雌激素β (ERs β)受体在褐家鼠卵巢功能减退模型中的表达及卵巢组织病理学改变

A. Firmawati, M. Hutabarat, H. Pratiwi
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引用次数: 1

摘要

在印度尼西亚的繁殖者中经常发现的生殖障碍之一是卵巢功能减退。卵巢功能减退是卵巢的一种病理状态,其特征是卵巢功能下降,导致卵泡发生抑制和排卵失败。本研究通过醋酸头孢瑞克诱导建立卵巢功能减退动物模型,观察其对卵巢雌激素β受体(Ers β)表达及组织病理学改变的影响。本研究选用三组雌性褐家鼠Wistar品系,年龄8 ~ 10周龄,体重150 ~ 180 g。本研究设对照组(KN),不加醋酸头孢瑞克,第一组(P1)为注射醋酸头孢瑞克0.009 mg/kg BW的治疗组,第二组(P2)为注射醋酸头孢瑞克0.0135 mg/kg BW的治疗组。采用免疫组化方法分析卵巢中β雌激素受体(Ers β)的表达,采用BNJ检验分析数据(p <0.05)。采用苏木精-伊红(HE)染色法分析卵巢组织病理变化,并进行定性分析。本研究结果表明,与阴性对照组相比,GnRH拮抗剂治疗组P1和P2有显著差异。P2治疗组雌激素受体与Ers β表达降低率最高,为92.2%。组织病理学结果显示,P1和P2治疗组均能抑制窦卵泡的发育。本研究的结论是,在卵巢组织病理学上,醋酸cetrorelix作为GnRH拮抗剂可以降低雌激素受体的表达,抑制卵泡的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of Estrogen Beta (ERs β) Receptor and Ovarian Histopathology Changes in Rats (Rattus norvegicus) Ovarian Hypofunction Model
: One of the reproductive disorders that are often found in breeders in Indonesia is ovarian hypofunction. Ovarian hypofunction is a pathological condition in the ovary that is characterized by a decrease in ovarian function that causes inhibition of folliculogenesis and failure of ovulation. The purpose of this study was to develop ovarian hypofunction animal models through cetrorelix acetate induction and observe their effects on the expression of estrogen beta receptors (Ers β ) and histopathological changes in the ovaries. This study used three groups of female Wistar strains (Rattus norvegicus), with ages 8-10 weeks, and body weight 150-180 grams. The treatments in this study included a control group (KN) without cetrorelix acetate, the first group (P1) was treatment group with an injection of cetrorelix acetate 0.009 mg/kg BW, and the second group (P2) was treatment group with an injection of cetrorelix acetate exposure 0.0135 mg/kg BW. Expression of beta estrogen receptors (Ers β ) in the ovaries was analyzed by immunohistochemical methods, and the data were analyzed using the BNJ test (p <0.05). The ovarian histopathological changes were analyzed by the hematoxylin-eosin (HE) staining method, then analyzed qualitatively. The results of this study indicate that the treatment groups P1 and P2 with GnRH antagonists differ significantly compared to the negative control group. The P2 treatment group had the highest reduction in estrogen receptor expression with Ers β by 92.2%. The result of histopathological in P1 and P2 treatment groups were able to inhibit the development of antral follicles. The conclusion of this study is that cetrorelix acetate as GnRH antagonists can reduce estrogen receptor expression and inhibit folliculogenesis in ovarian histopathology.
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