The α1- and α2-isoforms of Na-K-ATPase play different roles in skeletal muscle contractility

被引:114
作者
He, SW
Shelly, DA
Moseley, AE
James, PF
James, JH
Paul, RJ
Lingrel, JB [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Coll Med, Dept Cellular & Mol Physiol, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Coll Med, Dept Surg, Cincinnati, OH 45267 USA
关键词
sodium-potassium-adenosinetriphosphatase; extensor digitorum longus muscle; ouabain; muscle fatigue;
D O I
10.1152/ajpregu.2001.281.3.R917
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The Na-K-ATPase, which maintains the Na+ and K+ gradients across the plasma membrane, can play a major role in modulation of skeletal muscle contractility. Although both alpha (1)- and alpha (2)-isoforms of the Na-K-ATPase are expressed in skeletal muscle, the physiological significance of these isoforms in contractility is not known. Evaluation of the contractile parameters of mouse extensor digitorum longus (EDL) was carried out using gene-targeted mice lacking one copy of either the alpha (1)- or alpha (2)-isoform gene of the Na-K-ATPase. The EDL muscles from heterozygous mice contain approximately one-half of the alpha (1)- or alpha (2)-isoform, respectively, which permits differentiation of the functional roles of these isoforms. EDL from the alpha (+/-)(1) mouse shows lower force compared with wild type, whereas that from the alpha (+/-)(2) mouse shows greater force. The different functional roles of these two isoforms are further demonstrated because inhibition of the alpha (2)-isoform with ouabain increases contractility of alpha (+/-)(1) EDL. These results demonstrate that the Na-K-ATPase a,and alpha (2)-isoforms may play different roles in skeletal muscle contraction.
引用
收藏
页码:R917 / R925
页数:9
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