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牛黄体中内皮素-1表达的调节:前列腺素F2α使其升高。

Regulation of endothelin-1 expression in the bovine corpus luteum: elevation by prostaglandin F 2 alpha.

作者信息

Girsh E, Wang W, Mamluk R, Arditi F, Friedman A, Milvae R A, Meidan R

机构信息

Department of Animal Science, Section of Reproduction, The Hebrew University of Jerusalem, Rehovot, Israel.

出版信息

Endocrinology. 1996 Dec;137(12):5191-6. doi: 10.1210/endo.137.12.8940334.

Abstract

Prostaglandin F2alpha (PGF2alpha) has been recognized as the physiological luteolysin in ruminants and other species for more than three decades; however, the mechanisms involved in its action are poorly understood. We previously have shown that endothelin-1 (ET-1) mediates, at least in part, the action of PGF2alpha, and the current study examines the effect of PGF2alpha on the expression of ET-1 in bovine corpus luteum (CL). Endothelins (ETs) were extracted from CL, collected at various times of the estrous cycle, and highest levels were found during luteolysis. The expression of prepro-ET-1 was also highest in regressing CL, suggesting that PGF2alpha may have elevated ET-1 expression. This was confirmed by demonstrating that administration of PGF2alpha to heifers at midcycle elevated luteal ET-1 expression. Levels were induced as soon as 2 h after PGF2alpha treatment and 24 h later were 7-fold higher than preinjection levels. Endothelial cells isolated from bovine CL produced ET-1, and addition of PGF2alpha, oxytocin (OT), and vasopressin-augmented ET biosynthesis. Induction of ET-1 expression by PGF2alpha in these cells was evident after a short incubation time (15-90 min). Taken together, these data suggest that stimulation of luteal ET-1 expression by PGF2alpha may be achieved by several nonmutually exclusive mechanisms: 1) by acting directly on luteal endothelial cells; 2) indirectly, via OT release from large luteal cells; and 3) by causing hypoxia in the CL (as a result of ET-1-induced vasoconstriction). The latter mechanism may serve to augment ET-1 secretion in a positive-feedback process.

摘要

三十多年来,前列腺素F2α(PGF2α)一直被认为是反刍动物和其他物种中的生理性黄体溶解素;然而,其作用机制仍知之甚少。我们之前已经表明,内皮素-1(ET-1)至少部分介导了PGF2α的作用,并且当前研究考察了PGF2α对牛黄体(CL)中ET-1表达的影响。从发情周期不同时间收集的CL中提取内皮素(ETs),发现在黄体溶解期间含量最高。前内皮素原-1的表达在退化的CL中也最高,这表明PGF2α可能提高了ET-1的表达。给处于发情周期中期的小母牛注射PGF2α后黄体ET-1表达升高,证实了这一点。PGF2α处理后2小时内即可诱导其表达升高,24小时后比注射前水平高7倍。从牛CL中分离的内皮细胞产生ET-1,添加PGF2α、催产素(OT)和加压素可增强ET的生物合成。PGF2α在这些细胞中短时间孵育(15 - 90分钟)后即可明显诱导ET-1表达。综上所述,这些数据表明,PGF2α刺激黄体ET-1表达可能通过几种并非相互排斥的机制实现:1)直接作用于黄体内皮细胞;2)间接通过大黄体细胞释放OT;3)通过导致CL缺氧(由于ET-1诱导的血管收缩)。后一种机制可能在正反馈过程中增强ET-1的分泌。

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