Gangnerau M N, Picon R
Laboratoire de Physiologie du Développement, Université Paris 7, France.
Arch Androl. 1987;18(3):215-24. doi: 10.3109/01485018708988486.
The present study was performed to investigate in vitro the onset of steroidogenesis and the responsiveness to LH in rat fetal testes. The male gonads explanted on days 12.5, 13.5, and 14.5 of gestation in M199 produced testosterone from 15.5 days as is the case in vivo dcAMP (1 mM) induced an anticipated steroidogenesis on day 14.5 with secretions of testosterone (0.026 +/- 0.003 ng/gonad/24 h) and progesterone (0.078 +/- 0.005 ng/gonad/24 h), whereas LH (100 ng/ml) has no effect. Antiandrogens such as aminoglutethimide (2 mM), cyproterone acetate (1 microgram/ml), and hydroxyflutamide (1 microgram/ml) could not delay the responsiveness to LH on day 15.5. An anticipated production of testosterone on day 14.5 in presence of DHA (200 ng/ml) could not induce functional LH receptors. It would appear that: (a) the onset of testosterone production occurs without extrinsic stimulatory factors; (b) dcAMP initiates an early steroidogenesis; (c) the onset of functional receptors is likely free of the androgenic environment.
本研究旨在体外研究大鼠胎儿睾丸中类固醇生成的起始以及对促黄体生成素(LH)的反应性。在妊娠第12.5、13.5和14.5天取出的雄性性腺,在M199培养基中,从15.5天开始产生睾酮,这与体内情况相同。双丁酰环磷腺苷(dcAMP,1 mM)在第14.5天诱导了预期的类固醇生成,伴有睾酮(0.026±0.003 ng/性腺/24小时)和孕酮(0.078±0.005 ng/性腺/24小时)的分泌,而LH(100 ng/ml)无作用。抗雄激素药物如氨鲁米特(2 mM)、醋酸环丙孕酮(1μg/ml)和羟基氟他胺(1μg/ml)不能延迟第15.5天对LH的反应性。在存在二十二碳六烯酸(DHA,200 ng/ml)的情况下,第14.5天预期的睾酮产生不能诱导功能性LH受体。似乎:(a)睾酮产生的起始无需外在刺激因子;(b)dcAMP启动早期类固醇生成;(c)功能性受体的起始可能不受雄激素环境影响。