Na/K-ATPase-An Integral Player in the Adrenergic Fight-or-Flight Response

被引:48
作者
Bers, Donald M. [1 ]
Despa, Sanda [1 ]
机构
[1] Univ Calif Davis, Dept Pharmacol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
PROTEIN-KINASE-A; MOUSE VENTRICULAR MYOCYTES; CHANNEL RYANODINE RECEPTOR; AFFECT CALCIUM SPARKS; SR CA2+ LOAD; CARDIAC MYOCYTES; SARCOPLASMIC-RETICULUM; PUMP FUNCTION; PHOSPHORYLATION SITE; PHOSPHOLEMMAN FXYD1;
D O I
10.1016/j.tcm.2009.07.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
During activation of the sympathetic nervous system, cardiac performance is increased as part of the fight-or-flight stress response. The increase in contractility with sympathetic stimulation is an orchestrated combination of intrinsic inotropic, lusitropic, and chronotropic effects, mediated in part by activation of P-adrenergic receptors and protein kinase A. This causes phosphorylation of several Ca cycling proteins in cardiac myocytes (increasing Ca entry via L-type Ca channels, sarcoplasmic reticulum Ca pumping, and the dissociation rate of Ca from the myofilaments). Here, we discuss how stimulation of the Na/K-ATPase, mediated by phosphorylation of phospholemman (a small sarcolemmal protein that associates with and modulates Na/K-ATPase), is an additional important player in the sympathetic fight-or-flight response. Enhancement of Na/K-ATPase activity limits the rise in [Na](i) caused by the higher level of Na influx and by doing so limits the rise in cellular and sarcoplasmic reticulum Ca load by favoring Ca extrusion via the Na/Ca exchanger Thus, phospholemman-mediated activation of the Na/K-ATPase may prevent Ca. overload and triggered arrhythmias during stress. (Trends Cardiovasc Med 2009; 19:111-118) (C) 2009, Elsevier Inc.
引用
收藏
页码:111 / 118
页数:8
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