Cassidenti D L, Paulson R J, Lobo R A, Sauer M V
Department of Obstetrics and Gynecology, University of Southern California School of Medicine, Los Angeles.
Hum Reprod. 1992 Mar;7(3):344-8. doi: 10.1093/oxfordjournals.humrep.a137646.
Clomiphene citrate (CC), alone or in combination with exogenous gonadotrophins, has been widely used in ovulation induction. CC promotes endogenous release of gonadotrophins, yet when used in combination with exogenous gonadotrophins, its contribution to folliculogenesis is difficult to assess. In order to determine the contribution of CC-induced endogenous gonadotrophin production to the overall ovarian stimulation in cycles treated with CC/human menopausal gonadotrophin (HMG), Nal-Glu, a gonadotrophin-releasing hormone (GnRH) antagonist was administered. Fertile women (n = 10) undergoing ovarian stimulation and oocyte aspiration for the sole purpose of gamete donation were studied. Five women received CC (100 mg daily for 5 days) in conjunction with pure follicle stimulating hormone (FSH) 150 IU daily. Five women received HMG alone. Nal-Glu (50 micrograms/kg/day) was administered intramuscularly to both groups when the leading follicles reached a mean diameter of 16 mm. Human chorionic gonadotrophin (HCG) 10,000 IU was given when the largest follicles reached a mean diameter of 20-22 mm. A significant fall in serum oestradiol levels was observed in women given CC/FSH (37.9 +/- 7.3%) within the first 24 h of Nal-Glu administration. Serum luteinizing hormone (LH) decreased greater than 20% within 24 h of Nal-Glu administration and remained low throughout the rest of the treatment. No decrease in oestradiol levels was noted in cycles receiving HMG alone. With supplemental FSH, falling oestradiol levels in CC/FSH cycles rebounded and continued to rise until the day after HCG administration. Despite a drop in oestradiol in CC/FSH cycles, the aspirated oocytes exhibited no untoward effects. The fertilization and cleavage rates were similar, and pregnancies occurred in both groups.(ABSTRACT TRUNCATED AT 250 WORDS)
枸橼酸氯米芬(CC)单独使用或与外源性促性腺激素联合使用,已被广泛用于诱导排卵。CC可促进促性腺激素的内源性释放,然而,当与外源性促性腺激素联合使用时,其对卵泡发育的作用难以评估。为了确定在CC/人绝经期促性腺激素(HMG)治疗周期中,CC诱导的内源性促性腺激素产生对整体卵巢刺激的作用,给予促性腺激素释放激素(GnRH)拮抗剂那法瑞林(Nal-Glu)。研究了仅为配子捐赠而接受卵巢刺激和卵母细胞抽吸的可育女性(n = 10)。5名女性接受CC(每日100 mg,共5天)联合每日150 IU的纯促卵泡激素(FSH)。5名女性仅接受HMG。当主导卵泡平均直径达到16 mm时,两组均肌肉注射Nal-Glu(50微克/千克/天)。当最大卵泡平均直径达到20 - 22 mm时,给予10000 IU人绒毛膜促性腺激素(HCG)。在给予Nal-Glu的前24小时内,接受CC/FSH的女性血清雌二醇水平显著下降(37.9 +/- 7.3%)。血清促黄体生成素(LH)在给予Nal-Glu的24小时内下降超过20%,并在治疗的其余时间内保持较低水平。仅接受HMG的周期中未观察到雌二醇水平下降。补充FSH后,CC/FSH周期中下降的雌二醇水平反弹并持续上升,直至HCG给药后一天。尽管CC/FSH周期中雌二醇下降,但抽吸的卵母细胞未出现不良影响。受精率和卵裂率相似,两组均发生了妊娠。(摘要截短于250字)