|
|
|
|
Ask yourself the simple question: If you could create the ultimate sports supplement to boost your body and achieve higher performance, what would you want it to do? If your answer includes:
…then we have your prescription for achieving these results! DRIVE by Applied Nutriceuticals is simply the most versatile performance-enhancing sports supplement available. Whether it’s packing an inch of girth on your arms or shaving a second off your best time, DRIVE provides the goods to help you get there.
The synergistic compilation of constituents contained in this unique compound creates a very favorable anabolic environment through a variety of different mechanisms:
DRIVE is a synergistic blend of pharmaceutical-strength constituents that is designed to promote a highly anabolic state through a variety of different mechanisms. DRIVE combines cGMP and cAMP synergism, increased thyroid activity, a distinct AI effect, SHBG inhibition, endurance enhancement, elevated testosterone and luteinizing hormone activity and a marked improvement in the testosterone/estrogen and testosterone/cortisol ratios. DRIVE can be used as:
ORDER DRIVE NOW
Frequently Asked QuestionsQ: How long will it take to feel the positive benefits of DRIVE?A: You will feel the many benefits of DRIVE within 1 day of taking the first dose. Many users report increased strength and energy, increased stamina and endurance, as well as a boost in libido, within the first 24-48 hours of taking the product. Those taking DRIVE should expect to see marked gains in lean body mass and lowered body fat within 10 days of beginning the product, as well as constant fullness and noticeable increase in muscle density and vascularity. These effects continue to increase the longer DRIVE is used. When stacked with RPM™, numerous testers of DRIVE have reported setting personal records (PRs) on all major exercises within the first week of starting the stack. Users of the DRIVE/RPM stack report intense focus, heightened aggression towards training and an overall “hardening” effect, along with strong vasodilation and intense pumps. Q: How is DRIVE different from other testosterone boosters and NO-type products?A: DRIVE resides in a league of its own: It is a product that has been clinically proven to increase lean body mass, libido, strength, endurance and burn body fat, yet it is non-hormonal. The special aggregate mixture of the constituents in DRIVE yield results that no other test booster or NO product on the market can touch! DRIVE contains StAR 3,5 Anaplex™; a unique blend of pharmaceutical-grade icariin (50% extract vs. other brands’ 3-5% extracts) and forskolin (specially standardized to the highest potency available). The aformentioned blend is then combined with the A4E2 Endurance Complex™, an innovative blend of compounds that allows for energetic, non-stimulant ATP enhancement, heightened stamina, as well as an increased anabolic state.
Q: When should I take DRIVE? A: Take the first dose of DRIVE upon waking in the morning, and then take the second dose approximately one hour before your workout, or mid-afternoon. If you train in the evening, do not take within 3 hours of bedtime. If so, reduce your dosage by one capsule. Q: Has there been any scientific research on the product constituents of DRIVE?A: Absolutely. All of the components in DRIVE all have numerous clinical studies proving their efficacy, with documented properties including anabolic enhancement, anti-catabolism, increased thyroid activity, weight loss and PDE5 inhibition (the biochemical mechanism of Viagra®). All the product constituents of DRIVE have been studied extensively, and only the doses and standardizations used in research studies are used in the product. Q: Is it safe to use DRIVE for long periods of time, or should I cycle it?A: All research studies along with our own testing have indicated that it can be used continuously without any negative side effects. You will never want to go without DRIVE again - ask our product testers! However as with any product there is some degree of tolerance that can develop after extended use. If you experience this, we recommend cycling 8 weeks on / 4 weeks off. Q: What supplements should I take along with DRIVE, and are there any supplements I should avoid?A: We recommend whey protein supplementation, with a goal of attaining 1-1.5 grams of protein per day per lb. of bodyweight. Additionally we encourage the use of an EFA supplement with a proper ratio of omega 3/6/9, and a good multivitamin / multimineral. RPM stacks phenomenally well with DRIVE, and the two products can be considered THE most effective non-hormonal stack for sports performance/physique enhancement on the market today. Q: Who can benefit from DRIVE?A: Any man or woman over 18 years of age who is seeking to gain lean mass, and who wants to look and feel their best!!! The product is also a great contest-prep supplement; giving the user tighter skin, less water retention, harder muscle contractions and bulging pumps, even when living on limited carbs! Also, anyone looking to gain a competitive edge in athletics can benefit significantly from using DRIVE, from the strength and speed increases and the heightened concentration and focus; plus it is NCAA, NPC, IFBB, NFL, NBA, MLB and IOC compliant. Q: Who should not take DRIVE?A: Anyone sensitive to stimulants, under the age of 18, those who take MAOI’s or are on any other type of prescription medications, and if you are pregnant or nursing. Always check with your doctor before beginning any supplementation regimen.
