Department of Information Engineering, University of Padua, Padua, Italy.
Biophys J. 2010 Nov 17;99(10):3200-7. doi: 10.1016/j.bpj.2010.09.004.
Electrical activity in pancreatic β-cells plays a pivotal role in glucose-stimulated insulin secretion by coupling metabolism to calcium-triggered exocytosis. Mathematical models based on rodent data have helped in understanding the mechanisms underlying the electrophysiological patterns observed in laboratory animals. However, human β-cells differ in several aspects, and in particular in their electrophysiological characteristics, from rodent β-cells. Hence, from a clinical perspective and to obtain insight into the defects in insulin secretion relevant for diabetes mellitus, it is important to study human β-cells. This work presents the first mathematical model of electrical activity based entirely on published ion channel characteristics of human β-cells. The model reproduces satisfactorily a series of experimentally observed patterns in human β-cells, such as spiking and rapid bursting electrical activity, and their response to a range of ion channel antagonists. The possibility of Human Ether-a-Go-Go-related- and leak channels as drug targets for diabetes treatment is discussed based on model results.
胰腺 β 细胞的电活动在葡萄糖刺激的胰岛素分泌中起着关键作用,它将代谢与钙触发的胞吐作用联系起来。基于啮齿动物数据的数学模型有助于理解在实验室动物中观察到的电生理模式的机制。然而,人类 β 细胞在几个方面与啮齿动物 β 细胞不同,特别是在其电生理特性方面。因此,从临床角度来看,为了深入了解与糖尿病相关的胰岛素分泌缺陷,研究人类 β 细胞非常重要。这项工作提出了第一个完全基于已发表的人类 β 细胞离子通道特性的电活动数学模型。该模型令人满意地再现了一系列在人类 β 细胞中观察到的实验模式,如尖峰和快速爆发电活动,以及它们对一系列离子通道拮抗剂的反应。基于模型结果,讨论了人类 Ether-a-Go-Go-related 和泄漏通道作为糖尿病治疗药物靶点的可能性。