S-nitrosothiol inhibition of mitochondrial complex I causes a reversible increase in mitochondrial hydrogen peroxide production

被引:50
作者
Borutaite, Vilmante
Brown, Guy C.
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] Kaunas Univ Med, Inst Biomed Res, Kaunas, Lithuania
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2006年 / 1757卷 / 5-6期
关键词
mitochondria; reactive oxygen species; nitric oxide;
D O I
10.1016/j.bbabio.2006.02.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We found that reversible inactivation of mitochondrial complex I by S-nitroso-N-acetyl-D,L-penicillamine (SNAP) in isolated rat heart mitochondria resulted in a three-fold increase in H2O2 production, when mitochondria were respiring on pyruvate and malate, (but not when respiring on succinate or in the absence of added respiratory substrate). The inactivation of complex I and the increased H2O2 production were present in mitochondria, washed free of SNAP or NO, but were partially reversed by light or dithiothreitol, treatments known to reverse Snitrosation. Specific inhibition of complex I with rotenone increased H2O2 production to a similar extent as that caused by SNAP. The results suggest that S-nitrosation of complex I can reversibly increase oxidant production by mitochondria, which is potentially important in cell signalling and/or pathology. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:562 / 566
页数:5
相关论文
共 35 条
[1]
Mitochondrial dysfunction and oxidative damage in Alzheimer's and Parkinson's diseases and coenzyme Q10 as a potential treatment [J].
Beal, MF .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2004, 36 (04) :381-386
[2]
The free radical theory of aging matures [J].
Beckman, KB ;
Ames, BN .
PHYSIOLOGICAL REVIEWS, 1998, 78 (02) :547-581
[3]
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
[4]
Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues [J].
Birch-Machin, MA ;
Turnbull, DM .
METHODS IN CELL BIOLOGY, VOL 65: MITOCHONDRIA, 2001, 65 :97-117
[5]
Nitric oxide induces apoptosis via hydrogen peroxide, but necrosis via energy and thiol depletion [J].
Borutaite, V ;
Brown, GC .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (11) :1457-1468
[6]
Reversal of nitric oxide-, peroxynitrite- and S-nitrosothiol-induced inhibition of mitochondrial respiration or complex I activity by light and thiols [J].
Borutaite, V ;
Budriunaite, A ;
Brown, GC .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2000, 1459 (2-3) :405-412
[7]
Association between mitochondrial dysfunction and severity and outcome of septic shock [J].
Brealey, D ;
Brand, M ;
Hargreaves, I ;
Heales, S ;
Land, J ;
Smolenski, R ;
Davies, NA ;
Cooper, CE ;
Singer, M .
LANCET, 2002, 360 (9328) :219-223
[8]
Nitric oxide inhibition of mitochondrial respiration and its role in cell death [J].
Brown, GC ;
Borutaite, V .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (11) :1440-1450
[9]
Inhibition of mitochondrial respiratory complex I by nitric oxide, peroxynitrite and S-nitrosothiols [J].
Brown, GC ;
Borutaite, V .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1658 (1-2) :44-49
[10]
Cadenas Enrique, 2004, Molecular Aspects of Medicine, V25, P17, DOI 10.1016/j.mam.2004.02.005