DRIVE is a truly one-of-a-kind product and contains only the highest quality clinically proven doses for maximum effectiveness. The StAR Anaplex™ in DRIVE contains forskolin (7 beta-acetoxy-8, 13-epoxy-1 alpha,6 beta, 9 alpha-trihydroxy-labd-14-ene-11-one) and icariin (4H-1Benzopyran-4-one, 3-{(6-deoxy-a-L-mannopyranosyl)oxy}-7-(B-D-glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methy-2-butenyl). These two potent phytochemical (plant-derived) compounds have some SERM-like (selective estrogen receptor modulator) and also demonstrate SARM-like (selective androgen receptor modulating) properties, providing pronounced benefits on muscle mass, strength, bone, physical DRIVE and sexual function. Published research on icariin and forskolin support these hypotheses, however some experts are still divided as to the ability of these compounds to exert their effects on androgen and estrogen receptor modulation and tissue-specificity. Several studies further exploring these activities are currently underway that are sure to shed additional light on the many useful properties of these compounds.
Forskolin Forskolin has been the subject of large amounts of research in the health and wellness field since the early 1980s. Scientific studies have found that along with increasing thyroid activity and thermogenesis, forskolin is also a potent anabolic. This occurs primarily through elevation of 3,5 cyclic adenosine monophosphate (cAMP); a second messenger important in hormone signaling. cAMP elevation is a crucial piece of the puzzle in creating an anabolic and thermogenic state, and forskolin is one of the best compounds available for triggering dramatic increases in cAMP levels. One study (Bristow et al, 1984) showed that forskolin was able to increase cAMP levels 4.82 times more than a placebo. Another study (Litosch, 1982) demonstrates that forskolin can raise cAMP levels in fat cells. This is important because it demonstrates the ability of the compound to enhance lipolysis; meaning that forskolin exerts powerful fat-burning effects as well as being a potent anabolic agent; plus forskolin can also enhance endurance capacity as well. Another added bonus of forskolin is that it increases cAMP independently of epinephrine, thus providing increased energy without the need to take any type of traditional stimulant.
HPTA and Testosterone
So how does cAMP increase anabolism? cAMP is classified as a second messenger, meaning that it exerts its effects by acting in a manner secondary and in response to a first messenger signaling molecule. When a first messenger signaling molecule binds to a cell surface, another secondary (hence “second” messenger) pathway is activated that increases cAMP production. Increased cAMP production is responsible for the activation of protein kinase A, which is an enzyme that has positive effects androgen receptor binding even in the absence of other androgens. cAMP also is a signal for steroidogenesis (testosterone production) in the Leydig cells of the testes, by increasing levels of steroidogenic acute regulatory protein (StAR). Increased StAR production is noteworthy, because it is a Leydig cell cholesterol transfer protein and provides the building blocks for testosterone synthesis.
