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首页> 外文期刊>Molecular and Cellular Endocrinology >Identification of the somatostatin receptor subtypes involved in regulation of growth hormone secretion in chickens.
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Identification of the somatostatin receptor subtypes involved in regulation of growth hormone secretion in chickens.

机译:鉴定参与调节鸡生长激素分泌的生长抑素受体亚型。

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摘要

The effects of somatostatin (SRIF) are mediated through five distinct G-protein-coupled receptors (SSTR1-5). In the present study, pituitary cells from 6-week-old chickens were subjected to reverse hemolytic plaque assays for growth hormone (GH) in the presence of SSTR subtype specific nonpeptidyl agonists. A SSTR2 selective agonist (L-779,976) potently inhibited both basal and GH-releasing hormone (GHRH)-stimulated GH release at low nanomolar concentrations. A SSTR5 agonist (L-817,818) inhibited GH release only under basal conditions and in a subpopulation of somatotrophs. In contrast, a SSTR4 selective agonist (L-803,087) used at high nanomolar concentrations modestly stimulated GH release under basal conditions but did not influence GHRH-stimulated GH secretion. The SSTR1 and SSTR3 specific agonists did not affect GH secretion under any condition tested. Reverse transcription-polymerase chain reaction (RT-PCR) and Northern blot analysis using a partial cDNA for chicken SSTR2 showed relatively high levels of SSTR2 mRNA in the anterior pituitary (both in the caudal and cephalic lobes) and brain and detectable levels in liver, muscle, heart and small intestine. These results indicate that SSTR2 is the primary mediator of the inhibitory effects of SRIF on GH secretion in chickens.
机译:生长抑素(SRIF)的作用是通过五个不同的G蛋白偶联受体(SSTR1-5)介导的。在本研究中,在存在SSTR亚型特异性非肽基激动剂的情况下,对6周龄鸡的垂体细胞进行了逆溶血斑分析,以测定生长激素(GH)。在低纳摩尔浓度下,SSTR2选择性激动剂(L-779,976)可有效抑制基础和GH释放激素(GHRH)刺激的GH释放。 SSTR5激动剂(L-817,818)仅在基础条件下和生长体的亚群中抑制GH的释放。相反,以高纳摩尔浓度使用的SSTR4选择性激动剂(L-803,087)在基础条件下适度刺激了GH的释放,但不影响GHRH刺激的GH分泌。在任何测试条件下,SSTR1和SSTR3特异性激动剂均不影响GH分泌。鸡SSTR2的部分cDNA的逆转录聚合酶链反应(RT-PCR)和Northern blot分析显示,垂体前叶(尾叶和头叶)和大脑中SSTR2 mRNA的水平相对较高,肝脏中可检测到的水平,肌肉,心脏和小肠。这些结果表明,SSTR2是SRIF对鸡GH分泌的抑制作用的主要介质。

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