Division of Integrative Physiology, Department of Physiology, Jichi Medical University School of Medicine, Yakushiji 3311-1, Shimotsuke, Tochigi 329-0498, Japan.
FEBS Lett. 2012 Jul 30;586(16):2555-62. doi: 10.1016/j.febslet.2012.06.034. Epub 2012 Jun 29.
We studied interactive effects of insulinotropic GLP-1 and insulinostatic ghrelin on rat pancreatic islets. GLP-1 potentiated glucose-induced insulin release and cAMP production in isolated islets and Ca(2+) increases in single β-cells, and these potentiations were attenuated by ghrelin. Ghrelin suppressed Ca(2+) responses to an adenylate cyclase activator forskolin. Moreover, GLP-1-induced insulin release and cAMP production were markedly enhanced by [D-lys(3)]-GHRP-6, a ghrelin receptor antagonist, in isolated islets. These results indicate that both exogenous and endogenous islet-derived ghrelin counteracts glucose-dependent GLP-1 action to increase cAMP production, Ca(2+) and insulin release in islet β-cells, positioning ghrelin as a modulator of insulinotropic GLP-1.
我们研究了促胰岛素分泌的 GLP-1 和抑胰岛素分泌的 ghrelin 对大鼠胰岛的相互作用。GLP-1 增强了分离胰岛中葡萄糖诱导的胰岛素释放和 cAMP 产生,以及单个 β 细胞中的 Ca(2+) 增加,而 ghrelin 则减弱了这些增强作用。Ghrelin 抑制了对腺苷酸环化酶激活剂 forskolin 的 Ca(2+) 反应。此外,在分离的胰岛中,ghrelin 受体拮抗剂 [D-lys(3)]-GHRP-6 显著增强了 GLP-1 诱导的胰岛素释放和 cAMP 产生。这些结果表明,外源性和内源性胰岛衍生的 ghrelin 均拮抗葡萄糖依赖性 GLP-1 作用,增加胰岛 β 细胞中 cAMP 产生、Ca(2+) 和胰岛素释放,使 ghrelin 成为促胰岛素分泌 GLP-1 的调节剂。