Activity of the Na+/H+ exchanger contributes to cardiac damage following ischaemia and reperfusion

被引:8
作者
Allen, DG [1 ]
Xiao, XH [1 ]
机构
[1] Univ Sydney, Dept Physiol F13, Inst Biomed Res, Sydney, NSW 2006, Australia
关键词
ischaemia; Na+/H+ exchanger; NHE1; preconditioning; reperfusion;
D O I
10.1046/j.1440-1681.2000.03329.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The present review considers the evidence that Na+-H+ exchange activity contributes to cardiac damage following ischaemia and reperfusion, The basic mechanism involved is that protons are produced during ischaemia and leave the myocytes on the Na+/H+ exchanger during either ischaemia and/or reperfusion, The resulting elevation of [Na+](i) causes Ca2+ loading through the Na+/Ca2+ exchanger and the elevated [Ca2+](i) is thought to lead to myocardial damage, 2. Inhibition of the Na+/H+ exchanger during ischaemia and/or reperfusion produces a substantial cardioprotective effect by blocking the damage caused by the coupled exchanger mechanism described above. Preconditioning also produces a cardioprotective effect and the evidence that this also involves the Na+/H+ exchanger is reviewed, 3, The intracellular mechanisms associated with ischaemic damage and preconditioning are of great interest because they may provide targets for potential therapeutic interventions. The intracellular regulation of the Na+/H+ exchanger appears to be an important component of these pathways and may become a focus for therapeutic approaches.
引用
收藏
页码:727 / 733
页数:7
相关论文
共 73 条
[61]   MECHANISMS OF PH(I) RECOVERY AFTER GLOBAL-ISCHEMIA IN THE PERFUSED HEART [J].
VANDENBERG, JI ;
METCALFE, JC ;
GRACE, AA .
CIRCULATION RESEARCH, 1993, 72 (05) :993-1003
[62]   The role of the Na+ channel in the accumulation of intracellular Na+ during myocardial ischemia: Consequences for post-ischemic recovery [J].
VanEmous, JG ;
Nederhoff, MGJ ;
Ruigrok, TJC ;
VanEchteld, CJA .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (01) :85-96
[63]   EXTRACELLULAR H+ INACTIVATION OF NA+-H+ EXCHANGE IN THE SHEEP CARDIAC PURKINJE-FIBER [J].
VAUGHANJONES, RD ;
WU, ML .
JOURNAL OF PHYSIOLOGY-LONDON, 1990, 428 :441-466
[64]  
VAUGHANJONES RD, 1988, CIBA F SYMP, V139, P23
[65]   Molecular physiology of vertebrate Na+/H+ exchangers [J].
Wakabayashi, S ;
Shigekawa, M ;
Pouyssegur, J .
PHYSIOLOGICAL REVIEWS, 1997, 77 (01) :51-74
[66]   ALPHA-1-ADRENERGIC STIMULATION OF NA-H EXCHANGE IN CARDIAC MYOCYTES [J].
WALLERT, MA ;
FROHLICH, O .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (05) :C1096-C1102
[67]   THE PH OF SPONTANEOUSLY BEATING CULTURED RAT-HEART CELLS IS REGULATED BY AN ATP-CALMODULIN-DEPENDENT NA+/H+ ANTIPORT [J].
WEISSBERG, PL ;
LITTLE, PJ ;
CRAGOE, EJ ;
BOBIK, A .
CIRCULATION RESEARCH, 1989, 64 (04) :676-685
[68]   Role of Na+/H+ exchanger during ischemia and preconditioning in the isolated rat heart [J].
Xiao, XH ;
Allen, DG .
CIRCULATION RESEARCH, 1999, 85 (08) :723-730
[69]   NA+/H+ EXCHANGE AND REPERFUSION ARRHYTHMIAS - PROTECTION BY INTRACORONARY INFUSION OF A NOVEL INHIBITOR [J].
YASUTAKE, M ;
IBUKI, C ;
HEARSE, DJ ;
AVKIRAN, M .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1994, 267 (06) :H2430-H2440
[70]   Thrombin activates the sarcolemmal Na+-H+ exchanger - Evidence for a receptor-mediated mechanism involving protein kinase C [J].
Yasutake, M ;
Haworth, RS ;
King, A ;
Avkiran, M .
CIRCULATION RESEARCH, 1996, 79 (04) :705-715