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胰腺β细胞毒蕈碱受体激活后不同细胞内钙库的动员

Mobilization of different intracellular calcium pools after activation of muscarinic receptors in pancreatic beta-cells.

作者信息

Hellman B, Gylfe E

出版信息

Pharmacology. 1986;32(5):257-67. doi: 10.1159/000138178.

Abstract

Exposure to carbachol resulted in a biphasic stimulation of 45Ca efflux when beta-cell-rich pancreatic islets from ob/ob mice were perifused with a Ca2+-deficient medium. The pattern of stimulated 45Ca efflux was markedly modified by glucose. Whereas the initial carbachol-stimulated phase was conditional on previous exposure to glucose, the subsequent phase was completely suppressed by 20 mmol/l of the sugar. The stimulatory could be clearly separated also on the basis of a Na+ dependence. Removal of extracellular Na+ resulted in a disappearance of the second phase, but it was still possible to induce a prominent initial peak if depletion of intracellular K+ was prevented when Na+ was omitted. It is concluded that activation of muscarinic receptors in the pancreatic beta-cells results in mobilization of calcium from more than one intracellular pool. Whereas the second phase of stimulated efflux can be explained in terms of an increased entry of Na+ into the beta-cells, the initial stimulation may be due to receptor-mediated breakdown of polyphosphoinositides.

摘要

当用缺钙培养基对ob/ob小鼠富含β细胞的胰岛进行灌流时,暴露于卡巴胆碱会导致45Ca外流出现双相刺激。葡萄糖显著改变了刺激的45Ca外流模式。虽然最初卡巴胆碱刺激阶段取决于先前对葡萄糖的暴露,但随后的阶段被20 mmol/l的糖完全抑制。基于对Na+的依赖性,这种刺激也能被明显区分开来。去除细胞外Na+会导致第二阶段消失,但当省略Na+时,如果防止细胞内K+耗竭,仍有可能诱导出一个突出的初始峰值。结论是,胰腺β细胞中毒蕈碱受体的激活导致钙从多个细胞内池动员。虽然刺激外流的第二阶段可以用Na+进入β细胞增加来解释,但初始刺激可能是由于受体介导的多磷酸肌醇分解。

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