Spinucci G, Pasquali R
Dipartimento di Medicina interna e Gastroenterologia, Policlinico S. Orsola-Malpighi, Bologna.
Clin Ter. 1996 Jun;147(6):305-15.
Finasteride is a drug which inhibits the transformation of testosterone into its active metabolite, dihydrotestosterone, in the target organs, i.e. the skin, the scalp, the liver and the prostate. In the pathogenic mechanism of hirsutism and androgenetic alopecia, and important role is presumably played by alterations of the mechanisms which transform testosterone into dihydrotestosterone. In some conditions an increase in dihydrotestosterone has been demonstrated, due to increased activity of the enzyme 5 alpha-reductase. The effect of finasteride develops above all at the level of type II 5 alpha-reductase. Recent studies have evaluated the effect of finasteride in patients of both sexes with hirsutism and androgenetic alopecia. In women with various forms of hyperandrogenism, the use of the drug at the doses commonly used for the treatment of benign prostatic hyperplasia seems to have induced a significant reduction in the degree of hirsutism. Furthermore, both in animals and men with alopecia, the drug seems to have led to an increase in the number and an improvement in the shape of the follicles in the anagen phase, and a simultaneous decrease of dehydrotestosterone at the level of the scalp. This study represents a review of the main results obtained over the last two years and reports the prospects which the use of finasteride may have in this context.
非那雄胺是一种能抑制睾酮在靶器官(即皮肤、头皮、肝脏和前列腺)内转化为其活性代谢物双氢睾酮的药物。在多毛症和雄激素性脱发的发病机制中,睾酮向双氢睾酮转化机制的改变可能起着重要作用。在某些情况下,已证实由于5α-还原酶活性增加,双氢睾酮会增多。非那雄胺的作用主要在II型5α-还原酶水平发挥。最近的研究评估了非那雄胺对患有多毛症和雄激素性脱发的男女患者的疗效。在患有各种形式高雄激素血症的女性中,以治疗良性前列腺增生常用剂量使用该药物似乎已使多毛症程度显著降低。此外,在患有脱发的动物和男性中,该药物似乎已导致生长期毛囊数量增加且形态改善,同时头皮处的双氢睾酮水平降低。本研究对过去两年获得的主要结果进行了综述,并报告了在此背景下使用非那雄胺可能具有的前景。