Olsson J H, Dennefors B, Nilsson L
J Endocrinol Invest. 1986 Apr;9(2):109-14. doi: 10.1007/BF03348079.
In order to investigate the influence of danazol on steroidogenesis and gonadotropic responsiveness of human follicular cells, granulosa and thecal cells of preovulatory follicles were isolated and separately incubated for short term periods. Human chorionic gonadotropin (hCG) (100 IU/ml), FSH (0.5 IU/ml) and danazol (10 micrograms/ml) alone or in combination were added to the incubation medium. Following incubation the cellular cyclic adenosine 3'5' monophosphate (cAMP) levels and the medium content of progesterone (P), androstenedione (A) and 17 beta-estradiol (E2) were determined. All follicles included in the study were classified as nonatretic and well developed, i.e. less than 3 days before ovulation. Human chorionic gonadotropin caused an increase in cAMP formation in both cell-types and this effect was significantly counteracted by danazol in vitro. In granulosa cells danazol tended to counteract a stimulatory effect of FSH on cAMP formation. No significant influence of danazol was found on the basal steroid formation of both cell types during short term incubation. On the other hand, danazol significantly counteracted the FSH stimulated P formation of the granulosa cells and the hCG stimulated A and E2 formation of the thecal cells. It is concluded that danazol inhibits gonadotropin-stimulated steroidogenesis locally in the human follicular cells and that this effect of danazol is mediated via the cyclic AMP system.
为了研究达那唑对人卵泡细胞类固醇生成和促性腺激素反应性的影响,分离了排卵前卵泡的颗粒细胞和卵泡膜细胞,并分别进行短期培养。将人绒毛膜促性腺激素(hCG)(100 IU/ml)、促卵泡激素(FSH)(0.5 IU/ml)和达那唑(10微克/ml)单独或联合添加到培养液中。培养后,测定细胞内环磷酸腺苷(cAMP)水平以及培养液中孕酮(P)、雄烯二酮(A)和17β-雌二醇(E2)的含量。纳入研究的所有卵泡均被分类为非闭锁且发育良好,即排卵前不到3天。人绒毛膜促性腺激素使两种细胞类型中的cAMP生成增加,而在体外达那唑显著抵消了这种作用。在颗粒细胞中,达那唑倾向于抵消促卵泡激素对cAMP生成的刺激作用。在短期培养期间,未发现达那唑对两种细胞类型的基础类固醇生成有显著影响。另一方面,达那唑显著抵消了促卵泡激素刺激的颗粒细胞P生成以及人绒毛膜促性腺激素刺激的卵泡膜细胞A和E2生成。得出的结论是,达那唑在人卵泡细胞中局部抑制促性腺激素刺激的类固醇生成,并且达那唑的这种作用是通过环磷酸腺苷系统介导的。