Type 2 ryanodine receptor: A novel therapeutic target in myocardial ischemia/reperfusion

被引:43
作者
Fauconnier, Jeremy [1 ]
Roberge, Stephanie [1 ]
Saint, Nathalie [1 ]
Lacampagne, Alain [1 ]
机构
[1] Univ Montpellier 2, Univ Montpellier 1, CHRU Montpellier, INSERM,U1046, F-34295 Montpellier, France
关键词
Heart; Calcium; Oxidative stress; Mitochondria; Reperfusion injuries; CALCIUM-RELEASE CHANNEL; CARDIAC SARCOPLASMIC-RETICULUM; MITOCHONDRIAL PERMEABILITY TRANSITION; ISCHEMIA-REPERFUSION INJURY; CA2+ RELEASE; NITRIC-OXIDE; RAT-HEART; VENTRICULAR-ARRHYTHMIAS; ADRENERGIC REGULATION; MOLECULAR-MECHANISM;
D O I
10.1016/j.pharmthera.2013.01.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiac pathologies remain the main cause of mortality worldwide. Among them the most common cause is cardiac ischemia. The rapid reperfusion after coronary occlusion has considerably improved the cardiac outcome, however reperfusion per se has deleterious effect also called reperfusion injuries. Cytosolic calcium overload is now well admitted as an essential pathophysiological mechanism involved in reperfusion injuries although the source and origin of calcium remain to be determined. Recent works have pointed out the potential defect of sarcoplasmic reticulum calcium release channels (ryanodine receptor, RyR) as a primary cause of calcium overload during ischemia-reperfusion. This finding opens new pharmacological perspectives in limiting reperfusion injuries since allosteric modulators able to restore and prevents RyR dysfunction have been developed during the last decade. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:323 / 332
页数:10
相关论文
共 153 条
[61]   A NOVEL FK506 BINDING-PROTEIN CAN MEDIATE THE IMMUNOSUPPRESSIVE EFFECTS OF FK506 AND IS ASSOCIATED WITH THE CARDIAC RYANODINE RECEPTOR [J].
LAM, E ;
MARTIN, MM ;
TIMERMAN, AP ;
SABERS, C ;
FLEISCHER, S ;
LUKAS, T ;
ABRAHAM, RT ;
OKEEFE, SJ ;
ONEILL, EA ;
WIEDERRECHT, GJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) :26511-26522
[62]   Mechanisms of calcium signaling by cyclic ADP-ribose and NAADP [J].
Lee, HC .
PHYSIOLOGICAL REVIEWS, 1997, 77 (04) :1133-1164
[63]   Phosphodiesterase 4D deficiency in the ryanodine-receptor complex promotes heart failure and arrhythmias [J].
Lehnart, SE ;
Wehrens, XHT ;
Reiken, S ;
Warrier, S ;
Belevych, AE ;
Harvey, RD ;
Richter, W ;
Jin, SLC ;
Conti, M ;
Marks, AR .
CELL, 2005, 123 (01) :25-35
[64]   Leaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice [J].
Lehnart, Stephan E. ;
Mongillo, Marco ;
Bellinger, Andrew ;
Lindegger, Nicolas ;
Chen, Bi-Xing ;
Hsueh, William ;
Reiken, Steven ;
Wronska, Anetta ;
Drew, Liam J. ;
Ward, Chris W. ;
Lederer, W. J. ;
Kass, Robert S. ;
Morley, Gregory ;
Marks, Andrew R. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (06) :2230-2245
[65]   Modulation of cardiac ryanodine receptors by sorcin [J].
Lokuta, AJ ;
Meyers, MB ;
Sander, PR ;
Fishman, GI ;
Valdivia, HH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (40) :25333-25338
[66]   Removal of Fkbp12/12.6 from endothelial ryanodine receptors leads to an intracellular calcium leak and endothelial dysfunction [J].
Long, Cheng ;
Cook, Leslie G. ;
Wu, Gang-Yi ;
Mitchell, Brett M. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (07) :1580-1586
[67]   K201 modulates excitation-contraction coupling and spontaneous Ca2+ release in normal adult rabbit ventricular cardiomyocytes [J].
Loughrey, C. M. ;
Otani, N. ;
Seidler, T. ;
Craig, M. A. ;
Matsuda, R. ;
Kaneko, N. ;
Smith, G. L. .
CARDIOVASCULAR RESEARCH, 2007, 76 (02) :236-246
[68]   The inotropic adaptation during late preconditioning against myocardial stunning is associated with an increase in FKBP12.6 [J].
Lucats, Laurence ;
Vinet, Laurent ;
Bize, Alain ;
Monnet, Xavier ;
Morin, Didier ;
Su, Jin Bo ;
Rouet-Benzineb, Patricia ;
Cazorla, Olivier ;
Mercadier, Jean-Jacques ;
Hittinger, Luc ;
Berdeaux, Alain ;
Ghaleh, Bijan .
CARDIOVASCULAR RESEARCH, 2007, 73 (03) :560-567
[69]   MALIGNANT HYPERTHERMIA [J].
MACLENNAN, DH ;
PHILLIPS, MS .
SCIENCE, 1992, 256 (5058) :789-794
[70]   Sulfhydryl oxidation modifies the calcium dependence of ryanodine-sensitive calcium channels of excitable cells [J].
Marengo, JJ ;
Hidalgo, C ;
Bull, R .
BIOPHYSICAL JOURNAL, 1998, 74 (03) :1263-1277