EFFECTS OF TESTOSTERONE, TESTOSTERONE METABOLITES AND ANTI-ANDROGENS ON THE FUNCTION OF THE MALE ACCESSORY GLANDS IN THE RABBIT AND RAT

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Abstract
The androgenic potencies of testosterone, 5.alpha.-dihydrotestosterone, 5.alpha.-androstane-3.alpha.,17.beta.-diol and 5.alpha.-androstane-3.beta.,17.beta.-diol towards the prostate, glandula seminalis + glandula vesicularis, ampullae and epididymis were evaluated after administration to castrated rabbits. The influence of cyproterone acetate, stilbestrol and medrogestone on accessory gland function was also investigated in rabbits and rats. In the rabbit the minimum dose of testosterone propionate that would maintain the function of all accessory glands at normal levels was approximately 200 .mu.g/animal per day. Higher levels of testosterone propionate overstimulated the function of the prostate, glandula seminalis + glandula vesicularis and ampullae, but did not affect the epididymis. Testosterone propionate and 5.alpha.-dihydrotestosterone propionate were essentially equipotent in their capacity to support growth and secretory activity, and stimulated all the accessory glands; 5.alpha.-androstane-3.alpha.,17.beta.-diol dipropionate had a pronounced differential effect; it was considerably more potent than testosterone propionate in promoting secretion in the prostate, but was ineffective in maintaining the function of the epididymis. 5.alpha.-Androstane-3.beta.,17.beta.-diol dipropionate was the weakest androgen tested. The potency of a steroid probably depends on whether it is administered as its free or esterified form. Cyproterone acetate suppressed fructose secretion in the prostate of the rabbit but had no adverse effects on the function of the epididymis in either the rabbit or rat. Stilbestrol was the most potent anti-androgen tested and medrogestone the least effective.