Oxidative stress and aging reduce COX I RNA and cytochrome oxidase activity in Drosophila

被引:78
作者
Schwarze, SR
Weindruch, R
Aiken, JM [1 ]
机构
[1] Univ Wisconsin, Dept Anim Hlth & Biomed Sci, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Med, Madison, WI 53706 USA
[3] Univ Wisconsin, VA GRECC, Madison, WI 53706 USA
关键词
Drosophila; mitochondria; aging; mitochondrial RNA; cytochrome oxidase; catalase; superoxide dismutase; ATP; free radical;
D O I
10.1016/S0891-5849(98)00153-1
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
Drosophila melanogaster displays an age-associated increase in oxidative damage and a decrease in mitochondrial transcripts. To determine if these changes result in energy production deficiencies, we measured the electron transport system (ETS) enzyme activity, and ATP levels with age. No statistically significant influences of age on activities of complexes I and II or citrate synthase were observed. In contrast, from 2 to 45 days post-eclosion, declines were found in complex IV cytochrome c oxidase activity (COX, 40% decline) and ATP abundance (15%), while lipid peroxidation increased 71%. We next examined flies that were either genetically or chemically oxidatively stressed to determine the effect on levels of mitochondrial-encoded cytochrome oxidase I RNA (coxI) and COX activity. A catalase null mutant line had 48% of coxI RNA compared to the wild type. In Cu/Zn superoxide dismutase (cSOD) null flies, the rate of coxI RNA decline was greater than in controls. CoxI RNA also declined with increasing hydrogen peroxide (H2O2) treatment, which was reflected in reduced cytochrome c oxidase (COX) activity. These results show that oxidative stress is closely associated with reductions in mitochondrial transcript levels and support the hypothesis that oxidative stress may contribute to mitochondrial dysfunction and aging in D. melanogaster. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:740 / 747
页数:8
相关论文
共 36 条
[1]  
AEBI H, 1978, BASIS METABOLIC DIS, P1792
[2]   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
[3]   Factors contributing to the plasticity of the extended longevity phenotypes of Drosophila [J].
Arking, R ;
Force, AG ;
Dudas, SP ;
Buck, S ;
Baker, GT .
EXPERIMENTAL GERONTOLOGY, 1996, 31 (06) :623-643
[4]   THE MITOCHONDRIAL ELECTRON-TRANSFER ALTERATION AS A FACTOR INVOLVED IN THE BRAIN AGING [J].
BENZI, G ;
PASTORIS, O ;
MARZATICO, F ;
VILLA, RF ;
DAGANI, F ;
CURTI, D .
NEUROBIOLOGY OF AGING, 1992, 13 (03) :361-368
[5]   RNA MAPPING ON DROSOPHILA MITOCHONDRIAL-DNA - PRECURSORS AND TEMPLATE STRANDS [J].
BERTHIER, F ;
RENAUD, M ;
ALZIARI, S ;
DURAND, R .
NUCLEIC ACIDS RESEARCH, 1986, 14 (11) :4519-4533
[6]  
Blanc EM, 1997, J NEUROCHEM, V69, P570
[7]   EXTRAMITOCHONDRIAL RELEASE OF HYDROGEN-PEROXIDE FROM INSECT AND MOUSE-LIVER MITOCHONDRIA USING THE RESPIRATORY INHIBITORS PHOSPHINE, MYXOTHIAZOL, AND ANTIMYCIN AND SPECTRAL-ANALYSIS OF INHIBITED CYTOCHROMES [J].
BOLTER, CJ ;
CHEFURKA, W .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 278 (01) :65-72
[8]  
CALLEJA M, 1993, J BIOL CHEM, V268, P18891
[9]   Molecular organization of the glutathione reductase gene in Drosophila melanogaster [J].
Candas, M ;
Sohal, RS ;
Radyuk, SN ;
Klichko, VI ;
Orr, WC .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 339 (02) :323-334
[10]   Oxidative stress induces the levels of a mafG homolog in hamster HA-1 cells [J].
Crawford, DR ;
Leahy, KP ;
Wang, YH ;
Schools, GP ;
Kochheiser, JC ;
Davies, KJA .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (04) :521-525