Excitation-contraction coupling in skeletal muscle: Comparisons with cardiac muscle

被引:127
作者
Lamb, GD [1 ]
机构
[1] La Trobe Univ, Dept Zool, Bundoora, Vic 3083, Australia
来源
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY | 2000年 / 27卷 / 03期
关键词
calcium release channels; dihydropyridine receptor; excitation-contraction coupling; muscle fatigue; ryanodine receptor; skeletal muscle; voltage-sensor;
D O I
10.1046/j.1440-1681.2000.03224.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The present review describes the mechanisms involved in controlling Ca2+ release from the sarcoplasmic reticulum (SR) of skeletal muscle, which ultimately regulates contraction. 2. Comparisons are made between cardiac and skeletal muscle with respect to: (i) the role of the dihydropyridine receptors (DHPR) as Ca2+ channels and voltage-sensors; (ii) the regulation of the ryanodine receptor (RyR)/Ca2+-release channels in the SR; and (iii) the importance of Ca2+-induced Ca2+ release. 3. It is shown that the key differences of the skeletal muscle Ca2+-release channel (RyR1), namely the increase in its stimulation by ATP and its inhibition by Mg2+, are critical for its direct regulation by the associated DHPR and, consequently, for the Fast, accurate control of skeletal muscle contraction.
引用
收藏
页码:216 / 224
页数:9
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