StAR activation is necessary for the stimulation of steroidogenic enzymes involved in the transfer of cholesterol to testosterone. By increasing the intermediary between these two processes, a resulting positive shift in anabolism can occur. Therefore, high cAMP levels also equate to high levels of luteinizing hormone (the hormone responsible for mediating endogenous spermatogenesis), and when cAMP levels are elevated (DRIVE causes a marked elevation of cAMP), it serves as an intermediate in the signaling cascade that ranges from luteinizing hormone (LH) binding to testosterone production. By increasing the intermediate between these two processes, a resulting increase in anabolism and protein synthesis can occur. Numerous other studies have shown parallels between increased cAMP levels and increased anabolism, and a ground-breaking 2005 study in The Journal of Obesity Research found that obese men taking 250 mg of 10% forskolin a day for 12 weeks (roughly the dosage included in the daily dosage of DRIVE) experienced an averaged 33% increase in free testosterone levels, averaged a 10 lbs. fat loss per person and increased lean mass an average of 8 lbs! A 2001 study by Badmaev (see chart below) also yielded similar results.
Forskolin-Induced Lean Body Mass Gains (Badmaev et al. 2001)
These findings are extremely promising for another important reason: When an athlete uses anabolics for any length of time, impairment of the hypothalamo-pituitary gonadal axis (HPTA - the entity responsible for endogenous testosterone production) tends to occur. This is noteworthy because when HPTA shutdown occurs, it temporarily the diminishes the subject’s ability to synthesize testosterone. A large part of HPTA shutdown is due to decreased cAMP and LH levels, and forskolin increases both of these. By upping cAMP and LH post-cycle, it allows the body to resume testosterone production safely, potentially even beyond pre-cycle baseline levels. A 1997 study in the The Journal of Urology found that forskolin can also aid in erectile dysfunction. It is also notable to mention that forskolin also has measureable effects on the androgen receptor, and may exert some positive anabolic effects through this channel as well.
ICARIIN
Icariin is a potent phytochemical that has been documented to have profound effects on anabolism. Icariin exerts its efficacy through several different mechanisms of action: Via competition with glucocorticoids and increasing cAMP levels, by modulating estrogen receptor antagonism and by decreasing prolactin levels. Several studies have shown that icariin competes with glucocorticoids for various receptor sites, and thus improves the testosterone/cortisol ratio. A 2006 study by Pan et al. showed that icariin blocks glucocorticoids from binding to cortisol receptors, hence antagonizing the actions of cortisol. This alone creates an anabolic effect by positively skewing the testosterone/ cortisol ratio which is a trigger for greater anabolism, protein synthesis, increased aggression, and intensified muscle contractions. A 2006 study by Zhang found that icariin also has a testosterone mimetic effect on muscle tissue while increasing spermatogenesis however there is some disagreement among scientists on the mechanism by which icariin does this. A 2005 study conducted by Pan et al. concluded that icariin also has marked anti-depressant qualities through pituitary mediation, but the exact mechanism of action for this finding is also unknown.
Users of DRIVE report huge improvements in strength, physique hardness, sex drive and positive aggression while using this compound, an effect that can be at least partially attributed to the anabolic-mimicking qualities of icariin. DRIVE promotes higher dopamine levels and decreased prolactin levels, both of which are triggers for increased endogenous anabolism. Icariin can also enhance muscle contraction by decreasing the effects of acetylcholinesterase (AChE). Acetylcholine (Ach) is a neurotransmitter necessary for muscle contraction, and AChE is responsible for disabling ACh at the neuromuscular junction. Icariin blocks this disabling action, allowing for ACh to stay at the synapse and better exert its effects for a longer period of time- thus allowing for harder and stronger muscle contractions.
Action Potential/Muscle Contraction
Icariin is a selective inhibitor of cyclic guanitric oxidesine monitric oxidephosphate (cGMP) - specifically phosphodiasterase type 5 (PDE5). This is a notable characteristic, because PDE5 hydrolyzes cGMP into an inactive molecule. cGMP is important because nitric oxide requires cGMP to moderate vascular control and vasodilation. So essentially, no cGMP; no vasodilation (the “PUMP”), because nitric oxide requires cGMP to work. Conversely, the more cGMP; the more nitric oxide-induced vasodilation - therefore the greater the pumps. Icariin stops PDE5 from disabling cGMP and allows cGMP to extend its activity which increases the effects of nitric oxide in skeletal muscle and allows for a stronger muscle contraction and pump. This is the same way a popular pharmaceutical product – Viagra® – works; which is essentially the most well-known PDE5 inhibitor on the market.
