Role of the cardiac Na+ /H+ exchanger during ischemia and reperfusion

被引:102
作者
Allen, DG
Xiao, XH
机构
[1] Univ Sydney, Dept Physiol, Sydney, NSW 2006, Australia
[2] Univ Sydney, Inst Biomed Res, Sydney, NSW 2006, Australia
关键词
ischemia; Na/Ca-exchanger; Na/H-exchanger; reperfusion;
D O I
10.1016/S0008-6363(02)00836-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The coupled exchanger theory describes one of the central mechanisms of damage in the ischemic heart. The theory proposes that anaerobic glycolysis produces lactate and protons and that the protons can leave the cardiac cell on the cardiac Na+/H+ exchanger (NHE1). The subsequent rise in [Na+](i) stimulates the cardiac Na+/Ca2+ exchanger (NCX) and results in an increase in [Ca2+](i) which promotes myocardial cell damage. Although the general features of this theory are widely accepted, there is dispute about some aspects, specifically whether the NHE1 remains active during ischemia or not. We review the evidence on this issue and conclude that NHE1 is substantially inhibited during ischemia. This issue is central to the design of a clinical trial of NHE1 inhibitors in the treatment of human cardiac ischemia and the existing clinical trials are considered in this light. (C) 2003 European Society of Cardiology. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:934 / 941
页数:8
相关论文
共 63 条
[1]   ATP dependence is not an intrinsic property of Na+/H+ exchanger NHE1:: requirement for an ancillary factor [J].
Aharonovitz, O ;
Demaurex, N ;
Woodside, M ;
Grinstein, S .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (06) :C1303-C1311
[2]   Na+ entry during ischemia, reperfusion and preconditioning [J].
Allen, DG ;
Xiao, XH .
CARDIOVASCULAR RESEARCH, 2001, 50 (01) :164-166
[3]   Na+/H+ exchange in ischemia, reperfusion and preconditioning [J].
Avkiran, M ;
Gross, G ;
Karmazyn, M ;
Klein, H ;
Murphy, E ;
Ytrehus, K .
CARDIOVASCULAR RESEARCH, 2001, 50 (01) :162-163
[4]  
Avkiran M, 1999, AM J CARDIOL, V83, p10G
[5]   Na+/H+ exchange inhibitors for cardioprotective therapy:: Progress, problems and prospects [J].
Avkiran, M ;
Marber, MS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (05) :747-753
[6]   THE EFFECTS OF INSULIN ON MYOCARDIAL-METABOLISM AND ACIDOSIS IN NORMOXIA AND ISCHEMIA - A P-31-NMR STUDY [J].
BAILEY, IA ;
RADDA, GK ;
SEYMOUR, AML ;
WILLIAMS, SR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 720 (01) :17-27
[7]   MODULATION OF CARDIAC SODIUM-CHANNEL GATING BY LYSOPHOSPHATIDYLCHOLINE [J].
BURNASHEV, NA ;
UNDROVINAS, AI ;
FLEIDERVISH, IA ;
MAKIELSKI, JC ;
ROSENSHTRAUKH, LV .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1991, 23 :23-30
[8]   CHANGES IN MYOPLASMIC PH AND CALCIUM-CONCENTRATION DURING EXPOSURE TO LACTATE IN ISOLATED RAT VENTRICULAR MYOCYTES [J].
CAIRNS, SP ;
WESTERBLAD, H ;
ALLEN, DG .
JOURNAL OF PHYSIOLOGY-LONDON, 1993, 464 :561-574
[9]  
CASSEL D, 1986, J BIOL CHEM, V261, P5460
[10]   Slowly inactivating component of sodium current in ventricular myocytes is decreased by diabetes and partially inhibited by known Na+-H+ exchange blockers [J].
Chattou, S ;
Coulombe, A ;
Diacono, J ;
Le Grand, B ;
John, G ;
Feuvray, D .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (07) :1181-1192