inhibition of mitochondrial cytochrome oxidase by the gases carbon monoxide, nitric oxide, hydrogen cyanide and hydrogen sulfide: chemical mechanism and physiological significance

• Published in: Journal of bioenergetics and biomembranes 2008-10, Vol.40 (5), p.533-539, Article 533
• Main Authors: Cooper, Chris E, Brown, Guy C
• Format: Article
• Language: English
• Subjects: Animal Anatomy; Animal Biochemistry; Animals; Atmospheric chemistry; Biochemistry; Biocompatibility; Bioorganic Chemistry; Carbon monoxide; Carbon Monoxide - metabolism; Carbon Monoxide - pharmacology; Chemistry; Chemistry and Materials Science; Cyanides; Cytochrome; cytochrome-c oxidase; Cytochromes; Electron Transport Complex IV - antagonists & inhibitors; Enzyme Inhibitors - metabolism; Enzyme Inhibitors - pharmacology; Enzymes; Gases; Gases - metabolism; Gases - pharmacology; Histology; Humans; Hydrogen; Hydrogen cyanide; Hydrogen Cyanide - metabolism; Hydrogen Cyanide - pharmacology; Hydrogen sulfide; Hydrogen Sulfide - metabolism; Hydrogen Sulfide - pharmacology; Hypoxia - enzymology; Inhibition; Mitochondria; Mitochondria - drug effects; Mitochondria - enzymology; Models, Biological; Morphology; Nitric oxide; Nitric Oxide - metabolism; Nitric Oxide - physiology; Organic Chemistry; Oxidase; Oxidation; Oxygen consumption; Physiology; Signal Transduction - drug effects; Toxicity
• ISSN: 0145-479X; 1573-6881
• DOI: 10.1007/s10863-008-9166-6

The four gases, nitric oxide (NO), carbon monoxide (CO), hydrogen sulfide (H₂S) and hydrogen cyanide (HCN) all readily inhibit oxygen consumption by mitochondrial cytochrome oxidase. This inhibition is responsible for much of their toxicity when they are applied externally to the body. However, recently these gases have all been implicated, to greater or lesser extents, in normal cellular signalling events. In this review we analyse the chemistry of this inhibition, comparing and contrasting mechanism and discussing physiological consequences. The inhibition by NO and CO is dependent on oxygen concentration, but that of HCN and H₂S is not. NO and H₂S are readily metabolised by oxidative processes within cytochrome oxidase. In these cases the enzyme may act as a physiological detoxifier of these gases. CO oxidation is much slower and unlikely to be as physiologically important. The evidence for normal physiological levels of these gases interacting with cytochrome oxidase is equivocal, in part because there is little robust data about their steady state concentrations. A reasonable case can be made for NO, and perhaps CO and H₂S, inhibiting cytochrome oxidase in vivo, but endogenous levels of HCN seem unlikely to be high enough.