal environment that Test Ultra and Alpha Drive are optimizing is directly undermined by the blood sugar instability and cortisol elevation covered in Parts 1 through 3. Address the foundation and the stack works harder.

WHY PRIME CHOICE?

Both Test Ultra and Alpha Drive are NSF Certified and GMP Certified, manufactured in the USA, and independently lab tested for purity and label accuracy. In a testosterone supplement category notorious for proprietary blends that obscure underdosed ingredients, the transparency of Prime Choice's labeling and the independent verification of NSF certification ensures you're getting what the label states.

Through Prime Choice Club's membership model you get both products at up to 85% off retail. The $19.93 monthly membership includes a free product every month, effectively covering the membership cost. A complete two-product testosterone optimization stack, certified clean, made in the USA, at a price point that makes the full stack financially accessible.

REFERENCES
1. Peat R. Generative Energy. 1994. (pregnenolone steal, cortisol, and testosterone suppression)
2. Peat R. From PMS to Menopause. 1997. (estrogen as stress hormone, progesterone, and the HPG axis)
3. Doerr P, Pirke KM. Cortisol-induced suppression of plasma testosterone in normal adult males. Journal of Clinical Endocrinology and Metabolism. 1976;43(3):622-629.
4. Feldman HA, et al. Age trends in the level of serum testosterone and other hormones in middle-aged men. Journal of Clinical Endocrinology and Metabolism. 2002;87(2):589-598.
5. Longcope C, et al. The relationship of total and free estrogens and sex hormone-binding globulin with lipoproteins, glucose, and insulin in postmenopausal women. Journal of Clinical Endocrinology and Metabolism. 1996.
6. Anderson RA, et al. The effects of exogenous testosterone on sexuality and mood of normal men. Journal of Clinical Endocrinology and Metabolism. 1992.
7. Hamdi MM, Mutungi G. Dihydrotestosterone activates the MAPK pathway and modulates maximum isometric force through the EGF receptor in isolated intact mouse skeletal muscle fibres. Journal of Physiology. 2010.
8. Sharpe RM. Regulation of spermatogenesis. In: Knobil E, Neill JD, eds. The Physiology of Reproduction. Raven Press. 1994. (LH, FSH, and testosterone production)
9. Selye H. The Stress of Life. McGraw-Hill. 1956.
10. Cinar V, et al. Effects of magnesium supplementation on testosterone levels of athletes and sedentary subjects at rest and after exhaustion. Biological Trace Element Research. 2011;140(1):18-23.
11. Prasad AS, et al. Zinc status and serum testosterone levels of healthy adults. Nutrition. 1996;12(5):344-348.
12. Gauthaman K, Ganesan AP. The hormonal effects of Tribulus terrestris and its role in the management of male erectile dysfunction: an evaluation using primates, rabbit, and rat. Phytomedicine. 2008;15(1-2):44-54.
13. Pokrywka A, et al. Insights into supplements with Tribulus terrestris used by athletes. Journal of Human Kinetics. 2014;41:99-105.
14. Shukla KK, et al. Mucuna pruriens improves male fertility by its action on the hypothalamus-pituitary-gonadal axis. Fertility and Sterility. 2009. (referenced for LH/HPG axis context)
15. Talbott SM, et al. Effect of Tongkat Ali on stress hormones and psychological mood state in moderately stressed subjects. Journal of the International Society of Sports Nutrition. 2013;10(1):28.
16. Tambi MI, et al. Standardised water-soluble extract of Eurycoma longifolia, Tongkat Ali, as testosterone booster for managing men with late-onset hypogonadism. Andrologia. 2012;44(Suppl 1):226-230.
17. Shindel AW, et al. Epimedium-derived phytoestrogen flexibility of valence. Urology. 2010;75(5):1059-1065.
18. Gauthaman K, et al. Sexual effects of puncturevine (Tribulus terrestris) extract. Journal of Alternative and Complementary Medicine. 2003.
19. Suh SO, et al. Effects of epimedium on the central nervous system. Pharmacology Letters. 2006.
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21. Wilborn C, et al. Effects of a purported aromatase and 5α-reductase inhibitor on hormone profiles in college-age men. International Journal of Sport Nutrition and Exercise Metabolism. 2010;20(6):457-465. (fenugreek and testosterone)
22. Schottner M, et al. Lignans from the roots of Urtica dioica and their metabolites bind to human sex hormone binding globulin (SHBG). Planta Medica. 1997;63(6):529-532. (3,4-divanillyltetrahydrofuran SHBG binding)
23. Hryb DJ, et al. The effect of extracts of the roots of the stinging nettle (Urtica dioica) on the interaction of SHBG with its receptor on human prostatic membranes. Planta Medica. 1995;61(1):31-32.
24. Bradlow HL, et al. Indole-3-carbinol and its possible role in the pathogenesis and prevention of estrogen-sensitive cancers. Annals of the New York Academy of Sciences. 1995;768:180-200.
25. Reed GA, et al. Single-dose and multiple-dose administration of indole-3-carbinol to women: pharmacokinetics based on 3,3'-diindolylmethane. Cancer Epidemiology, Biomarkers and Prevention. 2006;15(12):2477-2481.
26. Kellis JT, Vickery LE. Inhibition of human estrogen synthetase (aromatase) by flavones. Science. 1984;225(4666):1032-1034. (chrysin as aromatase inhibitor)
27. Srinivasan K. Fenugreek. Food Reviews International. 2006.
28. Baur JA, et al. Resveratrol improves health and survival of mice on a high-calorie diet. Nature. 2006;444(7117):337-342. (resveratrol metabolic and hormonal effects)
29. Gehm BD, et al. Resveratrol, a polyphenolic compound found in grapes and wine, is an agonist for the estrogen receptor. PNAS. 1997;94(25):14138-14143. (resveratrol and estrogen receptor modulation)
30. Abenavoli L, et al. Milk thistle in liver diseases: past, present, future. Phytotherapy Research. 2010;24(10):1423-1432.
31. Vargas-Mendoza N, et al. Hepatoprotective effect of silymarin. World Journal of Hepatology. 2014;6(3):144-149.
32. Kraemer WJ, Ratamess NA. Hormonal responses and adaptations to resistance exercise and training. Sports Medicine. 2005;35(4):339-361.
33. West DW, Phillips SM. Associations of exercise-induced hormone profiles and gains in strength and hypertrophy in a large cohort after weight training. European Journal of Applied Physiology. 2012.
34. Raven PW, et al. Inter-relationships of free testosterone and sex hormone-binding globulin with other hormones in healthy middle-aged men. Annals of Clinical Biochemistry. 2006

DISCLAIMER

This is a sponsored advertorial. These statements have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat, cure, or prevent any disease. Results may vary. These products are not recommended for use during pregnancy or breastfeeding. Consult your healthcare provider before beginning any new supplement regimen, particularly if you have hormone-sensitive conditions or are taking medications including blood thinners or hormone therapies. The 14-day free trial offer requires a valid credit card and enrollment in the Prime Choice Club monthly membership program at $19.93/month after the trial period. Cancel anytime.

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