Pointis G, Latreille M T
J Reprod Fertil. 1987 May;80(1):321-6. doi: 10.1530/jrf.0.0800321.
In contrast to the strong stimulation of testosterone production by hCG, L-isoproterenol had little effect on freshly isolated Leydig cells from 18-day-old mouse fetuses. However, the ability of fetal Leydig cells to respond to L-isoproterenol exposure increased during culture (0-24 h). The response of the cultured cells to L-isoproterenol was dose-dependent with an ED50 at 2 X 10(-7) M. Adrenaline and noradrenaline at a concentration of 10(-5) M also increased testosterone production by cultured fetal Leydig cells. DL-Propranolol, a beta-antagonist, inhibited L-isoproterenol-stimulated testosterone production in a dose-dependent manner, while phentolamine, an alpha-adrenergic antagonist, had no effect. These results suggest that catecholamines may play an essential role in the control of testicular steroidogenesis during fetal development.
与hCG对睾酮生成的强烈刺激作用相反,L-异丙肾上腺素对从18日龄小鼠胎儿新鲜分离的睾丸间质细胞几乎没有影响。然而,胎儿睾丸间质细胞对L-异丙肾上腺素暴露的反应能力在培养过程中(0 - 24小时)有所增加。培养细胞对L-异丙肾上腺素的反应呈剂量依赖性,ED50为2×10(-7)M。浓度为10(-5)M的肾上腺素和去甲肾上腺素也能增加培养的胎儿睾丸间质细胞的睾酮生成。β受体拮抗剂DL-普萘洛尔以剂量依赖性方式抑制L-异丙肾上腺素刺激的睾酮生成,而α肾上腺素能拮抗剂酚妥拉明则无作用。这些结果表明,儿茶酚胺可能在胎儿发育过程中睾丸类固醇生成的控制中起重要作用。