Long-term usage of PDE5 inhibitors (more than 1 month of usage) has been shown to increase the testosterone/estrogen ratio, as evidenced by a 2006 study in The Journal of Sexual Medicine. This is very noteworthy for two reasons: It shows that PDE5 inhibitors have more than just an acute effect, and that they have anabolic tendencies as well. Pure icariin has been found to have roughly one-tenth the PDE5 inhibitory activity and nitric oxide productivity of Viagra®, and the dosage provided in DRIVE is tailored appropriately to provide similar effects. In short, the PDE5 inhibition displayed by icariin puts DRIVE in a class above all other nitric oxide enhancers- as “pharmaceutical-strength” results are commonly experienced.
Naringin (or
Naringenin-7-beta-neohesperidoside), and its
novel component Naringenin, also contribute profound effects of
DRIVE. Naringin (and Naringenin) exhibit remarkable anti-aromatase and estrogen-inhibiting
properties by decreasing the cytochrome P450arom isoform. The P450 enzyme also
allows for the oxidative metabolism for chemical modification and degradation of
oral medications. Therefore, the addition of naringin in DRIVE allows for
higher blood levels of the active ingredients to remain in the system of the
user, making for a more effective product. Naringin and naringenin have been
shown to slow the metabolism of caffeine and PDE5 inhibitors such as icariin,
allowing for these compounds to be much more effective on a per dose basis - by
up to 35%!!!
Cordyceps
Cordyceps Sinesis is another essential component of DRIVE. Cordyceps is a mushroom that grows on caterpillar larvae (but now re-created under laboratory conditions), and has been traditionally used to improve reproductive function, prevent fatigue and slow the effects of aging. It also helps you adapt to stress, and may be instrumental in increasing endurance, increasing anabolism and protein synthesis and improving general health. Cordyceps contains several notable actives, including some unique polysaccharides, proteins, fatty acids, flavones, 2'-deoxyadenosine, and cordycepin. Of main relevance to this product is the ability of cordyceps to do several things:
Dodder Seed Extract (or cuscuta chineses) is another important component of DRIVE, as it also activates the second messenger system, and subsequently allows greater amounts of cAMP to be generated from ATP. In a 2000 study by Qin in the Asian Journal of Andrology, dodder seed extract increased blood levels of testosterone and luteinizing hormone, and enhanced the growth of testes, epididymis and the pituitary gland which indicates an anabolic effect. In yet another study, combinations of icariin and dodder seed together were shown to increase cyclic AMP production, anabolism, and to also stimulate the growth of the testes, epididymis, and seminal vesicle in animals. Human clinical trials showed similar positive results. In one study, 50 patients with impotence were treated with a combination of icariin and dodder seed for 50 days. 76% (38 patients) experienced total recovery and 16% (8 patients) were improved for a total effectiveness rate of 92%.
In conclusion, the carefully selected and proportioned blend of constituents in DRIVE combine to create a truly synergistic compound that exploits a variety of different biochemical mechanisms of action to produce the most thoroughly researched, safe, effective and potent anabolic available.
