Permezel J M, Lenton E A, Roberts I, Cooke I D
Harris Birthright Centre for Reproductive Biology, Sheffield, United Kingdom.
J Clin Endocrinol Metab. 1989 May;68(5):960-5. doi: 10.1210/jcem-68-5-960.
Considerable controversy still exists concerning the role of progesterone in the initiation of the midcycle gonadotropin surge in humans. We, therefore, carried out a prospective randomized study to determine the potential of progesterone to initiate a gonadotropin surge and the acute effects of a potent progesterone antagonist (RU 486) on follicular phase gonadotropin secretion in normal women. The women underwent frequent blood sampling for 4 in the midfollicular (day 6) or late follicular phase (day 10). They then received either progesterone (10 mg, im) or RU 486 (10 or 100 mg, orally), and blood sampling was continued for an additional 8 h. Four women received each of the drug regimens in the early follicular phase, and four received each regimen in the late follicular phase. Two additional women were studied as control subjects at each stage of the cycle. Progesterone administration in the mid- and late follicular phases resulted in an acute increase in plasma LH and FSH concentrations, and the increases correlated with the base line plasma estradiol concentrations (P less than 0.05). In contrast to progesterone, the women who received RU 486 in the mid- and late follicular phases had a reduction in plasma LH and FSH concentrations after drug administration. The response in the mid-follicular phase was considerably less than that in the late follicular phase, and the extent of the response correlated with the baseline plasma estradiol concentrations (P less than 0.005). The changes were similar in response to both RU 486 doses. We conclude that progesterone can initiate a gonadotropin surge in the late follicular phase of the menstrual cycle. The inhibitory effect of the progesterone antagonist RU 486 suggests that a positive feedback mechanism involving progesterone may be influential some time before the surge onset.
关于孕酮在人类月经周期中期促性腺激素激增起始过程中的作用,目前仍存在相当大的争议。因此,我们进行了一项前瞻性随机研究,以确定孕酮引发促性腺激素激增的可能性,以及一种强效孕酮拮抗剂(RU 486)对正常女性卵泡期促性腺激素分泌的急性影响。这些女性在卵泡期中期(第6天)或卵泡期晚期(第10天)接受了4次频繁的血液采样。然后她们分别接受孕酮(10毫克,肌肉注射)或RU 486(10或100毫克,口服),并继续进行8小时的血液采样。4名女性在卵泡期早期接受每种药物方案,4名女性在卵泡期晚期接受每种方案。在月经周期的每个阶段,另外两名女性作为对照受试者进行研究。在卵泡期中期和晚期给予孕酮导致血浆促黄体生成素(LH)和促卵泡生成素(FSH)浓度急性升高,且升高与基线血浆雌二醇浓度相关(P<0.05)。与孕酮相反,在卵泡期中期和晚期接受RU 486的女性在给药后血浆LH和FSH浓度降低。卵泡期中期的反应明显小于卵泡期晚期,且反应程度与基线血浆雌二醇浓度相关(P<0.005)。两种RU 486剂量的反应变化相似。我们得出结论,孕酮可在月经周期的卵泡期晚期引发促性腺激素激增。孕酮拮抗剂RU 486的抑制作用表明,涉及孕酮的正反馈机制可能在激增开始前的一段时间内发挥作用。