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在使用马绒毛膜促性腺激素与促卵泡素进行超数排卵期间,牛体内编码促卵泡素(FSH)和促黄体素(LH)卵巢受体的信使核糖核酸水平。

Levels of messenger RNA encoding ovarian receptors for FSH and LH in cattle during superovulation with equine chorionic gonadotrophin versus FSH.

作者信息

Soumano K, Lussier J G, Price C A

机构信息

Centre de Recherche en Reproduction Animale, Faculté de Médecine Véterinaire, Université de Montréal, Quebec, Canada.

出版信息

J Endocrinol. 1998 Feb;156(2):373-8. doi: 10.1677/joe.0.1560373.

DOI:10.1677/joe.0.1560373
PMID:9518885
Abstract

This study tested the hypothesis that luteal LH receptor (LHr) and follicular LHr and FSH receptor (FSHr) steady-state mRNA levels are greater during superovulation with equine chorionic gonadotrophin (eCG) compared with that with FSH. Heifers were stimulated with eCG (n = 10) or FSH (n = 10), and ovaries were recovered the day before and at 12 and 24 h after luteolysis was induced with prostaglandin F2 alpha (PGF2 alpha). Total RNA was purified from individual follicles and corpora lutea. Steady-state levels of LHr and FSHr mRNA were assessed by slot blot analysis employing homologous cDNA probes. There were no differences in luteal LHr between FSH- and eCG-stimulated animals before luteolysis, and hybridization signals were detected in only one of six animals by 12 h after injection of PGF2 alpha. After PGF2 alpha injection, steady-state levels of follicular LHr were 4-fold lower (P < 0.05) and follicular FSHr mRNA levels were 2.4-fold lower (P < 0.05) in eCG- compared with FSH-treated cattle. In eCG-treated animals, induction of luteolysis led to a significant increase in follicular LHr mRNA levels (P < 0.01) and a significant decrease in follicular FSHr mRNA levels (P < 0.01). There was no such effect of luteolysis in FSH-treated animals. We conclude that superovulation with eCG, compared with FSH, results in lower follicular levels of LHr and FSHr mRNA but does not affect luteal LHr mRNA levels.

摘要

本研究检验了以下假设

与使用促卵泡素(FSH)相比,用马绒毛膜促性腺激素(eCG)进行超排时,黄体促黄体生成素受体(LHr)以及卵泡促黄体生成素受体和促卵泡素受体(FSHr)的稳态mRNA水平更高。用eCG(n = 10)或FSH(n = 10)刺激小母牛,在用前列腺素F2α(PGF2α)诱导黄体溶解前一天以及诱导后12小时和24小时采集卵巢。从单个卵泡和黄体中纯化总RNA。采用同源cDNA探针通过狭缝印迹分析评估LHr和FSHr mRNA的稳态水平。在黄体溶解前,FSH刺激组和eCG刺激组动物的黄体LHr没有差异,并且在注射PGF2α后12小时,仅在六只动物中的一只检测到杂交信号。注射PGF2α后,与FSH处理的牛相比,eCG处理的牛卵泡LHr的稳态水平低4倍(P < 0.05),卵泡FSHr mRNA水平低2.4倍(P < 0.05)。在eCG处理的动物中,黄体溶解诱导导致卵泡LHr mRNA水平显著增加(P < 0.01),卵泡FSHr mRNA水平显著降低(P < 0.01)。在FSH处理的动物中没有黄体溶解的这种效应。我们得出结论,与FSH相比,用eCG进行超排会导致卵泡LHr和FSHr mRNA水平降低,但不影响黄体LHr mRNA水平。

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