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体外葡萄糖诱导的双相胰岛素释放的胆碱能调节

Cholinergic modification of glucose-induced biphasic insulin release in vitro.

作者信息

Sharp R, Culbert S, Cook J, Jennings A, Burr I M

出版信息

J Clin Invest. 1974 Mar;53(3):710-6. doi: 10.1172/JCI107609.

Abstract

An in vitro system for perifusion of rat pancreatic islets has been utilized to define the effects of cholinergic agents on the dynamics of insulin release. In the absence of glucose the effects of either acetylcholine or acetyl-beta-methylcholine were minimal at concentrations up to 10(-5) mM. In the presence of low glucose concentration (2.4 mM), both of the muscarinic agents produced dose-dependent biphasic insulin release. Under these conditions significant insulin release was observed over both phases at concentrations of the muscarinic agents as low as 10(-8) mM. Further, the dose response curves relating muscarinic concentration to the total amount of insulin released in each of the two phases showed lack of parallelism between the curves. Nicotinic acid in concentrations up to 10(-5) mM had no effect on insulin release in the presence of 2.4 mM glucose. When the glucose concentration was increased to 16.4 mM, the effects of the muscarinic agents were significantly less than those observed in the presence of 2.4 mM glucose. This held true whether the effect was defined as absolute increment due to the muscarinic agent or as percentage of enhancement. Atropine inhibited insulin release induced by both acetylcholine and by 16.4 mM glucose. These data indicate that cholinergic stimulation can play a significant role in modifying insulin release patterns.

摘要

一种用于大鼠胰岛灌流的体外系统已被用于确定胆碱能药物对胰岛素释放动力学的影响。在无葡萄糖的情况下,乙酰胆碱或乙酰-β-甲基胆碱在浓度高达10^(-5) mM时作用极小。在低葡萄糖浓度(2.4 mM)存在时,两种毒蕈碱样药物均产生剂量依赖性双相胰岛素释放。在这些条件下,在低至10^(-8) mM的毒蕈碱样药物浓度下,两个阶段均观察到显著的胰岛素释放。此外,将毒蕈碱浓度与两个阶段中每个阶段释放的胰岛素总量相关的剂量反应曲线显示曲线之间缺乏平行性。在存在2.4 mM葡萄糖的情况下,浓度高达10^(-5) mM的烟酸对胰岛素释放无影响。当葡萄糖浓度增加到16.4 mM时,毒蕈碱样药物的作用明显小于在2.4 mM葡萄糖存在时观察到的作用。无论将该作用定义为毒蕈碱样药物引起的绝对增量还是增强百分比,都是如此。阿托品抑制由乙酰胆碱和16.4 mM葡萄糖诱导的胰岛素释放。这些数据表明胆碱能刺激在改变胰岛素释放模式中可发挥重要作用。

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