IRREVERSIBLE INHIBITION OF MITOCHONDRIAL COMPLEX-I BY 1-METHYL-4-PHENYLPYRIDINIUM - EVIDENCE FOR FREE-RADICAL INVOLVEMENT

被引:343
作者
CLEETER, MWJ
COOPER, JM
SCHAPIRA, AHV
机构
[1] ROYAL FREE HOSP,SCH MED,DEPT NEUROSCI,ROWLAND HILL ST,LONDON NW3 2PF,ENGLAND
[2] ROYAL FREE HOSP,SCH MED,DEPT PROT & MOLEC BIOL,LONDON NW3 2PF,ENGLAND
[3] UNIV LONDON,INST NEUROL,DEPT CLIN NEUROL,LONDON,ENGLAND
关键词
1-METHYL-4-PHENYLPYRIDINIUM; COMPLEX-I; FREE RADICALS; PARKINSONS DISEASE;
D O I
10.1111/j.1471-4159.1992.tb09789.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
Incubation of 10 mM 1-methyl-4-phenylpyridinium (MPP+) with sonicated beef heart mitochondria caused an irreversible time-dependent decrease in NADH-ubiquinone-1 (CoQ1) reductase activity (52% inhibition after 1 h). Inclusion of glutathione, ascorbate, or catalase in the incubation mixture protected the NADH-CoQ1 reductase activity. These results suggest that the interaction of MPP+ with complex I induces free radical generation, which in turn leads to the irreversible inhibition of complex I activity. The generation of free radicals by neurotoxin-induced inhibition of complex I has important implications for our interpretation of the increased oxidative stress observed in Parkinson's disease substantia nigra and for our understanding of the cause(s) of dopaminergic cell death in this disorder.
引用
收藏
页码:786 / 789
页数:4
相关论文
共 30 条
[1]  
ADAMS JD, 1989, RES COMMUN SUBSTANCE, V10, P169
[2]  
ADAMS JD, 1986, MPTP NEUROTOXIN PROD, P571
[3]   MITOCHONDRIAL GENERATION OF HYDROGEN-PEROXIDE - GENERAL PROPERTIES AND EFFECT OF HYPERBARIC-OXYGEN [J].
BOVERIS, A ;
CHANCE, B .
BIOCHEMICAL JOURNAL, 1973, 134 (03) :707-716
[4]   CHEMICALLY-INDUCED PARKINSONS-DISEASE .2. INTERMEDIATES IN THE OXIDATION AND REDUCTION REACTIONS OF THE 1-METHYL-4-PHENYL-2,3-DIHYDROPYRIDINIUM ION AND ITS DEPROTONATED FORM [J].
CHACON, JN ;
CHEDEKEL, MR ;
LAND, EJ ;
TRUSCOTT, TG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 158 (01) :63-71
[5]   CHEMICALLY-INDUCED PARKINSONS-DISEASE - INTERMEDIATES IN THE OXIDATION OF 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE TO THE 1-METHYL-4-PHENYL-PYRIDINIUM ION [J].
CHACON, JN ;
CHEDEKEL, MR ;
LAND, EJ ;
TRUSCOTT, TG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 144 (02) :957-964
[6]  
Davis G. C., 1979, PSYCHIAT RES, V1, P649
[7]   BASAL LIPID-PEROXIDATION IN SUBSTANTIA NIGRA IS INCREASED IN PARKINSONS-DISEASE [J].
DEXTER, DT ;
CARTER, CJ ;
WELLS, FR ;
JAVOYAGID, F ;
AGID, Y ;
LEES, A ;
JENNER, P ;
MARSDEN, CD .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (02) :381-389
[8]   MODEL STUDY ON THE BIOREDUCTION OF PARAQUAT, MPP+, AND ANALOGS - EVIDENCE AGAINST A REDOX CYCLING MECHANISM IN MPTP NEUROTOXICITY [J].
FRANK, DM ;
ARORA, PK ;
BLUMER, JL ;
SAYRE, LM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 147 (03) :1095-1104
[9]   A LARGE KINDRED WITH AUTOSOMAL DOMINANT PARKINSONS-DISEASE [J].
GOLBE, LI ;
DIIORIO, G ;
BONAVITA, V ;
MILLER, DC ;
DUVOISIN, RC .
ANNALS OF NEUROLOGY, 1990, 27 (03) :276-282
[10]   1-METHYL-4-PHENYLPYRIDINIUM (MPP+) INDUCES NADH-DEPENDENT SUPEROXIDE FORMATION AND ENHANCES NADH-DEPENDENT LIPID-PEROXIDATION IN BOVINE HEART SUBMITOCHONDRIAL PARTICLES [J].
HASEGAWA, E ;
TAKESHIGE, K ;
OISHI, T ;
MURAI, Y ;
MINAKAMI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :1049-1055