Rittmaster R S, Antonian L, New M I, Stoner E
Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
J Androl. 1994 Jul-Aug;15(4):298-301.
Finasteride, a 5 alpha-reductase inhibitor, does not bind to the androgen receptor and has no other known hormonal activity. To determine what effect, if any, it has on adrenal steroidogenesis, 10 healthy men received 5 mg finasteride daily for 28 days. Adrenocorticotropic hormone (ACTH) stimulation tests were performed before and after 4 weeks of finasteride administration (5 mg daily). Serum levels of 17-hydroxypregnenolone, 17-hydroxyprogesterone, deoxycorticosterone, corticosterone, aldosterone, cortisol, dehydroepiandrosterone, and androstenedione were measured before and 60 minutes after i.v. ACTH. Finasteride decreased serum dihydrotestosterone levels from 31 +/- 5 to 4.4 +/- 1.2 ng/dl (P < 0.001). There were no significant changes in basal or ACTH-stimulated serum levels of adrenal steroids. There was also no significant decrease in the product to precursor ratio for the seven adrenal enzymes tested. Finasteride increased mean serum androstenedione levels by 17% (P = 0.10) and significantly increased the androstenedione to 17-hydroxyprogesterone ratio (P = 0.02 before ACTH and 0.05 after ACTH). These changes are most likely due to inhibition of androstenedione metabolism by 5 alpha-reductase. In conclusion, finasteride has no detectable effect on adrenal steroidogenesis, other than that which can be explained by inhibition of the 5 alpha-reductase enzyme.
非那雄胺是一种5α-还原酶抑制剂,不与雄激素受体结合,也没有其他已知的激素活性。为了确定它对肾上腺类固醇生成是否有影响(如果有影响,影响如何),10名健康男性每天服用5毫克非那雄胺,持续28天。在服用非那雄胺4周(每日5毫克)前后进行促肾上腺皮质激素(ACTH)刺激试验。在静脉注射ACTH前及注射后60分钟测量血清中17-羟孕烯醇酮、17-羟孕酮、脱氧皮质酮、皮质酮、醛固酮、皮质醇、脱氢表雄酮和雄烯二酮的水平。非那雄胺使血清双氢睾酮水平从31±5降至4.4±1.2纳克/分升(P<0.001)。肾上腺类固醇的基础水平或ACTH刺激后的血清水平没有显著变化。所检测的七种肾上腺酶的产物与前体比值也没有显著下降。非那雄胺使平均血清雄烯二酮水平升高了17%(P=0.10),并显著提高了雄烯二酮与17-羟孕酮的比值(ACTH注射前P=0.02,注射后P=0.05)。这些变化很可能是由于5α-还原酶对雄烯二酮代谢的抑制作用。总之,非那雄胺对肾上腺类固醇生成没有可检测到的影响,除非可以用5α-还原酶的抑制作用来解释。