ATP-sensitive K+ channels and disease:: from molecule to malady

被引:88
作者
Ashcroft, Frances M.
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, Ctr Gene Funct, Oxford OX1 3PT, England
[2] Univ Oxford, Henry Wellcome Ctr Gene Fucnt, Oxford OX1 2JD, England
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2007年 / 293卷 / 04期
基金
英国惠康基金;
关键词
Kir6.2; SUR1; neonatal diabetes; hyperinsulinism;
D O I
10.1152/ajpendo.00348.2007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This essay is based on a lecture given to the American Physiological Society in honor of Walter B. Cannon, an advocate of homeostasis. It focuses on the role of the ATP-sensitive potassium K+ (K-ATP) channel in glucose homeostasis and, in particular, on its role in insulin secretion from pancreatic beta-cells. The beta-cell K-ATP channel comprises pore-forming Kir6.2 and regulatory SUR1 subunits, and mutations in either type of subunit can result in too little or too much insulin release. Here, I review the latest information on the relationship between K-ATP channel structure and function, and consider how mutations in the K-ATP channel genes lead to neonatal diabetes or congenital hyperinsulinism.
引用
收藏
页码:E880 / E889
页数:10
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