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雌性大鼠卵巢卵泡发育失调:LH 在窦前卵泡-早窦卵泡过渡期间降低了 FSH 的敏感性。

Dysregulation of ovarian follicular development in female rat: LH decreases FSH sensitivity during preantral-early antral transition.

机构信息

Department of Obstetrics and Gynecology, University of Fukui, Fukui, Japan 910-1193.

出版信息

Endocrinology. 2013 Aug;154(8):2870-80. doi: 10.1210/en.2012-2173. Epub 2013 May 24.

DOI:10.1210/en.2012-2173
PMID:23709086
Abstract

Several clinical studies have shown a correlation of hypersecretion of LH and polycystic ovary syndrome (PCOS), infertility, and miscarriage in women, suggesting that chronically elevated LH impairs fertility. Growth arrest of small antral follicles in PCOS is also assumed to be associated with an abnormal endocrine environment involving increased LH stimulation, a hyperandrogenic milieu, and subsequent dysregulated FSH action in the ovarian follicles. In this study, we examined whether and how LH modulates follicular development and steroid production during preantral-early antral follicle transition by using a rat preantral follicle culture system. LH augments testosterone and estradiol production in preantral follicles via up-regulating mRNA abundance of CYP17A1 and CYP19A1. LH promotes rat preantral follicle growth, and the follicular size reaches that of early antral follicles in vitro, a response attenuated by the specific androgen receptor antagonist and a targeted disruption of androgen receptor gene. Sustained follicle stimulation by LH, but not by androgen, decreases FSH receptor mRNA levels and FSH receptor signaling and inhibits FSH-induced follicular growth. The data suggest that LH promotes preantral-early antral transition via the increased synthesis and growth-promoting action of androgen. However, chronic LH stimulation impairs FSH-dependent antral follicle growth by suppressing granulosa cell FSHR expression via the modulation of intraovarian regulators, including LH-induced thecal factors.

摘要

几项临床研究表明,黄体生成素(LH)分泌过多与多囊卵巢综合征(PCOS)、不孕和流产有关,这表明慢性 LH 升高会损害生育能力。PCOS 中小窦卵泡的生长停滞也被认为与异常的内分泌环境有关,涉及增加的 LH 刺激、高雄激素环境以及随后的卵巢卵泡中 FSH 作用失调。在这项研究中,我们使用大鼠小窦前卵泡培养系统,研究了 LH 是否以及如何在窦前-小窦卵泡过渡期间调节卵泡发育和类固醇生成。LH 通过上调 CYP17A1 和 CYP19A1 的 mRNA 丰度来增加小窦前卵泡中的睾酮和雌二醇的产生。LH 促进大鼠小窦前卵泡的生长,并且卵泡大小在体外达到小窦卵泡的大小,这种反应被特异性雄激素受体拮抗剂和雄激素受体基因靶向敲除所减弱。LH 的持续卵泡刺激,而不是雄激素刺激,会降低 FSH 受体 mRNA 水平和 FSH 受体信号,并抑制 FSH 诱导的卵泡生长。数据表明,LH 通过增加雄激素的合成和促进生长作用来促进窦前-小窦过渡。然而,慢性 LH 刺激通过调节卵巢内的调节剂(包括 LH 诱导的间质因子)来抑制颗粒细胞 FSHR 表达,从而损害了依赖 FSH 的窦卵泡生长。

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