Regulation of mitochondrial respiration by oxygen and nitric oxide

被引:0
|
作者
Boveris, A [1 ]
Costa, LE
Poderoso, JJ
Carreras, MC
Cadenas, E
机构
[1] Univ Buenos Aires, Sch Pharm & Biochem, Lab Free Rad Biol, Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Cardiol Res Inst, Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Univ Hosp, Sch Med, Buenos Aires, DF, Argentina
[4] Univ So Calif, Sch Pharm, Dept Mol Pharmacol & Toxicol, Los Angeles, CA 90033 USA
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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
Although the regulation of mitochondrial respiration and energy production in mammalian tissues has been exhaustively studied and extensively reviewed, a clear understanding of the regulation of cellular respiration has not yet been achieved. In particular, the role of tissue pO(2) as a factor regulating cellular respiration remains controversial. The concept of a complex and multisite regulation of cellular respiration and energy production signaled by cellular and intercellular messengers has evolved in the last few years and is still being researched, A recent concept that regulation of cellular respiration is regulated by ADP, O-2 and NO preserves the notion that energy demands drive respiration but places the kinetic control of both respiration and energy supply in the availability of ADP to F-1-ATPase and of O-2 and NO to cytochrome oxidase, In addition, recent research indicates that NO participates in redox reactions in the mitochondrial matrix that regulate the intramitochondrial steady state concentration of NO itself and other reactive species such as superoxide radical (O-2(-)) and peroxynitrite (ONOO-). In this way, NO acquires an essential role as a mitochondrial regulatory metabolite. NO exhibits a rich biochemistry and a high reactivity and plays an important role as intercellular messenger in diverse physiological processes, such as regulation of blood flow, neurotransmission, platelet aggregation and immune cytotoxic response.
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页码:121 / 135
页数:15
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