Smals A G, Kloppenborg P W, Lequin R M, Benraad T J
Acta Endocrinol (Copenh). 1976 Dec;83(4):829-38. doi: 10.1530/acta.0.0830829.
The mean basal plasma LH and FSH levels in 8 patients with Klinefelter's syndrome were respectively 5 and 15-fold higher than in 8 eugonadal males, whereas plasma testosterone concentration were half the normal value. After an intravenous bolus injection of gonadotrophin releasing hormone (100 mug of LH-RH) the gonadotrophin increase in the Klinefelter patients was more marked than in the control subjects, but in both groups the plasma testosterone levels remained essentially unchanged. In contrast to the bolus injection, an 8 h infusion of LH-RH after the bolus elicited a significant plasma testosterone increase in both the eugonadal males (59%) and the Klinefelter patients (51%). These findings indicate that despite an impressive endogenous hyper-gonadotrophism, Leydig cells in Klinefelter's syndrome can still respond to a sustained further increase of these endogenous gonadotrophins and thus still have functional reserve.
8例克兰费尔特综合征患者的基础血浆促黄体生成素(LH)和促卵泡生成素(FSH)水平分别比8例性腺功能正常男性高5倍和15倍,而血浆睾酮浓度仅为正常值的一半。静脉推注促性腺激素释放激素(100μg促黄体生成素释放激素)后,克兰费尔特综合征患者促性腺激素的升高比对照组更为明显,但两组的血浆睾酮水平基本保持不变。与推注不同,推注后8小时输注促黄体生成素释放激素会使性腺功能正常男性(59%)和克兰费尔特综合征患者(51%)的血浆睾酮显著升高。这些发现表明,尽管存在明显的内源性促性腺激素过多,但克兰费尔特综合征患者的睾丸间质细胞仍能对这些内源性促性腺激素的持续进一步升高做出反应,因此仍具有功能储备。