Nitric oxide and mitochondrial signaling: From physiology to pathophysiology

Jorge D. Erusalimsky*, Salvador Moncada

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

276 Citations (Scopus)

Abstract

Nitric oxide (NO) has been known for many years to bind to cytochrome C oxidase, the terminal acceptor in the mitochondrial electron transport chain, in competition with oxygen. This interaction may be significant in vivo and explain some of the biological actions of NO. In this article we review the evidence showing that binding of NO to cytochrome C oxidase elicits intracellular signaling events, including the diversion of oxygen to nonrespiratory substrates and the generation of reactive oxygen species. We discuss findings indicating that these NO-elicited events act as triggers by which mitochondria modulate signal transduction cascades involved in the induction of cellular defense mechanisms and adaptive responses. We also discuss instances in which the effects of NO on the electron transport chain might lead to mitochondrial dysfunction and pathology.

Original languageEnglish
Pages (from-to)2524-2531
Number of pages8
JournalArteriosclerosis, thrombosis, and vascular biology
Volume27
Issue number12
DOIs
Publication statusPublished - Dec 2007

Keywords

  • Cytoprotection
  • Mitochondria
  • Nitric oxide
  • Reactive oxygen species
  • Signal transduction

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