McDermott A M, Sharp G W
Department of Pharmacology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.
Cell Signal. 1993 May;5(3):229-34. doi: 10.1016/0898-6568(93)90014-d.
Insulin secretion from the beta-cells of the endocrine pancreas is subject to a pot-pourri of stimulatory, modulatory and inhibitory influences. beta-Cell secretion is reduced or blocked by a variety of inhibitors (including galanin, somatostatin and noradrenaline) which reach the cells either via the islet vascular system or are released locally from sympathetic and peptidergic nerves terminating in the pancreas. It is now becoming clear that among these many inhibitors, several have multiple mechanisms by which they inhibit release at the cellular level. Indeed, with multiple inhibitors (some of which are co-secreted) and multiple mechanisms of inhibition, the latter including a late effect in stimulus secretion coupling (perhaps on the exocytotic step per se), inhibition of insulin secretion has the characteristics of a fail-safe system.
内分泌胰腺β细胞的胰岛素分泌受到多种刺激、调节和抑制性影响。多种抑制剂(包括甘丙肽、生长抑素和去甲肾上腺素)可降低或阻断β细胞分泌,这些抑制剂可通过胰岛血管系统到达细胞,或从终止于胰腺的交感神经和肽能神经局部释放。现在越来越清楚的是,在这些众多抑制剂中,有几种具有多种在细胞水平抑制释放的机制。事实上,存在多种抑制剂(其中一些是共同分泌的)和多种抑制机制,后者包括刺激分泌偶联中的晚期效应(可能作用于胞吐步骤本身),胰岛素分泌的抑制具有故障安全系统的特征。