Moderate dependence of ROS formation on Δψm in isolated brain mitochondria supported by NADH-linked substrates

被引:31
作者
Tretter, Laszlo
Adam-Vizi, Vera
机构
[1] Semmelweis Univ, Dept Biochem Med, H-1444 Budapest, Hungary
[2] Hungarian Acad Sci, Neurobiochem Grp, H-1051 Budapest, Hungary
[3] Szetagothai Janos Knowledge Ctr, Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
mitochondria; reactive oxygen species; membrane potential; amplex red; glutamate-malate; respiratory chain; NADH; Complex I; hydrogen peroxide; superoxide; bovine serum albumin; brain; guinea pig;
D O I
10.1007/s11064-006-9130-y
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
The membrane potential (Delta Psi m) dependence of the generation of reactive oxygen species (ROS) in isolated guinea-pig brain mitochondria respiring on NADH-linked substrates (glutamate plus malate) was addressed. Depolarization by FCCP was without effect on H2O2 formation in the absence of bovine serum albumin (BSA). Addition of BSA (0.025%) to the assay medium hyperpolarized mitochondria by 6.1 +/- 0.9 mV (from 169 +/- 3 to 175.1 +/- 2.1 mV) and increased the rate of H2O2 formation from 207 +/- 4.5 to 312 +/- 12 pmol/min/mg protein. Depolarization by FCCP (5-250 nM) in the presence of BSA decreased H2O2 formation but only to the level observed in the absence of BSA. Rotenone stimulated the formation of H2O2 both in the absence and presence of BSA. It is suggested that H2O2 formation in mitochondria supported by NADH-linked substrates is sensitive to changes in Delta psi m only when mitochondria are highly polarized and even then, 60% of ROS generation is independent of Delta Psi m. This is in contrast to earlier reports on the highly Delta Psi m sensitive ROS formation related to reverse electron flow observed in well-coupled succinate-supported mitochondria.
引用
收藏
页码:569 / 575
页数:7
相关论文
共 35 条
[21]   Mitochondria in neurodegeneration: Bioenergetic function in cell life and death [J].
Murphy, AN ;
Fiskum, G ;
Beal, MF .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1999, 19 (03) :231-245
[22]   Mitochondria and neuronal survival [J].
Nicholls, DG ;
Budd, SL .
PHYSIOLOGICAL REVIEWS, 2000, 80 (01) :315-360
[23]   Mitochondria, oxygen free radicals, disease and ageing [J].
Raha, S ;
Robinson, BH .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (10) :502-508
[24]   The production of reactive oxygen species in intact isolated nerve terminals is independent of the mitochondrial membrane potential [J].
Sipos, I ;
Tretter, L ;
Adam-Vizi, V .
NEUROCHEMICAL RESEARCH, 2003, 28 (10) :1575-1581
[25]   Regulation of brain mitochondrial H2O2 production by membrane potential and NAD(P)H redox state [J].
Starkov, AA ;
Fiskum, G .
JOURNAL OF NEUROCHEMISTRY, 2003, 86 (05) :1101-1107
[26]   Mitochondrial α-ketoglutarate dehydrogenase complex generates reactive oxygen species [J].
Starkov, AA ;
Fiskum, G ;
Chinopoulos, C ;
Lorenzo, BJ ;
Browne, SE ;
Patel, MS ;
Beal, MF .
JOURNAL OF NEUROSCIENCE, 2004, 24 (36) :7779-7788
[27]   Initiation of neuronal damage by complex I deficiency and oxidative stress in Parkinson's disease [J].
Tretter, L ;
Sipos, I ;
Adam-Vizi, V .
NEUROCHEMICAL RESEARCH, 2004, 29 (03) :569-577
[28]   Alpha-ketoglutarate dehydrogenase: a target and generator of oxidative stress [J].
Tretter, L ;
Adam-Vizi, V .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2005, 360 (1464) :2335-2345
[29]   Generation of reactive oxygen species in the reaction catalyzed by α-ketoglutarate dehydrogenase [J].
Tretter, L ;
Adam-Vizi, V .
JOURNAL OF NEUROSCIENCE, 2004, 24 (36) :7771-7778
[30]  
TRETTER L, 2006, IN PRESS NEUROCHEM I