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 About | Disclaimer | Links | Contact | Home | Bodybuilding Supersite 9:22 am | 7.04.09 
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Jun 17 2009 - Women in Steroids


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Andractim



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Andractim

Topical Dihydrotestosterone

Although DHT is much more potent than testosterone, in terms of both anabolic and androgenic effects, it has several possible nasty side effects, and several problems inherent with the form of administration (topical) as well as a couple of possible advantages due to those same factors.

First, a brief discussion of DHT is probably in order, so bear with me.

For starters, pure DHT is a very poor choice for anabolism of any sort. I know we can all look at the anabolic/androgenic rating of it and say that it´s a very good anabolic steroid, but in actuality, what happens to DHT in the body is far different than what we´d want& .but first I´ll give you the good news about it.

DHT is a non-aromatizing androgen, which as you know, means it doesn´t convert to estrogen at all. This is important because estrogen is suppressive of LH production (1), which is of course going to be an aggravating factor in lowering your endogenous testosterone production. DHT, in addition to not converting to that nasty test-suppressive-estrogen, will not inhibit LH production or testosterone production (1) (2) (3). DHT may even have a suppressive effect on estrogen, in some cases. This would certainly account for its ability to actually have a positive effect (again, in some cases) on LH and testosterone.

This is all very good news, but unfortunately, there´s a catch. Your body reduces DHT to inactive metabolites by way of the 3-alpha-hydroxysteroid dehydrogenase enzyme before alot of it can reach the androgen receptors in skeletal tissue. This means while it reaches your scalp and prostate relatively intact, it doesn´t make it to your muscles that way. This is why we see so many different alterations of DHT available on the market, from Anadrol 50 to Anavar, with so many different uses. Andractim has the most unique use, though, I think.

Andractim has been used with some success to reduce gyno in males. It´s possible that a lowering of circulating DHT-levels can cause Gyno (5)(6), and certainly androgen therapy with DHT derivatives has been found useful for treatment of gyno... so it´s very logical that a topical DHT would be a good bet for Anabolic/Androgenic Steroid induced Gyno. Here´s the creepy part:

You´ll need to rub it on your nipples several times per day.

Obviously this is problematic for someone with a job, who can´t be going to the restroom and rubbing their nipples a couple of times every day. Unless rubbing your nipples is part of your job, anyway..

Andractim Testosterone Gel

Andractim testosterone gel is a topical gel, which comes in a tube, containing 80x 25mg doses of DHT. Absorption rate is going to be similar to testosterone gel, or roughly 10%, so you´re applying 2.5mgs of pure DHT to your nips every time you use this stuff. I´d say you want to be doing this 2x per day with an equal amount per nipple, using 25-5 mgs of gel each time.

References:

 

  1. Hypothalamic sites of action for testosterone, dihydrotestosterone, and estrogen in the regulation of luteinizing hormone secretion in male sheep. Endocrinology. 1997 Sep;138(9):3686-94.
  2. Inhibition of LH Secretion by Localized Administration of Estrogen, but not Dihydrotestosterone, Is Enhanced in the Ventromedial Hypothalamus During Feed Restriction in the Young Wether. Biol Reprod. 2005 Jun 22; [Epub ahead of print]
  3. Crystalline dihydrotestosterone implants in the lateral septum of male rats. A positive effect on LH and FSH. Endocr Res. 2001 Feb-May;27(1-2):35-40.
  4. Significant role of 5 alpha-reductase on feedback effects of androgen in rat anterior pituitary cells demonstrated with a nonsteroidal 5 alpha-reductase inhibitor ONO-3805. J Androl. 1994 Nov-Dec;15(6):521-7.
  5. Case report: finasteride-induced gynecomastia in a 62-year-old man. Am J Med Sci. 1995 Jun;309(6):322-5.
  6. Male pseudohermaphroditism due to 5 alpha reductase deficiency associated with gynecomastia. Rev Hosp Clin Fac Med Sao Paulo. 1987 Mar-Apr;42(2):66-8.


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