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Keywords :
Androgen Antagonists/pharmacology; Androstanes/pharmacology; Androstatrienes/pharmacology; Animals; Azasteroids/pharmacology; Cloaca/drug effects/metabolism; Coturnix/physiology; Cyproterone/analogs & derivatives/pharmacology; Cyproterone Acetate; Estrogen Antagonists/pharmacology; Flutamide/pharmacology; Hypothalamus/drug effects/metabolism; Male; Nitromifene/pharmacology; Quail/physiology; Tamoxifen/pharmacology; Testosterone/metabolism/pharmacology
Abstract :
[en] The effects of antioestrogens, antiandrogens and of various inhibitors of testosterone metabolism on testosterone metabolism in the quail hypothalamus and cloacal gland were studied by an in-vitro radioenzymatic assay. It was found that antioestrogens and antiandrogens generally had little or no effect on aromatase and 5 alpha- and 5 beta-reductases of testosterone, except when used at very high doses. The 5 alpha-reductase inhibitor, 17 beta-N,N-diethylcarbamoyl-4-methyl-4-aza-5 alpha-androstan-3-one, inhibited both 5 alpha- and 5 beta-dihydrotestosterone production without markedly affecting aromatase activity. Surprisingly, the aromatase inhibitor, 1,4,6-androstatriene-3,17-dione, inhibited not only the production of oestradiol but also that of 5 beta-dihydrotestosterone and, to a lesser extent, 5 alpha-dihydrotestosterone. These unexpected properties should be taken into account when interpreting the results of in-vivo experiments using these compounds.
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