References 1. Ying, Pan, Wei-Yun Zhang, Xing Xia, and Ling-Dong Kong, “Effects of Icariin on Hypothalamic-Pituitary-Adrenal Axis Action and Cytokine Levels in Stressed Sprague-Dawley Rats” Biol. Pharm. Bull., Vol. 29, 2399-2403. 2. Aghdasi B, Reid MB, and Hamilton SL. (1997) Nitric oxide protects the skeletal muscle Ca2+ release channel from oxidation induced activation. J Biol Chem 272:25462-25467 3. Balon TW, Nadler JL. (1997)Evidence that nitric oxide increases glucose transport in skeletal muscle. J Appl Physiol. 1997 Jan;82(1):359-63. 4. Etgen GJ Jr, Fryburg DA, Gibbs EM. (1997) Nitric oxide stimulates skeletal muscle glucose transport through a calcium/contraction- and phosphatidylinitric oxidesitol-3-kinase-independent pathway. Diabetes Nitric oxidev; 46(11):1915-9. 5. McAllister RM, Hirai T, Musch TI. (1995) Contribution of endothelium-derived nitric oxide (EDNO) to the skeletal muscle blood flow response to exercise. Med Sci Sports Exerc. Aug;27(8):1145-51 6. Wilson, JR and Kapoor S. (1993) Contribution of endothelium-derived relaxing factor to exercise-induced vasodilation in humans. J. Appl. Physiol. 75:2740-2744. 7. Young ME, Leighton B.(1998) Evidence for altered sensitivity of the nitric oxide/cGMP signaling cascade in insulin-resistant skeletal muscle. Biochem J. Jan 1;329 ( Pt 1):73-9 8. Liu, HJ et al. [The effect of icariin and astragalosid I on the proliferation and differentiation of bone marrow stromal cells] Zhong Yao Cai. 2006 Oct;29(10):1062-5. 9. Ning, H et al. Effects of icariin on phosphodiesterase-5 activity in vitro and cyclic guanosine monophosphate level in cavernous smooth muscle cells. Urology. 2006 Dec;68(6):1350-4. 10. Jiang, Z. et al Effects of icariin on hypothalamic-pituitary-adrenal axis action and cytokine levels in stressed Sprague-Dawley rats. Biol Pharm Bull. 2006 Dec;29(12):2399-403. 11. Zhang, Z. et al The testosterone mimetic properties of icariin. Asian J Androl. 2006 Sep;8(5):601-5. Epub 2006 Jun 5. 12. Liu, W. Effects of icariin on erectile function and expression of nitric oxide synthase isoforms in castrated rats. Asian J Androl. 2005 Dec;7(4):381-8. 13. Xin, ZC Effects of icariin on cGMP-specific PDE5 and cAMP-specific PDE4 activities. Asian J Androl. 2003 Mar;5(1):15-8. 14. Yap, SP, Shen P, Li, J, Lee, LS, Yong, EL. . J Ethnopharmacol. 2007 Jun 2: 17628368 Molecular and pharmacodynamic properties of estrogenic extracts from the traditional Chinese medicinal herb, Epimedium. J Ethnopharmacol. 15. Tian L, Xin ZC, Yuan YM, Fu J, Liu WJ, Wang LL. Zhonghua Yi Xue Za Zhi. 2004 Jun 2;84(11):954-7. Effects of icariin on the erectile function and expression of nitrogen oxide synthase isoforms in corpus cavernitric oxidesum of arterigenic erectile dysfunction rat model 16. Xin ZC, Kim EK, Lin CS, Liu WJ, Tian L, Yuan YM, Fu J. Asian J Androl. 2003 Mar;5(1):15-8. Effects of icariin on cGMP-specific PDE5 and cAMP-specific PDE4 activities. 17. Tian L, Xin ZC, Yuan YM, Fu J, Liu WJ, Wang LL. Zhonghua Yi Xue Za Zhi. 2004 Jan 17;84(2):142-5. [Article in Chinese] Effects of icariin on intracavernitric oxidesal pressure and systematic arterial blood pressure of rat. 18. Hull EM, Muschamp JW, Sato S. Dopamine and serotonin: influences on male sexual behavior. Physiol Behav. 