sseing its not being used as an ancillery on cycle, im interested in form for its ai properties, cutting water and its leaning effects
i know its apples and oranges, but for my goals, the products would serve the same purpose.....its a planned 8wk attack give or take, id even do 1month erase 1 month form, stacked with the other stuff
the goal is to really tighten **** up (im coming off a canadian winter so.....)and may-ish plan to cycle before the summer, i like being in very good conditioning, the 10% range, 12 max, before i touch anything.....im 15% give or take now
FORMA-STANOZOLOL really is an amazing compound that should be a part of EVERY cycle - not only for muscle gains and fat loss, but for longevity and health. It's one of the world's most potent aromatase inhibitors that Started out a a prescription drug here in the U.S and is still a prescription drug in other countries under the brand name of Lentaron I.M. Depot®.
The amazing part is Lentaron I.M. Depot® use to be available in the USA, but the government removed it because it was
"too anabolic" and it put on muscle. Mrsupps.com FORMA-STANOZOLOL is the EXACT compound found in Lentaron I.M. Depot® and we've attained it due to the current legal loopholes in America. What else have we done? We have enhanced its effects by adding
25mgs DIM
7,8 - Benzoflavone (99%) 25mg
chrysin 4mg
Horse Chestnut seed extract 8mg
Because of the formatane and now added compounds Its anabolic/androgen effects are similar to that of the steroid
Primobolan Depot. It also increases IGF-1 levels by an amazing 26%. It also increases HPTA activity and testicular activity similar to a combination of HCG and Clomid!
All of this is backed up by " human" studies. Yes Real human studies don by well known Universities and agencies. Because for the longest time Lentaron I.M. Depot® was a
proscrition drug . This was not a drug that got scrapped because it did not work or because other drugs worked better. No this drug lost favor because many years ago the only way to use the drug was through injections. But because of the advancements in Trans dermal delivery Lentaron I.M. Depot® is back. With the help of NTBM and MRsupps.com its more powerful then ever.
Now you cn understand why I will recommend this to be a part of any and every cycle from this day forward. Whether it's to keep your estrogen under control, prevent deca and tren libido [rpblems or to simply create an environment that is more anabolic and beneficial for muscular gains and fat loss.
Its now a fact! The science and studies prove FORMA-STANOZOLOL works better then current prescription aromatase inhibitors on the market (such as Arimidex, Femara, Aromasin, Cytadren, etc.) but at a
FRACTION OF THE COST! If one wanted to prevent prolactin,estrogen,progesterone induced gyno and or cycle side effects they may need 2-3 and some times 4 different drugs. Of course each one of these drugs comes with its own set of negative side effects. Some Ai's raise SHBG, some lower IGF-1 and almost all of them leave you feeling weak and brittle.
FORMA-STANOZOLOL decreases SHBG 34% thus increasing androgen activity, which basically makes androgens/steroids in your systems MORE effective WITHOUT any increase in dosage. FORMA-STANOZOLOL Increases IGF-1 levels by a whopping 26% In doing so creates the perfect anabolic muscle building environment on cycle, off cycle and during pct.
FORMA-STANOZOLOL Decreases the number of progesterone receptors (inhibits the trenbolone and “deca-****” type side effects and increases fat loss. Through "clinical studies its been proven to lower progesterone.
Effect of 4-Hydroxyandrostenedione on Murine Leydig Tumor Cell Steroidogenesis -- Zimniski et al. 51 (14): 3663 -- Cancer Research
Effect of 4-hydroxyandrostenedione on murine Leydig tumor cell steroidogenesis.
Zimniski SJ, Brandt ME, Melner MH, Brodie AM, Puett D.
Department of Biochemistry and Molecular Biology, University of Miami School of Medicine, Florida 33101.
The murine Leydig cell tumor (M5480A) possesses high levels of estrogen receptor and is known to produce estrogens. In these studies we examined the effects of the potent aromatase inhibitor 4-hydroxyandrostenedione (4-OHA) on Leydig tumor cell steroidogenesis both in vitro and in vivo. The addition of 4-OHA to Leydig tumor cells in primary culture resulted in a dose- and a time-dependent decrease in media progesterone levels. The observed decrease was most likely due to impaired synthesis of progesterone, inasmuch as no alteration in progesterone metabolism was seen when progesterone levels were diminishing. However, 4-OHA inhibited progesterone conversion to testosterone following 1 h of incubation, but this effect disappeared coincident with 4-OHA metabolism. Analysis of pregnenolone production revealed a biphasic dose-dependent effect of 4-OHA. At low doses (0.01-0.1 microM), 4-OHA was found to decrease pregnenolone concentrations, while at higher doses (1-10 microM) pregnenolone levels were elevated. Therefore, the actions of 4-OHA on Leydig cell steroidogenesis in vitro appear to be multifocal. Other experiments were performed to evaluate the effects of 4-OHA on tumor-bearing male mice in vivo. In these studies, the predominant effects of 4-OHA were to act as an aromatase inhibitor and to inhibit progesterone production. Thus, while 4-OHA is a potent aromatase inhibitor, we have found that this compound may alter steroidogenesis in Leydig tumor cells at several sites prior to aromatization.
PMID: 2065323 [PubMed - indexed for MEDLINE]
Aromatase inhibition: 4-hydroxyandrostenedione (4-OHA, CGP 32349) in advanced prostatic cancer.
Comparison of the pharmacokinetics and pharmacodyn... [Cancer Chemother Pharmacol. 1990] - PubMed result
Biochemistry and function of sterols - Google Books
Pharmacokinetics of 4-hydroxyandrostenedione in ma... [J Steroid Biochem Mol Biol. 1993] - PubMed result