Low-dose γ-ray irradiation reduces oxidative damage induced by CCl4 in mouse liver

被引:34
作者
Nomura, T
Yamaoka, K
机构
[1] Cent Res Inst Elect Power Ind, Dept Biosci, Komae Branch, Abiko Res Lab, Komae, Tokyo 2018511, Japan
[2] Okayama Univ, Sch Med, Fac Hlth Sci, Okayama 7008558, Japan
关键词
gamma-ray irradiation; mouse liver; carbon tetrachloride; glutathione; glutathione-related enzymes; antioxidant enzymes; free radical;
D O I
10.1016/S0891-5849(99)00180-X
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
We examined the effects of irradiation (50 cGy of gamma-ray) reducing the oxidative damage in carbon tetrachloride (CCl4)-hepatopathy mice. We made pathological examinations and analyzed transaminase activity (glutamic oxaloacetic transaminase and glutamic pyruvic transaminase), lipid peroxide level and the activities of endogenous antioxidants in the mouse. The irradiation was found to accelerate the recovery. Based on pathological examination as well as changes in each transaminase activity and lipid peroxide levels, it was shown that hepatopathy improved 3 d after the irradiation. The activities of glutathione reductase and glutathione peroxidase rapidly elevated after irradiation, and the total glutathione content gradually increased in the irradiation group. Both activities of gamma-glutamylcysteine synthetase and catalase were higher than normal at all times after the irradiation and gradually increased. In addition, the gamma-glutamylcysteine synthetase activity changed In a similar fashion to the total glutathione content. However, superoxide dismutase activity in bath groups decreased and that of the irradiation group was significantly lower than that of the sham-irradiation group. These findings suggest that low-dose radiation relieved functional disorder at least in the liver of mice with active oxygen diseases. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:1324 / 1333
页数:10
相关论文
共 41 条
[1]   PROPERTIES OF ERYTHROCYTE CATALASE FROM HOMOZYGOTES AND HETEROZYGOTES FOR SWISS-TYPE ACATALASEMIA [J].
AEBI, H ;
WYSS, SR ;
SCHERZ, B ;
GROSS, J .
BIOCHEMICAL GENETICS, 1976, 14 (9-10) :791-807
[3]   OPTIMIZED SEMIAUTOMATIC RATE METHOD FOR SERUM GLUTATHIONE REDUCTASE-ACTIVITY AND ITS APPLICATION TO PATIENTS WITH MALIGNANT DISEASE [J].
DELIDES, A ;
SPOONER, RJ ;
GOLDBERG, DM ;
NEAL, FE .
JOURNAL OF CLINICAL PATHOLOGY, 1976, 29 (01) :73-77
[4]  
FLOHE L, 1979, GLUTATHIONE METABOLI, P17
[5]  
FUJII J, 1991, J BIOL CHEM, V266, P23142
[6]  
GORLA N, 1983, BRIT J EXP PATHOL, V64, P388
[7]  
GOTO S, 1995, CANCER RES, V55, P4297
[8]   Synthesis and role of glutathione in protection against oxidative stress in yeast [J].
Grant, CM ;
Dawes, IW .
REDOX REPORT, 1996, 2 (04) :223-229
[9]   CHARACTERIZATION OF THE IN-VITRO HEPATOCYTE MODEL FOR TOXICOLOGICAL EVALUATION - REPEATED GROWTH-STIMULATION AND GLUTATHIONE RESPONSE [J].
GUILLEMETTE, J ;
MARION, M ;
DENIZEAU, F ;
FOURNIER, M ;
BROUSSEAU, P .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1993, 71 (1-2) :7-13
[10]   INCREASED SUPEROXIDE-DISMUTASE ACTIVITY IN AGED HUMAN CEREBROSPINAL-FLUID AND RAT-BRAIN DETERMINED BY ELECTRON-SPIN-RESONANCE SPECTROMETRY USING THE SPIN TRAP METHOD [J].
HIRAMATSU, M ;
KOHNO, M ;
EDAMATSU, R ;
MITSUTA, K ;
MORI, A .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (03) :1160-1164