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前列腺素F(2α)在黄体早期和中期对牛黄体内皮素系统的调节作用

Prostaglandin F(2alpha) regulation of the bovine corpus luteum endothelin system during the early and midluteal phase.

作者信息

Wright M F, Sayre B, Keith Inskeep E K, Flores J A

机构信息

Department of Biology, West Virginia University, Morgantown, West Virginia 26506-6057, USA.

出版信息

Biol Reprod. 2001 Dec;65(6):1710-7. doi: 10.1095/biolreprod65.6.1710.

Abstract

Recent evidence in the cow suggests that endothelin-1 (ET-1) plays a role during prostaglandin (PG) F(2alpha)-induced luteal regression. We have examined the effects of treatment with PGF(2alpha) during the early and midluteal phases on three components of the endothelin system: endothelin-converting enzyme-1 (ECE-1), ET type A receptor (ET(A)), and ET-1 in the bovine corpus luteum (CL). Cyclic beef cows were injected (0 h) on Day 4 or 10 with either saline or the PGF(2alpha) analogue Lutalyse (15 mg). The CL were collected at 2 (n = 11), 10 (n = 23), 24 (n = 15), or 48 h (n = 12) after treatment. The cows in which CL were removed after 10 h comprised of two experimental groups. The first group (n = 11) received one injection; the second group (n = 12) received two injections, one at 0 h and one at 8 h. The cows in which CL were collected after 24 and 48 h received one injection every 8 h. Semiquantitative reverse transcriptase-polymerase chain reaction was used to evaluate the mRNA encoding ECE-1, ET(A), and ET-1. The ECE-1 and ET(A) proteins were evaluated by semiquantitative Western blot analysis. The ET-1 was the most likely component of the endothelin system target for PGF(2alpha) regulation during the midluteal phase. The ET(A) and ECE-1 genes were constitutively expressed in the Day 4 and Day 10 CL. A practical application of this observation is that it may be possible to target the ET-1 gene as a way to manipulate the luteolytic action of PGF(2alpha).

摘要

近期在奶牛身上的研究证据表明,内皮素-1(ET-1)在前列腺素(PG)F2α诱导的黄体退化过程中发挥作用。我们研究了在黄体早期和中期用PGF2α处理对内皮素系统三个组成部分的影响:内皮素转换酶-1(ECE-1)、A型内皮素受体(ET(A))和牛黄体(CL)中的ET-1。在第4天或第10天,对发情周期的肉牛注射(0小时)生理盐水或PGF2α类似物氯前列烯醇(15毫克)。在处理后2小时(n = 11)、10小时(n = 23)、24小时(n = 15)或48小时(n = 12)采集黄体。在10小时后切除黄体的奶牛分为两个实验组。第一组(n = 11)接受一次注射;第二组(n = 12)接受两次注射,一次在0小时,一次在8小时。在24小时和48小时后采集黄体的奶牛每8小时接受一次注射。采用半定量逆转录-聚合酶链反应评估编码ECE-1、ET(A)和ET-1的mRNA。通过半定量蛋白质免疫印迹分析评估ECE-1和ET(A)蛋白。ET-1最有可能是黄体中期PGF2α调节的内皮素系统靶点。ET(A)和ECE-1基因在第4天和第10天的黄体中组成性表达。这一观察结果的实际应用是,有可能将ET-1基因作为一种调节PGF2α黄体溶解作用的方法。

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