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人颗粒黄体细胞中17β-雌二醇与孕酮生成的相互作用

Interaction of 17 beta-estradiol and progesterone production in human granulosa-luteal cells.

作者信息

Jalkanen J

机构信息

Department I of Obstetrics and Gynecology, Helsinki University Central Hospital, Finland.

出版信息

Eur J Obstet Gynecol Reprod Biol. 1990 Nov;37(2):143-53. doi: 10.1016/0028-2243(90)90107-c.

Abstract

The secretion of 17 beta-estradiol (E2) and the effect of exogenous E2 on progesterone (P) production by granulosa-luteal cells from 18 women attending an in vitro fertilization (IVF) program were studied. The cells were separated from follicular fluid and precultured in medium containing fetal calf serum. On the third day of culture E2 (0.25-2.0 micrograms/ml) was added onto the cells and its effect on both hCG-stimulated and basal P production was measured. E2 inhibited both basal and hCG-stimulated P production. 1 microgram/ml of E2 caused mean decrements of 55 and 56% in basal and hCG-stimulated P production, respectively. The maximal inhibition by E2 occurred at 6 hours of incubation, but when the cells were allowed to react with E2 for longer periods of time the effect became less significant and more variable. At 48 h no inhibition was observed. At 6 h E2 (1.0 microgram/ml) increased both basal and hCG-stimulated pregnenolone production by approx. 10-fold, suggesting that the suppression of P production was due to inhibition of 3 beta-hydroxysteroid dehydrogenase. Exogenous androgen, 5-Androsten-3 beta-ol-17-one sulfate, dehydroepiandrosterone sulfate (DHEAS), in a dose-dependent manner increased granulosa-luteal cell E2 production. The maximal response was about 1000-fold above the E2 production of unstimulated cells and was not affected by hCG. However, the maximal amount of E2 produced was minor in comparison to exogenous doses required for the suppression of P production and did not have the inhibitory effect. It is concluded that the production of E2 by granulosa-luteal cells is mainly regulated by the availability of androgen substrate, and that E2 functions as a modulator of luteal P production.

摘要

研究了18名接受体外受精(IVF)治疗的女性颗粒黄体细胞分泌17β-雌二醇(E2)的情况以及外源性E2对其孕酮(P)产生的影响。从卵泡液中分离出细胞,并在含有胎牛血清的培养基中预培养。在培养的第三天,将E2(0.25 - 2.0微克/毫升)添加到细胞中,并测量其对hCG刺激的和基础P产生的影响。E2抑制基础和hCG刺激的P产生。1微克/毫升的E2分别使基础和hCG刺激的P产生平均降低55%和56%。E2的最大抑制作用出现在孵育6小时时,但当细胞与E2反应更长时间时,这种作用变得不那么显著且更具变异性。在48小时时未观察到抑制作用。在6小时时,E2(1.0微克/毫升)使基础和hCG刺激的孕烯醇酮产生增加约10倍,表明P产生的抑制是由于3β-羟基类固醇脱氢酶的抑制。外源性雄激素5-雄烯-3β-醇-17-酮硫酸盐、硫酸脱氢表雄酮(DHEAS)以剂量依赖的方式增加颗粒黄体细胞E2的产生。最大反应比未刺激细胞的E2产生高约1000倍,且不受hCG影响。然而,与抑制P产生所需的外源性剂量相比,产生的最大E2量较小,且没有抑制作用。结论是颗粒黄体细胞产生E2主要受雄激素底物可用性的调节,并且E2作为黄体P产生的调节剂发挥作用。

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