KINETICS OF HYDROPEROXIDE DEGRADATION BY NADP-GLUTATHIONE SYSTEM IN MITOCHONDRIA

被引:30
作者
KUROSAWA, K
SHIBATA, H
HAYASHI, N
SATO, N
KAMADA, T
TAGAWA, K
机构
[1] OSAKA UNIV,SCH MED,DEPT PHYSIOL CHEM,KITA KU,OSAKA 530,JAPAN
[2] OSAKA UNIV,SCH MED,DEPT MED 1,KITA KU,OSAKA 530,JAPAN
关键词
D O I
10.1093/oxfordjournals.jbchem.a123169
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
Hydroperoxide decomposition by the NADP-glutathione system in rat liver mitochondria was analyzed. Mitochondria were found to contain high concentrations of the reduced form of glutathione (GSH) (4.32±0.50nmol/mg) and NADPH (4.74±0.64nmol/mg), and high activities of glutathione peroxidase and reductase. In the initial phase of the reaction, the rate of hydroperoxide decomposition was proportional to both the GSH level and the activity of GSH peroxidase. However, in the later steady state, the step of NADP reduction was rate-limiting, and the overall reaction rate was independent of the initial concentration of GSH, and activities of glutathione peroxidase and reductase. Some GSH was released from mitochondria during incubation, but the rate of the decomposition could be simply expressed as k [GSH]/2, where k is the first-order rate constant of the peroxidase and [GSH] is the intramitochondrial level of GSH in the steady state. The rate of the reaction in the steady state was also dependent on the NADPH level, its reciprocal being linearly correlated with [NADPH]-1. The rate of decomposition of hydroperoxide was influenced by the respiratory state. During state 3 respiration, the rate was greatly depressed, but was still considered to exceed by far the rate of physiological generation of hydroperoxide. © 1990 Copyright, 1990 by the Journal of Biochemistry.
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页码:9 / 16
页数:8
相关论文
共 29 条
[1]  
BEATRICE MC, 1984, J BIOL CHEM, V259, P1279
[2]  
BEAVIS AD, 1985, J BIOL CHEM, V260, P3424
[3]   PYRIDINE-NUCLEOTIDE OXIDATION, CA-2+ CYCLING AND MEMBRANE DAMAGE DURING TERT-BUTYL HYDROPEROXIDE METABOLISM BY RAT-LIVER MITOCHONDRIA [J].
BELLOMO, G ;
MARTINO, A ;
RICHELMI, P ;
MOORE, GA ;
JEWELL, SA ;
ORRENIUS, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 140 (01) :1-6
[4]   CELLULAR PRODUCTION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CHANCE, B ;
OSHINO, N .
BIOCHEMICAL JOURNAL, 1972, 128 (03) :617-&
[5]  
CARLBERG I, 1975, J BIOL CHEM, V250, P5475
[6]   HYDROPEROXIDE METABOLISM IN MAMMALIAN ORGANS [J].
CHANCE, B ;
SIES, H ;
BOVERIS, A .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :527-605
[7]   REDUCTION OF LINOLENIC ACID HYDROPEROXIDE BY A GLUTATHIONE PEROXIDASE [J].
CHRISTOP.BO .
BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 176 (03) :463-&
[8]   OXIDATION OF GLUTATHIONE DURING HYDROPEROXIDE METABOLISM - A STUDY USING ISOLATED HEPATOCYTES AND THE GLUTATHIONE-REDUCTASE INHIBITOR 1,3-BIS(2-CHLOROETHYL)-1-NITROSOUREA [J].
EKLOW, L ;
MOLDEUS, P ;
ORRENIUS, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1984, 138 (03) :459-463
[9]  
GLASER L, 1955, J BIOL CHEM, V216, P67
[10]   ORIGIN AND TURNOVER OF MITOCHONDRIAL GLUTATHIONE [J].
GRIFFITH, OW ;
MEISTER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (14) :4668-4672