Department of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Exp Physiol. 2011 Sep;96(9):957-65. doi: 10.1113/expphysiol.2011.058453. Epub 2011 Jun 10.
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.
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。