2004 Nitric oxidev 15;83(2):291-307 19. Pavone C, Curto F, Anello G, Serretta V, Almasio PL, Pavone-Macaluso M. J Urol. 2004 Dec;172(6 Pt 1):2347-9. Prospective, crossover comparison of sublingual apomorphine (3mg) with oral sildenafil (50mg) for male erectile dysfunction. 20. Kruger TH, Haake P, Hartmann U, Schedlowski M, Exton MS. Orgasm-induced prolactin secretion: feedback control of sexual DRIVE? Neurosci Biobehav Rev. 2002 Jan;26(1):31-44. 21. LeBail, JC et al Chalcones are potent inhibitors of aromatase and 17beta-hydroxysteroid dehydrogenase activities.Life Sci. 2001 Jan 5;68(7):751-61. 22. LeBail, JC et al Effects of phytoestrogens on aromatase, 3beta and 17beta-hydroxysteroid dehydrogenase activities and human breast cancer cells. Life Sci. 2000 Feb 25;66(14):1281-91. 23. LeBail, JC et al Aromatase and 17beta-hydroxysteroid dehydrogenase inhibition by flavonitric oxideids. .Cancer Lett. 1998 Nitric oxidev 13;133(1):101-6. 24. Arayne, LS. Et al Grape fruit juice-drug interactions.Pak J Pharm Sci. 2005 Oct;18(4):45-57. Review. 25. Ho, PC et al. Inhibition of human CYP3A4 activity by grapefruit flavonoids, furanocoumarins and related compounds. J Pharm Pharm Sci. 2001 Sep-Dec;4(3):217-27. 26. Fuhr, U Inhibitory effect of grapefruit
juice and its bitter principal, naringenin, on CYP1A2 dependent metabolism of
caffeine in man. 27. Jetter, A. et al Effects of grapefruit juice on the pharmacokinetics of sildenafil. Clin Pharmacol Ther. 2002 Jan;71(1):21-9. 28. Asano Tsuguyoshi (2001). Clinical report on root extract of perilla plant (Coleus forskohlii) ForsLean ® in reducing body fat. Asano Institute. Tokyo , Japan. 29. Kreider RB, et al. Effects of Coleus forskohlii supplementation on body composition and markers of health in sedentary overweight females. Experimental Biology 2002 Late Breaking Abstracts. LB305: 2002. 30. Debes, J. D., Schmidt, L. J., Huang, H., and Tindall, D. J. p300 mediates androgen-independent transactivation of the androgen receptor by interleukin 6. Cancer Res., 62: 5632–5636, 2002. 31. Pratt, W. B. and Toft, D. O. Steroid
receptor interactions with heat shock protein and immunophilin chaperones.
Endocr. Rev., 18: 306–360, 1997. 33. Rosenfeld, M. G. and Glass, C. K.
Coregulator codes of transcriptional regulation by nuclear receptors. J. Biol.
Chem., 276: 36865–36868, 2001. 35. Farmer, G., Connolly, E. S., Jr., Mocco, J., and Freedman, L. P. Molecular analysis of the prostate-specific antigen upstream gene enhancer. Prostate, 46: 76–85, 2001. 36. Huang, W., Shostak, Y., Tarr, P., Sawyers, C., and Carey, M. Cooperative assembly of androgen receptor into a nucleoprotein complex that regulates the prostate-specific antigen enhancer. J. Biol. Chem., 274: 25756–25768, 1999. 37. Shang, Y., Myers, M., and Brown, M. Formation of the androgen receptor transcription complex. Mol. Cell, 9: 601–610, 2002. 38. Ma, H., Hong, H., Huang, S. M., Irvine, R. A., Webb, P., Kushner, P. J., Coetzee, G. A., and Stallcup, M. R. Multiple signal input and output domains of the 160-kilodalton nuclear receptor coactivator proteins. Mol. Cell. Biol., 19: 6164–6173, 1999. 39. Irvine, R. A., Ma, H., Yu, M. C., Ross, R. K., Stallcup, M. R., and Coetzee, G. A. Inhibition of p160-mediated coactivation with increasing androgen receptor polyglutamine length. Hum. Mol. Genet., 9: 267–274, 2000. 40. LEAMON, KB; PADGETT, W; DALY, JW. "Forskolin:
