Closing in on the Mechanisms of Pulsatile Insulin Secretion

被引:58
|
作者
Bertram, Richard [1 ,2 ,3 ]
Satin, Leslie S. [4 ,5 ]
Sherman, Arthur S. [6 ]
机构
[1] Florida State Univ, Dept Math, Tallahassee, FL 32306 USA
[2] Florida State Univ, Program Neurosci, Tallahassee, FL 32306 USA
[3] Florida State Univ, Program Mol Biophys, Tallahassee, FL 32306 USA
[4] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Brehm Ctr Diabet Res, Ann Arbor, MI USA
[6] NIDDK, Lab Biol Modeling, NIH, Bethesda, MD 20892 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PANCREATIC BETA-CELLS; METABOLIC OSCILLATIONS; ELECTRICAL-ACTIVITY; GLYCOLYTIC OSCILLATIONS; CALCIUM OSCILLATIONS; SLOW OSCILLATIONS; PORTAL-VEIN; CA2+; GLUCOSE; ISLETS;
D O I
10.2337/dbi17-0004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin secretion from pancreatic islet beta-cells occurs in a pulsatile fashion, with a typical period of similar to 5 min. The basis of this pulsatility in mouse islets has been investigated for more than four decades, and the various theories have been described as either qualitative or mathematical models. In many cases the models differ in their mechanisms for rhythmogenesis, as well as other less important details. In this Perspective, we describe two main classes of models: those in which oscillations in the intracellular Ca2+ concentration drive oscillations in metabolism, and those in which intrinsic metabolic oscillations drive oscillations in Ca2+ concentration and electrical activity. We then discuss nine canonical experimental findings that provide key insights into the mechanism of islet oscillations and list the models that can account for each finding. Finally, we describe a new model that integrates features from multiple earlier models and is thus called the Integrated Oscillator Model. In this model, intracellular Ca2+ acts on the glycolytic pathway in the generation of oscillations, and it is thus a hybrid of the two main classes of models. It alone among models proposed to date can explain all nine key experimental findings, and it serves as a good starting point for future studies of pulsatile insulin secretion from human islets.
引用
收藏
页码:351 / 359
页数:9
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