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首页> 外文期刊>Molecular reproduction and development >Changes in expression of 11beta-hydroxysteroid dehydrogenase type-1, type-2 and glucocorticoid receptor mRNAs in porcine corpus luteum during the estrous cycle.
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Changes in expression of 11beta-hydroxysteroid dehydrogenase type-1, type-2 and glucocorticoid receptor mRNAs in porcine corpus luteum during the estrous cycle.

机译:发情周期中猪黄体中11β-羟类固醇脱氢酶1、2和糖皮质激素受体mRNA表达的变化。

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摘要

The objective of the present study was to determine whether glucocorticoid (GC) and its receptor (GC-R) are expressed in the porcine corpus luteum (CL), and whether GC influences porcine luteal hormone production. The gene expressions of 11beta-hydroxysteroid dehydrogenase type 1 (11-HSD1), type 2 (11-HSD2), GC-R, and the concentrations of GC were determined in the CL of Chinese Meishan pigs during the estrous cycle. Moreover, the effects of GC on progesterone (P(4)), estradiol-17beta (E(2)), and prostaglandin (PG) F2alpha secretion by cultured luteal cells were investigated. Messenger RNAs of the 11-HSD1, 11-HSD2, and GC-R were clearly expressed in the CL throughout the estrous cycle. The 11-HSD1 mRNA level in the CL was higher at the regressed stage than at the other stages (P < 0.05), whereas 11-HSD2 mRNA was lower at the regressed stage than at the other stages (P < 0.05). GC-R mRNA level was higher at the regressed stages than at the other stages (P < 0.01). Concentrations of GC were lower in the regressed CL than in the other stages (P < 0.01). When the cultured luteal cells obtained from mid-stage CL (Days 8-11) were exposed to GC (50-5,000 ng/ml), P(4) and PGF2alpha secretion by the cells were reduced (P < 0.05), whereas GC had no effect on E(2) secretion by the cells. The overall results suggest that GC is regulated locally by 11-HSD1 and 11-HSD2 in the porcine CL. GC inhibits P(4) and PGF2alpha production from luteal cells via their specific receptors, implying GC plays some roles in regulating porcine CL function throughout the estrous cycle.
机译:本研究的目的是确定糖皮质激素(GC)及其受体(GC-R)是否在猪黄体(CL)中表达,以及GC是否影响猪黄体激素的产生。在发情周期中,测定中国眉山猪CL中11β-羟类固醇脱氢酶1型(11-HSD1),2型(11-HSD2),GC-R的基因表达以及GC的浓度。此外,还研究了GC对黄体细胞培养黄体酮(P(4)),雌二醇-17beta(E(2))和前列腺素(PG)F2alpha分泌的影响。在整个动情周期中,CL中清楚地表达了11-HSD1、11-HSD2和GC-R的信使RNA。 CL的11-HSD1 mRNA水平在回归阶段高于其他阶段(P <0.05),而11-HSD2 mRNA在回归阶段低于其他阶段(P <0.05)。回归阶段的GC-R mRNA水平高于其他阶段(P <0.01)。回归CL中GC的浓度低于其他阶段(P <0.01)。当从CL中期(第8-11天)获得的培养的黄体细胞暴露于GC(50-5,000 ng / ml)时,细胞分泌的P(4)和PGF2alpha减少(P <0.05)对细胞的E(2)分泌没有影响。总体结果表明,GC在猪CL中受到11-HSD1和11-HSD2的局部调节。 GC抑制黄体细胞通过其特定受体的P(4)和PGF2alpha生产,这意味着GC在整个发情周期中调节猪CL功能中发挥了一定作用。

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