Unique diterpene activator of adenylate cyclase in membrane and intact cells"
Proc. 41. DE SOUZA, NJ; DOHADWALLA, AN; REDEN, J;
Forskolin, A. "Labdane Diterpenoid with Antihypertensive, Positive Inotropic,
Platelet 42. GIRARDIER, L. "Brown Fat: An Energy Dissipating Tissue"; In: Mammalian Thermogenesis; Girardier, L.; Sock M.J. Eds.; Chapman and Hall Ltd. London and New York, 1983, pp 50-98. 43. Badmaev, V. Majeed, M. Conte, A,
Parker, J. “Diterpene Forskolin (Coleus forskohlii, Benth.): A possible new
compound for reduction of body weight by 44. K. S. R. Sastry, Y. Karpova, S. Prokopovich,
A. J. Smith, B. Essau, A. Gersappe, J. P. Carson, M. J. Weber, T. C. Register,
Y. Q. Chen, R. B. Penn, and G. Kulik
Epinephrine Protects Cancer Cells from Apoptosis via Activation of cAMP-dependent
Protein Kinase and BAD Phosphorylation 45. L. Jia, H. C. Shen, M. Wantroba, O. Khalid,
G. Liang, Q. Wang, E. Gentzschein, J. K. Pinski, F. Z. Stanczyk, P. A. Jones,
and G. A. Coetzee 46. G. Chen, M. Nomura, H. Morinaga, E.
Matsubara, T. Okabe, K. Goto, T. Yanase, H. Zheng, J. Lu, and H. Nawata 47. Induction of Drug Metabolism by Forskolin, the Role of The Pregnane X Receptor and the PKA Signal Transduction Pathway. J Pharmacol Exp Ther. 2004 Sep 30 Ding X, Staudinger J. University of Kansas. 48. Bersudsky Y, et al. A preliminary study of
possible psychoactive effects of intravenous forskolin in depressed and
schizophrenic patients. Short
communication. J Neural Transm 1996;103(12):1463-7. 50. Relaxant effects of forskolin on guinea pig
tracheal smooth muscle. 53. The positive inotropic-acting forskolin, a
potent adenylate cyclase activator. 54. An experimental study on anti-aging action
of Cordyceps extract 60. Cordyceps sinensis mycelium activates PKA
and PKC signal pathways to stimulate steroidogenesis in MA-10 mouse Leydig tumor
cells. Int J Biochem Cell Biol. 2005 Jan;37(1):214-23.
70.2002 Dec;25(12):886-8. [Effects of
flavonoids from semen Cuscutae on changes of beta-EP in hypothalamuses and FSH
and LH in anterior pituitaries in female rats exposed to psychologic stress]
Wang J, Wang M,Ou Y, Wu Q. 71. J Pharm Biomed Anal. 2002 May 15;28(3-4):621-8. Determination of flavonoids in Semen Cuscutae by RP-HPLC. Ye M, Li Y, Yan Y, Liu H, Ji X.. Department of Pharmaceutical Biotechnology, Health Science Center, Peking University, Beijing 100083, People's Republic of China. ORDER DRIVE NOW
|
SPORTS CLUBS & GYMS If you are buying for members of your club in bulk or to re-sell in your gym then call us on 01289 303111 ask for Supplement Sales Division & get our SPECIAL OFFER Bulk Discount Prices Sports Nutrition has developed dramatically during the last few years. Whilst Creatine is still the best selling line – Creatine itself has developed and is now available as the SUPER POTENT Formula NEOVAR. In the past it was necessary to resort to chemical anabolic steroids in order to achieve serious muscle growth – with next generational supplements such as RPM & IGF-2 Natural Muscle Building has reached new grounds with results on a par with those previously only achieved by chemical users – so be the best you can be with the highest quality sports performance enhancement supplements you can buy! Order on-line OR Call us FREE in the UK on 0800 917 4073 Free UK Delivery on all Applied Nutriceutical lines.
|
|
SALES
ORDER HOTLINE |
