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前列腺素F2α促进内皮素-1在体外对牛黄体功能的抑制作用。

Prostaglandin F2 alpha promotes the inhibitory action of endothelin-1 on the bovine luteal function in vitro.

作者信息

Miyamoto A, Kobayashi S, Arata S, Ohtani M, Fukui Y, Schams D

机构信息

Department of Animal Genetics and Reproduction, University Farm, Obihiro University of Agriculture and Veterinary Medicine, Japan.

出版信息

J Endocrinol. 1997 Feb;152(2):R7-11. doi: 10.1677/joe.0.152r007.

Abstract

Prostaglandin F2 alpha (PGF2 alpha) is a primary luteolysin in the cow. Although the mechanisms involved in luteolysis are thought to be a complex of its direct action on luteal cells and indirect effect on luteal blood flow, the detailed mechanisms remain to be elucidated. This study focuses on the possible interaction of endothelial cells-derived endothelin-1 (ET-1) with PGF2 alpha in the rapid suppression of progesterone release from the bovine corpus luteum (CL). In in vitro microdialysis system (MDS) of CL, PGF2 alpha acutely stimulated the release of progesterone and oxytocin during infusion and ET-1 release after infusion. Moreover, PGF2 alpha induced slight decrease of progesterone release during the last period of the experiment (8-11 h after PGF2 alpha exposure). Two 1 h-perfusions of ET-1 at 3 h intervals induced only a slight decrease of progesterone release after the second perfusion. This treatment also affected the oxytocin release; the first ET-1 perfusion produced an acute stimulation, whereas the second ET-1 perfusion inhibited the release to below 50%. When the CL pieces were pre-perfused with PGF2 alpha for 2 h, the two consecutive perfusion of ET-1 at 3 h intervals induced drastic decrease in progesterone and oxytocin release only after the second ET-1 perfusion. Thus, a pre-exposure with PGF2 alpha clearly potentiated the inhibiting activity of ET-1 in the progesterone release. These results suggest a physiological impact of PGF2 alpha and ET-1 in the rapid cascade of functional luteolysis in vivo, and a possible interaction between endothelial cells and luteal cells.

摘要

前列腺素F2α(PGF2α)是奶牛黄体溶解的主要溶黄体素。尽管黄体溶解涉及的机制被认为是其对黄体细胞的直接作用和对黄体血流的间接影响的复合体,但详细机制仍有待阐明。本研究聚焦于内皮细胞衍生的内皮素-1(ET-1)与PGF2α在快速抑制牛黄体(CL)孕酮释放中的可能相互作用。在CL的体外微透析系统(MDS)中,PGF2α在灌注期间急性刺激孕酮和催产素的释放以及灌注后ET-1的释放。此外,PGF2α在实验的最后阶段(PGF2α暴露后8-11小时)诱导孕酮释放略有下降。以3小时间隔进行两次1小时的ET-1灌注,仅在第二次灌注后诱导孕酮释放略有下降。这种处理也影响催产素的释放;第一次ET-1灌注产生急性刺激,而第二次ET-1灌注将释放抑制至50%以下。当CL组织块用PGF2α预灌注2小时时,以3小时间隔进行的两次连续ET-1灌注仅在第二次ET-1灌注后诱导孕酮和催产素释放急剧下降。因此,PGF2α的预先暴露明显增强了ET-1对孕酮释放的抑制活性。这些结果表明PGF2α和ET-1在体内功能性黄体溶解的快速级联反应中的生理影响,以及内皮细胞和黄体细胞之间可能的相互作用。

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