INCREASED RESISTANCE AGAINST OXIDATIVE STRESS IS OBSERVED DURING A SHORT-PERIOD OF RENAL REPERFUSION AFTER A TEMPORAL ISCHEMIA

被引:4
作者
CAMPOS, R [1 ]
GARRIDO, A [1 ]
GUERRA, R [1 ]
VALENZUELA, A [1 ]
机构
[1] UNIV CHILE,INST NUTR & TECNOL ALIMENTOS,UNIDAD BIOQUIM FARMACOL,CASILLA 13811,SANTIAGO,CHILE
来源
FREE RADICAL RESEARCH COMMUNICATIONS | 1990年 / 10卷 / 4-5期
关键词
Ischaemia-reperfusion damage; Microsomal free radicals; Renal ischaemia; Tissue oxidative damage;
D O I
10.3109/10715769009149894
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reperfusion of rat kidney submitted to temporal ischaemia induces a decrease in glutathione content. Lipid peroxidation is not detected in kidney homogenates but microsomes obtained after periods of reperfusion longer than 60 minutes show increased malondialdehyde values correlated with high oxygen consumption and superoxide free radical generation. Microsomes obtained from kidneys submitted to 15 or 60 minutes of reperfusion are resistant to NADPH-induced lipid peroxidation but after 120 minutes of reperfusion an increased lipid peroxidative response is observed. Although the mechanism of the protection found in microsomes against the induction of oxidative stress in the first 60 minutes of reperfusion is unknown, it is postulated that this subcellular fraction plays an important role in the oxidative stress observed after longer periods of reperfusion. © 1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
引用
收藏
页码:259 / 264
页数:6
相关论文
共 26 条
[1]   RAPID ISOLATION OF MICROSOMES FOR STUDIES OF LIPID-PEROXIDATION [J].
ALBRO, PW ;
CORBETT, JT ;
SCHROEDER, JL .
LIPIDS, 1987, 22 (10) :751-756
[2]  
Aust S.D., 1985, HDB METHODS OXYGEN R, P203
[4]   ISCHEMIC ACUTE RENAL-FAILURE AND ANTIOXIDANT THERAPY IN THE RAT - THE RELATION BETWEEN GLOMERULAR AND TUBULAR DYSFUNCTION [J].
BIRD, JE ;
MILHOAN, K ;
WILSON, CB ;
YOUNG, SG ;
MUNDY, CA ;
PARTHASARATHY, S ;
BLANTZ, RC .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (05) :1630-1638
[5]   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
[6]   MECHANISM OF PROTECTION BY VERAPAMIL AND NIFEDIPINE FROM ANOXIC INJURY IN ISOLATED CARDIAC MYOCYTES [J].
CHEUNG, JY ;
LEAF, A ;
BONVENTRE, JV .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (03) :C323-C329
[7]   LIPID-PEROXIDATION IN RAT UTERUS [J].
DEVASAGAYAM, TPA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 876 (03) :507-514
[8]  
FANTONE JC, 1982, AM J PATHOL, V107, P396
[9]   EVIDENCE THAT SUPEROXIDE DISMUTASE PLAYS A ROLE IN PROTECTING RED BLOOD-CELLS AGAINST PEROXIDATIVE HEMOLYSIS [J].
FEE, JA ;
TEITELBAUM, HD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1972, 49 (01) :150-+
[10]   SUPEROXIDE RADICAL GENERATION, NADPH OXIDASE ACTIVITY, AND CYTOCHROME-P-450 CONTENT OF RAT-LIVER MICROSOMAL FRACTIONS IN AN EXPERIMENTAL HYPERTHYROID STATE - RELATION TO LIPID-PEROXIDATION [J].
FERNANDEZ, V ;
BARRIENTOS, X ;
KIPREOS, K ;
VALENZUELA, A ;
VIDELA, LA .
ENDOCRINOLOGY, 1985, 117 (02) :496-501