首页> 外文期刊>Clinical and experimental pharmacology & physiology >Involvement of somatostatin receptor subtypes in membrane ion channel modification by somatostatin in pituitary somatotropes.
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Involvement of somatostatin receptor subtypes in membrane ion channel modification by somatostatin in pituitary somatotropes.

机译:生长抑素受体亚型参与垂体生长激素促生长素抑制素在膜离子通道修饰中的作用。

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摘要

1. Growth hormone (GH) secretion from pituitary somatotropes is mainly regulated by two hypothalamic hormones, GH-releasing hormone (GHRH) and somatotrophin releasing inhibitory factor (SRIF). 2. Somatotrophin releasing inhibitory factor inhibits GH secretion via activation of specific membrane receptors, somatostatin receptors (SSTRs) and signalling transduction systems in somatotropes. 3. Five subtypes of SSTRs, namely SSTR1, 2, 3, 4 and 5, have been identified, with the SSTR2 subtype divided into SSTR2A and SSTR2B. All SSTRs are G-protein-coupled receptors. 4. Voltage-gated Ca(2+) and K(+) channels on the somatotrope membrane play an important role in regulating GH secretion and SRIF modifies both channels to reduce intracellular free Ca(2+) concentration and GH secretion. 5. Using specific SSTR subtype-specific agonists, it has been found that reduction in Ca(2+) currents by SRIF is mediated by SSTR2 and an increase in K(+) currents is mediated by both SSTR2 and SSTR4 in rat somatotropes.
机译:1.垂体生长激素分泌的生长激素(GH)主要受两种下丘脑激素(生长激素释放激素(GHRH)和生长激素释放抑制因子(SRIF))的调节。 2.生长激素释放抑制因子通过激活生长激素中特定的膜受体,生长抑素受体(SSTR)和信号转导系统来抑制GH分泌。 3.已经确定了SSTR的五个亚型,即SSTR1、2、3、4和5,其中SSTR2亚型分为SSTR2A和SSTR2B。所有的SSTR都是G蛋白偶联受体。 4.体细胞膜上的电压门控Ca(2+)和K(+)通道在调节GH分泌中起重要作用,SRIF修饰这两个通道以减少细胞内游离Ca(2+)浓度和GH分泌。 5.使用特定的SSTR亚型特异性激动剂,已发现SRIF介导的钙离子电流减少是由SSTR2介导的,而K(+)电流的增加是由大鼠生长激素中的SSTR2和SSTR4介导的。

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