首页> 外文期刊>Journal of reproduction and fertility >Regulation of prostaglandin F2α and E receptor mRNA by prostaglandin F2α in ovine corpora lutea
【24h】

Regulation of prostaglandin F2α and E receptor mRNA by prostaglandin F2α in ovine corpora lutea

机译:绵羊黄体中前列腺素F2α对前列腺素F2α和E受体mRNA的调控

获取原文
获取外文期刊封面目录资料

摘要

Prostaglandins regulate many physiological functions, including reproduction, by binding to specific plasma membrane receptors. In this study we evaluated the regulation of PGF2α (FP) and PGE (EP3 subtype) receptors in ovine corpora lutea. In the first study, tissue distribution of FP and EP3 receptors was evaluated in 13 ovine tissues. FP receptor mRNA was present in 100-fold higher concentration in corpora lutea than in other tissues. Similarly, [3H]PGF2α binding was much greater in luteal plasma membranes than in membranes from other tissues. In contrast, EP3 receptor mRNA was more uniformly distributed, with high concentrations in adrenal medulla, inner myometrium, kidney medulla and heart. The distribution of [3H]PGE1 binding was generally similar to EP3 mRNA, with the exception that ovarian stroma, endometrium and outer myometrium had high [3H]PGE1 binding but low concentrations of EP3 receptor mRNA. The second study evaluated the action of PGF2α on luteal mRNA encoding FP and EP3 receptors. Ewes had PGF2α or saline infused into the ovarian artery and corpora lutea were removed at 0, 1, 4, 12 and 24 h. FP receptor mRNA decreased by 50% at 12 and 24 h after infusion with PGF2α, whereas EP3 mRNA was unchanged. Treatment of large luteal cells with PGF2α, phorbol didecanoate (protein kinase C activator), or ionomycin (calcium ionophore) decreased FP receptor mRNA after 24 h (P < 0.05). Glyceraldehyde 3-phosphate dehydrogenase mRNA was not changed by any treatment. These results show that EP3 receptors are expressed in many tissues and expression is not regulated by PGF2α. In contrast, FP receptors are primarily expressed in corpora lutea and expression is inhibited by PGF2α.
机译:前列腺素通过结合特定的质膜受体来调节许多生理功能,包括生殖。在这项研究中,我们评估了绵羊黄体中PGF2α(FP)和PGE(EP3亚型)受体的调节。在第一项研究中,评估了FP和EP3受体在13个绵羊组织中的组织分布。黄体中的FP受体mRNA浓度比其他组织高100倍。同样,黄体质膜中的[3H]PGF2α结合要比其他组织的膜中的高得多。相反,EP3受体mRNA更均匀地分布,在肾上腺髓质,子宫内膜,肾髓质和心脏中浓度较高。 [3H] PGE1结合的分布通常类似于EP3 mRNA,除了卵巢间质,子宫内膜和子宫外膜具有高[3H] PGE1结合而低浓度的EP3受体mRNA。第二项研究评估了PGF2α对编码FP和EP3受体的黄体mRNA的作用。在0、1、4、12和24小时将母羊的PGF2α或盐水注入卵巢动脉,并取出黄体。输注PGF2α后12和24小时,FP受体mRNA下降50%,而EP3 mRNA不变。用PGF2α,佛波二癸酸酯(蛋白激酶C激活剂)或离子霉素(钙离子载体)处理大黄体细胞后24小时可降低FP受体mRNA(P <0.05)。甘油醛3-磷酸脱氢酶mRNA没有任何改变。这些结果表明EP3受体在许多组织中表达并且表达不受PGF2α调节。相反,FP受体主要在黄体中表达,并且表达被PGF2α抑制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号