EFFECT OF VITAMIN-A AND VITAMIN-E ON ISCHEMIA-REPERFUSION DAMAGE IN RABBIT HEART

被引:15
作者
LLESUY, S [1 ]
MILEI, J [1 ]
PICONE, V [1 ]
FLECHA, BG [1 ]
BEIGELMAN, R [1 ]
BOVERIS, A [1 ]
机构
[1] UNIV SALVADOR,CARDIOPSIS & FAC MED,BUENOS AIRES,DF,ARGENTINA
关键词
ANTIOXIDANTS; CHEMILUMINESCENCE; ISCHEMIA-REPERFUSION; VITAMIN-A; VITAMIN-E;
D O I
10.1007/BF00925712
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of this study was to test the effect of vitamins A and E in reducing oxyradical effects and myocardial damage after ischemia - reperfusion in the rabbit heart. Oxyradical effects were indirectly assessed by hydroperoxide initiated chemiluminescence and myocardial damage was evaluated by qualitative and quantitative electron microscopy. Left anterior coronary artery was ligated in control and vitamin-treated rabbits for 30 min and then reperfused for 10 min. Rabbits were pretreated with 150 mg vitamin E and 60000 IU vitamin A 24 h before surgery, After 10 min of reperfusion full-thickness needle samples were obtained from five different myocardial areas (three ventricular and two septal areas) and used for the determination of hydroperoxide-initiated chemiluminescence and ultrastructural damage. In the control group, hydroperoxide-initiated chemiluminescence was 18400 +/- 500 cpm/mg protein for the non-ischemic and non-reperfused ventricular areas, and 40500 +/- 1800 cpm/mg protein for ischemic-reperfused ventricular areas. In the vitamin-treated group, hydroperoxide-initiated chemiluminescence was decreased by 8% in the non ischemic acid non reperfused ventricular areas and by 51-75% in the ventricular ischemic and reperfused areas. The two septal areas in the control group gave chemiluminescences of 6800 +/- 1200 cmp/mg protein (non ischemic-non reperfused) and 17000 +/- 2000 cpm/mg protein (ischemia-reperfusion). In the vitamin-treated group, chemiluminescence decreased by 4 and 58%, respectively. The ischemia-reperfused areas showed extensive edema, margination of nuclear chromatin and swollen mitochondria with disrupted cristae including rupture of the inner and outer mitochondrial membranes. Assessment of mitochondrial damage in electron micrographs by stereological counting and grading indicated 77% of damaged mitochondria. These hearts displayed the early signs of irreversible damage and infarction. Rabbits pretreated with vitamins A and E showed a 18% of damaged mitochondria in the same areas (p < 0.001) and relative preservation of myocyte subcellular structures. The results indicated that vitamins A and E reduce hydroperoxide-initiated chemiluminescence and myocardial cell damage during ischemia-reperfusion in the rabbit.
引用
收藏
页码:45 / 51
页数:7
相关论文
共 47 条
[1]   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
[2]   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
[3]   INCREASED CHEMI-LUMINESCENCE AND SUPEROXIDE PRODUCTION IN THE LIVER OF CHRONICALLY ETHANOL-TREATED RATS [J].
BOVERIS, A ;
FRAGA, CG ;
VARSAVSKY, AI ;
KOCH, OR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 227 (02) :534-541
[4]  
Boveris A, 1985, J Free Radic Biol Med, V1, P131, DOI 10.1016/0748-5514(85)90017-0
[5]  
BOVERIS A, 1973, BIOCHEM J, V134, P107
[6]  
BREED JGS, 1980, CANCER RES, V40, P2033
[7]   XANTHINE-OXIDASE AS A SOURCE OF FREE-RADICAL DAMAGE IN MYOCARDIAL ISCHEMIA [J].
CHAMBERS, DE ;
PARKS, DA ;
PATTERSON, G ;
ROY, R ;
MCCORD, JM ;
YOSHIDA, S ;
PARMLEY, LF ;
DOWNEY, JM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1985, 17 (02) :145-152
[8]   XANTHINE-OXIDASE IS NOT A SOURCE OF FREE-RADICALS IN THE ISCHEMIC RABBIT HEART [J].
DOWNEY, JM ;
MIURA, T ;
EDDY, LJ ;
CHAMBERS, DE ;
MELLERT, T ;
HEARSE, DJ ;
YELLON, DM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1987, 19 (11) :1053-1060
[9]   FREE RADICAL-PRODUCING ENZYME, XANTHINE-OXIDASE, IS UNDETECTABLE IN HUMAN HEARTS [J].
EDDY, LJ ;
STEWART, JR ;
JONES, HP ;
ENGERSON, TD ;
MCCORD, JM ;
DOWNEY, JM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (03) :H709-H711
[10]  
FEHDER J, 1987, CHEM FREE RADICAL RE, P2