Melatonin increases the activity of the oxidative phosphorylation enzymes and the production of ATP in rat brain and liver mitochondria

被引:215
作者
Martín, M [1 ]
Macías, M [1 ]
León, J [1 ]
Escames, G [1 ]
Khaldy, H [1 ]
Acuña-Castroviejo, D [1 ]
机构
[1] Univ Granada, Inst Biotecnol, Dept Fisiol, E-18012 Granada, Spain
关键词
melatonin; mitochondria; ATP; electron chain transport; complex I; complex IV; oxidative stress;
D O I
10.1016/S1357-2725(01)00138-8
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
We recently showed that melatonin counteracted mitochondrial oxidative stress and increased the activity of the mitochondrial oxidative phosphorylation (OXPHOS) enzymes both in vivo and in vitro. To further clarify these effects, we studied here the activity of OXPHOS enzymes and the synthesis of ATP in rat liver and brain mitochondria in vitro. In sub-mitochondrial particles, melatonin increases the activity of the complexes I and IV dose-dependently, the effect being significant between I and 10 nM. Blue native-PAGE followed by histochemical analysis of the OXPHOS enzymes further showed the melatonin-induced increase of complex I activity. Titration studies show that melatonin counteracts the partial inhibition of complex IV induced by 5 muM potassium cyanide. However, melatonin (up to 5 mM) was unable to recover the activity of complex IV when it was completely blocked by 100 muM cyanide. These data suggest that the indoleamine could stimulate the activity of the non-inhibited part of the complex IV. Melatonin also increases the production of ATP in control mitochondria and counteracts the cyanide-induced inhibition of ATP synthesis. These results provide new hormonal mechanism regulating mitochondrial homeostasis and may explain, at least in part, the anti-aging and neuroprotective properties of melatonin. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:348 / 357
页数:10
相关论文
共 40 条
[1]   Melatonin, mitochondria, and cellular bioenergetics [J].
Acuña-Castroviejo, D ;
Martín, M ;
Macías, M ;
Escames, G ;
León, J ;
Khaldy, H ;
Reiter, RJ .
JOURNAL OF PINEAL RESEARCH, 2001, 30 (02) :65-74
[2]  
ACUNACASTROVIEJ.D, 1997, LIFE SCI, V60, P3
[3]  
[Anonymous], LIFE SCI
[4]   Rapid reduction of nitric oxide by mitochondria, and reversible inhibition of mitochondrial respiration by nitric oxide [J].
Borutaite, V ;
Brown, GC .
BIOCHEMICAL JOURNAL, 1996, 315 :295-299
[5]  
BOVERIS A, 1984, METHOD ENZYMOL, V105, P429
[6]  
BROWN GC, 1992, BIOCHEM J, V284, P1
[7]   An evaluation of the role of mitochondria in neurodegenerative diseases: mitochondrial mutations and oxidative pathology, protective nuclear responses, and cell death in neurodegeneration [J].
Cassarino, DS ;
Bennett, JP .
BRAIN RESEARCH REVIEWS, 1999, 29 (01) :1-25
[8]   How melatonin interacts with lipid bilayers: a study by fluorescence and ESR spectroscopies [J].
Costa, EJX ;
Shida, CS ;
Biaggi, MH ;
Ito, AS ;
LamyFreund, MT .
FEBS LETTERS, 1997, 416 (01) :103-106
[9]   Melatonin protects against 6-OHDA-induced neurotoxicity in rats: a role for mitochondrial complex I activity [J].
Dabbeni-Sala, F ;
Di Santo, S ;
Franceschini, D ;
Skaper, SD ;
Giusti, P .
FASEB JOURNAL, 2001, 15 (01) :164-170
[10]  
de Grey, 1999, MITOCHONDRIAL FREE R