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人绒毛膜促性腺激素和前列腺素F2α对人黄体细胞孕酮分泌的影响。

Effect of human chorionic gonadotropin and prostaglandin F2a on progesterone production by human luteal cells.

作者信息

Khan-Dawood F S, Huang J C, Dawood M Y

机构信息

Department of Obstetrics and Gynecology, University of Illinois College of Medicine, Chicago 60612.

出版信息

J Steroid Biochem. 1989 Nov;33(5):941-7. doi: 10.1016/0022-4731(89)90244-6.

Abstract

To determine and compare the direct effects of prostaglandin F2a (PGF2a) and human chorionic gonadotropin (hCG) on luteal cell progesterone production in vitro, 9 human corpora lutea obtained at tubal ligation were minced and treated with collagenase to disaggregate luteal cells. Dispersed luteal cells (80% viable) were incubated in air at 37 degrees C in a shaking water bath for 3 h and total progesterone in the media and cells was determined by radioimmunoassay. Optimum progesterone production was obtained using 25,000 or more cells per incubate and an incubation time of 2-4 h. hCG-stimulated progesterone production increased significantly with 0.01 IU to as high as 100 IU. In the early luteal phase (days 1-5 post ovulation or days 15-20 of the luteal phase), PGF2a (10-1000 ng) significantly inhibited progesterone production but significantly stimulated progesterone production in the mid-luteal phase (days 21-25). PGF2a had no effect on luteal cell progesterone production in the late luteal phase (days 26-30). This age-dependent direct effect of PGF2a on human luteal cell progesterone production in vitro indicates a role for PGF2a in the total intragonadal regulation of progesterone output, possibly through a paracrine or autocrine manner directed towards synchronizing luteal progesterone secretion and endometrial preparation for nidation.

摘要

为了确定并比较前列腺素F2α(PGF2α)和人绒毛膜促性腺激素(hCG)对体外黄体细胞孕酮生成的直接作用,将9个在输卵管结扎时获得的人黄体切碎,并用胶原酶处理以分离黄体细胞。将分散的黄体细胞(80%存活)在37℃的空气中于振荡水浴中孵育3小时,通过放射免疫测定法测定培养基和细胞中的总孕酮。每个培养物使用25000个或更多细胞以及2 - 4小时的孵育时间可获得最佳孕酮生成。hCG刺激的孕酮生成在0.01 IU至高达100 IU时显著增加。在黄体早期(排卵后第1 - 5天或黄体期第15 - 20天),PGF2α(10 - 1000 ng)显著抑制孕酮生成,但在黄体中期(第21 - 25天)显著刺激孕酮生成。PGF2α在黄体晚期(第26 - 30天)对黄体细胞孕酮生成无影响。PGF2α对体外人黄体细胞孕酮生成的这种年龄依赖性直接作用表明PGF2α在孕酮输出的性腺内整体调节中发挥作用,可能通过旁分泌或自分泌方式来协调黄体孕酮分泌和子宫内膜着床准备。

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