Regulation of mitochondrial respiration by nitric oxide inhibition of cytochrome c oxidase

被引:505
作者
Brown, GC [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2001年 / 1504卷 / 01期
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
nitric oxide; mitochondrion; cytochrome oxidase; respiration; oxygen consumption;
D O I
10.1016/S0005-2728(00)00238-3
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
Nitric oxide (NO) and its derivatives inhibit mitochondrial respiration by a variety of means. Nanomolar concentrations of NO immediately, specifically and reversibly inhibit cytochrome oxidase in competition with oxygen, in isolated cytochrome oxidase, mitochondria, nerve terminals, cultured cells and tissues. Higher concentrations of NO and its derivatives (peroxynitrite, nitrogen dioxide or nitrosothiols) can cause irreversible inhibition of the respiratory chain, uncoupling, permeability transition, and/or cell death. Isolated mitochondria, cultured cells, isolated tissues and animals in vivo display respiratory inhibition by endogenously produced NO from constitutive isoforms of NO synthase (NOS), which may be largely mediated by NO inhibition of cytochrome oxidase. Cultured cells expressing the inducible isoform of NOS (iNOS) can acutely and reversibly inhibit their own cellular respiration and that of co-incubated cells due to NO inhibition of cytochrome oxidase, but after longer-term incubation result in irreversible inhibition of cellular respiration due to NO or its derivatives. Thus the NO inhibition of cytochrome oxidase may be involved in the physiological and/or pathological regulation of respiration rate, and its affinity for oxygen. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:46 / 57
页数:12
相关论文
共 97 条
[1]   OXYGEN ACTIVATION AND THE CONSERVATION OF ENERGY IN CELL RESPIRATION [J].
BABCOCK, GT ;
WIKSTROM, M .
NATURE, 1992, 356 (6367) :301-309
[2]   CONTROL OF CARDIAC-MUSCLE CELL-FUNCTION BY AN ENDOGENOUS NITRIC-OXIDE SIGNALING SYSTEM [J].
BALLIGAND, JL ;
KELLY, RA ;
MARSDEN, PA ;
SMITH, TW ;
MICHEL, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :347-351
[3]   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
[4]   Mitochondrial nitric oxide synthase: A ubiquitous regulator of oxidative phosphorylation? [J].
Bates, TE ;
Loesch, A ;
Burnstock, G ;
Clark, JB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 218 (01) :40-44
[5]  
BATES TE, 1995, BIOCHEM BIOPH RES CO, V213, P869
[6]   Oxidative stress and S-nitrosylation of proteins in cells [J].
Beltrán, B ;
Orsi, A ;
Clementi, E ;
Moncada, S .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (05) :953-960
[7]  
BLACKMORE RS, 1991, J BIOL CHEM, V266, P19245
[8]   AN ELECTRON-PARAMAGNETIC-RES STUDY OF THE PHOTO-DISSOCIATION REACTIONS OF OXIDIZED CYTOCHROME-C OXIDASE NITRIC-OXIDE COMPLEXES [J].
BOELENS, R ;
WEVER, R ;
VANGELDER, BF ;
RADEMAKER, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 724 (02) :176-183
[9]  
BOLANOS JP, 1994, J NEUROCHEM, V63, P910
[10]  
BOLANOS JP, 1995, J NEUROCHEM, V64, P1965