Guerrero H E, Stein P, Asch R H, de Fried E P, Tesone M
Instituto de Biología y Medicina Experimental, Buenos Aires, Argentina.
Fertil Steril. 1993 Apr;59(4):803-8.
To examine the effect of a gonadotropin-releasing hormone agonist (GnRH-a), leuprolide acetate (LA), on human chorionic gonadotropin/luteinizing hormone (LH) receptors content and progesterone (P) and estradiol (E2) production in cultured granulosa or luteal cells.
Prospective.
Private Fertility Clinic and National Research Institute.
Twenty patients undergoing in vitro fertilization or gamete intrafallopian transfer programs.
Human chorionic gonadotropin/LH receptors in human granulosa cells increased after 48 hours of culture, and LA inhibited such effect. Leuprolide acetate, 1 ng/mL, in the cultures produced an increase in P production. On the contrary, LA inhibited E2 production. Additionally, the in vivo effect of LA (2 micrograms/rat per 7 days) was studied in corpus luteum of superovulated rats. Luteal cells from LA-treated rats in culture produced lower P than the controls but showed an increase in aromatase activity. Luteal LH receptors declined after 48 hours of culture with LA.
The high doses of gonadotropin necessary to induce ovarian hyperstimulation when GnRH-a is administered could be related with an inhibitory effect of these agonists on LH receptors and aromatase activity.
研究促性腺激素释放激素激动剂(GnRH-a)醋酸亮丙瑞林(LA)对培养的颗粒细胞或黄体细胞中人绒毛膜促性腺激素/促黄体生成素(LH)受体含量以及孕酮(P)和雌二醇(E2)生成的影响。
前瞻性研究。
私立生育诊所和国家研究所。
20例行体外受精或配子输卵管内移植手术的患者。
人颗粒细胞中的人绒毛膜促性腺激素/LH受体在培养48小时后增加,而LA抑制了这种作用。培养物中1 ng/mL的醋酸亮丙瑞林使P生成增加。相反,LA抑制E2生成。此外,还研究了LA(每7天2微克/大鼠)在超排卵大鼠黄体中的体内作用。培养的LA处理大鼠的黄体细胞产生的P低于对照组,但芳香化酶活性增加。用LA培养48小时后,黄体LH受体减少。
给予GnRH-a时诱导卵巢过度刺激所需的高剂量促性腺激素可能与这些激动剂对LH受体和芳香化酶活性的抑制作用有关。