Martikainen H, Vihko R
Clin Endocrinol (Oxf). 1982 Mar;16(3):227-34. doi: 10.1111/j.1365-2265.1982.tb00711.x.
In order to elucidate the role of prolactin in the regulation of testicular steroidogenesis in man, hyper- and hypoprolactinaemia were induced by sulpiride (group 2) and bromocriptine (group 3) administration in eight and nine young adults, respectively, and the responses of testosterone and six other steroids to a single dose of 5000 iu hCG were compared with those obtained under basal conditions (group 1) in eight men. During hyperprolactinaemia (group 2) the responses of pregnenolone, progesterone, 17-hydroxyprogesterone, testosterone and 5 alpha-dihydrotestosterone tended to be greater than in the control and hypoprolactinaemia groups, but these changes were not statistically significant. In contrast to the behaviour of these steroids, oestradiol showed diminished peak values at 24-36 hCG in the sulpiride-treated group and the response was significantly smaller (P less than 0 . 01) than during hypoprolactinaemia. These findings suggest that testicular aromatization is modulated by prolactin and thus the partial inhibition of oestradiol production, observed during short-term hyperprolactinaemia, may result in a better androgen response to hCG.
为了阐明催乳素在男性睾丸类固醇生成调节中的作用,分别对8名和9名年轻男性使用舒必利(第2组)和溴隐亭(第3组)诱导高催乳素血症和低催乳素血症,并将睾酮和其他6种类固醇对单次5000国际单位人绒毛膜促性腺激素(hCG)的反应与8名男性在基础条件下(第1组)获得的反应进行比较。在高催乳素血症期间(第2组),孕烯醇酮、孕酮、17-羟孕酮、睾酮和5α-二氢睾酮的反应往往大于对照组和低催乳素血症组,但这些变化无统计学意义。与这些类固醇的表现相反,在舒必利治疗组中,雌二醇在hCG注射后24 - 36小时的峰值降低,且反应明显小于低催乳素血症期间(P < 0.01)。这些发现表明,催乳素可调节睾丸芳香化作用,因此在短期高催乳素血症期间观察到的雌二醇生成的部分抑制可能导致对hCG的雄激素反应更好。