Functional modulation of cardiac ATP-sensitive K+ channels

被引:0
|
作者
Hiraoka, M
Furukawa, T
机构
[1] Tokyo Med & Dent Univ, Med Res Inst, Dept Cardiovasc Dis, Bunkyo Ku, Tokyo 113, Japan
[2] Tokyo Med & Dent Univ, Med Res Inst, Dept Auton Physiol, Bunkyo Ku, Tokyo 113, Japan
来源
NEWS IN PHYSIOLOGICAL SCIENCES | 1998年 / 13卷
关键词
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
ATP-sensitive K+ (K-ATP) channels are inhibited by intracellular ATP, but MgATP is necessary to maintain the channel activity. Numerous cofactors modulate channel function. K+ channel openers activate and sulfonylureas inhibit K-ATP channels. The structure of cardiac K-ATP channel is a complex of mainly K(IR)6.2 and SUR2a. Activation of cardiac K-ATP channels contributes to action potential shortening during ischemia and plays a role in cardioprotection.
引用
收藏
页码:131 / 137
页数:7
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