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血管紧张素-(1-7)可诱导兔离体卵巢排卵和类固醇生成。

Angiotensin-(1-7) induces ovulation and steroidogenesis in perfused rabbit ovaries.

机构信息

Department of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Exp Physiol. 2011 Sep;96(9):957-65. doi: 10.1113/expphysiol.2011.058453. Epub 2011 Jun 10.

Abstract

A local renin-angiotensin system has been described in several organs, including the ovary; however, data indicating a role for angiotensin II in the induction of ovulation are controversial. We have previously shown the presence of a novel peptide, angiotensin-(1-7) [Ang-(1-7)], in the rat ovary and its effect on steroidogenesis. The objective of the present study was to determine whether Ang-(1-7) plays a role in ovulation. We first determined the presence and distribution of Ang-(1-7) and the receptor Mas in rabbit ovaries by immunohistochemistry. Angiotensin-(1-7) and Mas immunoreactivity were observed in interstitial cells and oocytes of immature ovaries. Immunoreactivity for Ang-(1-7) and Mas was also observed in theca and granulosa cells of preovulatory follicles in ovaries of gonadotrophin-stimulated rabbits. To verify the effect of Ang-(1-7) in ovulation and steroidogenesis, we used isolated ovaries from immature rabbits pretreated with equine chorionic gonadotrophin (50 i.u., 48 h before the experiment) and then perfused in vitro. The ovulatory efficiency was determined by the number of oocytes compared with the number of preovulatory follicles present in the ovary. Angiotensin-(1-7) stimulated oestradiol production and enhanced ovulatory efficiency, which was blocked by the specific Ang-(1-7) antagonist, A-779. Ovulation induced by human chorionic gonadotrophin was also antagonized by A-779. These results show, for the first time, the involvement of a novel regulatory peptide system, Ang-(1-7) and Mas, in the ovulatory process. More importantly, because A-779 antagonized hCG-induced ovulation, it may be inferred that Ang-(1-7) plays an important role in ovulation, possibly as a mediator of gonadotrophin action.

摘要

在包括卵巢在内的几种器官中已经描述了局部肾素-血管紧张素系统;然而,关于血管紧张素 II 在诱导排卵中的作用的数据存在争议。我们之前已经证明了一种新型肽,血管紧张素-(1-7)[Ang-(1-7)],在大鼠卵巢中的存在及其对类固醇生成的影响。本研究的目的是确定 Ang-(1-7)是否在排卵中起作用。我们首先通过免疫组织化学法确定兔卵巢中 Ang-(1-7)和 Mas 受体的存在和分布。在未成熟卵巢的间质细胞和卵母细胞中观察到 Ang-(1-7)和 Mas 免疫反应性。在促性腺激素刺激的兔卵巢中,预排卵卵泡的卵泡膜和颗粒细胞中也观察到 Ang-(1-7)和 Mas 的免疫反应性。为了验证 Ang-(1-7)在排卵和类固醇生成中的作用,我们使用预先用马绒毛膜促性腺激素(50 i.u.,实验前 48 小时)处理的未成熟兔的离体卵巢进行体外灌流。通过与卵巢中存在的预排卵卵泡数相比,确定排卵效率。血管紧张素-(1-7)刺激雌二醇的产生并增强排卵效率,这被特异性 Ang-(1-7)拮抗剂 A-779 阻断。人绒毛膜促性腺激素诱导的排卵也被 A-779 拮抗。这些结果首次表明,一种新型调节肽系统 Ang-(1-7)和 Mas 参与了排卵过程。更重要的是,因为 A-779 拮抗 hCG 诱导的排卵,所以可以推断 Ang-(1-7)在排卵中起重要作用,可能作为促性腺激素作用的介质。

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