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It might, but the aromatase enzyme in all of our bodies creates estrogen from testosterone, and higher estrogen levels can lead to problems like gynecomastia as well as water retention, steroid oral fluticasone.

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Steroid oral fluticasone, legal steroids for sale gain muscle. For this reason, it is logical to summarize this approach, based on growth of a particular skeletal muscle called the levator ani relative to that of androgenic target tissue, usually the prostate gland, and attempt to explain the underlying mechanism of dissociation of the growth of the two tissues (compared with controls). Eisenberg and Gordan (1950) proposed the use of the rat levator ani muscle as a bioassay of protein anabolic activity; the anatomical drawings from the dissection of the male rat, displaying the location of this muscle, the prostate and seminal vesicles are displayed in this paper. The rat levator ani muscle is part of the perineal complex of striated muscles that envelope the rectum. This muscle was chosen because previous workers had reported that testosterone propionate stimulated the growth of the perineal complex in infantile rats, and, additionally, this complex was easily separated from other tissues. In contrast, there was a much smaller unparalleled increase in the weight of the seminal vesicles. The foundation of the commonly used procedure of the myotrophic’androgenic index was based on a modification of the Eisenberg and Gordan method by Hershberger et al. Hershberger and co-workers preferred the use of the ventral part of the prostate rather than the seminal vesicles as a measure of tissue androgenic response in immature gonadectomized rats. They proposed a measure of hormonal myotrophic-to-androgenic activity using the following ratio: Index ratio=(experimental levator ani weight?control levator ani weight)/(experimental ventral prostate weight?control ventral prostate weight) =increase in levator ani weight/increase in ventral prostate weight. Many investigators employed the approach proposed by Hershberger et al. Like the index value, the myotrophic or androgenic effects were themselves expressed as ratios to other reference steroids, for example, 17?-methyl testosterone or testosterone for oral routes and testosterone propionate for parenteral routes. A comprehensive comparison of the anabolic and androgenic activities of many anabolic steroids and their dissociation index is given elsewhere (Potts et al. Comparison of myotrophic and androgenic activities of anabolic steroids’examples were drawn from a much more comprehensive table (with referenced papers) presented by Potts et al, steroid oral fluticasone. Kruskemper (1968) discusses the many failings of the procedures used for determining the myotrophic’androgenic index, for example, the seminal vesicles react more slowly to certain androgens, so that with short test administration, distortions can arise in favour of the myotrophic effect. The harshest criticism of this index was given by Nimni and Geiger (1957), Scow and Hagan (1957) and Hayes (1965). Testosterone administration for 56 days to young gonadectomized rats (castrated at 20’23 days of age) had no effect on the growth of the thigh muscle compared with controls, yet there was considerable growth in the perineal musculature (Scow, 1952; Scow and Hagan, 1957). Testosterone propionate or norethandrolone (17?-ethyl-19-nortestosterone; also an anabolic steroid) administration promoted the growth of the levator ani muscle even in young normal or castrated rats on a protein-free diet, that is, a local anabolic effect proceeding at the expense of catabolic processes in other organs. Hayes (1965) stated that the rat levator ani muscle is not homologous to this muscle in other species, that is, it is not a typical sphincter muscle and does not lift the anus in rodents but is part of the male reproductive system. Thus, Hayes renamed the levator ani muscle, calling it the dorsal bulbocavernosus. All three groups of workers showed that the levator ani muscle reflects a general genitomyotrophic response rather than an overall response to androgens. Later, Hervey (1982) claimed that the male rat’s characteristics are determined shortly after birth (due to a brief secretion of testosterone), and, thereafter, any increase in body mass is not affected by androgens. Contrary to the opinions described above, there is nonetheless biochemical evidence that suggests that the genitomyotrophic response of the levator ani muscle may serve as an indicator of the general myotrophic responses in the developing rat for the following reasons. The same classic androgen receptor can be characterized in the prostate, the bulbocavernosus/levator ani muscle and typical skeletal muscles of the rat (Krieg and Voigt, 1977). Nandrolone (19-nortestosterone) and 5?-DHT have a higher binding affinity than testosterone with the receptor. The prostate has 7 times the concentration of androgen receptors than the bulbocavernosus/levator ani muscles which in turn has 10 times more than other skeletal muscle. In vitro studies by Gloyna and Wilson (1969) and Massa and Martini (1974) have shown that 5?-reductase activity is very high in rat sexual tissue such as the prostate and seminal vesicles but negligible, if at all, in skeletal muscle such as the levator ani and thigh muscle.

 

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