Nagler H M, deVere White R, Dyrenfurth I, Hembree W C
Fertil Steril. 1983 Dec;40(6):818-22. doi: 10.1016/s0015-0282(16)47487-x.
delta 1-Testolactone, an androgen derivative without intrinsic hormonal action, is known to block the aromatization of androgens to estrogens. This study was designed to assess its effect upon serum testosterone (T) and estradiol (E2) in the adult male rat. By itself, testolactone (TL) did not affect T/E2 levels in the dosages utilized. Daily injections of human chorionic gonadotropin (hCG) for 15 days caused a tenfold rise in serum T, although there was no increase in serum E2. When given along with hCG, TL did not alter the Leydig cell response. However, pretreatment of animals with TL increased the testicular response to hCG over that of saline-treated animals. Studies were also carried out to delineate the sources of estrogen in the adult male rat. These experiments demonstrate that (1) the majority of E2 is not testicular in origin but is derived from the adrenal; (2) the conversion of androgen precursors to E2 in the rat is not affected by TL; and (3) in spite of no demonstrable inhibition of E2 production, TL causes an increased Leydig cell responsiveness to hCG.
δ1-睾酮内酯是一种无内在激素作用的雄激素衍生物,已知它能阻断雄激素向雌激素的芳香化作用。本研究旨在评估其对成年雄性大鼠血清睾酮(T)和雌二醇(E2)的影响。就其本身而言,在所使用的剂量下,睾酮内酯(TL)不影响T/E2水平。每日注射人绒毛膜促性腺激素(hCG)15天可使血清T升高10倍,尽管血清E2没有增加。当与hCG一起给予时,TL不会改变睾丸间质细胞的反应。然而,用TL对动物进行预处理会使睾丸对hCG的反应比用生理盐水处理的动物增强。还进行了研究以确定成年雄性大鼠中雌激素的来源。这些实验表明:(1)大部分E2并非来源于睾丸,而是来自肾上腺;(2)大鼠中雄激素前体向E2的转化不受TL影响;(3)尽管没有明显抑制E2的产生,但TL会使睾丸间质细胞对hCG的反应性增强。