Dependence of H2O2 formation by rat heart mitochondria on substrate availability and donor age

被引:374
作者
Hansford, RG [1 ]
Hogue, BA [1 ]
Mildaziene, V [1 ]
机构
[1] KAUNAS MED ACAD, INST BIOMED RES, LT-3007 KAUNAS, LITHUANIA
关键词
respiratory chain; reactive oxygen species;
D O I
10.1023/A:1022420007908
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We have examined the substrate specificity and inhibitor sensitivity of H2O2 formation by rat heart mitochondria. Active H2O2 production requires both a high fractional reduction of Complex I (indexed by NADH/NAD(+) + NADH ratio) and a high membrane potential, Delta psi. These conditions are achieved with supraphysiological concentrations of succinate. With physiological concentrations of NAD-linked substrates, rates of H2O2 formation are much lower (less than 0.1% of respiratory chain electron flux) but may be stimulated by the Complex III inhibitor antimycin A, but not by myxothiazol. Addition of Mn2+ to give 10 nmol/mg of mitochondrial protein enhances H2O2 production with all substrate combinations, possibly by repleting mitochondrial superoxide dismutase with this cation. Contrary to previously published work, no increased activity of H2O2 production was found with heart mitochondria from senescent (24 month) rats, relative to young adults (6 month).
引用
收藏
页码:89 / 95
页数:7
相关论文
共 27 条
[1]   DNA OXIDATIVE DAMAGE AND LIFE EXPECTANCY IN HOUSEFLIES [J].
AGARWAL, S ;
SOHAL, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12332-12335
[2]   OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[3]   LOW MITOCHONDRIAL FREE-RADICAL PRODUCTION PER UNIT O-2 CONSUMPTION CAN EXPLAIN THE SIMULTANEOUS PRESENCE OF HIGH LONGEVITY AND HIGH AEROBIC METABOLIC-RATE IN BIRDS [J].
BARJA, G ;
CADENAS, S ;
ROJAS, C ;
PEREZCAMPO, R ;
LOPEZTORRES, M .
FREE RADICAL RESEARCH, 1994, 21 (05) :317-327
[4]   MITOCHONDRIAL GENERATION OF HYDROGEN-PEROXIDE - GENERAL PROPERTIES AND EFFECT OF HYPERBARIC-OXYGEN [J].
BOVERIS, A ;
CHANCE, B .
BIOCHEMICAL JOURNAL, 1973, 134 (03) :707-716
[5]   ROLE OF UBIQUINONE IN MITOCHONDRIAL GENERATION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CADENAS, E ;
STOPPANI, AOM .
BIOCHEMICAL JOURNAL, 1976, 156 (02) :435-444
[6]  
BOVERIS A, 1984, METHOD ENZYMOL, V105, P429
[7]   CELLULAR PRODUCTION OF HYDROGEN-PEROXIDE [J].
BOVERIS, A ;
CHANCE, B ;
OSHINO, N .
BIOCHEMICAL JOURNAL, 1972, 128 (03) :617-&
[8]   MOLECULAR-BASIS OF MITOCHONDRIAL-DNA DISEASE [J].
BROWN, MD ;
WALLACE, DC .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1994, 26 (03) :273-289
[9]   HYDROPEROXIDE METABOLISM IN MAMMALIAN ORGANS [J].
CHANCE, B ;
SIES, H ;
BOVERIS, A .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :527-605
[10]  
CUTLER RG, 1984, FREE RADICALS MOL BI, P235