Impairment of brain mitochondrial function by reactive nitrogen species:: the role of glutathione in dictating susceptibility

被引:60
作者
Heales, SJR
Bolaños, JP
机构
[1] Inst Neurol, Dept Neurochem, London WC1N 3BG, England
[2] Inst Neurol, Dept Clin Biochem, London WC1N 3BG, England
[3] Natl Hosp, London WC1N 3BG, England
[4] Univ Salamanca, Dept Bioquim & Biol Mol, Salamanca 37007, Spain
基金
英国医学研究理事会;
关键词
glutathione; mitochondrial enzyme; reactive nitrogen species;
D O I
10.1016/S0197-0186(01)00117-6
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
Mitochondrial enzymes involved in energy metabolism display varying degrees of sensitivity towards reactive nitrogen species such as peroxynitrite (ONOO-). With regards to the electron transport chain, cytochrome oxidase appears particularly sensitive. Inhibition of this component may lead to an increase in mitochondrial superoxide formation, exacerbation of cellular oxidative stress and further mitochondrial damage. Impairment of the electron transport chain may lead to a loss of membrane potential, ATP deficiency, opening of the permeability transition pore and the release of factors capable of initiating apoptosis. Reduced glutathione will react, via a number of diverse reactions, with reactive nitrogen species and hence is capable of limiting mitochondiral damage. Loss of brain glutathione may therefore be an important factor in those neurological conditions in which there is evidence of excessive nitric oxide formation and mitochondrial damage. (C) 2002 Published by Elsevier Science Ltd.
引用
收藏
页码:469 / 474
页数:6
相关论文
共 58 条
[1]   Nitric oxide mediates glutamate induced mitochondrial depolarization in rat cortical neurons [J].
Almeida, A ;
Bolaños, JP ;
Medina, JM .
BRAIN RESEARCH, 1999, 816 (02) :580-586
[2]   Glutamate neurotoxicity is associated with nitric oxide-mediated mitochondrial dysfunction and glutathione depletion [J].
Almeida, A ;
Heales, SJR ;
Bolaños, JP ;
Medina, JM .
BRAIN RESEARCH, 1998, 790 (1-2) :209-216
[3]   Activation of the inducible form of nitric oxide synthase in the brains of patients with multiple sclerosis [J].
Bagasra, O ;
Michaels, FH ;
Zheng, YM ;
Bobroski, LE ;
Spitsin, SV ;
Fu, ZF ;
Tawadros, R ;
Koprowski, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) :12041-12045
[4]   Depletion of brain glutathione results in a decrease of glutathione reductase activity; An enzyme susceptible to oxidative damage [J].
Barker, JE ;
Heales, SJR ;
Cassidy, A ;
Bolanos, JP ;
Land, JM ;
Clark, JB .
BRAIN RESEARCH, 1996, 716 (1-2) :118-122
[5]   Glutathione protects astrocytes from peroxynitrite-mediated mitochondrial damage: Implications for neuronal astrocytic trafficking and neurodegeneration [J].
Barker, JE ;
Bolanos, JP ;
Land, JM ;
Clark, JB ;
Heales, SJR .
DEVELOPMENTAL NEUROSCIENCE, 1996, 18 (5-6) :391-396
[6]   Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis [J].
Beal, MF ;
Ferrante, RJ ;
Browne, SE ;
Matthews, RT ;
Kowall, NW ;
Brown, RH .
ANNALS OF NEUROLOGY, 1997, 42 (04) :644-654
[7]  
Bolanos JP, 1997, J NEUROCHEM, V68, P2227
[8]  
BOLANOS JP, 1994, J NEUROCHEM, V63, P910
[9]   Roles of nitric oxide in brain hypoxia-ischemia [J].
Bolaños, JP ;
Almeida, A .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1999, 1411 (2-3) :415-436
[10]  
BOLANOS JP, 1995, J NEUROCHEM, V64, P1965