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PMID: 8670121 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Rapid reduction of nitric oxide by mitochondria, and reversible inhibition of mitochondrial respiration by nitric oxide.

The Biochemical journal ·Vol. 315 ( Pt 1) ·1996-04-01 ·Pages 295-9

Borutaité V, Brown GC

Abstract

Nitric oxide (NO) inhibited the respiration rate of mitochondria isolated from rat heart at sub-micromolar concentrations of NO. The inhibition was rapidly and completely reversible, indicating that NO does not damage mitochondria. The sensitivity of respiration to NO depended on the oxygen concentration, substrate type and respiratory state of the mitochondria, consistent with NO competing with oxygen at cytochrome oxidase. Mitochondria catalysed a rapid rate of NO breakdown, which was greater in the absence of oxygen and was partly inhibited by cyanide and azide, suggesting that at least part of the NO breakdown was due to reduction of NO by cytochrome oxidase. The rapid rate of this breakdown suggests that mitochondrial breakdown of NO may be significant physiologically.

MeSH Terms
Animals Electrodes Electron Transport Complex IV/metabolism,pharmacology Mitochondria, Heart/drug effects,metabolism Nitric Oxide/metabolism,pharmacology Oxidation-Reduction Oxygen/pharmacology Oxygen Consumption/drug effects Rats Rats, Wistar
Chemicals
Nitric Oxide Electron Transport Complex IV Oxygen
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Borutaité V
Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Brown G C
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26 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1996-04-01
Pages
295-9
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1217185
Subset
IM
Grants
Wellcome Trust · United Kingdom
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