Purus Labs Recycle All Natural Hormone Exhilirator- 100 Capsules ReCycle
A plethora of medical research has been combed through tenaciously to formulate the most avant-garde, natural endogenous testosterone amplifier this industry has ever seen. Purus Labs ReCycle™ was strategically designed to address all the major endocrinological issues associated with optimizing testosterone levels. ReCycle™ elevates free testosterone by increasing natural production of Lutenizing Hormone, inhibits estrogen by blocking the nasty aromatase enzyme, cripples SHBG (sex hormone binding globulin) so testosterone molecules can be unbound to exert their anabolic effects, blocks DHT by preventing it from binding to the androgen receptor, lowers cortisol, and fully rejuvenates the HPTA (Hypothalamus-Pituitary-Testicular Axis) allowing for maximum anabolism and minimal catabolism. ALL constituents of the ReCycle™ hormone exhilaration matrix have been substantiated through peer reviewed medical/scientific research and testing. Consider all other natural testosterone boosters OBSOLETE! Purus Labs Recycle Key Features:
- Propel Test Production.
- Rejuvenate HPTA.
- Inhibit Estrogen.
- Block DHT.
- Blunt Cortisol.
- Cripple SHBG.
- 9 proven compoundsbacked by peer-reviewedmedical research!
- Can be used for bothnatural test elevation orp ost-cycle therapy (PCT).
Recycle represents a new breed of all natural testosterone boosters. The days of ineffectiveTribulus Terrestris, Avena Sativa, and Longjack formulas are long gone. Every single cuttingedgecomponent of Recycle is backed by peer-reviewed medical research to elicit exactly theeffects we claim. Perfect for all natural Testosterone elevation or post cycle therapy (PCT).HPTA Upregulating Matrix –
(SHBG Inhibition/ Cortisol Suppression) (Lutenizing Hormone Elevation/ Free Testosterone Elicitation)
Basella Alba (10:1) has shown to have androgenic bioactive components increasing the Testosterone production in testes slices 34-60%. A separate study showed significant Testosterone elevation in leydig cells of bull testes while another study recorded a 17% weight gain amongst rats and a concurrent 80% increase in serum Testosterone in just 15 days! Aromatase Inhibition/ Estrogen Modulation/ DHT Block
Icariin (40% std. from Epimedium) is the most touted flavanoid found in horny goat weed. Lab studies have verified its Testosterone mimetic capabilities by improving circulating levels of Testosterone and the condition of reproductive organs. This wonder ingredient has also been shown in vivo to be an estrogen receptor antagonist (blocking estrogen thus increasing testosterone), a vasodilator (allowing more nutrient carrying blood to the muscles), and an effective inhibitor of PDE-5, a la Viagra!
3, 4-Divanillyltetrahydrofuran (95% std. from Nettle Root), extracted at the highest purity from stinging nettle root, has shown in multiple studies to have the highest binding affinity for SHBG of all lignans investigated thus far. As aforementioned, less SHBG allows greater amounts of free Testosterone!
Now we have an abundance of FREE, muscle building Testosterone floating around ready to engage cell receptors, yet we encounter another obstacle…Aromatase. This nuisance to our precious Testosterone is an enzyme that binds to androgens and “aromatizes” (converts) them into estrogen. We must protect our precious Testosterone from aromatization much like we did earlier from SHBG.
Less Aromatase = Less Estrogen Conversion = More Testosterone Salvaged.
stosterone converting it into DHT. Too much DHT is most commonly associated with causing androgenic alopecia (male pattern baldness), benign prostate hypertrophy (BPH), and prostate cancer. Obviously, we need to prevent the 5-alpha-reductase enzyme from binding to our Testosterone as well as excessive amounts of DHT from binding to the androgen receptor to alleviate potential side effects of increased Testosterone levels.
So now we know we need to inhibit aromatase, thus decreasing estrogen conversion, prevent excessive amounts of DHT from binding to the androgen receptor, and prevent the enzyme 5-alpha-reductase from binding to our Testosterone. The second strategic portion of the Recycle™ matrix handles all of this with ease!
Bladderwrack (Fucus Vesiculosis) has been shown to prevent the binding of estradiol and progesterone to their receptor sites thus lowering endogenous levels of both.Absorption Amplification/ Glucoronidation Prevention/ CYP3A4 Inhibition.
White Button Mushroom Extract (Agaricus Bisporis) is loaded with aromatase inhibiting phytochemicals that are postulated to work through multiple inhibitory mechanisms. These compounds are so noteworthy Beckman Research Institute is presently studying for prostate and estrogen dependent breast cancer prevention! It has also been shown to inhibit the 5-alpha- reductase enzyme from binding to Testosterone and converting it to DHT.
Trans-3,4’,5-trihydroxystilbene (Resveratrol), a polyphenolic compound structurally similar to estrogen, has been receiving mounds of attention as of late due to its anti-cancer, anti-estrogen, life extension, and cardiovascular benefits. For our purposes, it is included for its proven testosterone boosting, anti-aromatization, and vasodilating properties. Resveratrol has been shown in lab studies to elicit 51.6% blood Testosterone increases, and 15.8% increases in testicular sperm count. Another study displayed its inhibition of aromatase at the enzyme and mRNA level. Countless other peer reviewed research studies support and substantiate this powerful ingredients’ positive effects. As mentioned above, the less aromatase we have the greater circulating Testosterone we can achieve!
Indole-3-carbinol (40% std. for 3,3-Diindolylmethane ) is a phytochemical found largely in cruciferous vegetables. One of its major metabolites is DIM (3,3-Diindolylmethane) which has been shown to steer estrogen metabolism in favor of “good” estrogen (2-hydroxyestrone/estradiol) and away from “bad” estrogen, such as 4-hydroxyestradiol. DIM represents a class of relatively non-toxic AhR-based anti-estrogens with SERM type qualities. A study done by University of California, Berkeley, showed through receptor binding assays that DIM is a strong competitive inhibitor of DHT binding to the androgen receptor.
Quercetin & Piperine (Piper nigrum) increase bioavailability either by promoting rapid absorption from the gastrointestinal tract, by protecting the drug from being metabolized/oxidized in its first passage through the liver after being absorbed, or by a combination of these two mechanisms. They have been proven to inhibit glucoronidation in gastrointestinal transit and be CYP3A4 inhibitor, thus increasing the bioavailability of compounds. Specific studies have noted Quercetin’s ability to substantially increase the bioavailability of Resveratrol in vivo.