Schreiber J R, Nakamura K, Erickson G F
Mol Cell Endocrinol. 1980 Aug;19(2):165-73. doi: 10.1016/0303-7207(80)90019-2.
It has been hypothesized that progesterone (P) exerts a direct inhibitory effect on ovarian follicular development, an effect which could be mediated by P receptors located in granulosa cells. We tested this hypothesis by examining the effect of several progestins on FSH-stimulated estrogen (E), P, and 20 alpha-dihydroprogesterone (DHP) production by cultured rat granulosa cells, and correlated the results with the ability of the progestins to bind to the granulosa cell P receptor. Granulosa cells from immature hypophysectomized DES-treated rat produced 9 ng/ml E, 21 ng/ml P and 29 ng/ml DHP during a 2-day incubation in McCoy's 5a medium containing 10(-7) M androstenedione and 10 ng/ml of FSH. The FSH-induced increase in E production was inhibited by 50 and 95% following concomitant treatment with 3 x 10(-6) and 10(-5) M resp. of R5020, a potent synthetic progestin. Added R5020 at these concentrations also significantly inhibited P and DHP production. R5020 had no effect on granulosa cell viability or plating efficiency, and the inhibitory action of R50920 on E production was reversible. In studies of the specificity of the progestin inhibitory action, the relative abilities of various progestins to inhibit E production were R5020 > P > DHP > 17 alpha-hydroxyprogesterone (17OHP). The relative abilities of these progestins to bind to the ovary P receptor were also: R5020 > P > DHP > 17OHP. These results indicate that exogenous progestins directly inhibit the FSH-stimulation of granulosa cell steroidogenesis in vitro and suggest that the progestin effect may be mediated by the P receptor. Such results offer a possible mechanism whereby progesterone could exert a direct but reversible inhibitory action on ovarian follicular development.
据推测,孕酮(P)对卵巢卵泡发育具有直接抑制作用,该作用可能由颗粒细胞中的P受体介导。我们通过检测几种孕激素对培养的大鼠颗粒细胞中促卵泡激素(FSH)刺激的雌激素(E)、P和20α-二氢孕酮(DHP)产生的影响来验证这一假设,并将结果与孕激素与颗粒细胞P受体结合的能力相关联。来自未成熟垂体切除且经己烯雌酚处理的大鼠的颗粒细胞,在含有10⁻⁷M雄烯二酮和10 ng/ml FSH的 McCoy's 5a培养基中培养2天时,产生9 ng/ml E、21 ng/ml P和29 ng/ml DHP。分别用3×10⁻⁶M和10⁻⁵M的强效合成孕激素R5020同时处理后,FSH诱导的E产生增加分别被抑制了50%和95%。添加这些浓度的R5020也显著抑制了P和DHP的产生。R5020对颗粒细胞活力或接种效率没有影响,并且R50920对E产生的抑制作用是可逆的。在孕激素抑制作用特异性的研究中,各种孕激素抑制E产生的相对能力为:R5020 > P > DHP > 17α-羟孕酮(17OHP)。这些孕激素与卵巢P受体结合的相对能力也为:R5020 > P > DHP > 17OHP。这些结果表明,外源性孕激素在体外直接抑制FSH对颗粒细胞类固醇生成的刺激,并提示孕激素的作用可能由P受体介导。这些结果提供了一种可能机制,据此孕酮可对卵巢卵泡发育发挥直接但可逆的抑制作用。