ISCHEMIC-HEART-DISEASE AND ANTIOXIDANTS - MECHANISTIC ASPECTS OF OXIDATIVE INJURY AND ITS PREVENTION

被引:20
作者
JANERO, DR
机构
[1] NitroMed, Inc., NitroMed Research Laboratories, Boston, MA 02118
关键词
ISCHEMIA-REPERFUSION; MYOCARDIUM; CARDIOMYOCYTES; OXIDATIVE STRESS; FREE RADICALS; ARRHYTHMIA; STUNNING; INFARCTION; CELL PATHOLOGY; PEROXIDATION; MEMBRANES; METABOLISM;
D O I
10.1080/10408399509527688
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The disease state of myocardial ischemia results from a hypoperfusion-induced insufficiency of heart-muscle oxidative metabolism due to inadequate coronary circulation. Myocardial ischemia is an important, lifespan-limiting medical problem and a major economic health-care concern. Reperfusion, although avidly pursued in the clinic as essential to the ultimate survival of acutely ischemic heart muscle, may itself carry an injury component Cardiac reperfusion injury appears to reflect, at feast in part, an oxidant burden established upon reoxygenation of ischemic myocardium. Laboratory evidence demonstrates that oxidative stress to the heart-muscle cell (cardiomyocyte) can elicit the three known types of ischemia-reperfusion injury that directly affect the myocardium: arrhythmia, stunning, and infarction. The limited clinical occurrence of serious reperfusion arrhythmias has restricted the importance of antioxidants as antiarrhythmic agents against this form of myocardial ischemia-reperfusion damage. Despite the utmost clinical significance of lethal cardiomyocyte injury as a negative prognostic indicator for the ischemic heart-disease patient, inconsistent results of antioxidant interventions in reducing infarct size have somewhat tempered interest in antioxidant infarct trials. By contrast, the negative clinical consequences of stunning may indeed be preventable by utilizing antioxidants to help restore postischemic cardiac pump function. Several as yet unanswered questions remain regarding oxidative stress in the reperfused heart, its significance to cardiomyocyte damage, and its ability to elicit specific postischemic myocardial derangements. Targeted mechanistic studies are required to address these questions and to define the pathogenic role of oxidative stress (and hence, the therapeutic potential of antioxidant intervention) in myocardial ischemia-reperfusion injury. The overall aim of current research in this area is to enable the cardiac surgeon/cardiologist to advance beyond the largely palliative drugs now available for management of the coronary heart-disease patient and attack directly the pathogenic determinants of heart-muscle ischemia-reperfusion injury. Optimal use of antioxidants may help address this important medical need.
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页码:65 / 81
页数:17
相关论文
共 120 条
[1]  
AMBROSIO G, 1991, AM J MED, V91, P86
[2]   MYOCYTE MITOTIC DIVISION IN THE AGING MAMMALIAN RAT-HEART [J].
ANVERSA, P ;
FITZPATRICK, D ;
ARGANI, S ;
CAPASSO, JM .
CIRCULATION RESEARCH, 1991, 69 (04) :1159-1164
[3]   REPERFUSION VENTRICULAR TACHYARRHYTHMIAS - CORRELATION WITH ANTECEDENT CORONARY-ARTERY OCCLUSION TACHYARRHYTHMIAS AND DURATION OF MYOCARDIAL ISCHEMIA [J].
BALKE, CW ;
KAPLINSKY, E ;
MICHELSON, EL ;
NAITO, M ;
DREIFUS, LS .
AMERICAN HEART JOURNAL, 1981, 101 (04) :449-456
[4]   REACTIVE OXYGEN SPECIES AND AIRWAY INFLAMMATION [J].
BARNES, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (03) :235-243
[5]   MYOCARDIAL VITAMIN-E IS CONSUMED DURING CARDIOPULMONARY BYPASS - INDIRECT EVIDENCE OF FREE-RADICAL GENERATION IN HUMAN ISCHEMIC HEART [J].
BARSACCHI, R ;
PELOSI, G ;
MAFFEI, S ;
BARONI, M ;
SALVATORE, L ;
URSINI, F ;
VERUNELLI, F ;
BIAGINI, A .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 1992, 37 (03) :339-343
[6]   URIC-ACID AS RADICAL SCAVENGER AND ANTIOXIDANT IN THE HEART [J].
BECKER, BF ;
REINHOLZ, N ;
OZCELIK, T ;
LEIPERT, B ;
GERLACH, E .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1989, 415 (02) :127-135
[7]   REVERSAL OF DYSFUNCTION IN POSTISCHEMIC STUNNED MYOCARDIUM BY EPINEPHRINE AND POSTEXTRASYSTOLIC POTENTIATION [J].
BECKER, LC ;
LEVINE, JH ;
DIPAULA, AF ;
GUARNIERI, T ;
AVERSANO, T .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1986, 7 (03) :580-589
[8]   REPERFUSION ARRHYTHMIAS - DOSE-RELATED PROTECTION BY ANTI-FREE RADICAL INTERVENTIONS [J].
BERNIER, M ;
MANNING, AS ;
HEARSE, DJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (05) :H1344-H1352
[9]   REPERFUSION-INDUCED ARRHYTHMIAS AND OXYGEN-DERIVED FREE-RADICALS - STUDIES WITH ANTI-FREE RADICAL INTERVENTIONS AND A FREE RADICAL-GENERATING SYSTEM IN THE ISOLATED PERFUSED RAT-HEART [J].
BERNIER, M ;
HEARSE, DJ ;
MANNING, AS .
CIRCULATION RESEARCH, 1986, 58 (03) :331-340
[10]  
BIGGER JT, 1984, ANNU REV MED, V35, P127