Wollheim C B, Siegel E G, Sharp G W
Endocrinology. 1980 Oct;107(4):924-9. doi: 10.1210/endo-107-4-924.
The dependency of acetylcholine-induced insulin release on Ca++ uptake from extracellular fluid has been investigated in isolated rat pancreatic islets. Islets were maintained for 46 h in tissue culture, and 45Ca++ uptake and insulin release were measured over 5 min on the same batches of islets. Acetylcholine (10(-10)--10(-6) M) at 2.8 mM glucose stimulated insulin release and Ca++ uptake. Both effects were inhibited by atropine. When acetylcholine-stimulated Ca++ uptake was inhibited by verapamil, a blocker of the voltage-dependent Ca++ channel, acetylcholine-induced insulin release was abolished. In a previous report, verapamil did not inhibit glucose-stimulated insulin release over 5 min despite inhibition of the accompanying Ca++ uptake. Glucose (16.7 mM) stimulated insulin release to a similar extent as acetylcholine. Acetylcholine further enhanced glucose-stimulated insulin release without changing glucose-stimulated Ca++ uptake. Acetylcholine did not significantly alter cAMP levels in the islets. It is concluded that acetylcholine, in contrast to glucose, appears to stimulate the early phase of insulin release by enhancing Ca++ uptake from extracellular fluid. An additional effect of acetylcholine in the presence of high glucose may be operative.
在分离的大鼠胰岛中,已对乙酰胆碱诱导的胰岛素释放对细胞外液中钙离子摄取的依赖性进行了研究。胰岛在组织培养中维持46小时,对同一批胰岛在5分钟内测量45钙离子摄取和胰岛素释放。在2.8 mM葡萄糖存在下,乙酰胆碱(10(-10)-10(-6)M)刺激胰岛素释放和钙离子摄取。两种效应均被阿托品抑制。当乙酰胆碱刺激的钙离子摄取被维拉帕米(一种电压依赖性钙离子通道阻滞剂)抑制时,乙酰胆碱诱导的胰岛素释放被消除。在先前的一份报告中,尽管维拉帕米抑制了伴随的钙离子摄取,但在5分钟内并未抑制葡萄糖刺激的胰岛素释放。葡萄糖(16.7 mM)刺激胰岛素释放的程度与乙酰胆碱相似。乙酰胆碱在不改变葡萄糖刺激的钙离子摄取的情况下,进一步增强了葡萄糖刺激的胰岛素释放。乙酰胆碱并未显著改变胰岛中的环磷酸腺苷水平。结论是,与葡萄糖相反,乙酰胆碱似乎通过增强细胞外液中的钙离子摄取来刺激胰岛素释放的早期阶段。在高葡萄糖存在下,乙酰胆碱可能还有其他作用。