4.6 Article

Sites of Superoxide and Hydrogen Peroxide Production by Muscle Mitochondria Assessed ex Vivo under Conditions Mimicking Rest and Exercise

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 290, Issue 1, Pages 209-227

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M114.619072

Keywords

Exercise; Hydrogen Peroxide; Mitochondria; Mitochondrial Respiratory Chain Complex; Reactive Oxygen Species (ROS); Rat Skeletal Muscle; Superoxide

Funding

  1. National Institutes of Health [TL1 AG032116]
  2. Brazilian Government through the Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) e ao Conselho de Nacional de Desenvolvimento Cientifico e Tecnologico programa Ciencias Sem Fronteiras (CNPq-CSF)
  3. Glenn Foundation
  4. Carlsberg Foundation

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Background: Ten mitochondrial sites of superoxide/H2O2 generation are known, but their contributions in vivo are undefined. Results: We assessed their rates ex vivo in conditions mimicking rest and exercise. Conclusion: Sites I-Q and IIF generated half the signal at rest. During exercise, rates were lower, and site I-F dominated. Significance: Contributing sites ex vivo probably reflect those in vivo. The sites and rates of mitochondrial production of superoxide and H(2)O(2)in vivo are not yet defined. At least 10 different mitochondrial sites can generate these species. Each site has a different maximum capacity (e.g. the outer quinol site in complex III (site IIIQo) has a very high capacity in rat skeletal muscle mitochondria, whereas the flavin site in complex I (site I-F) has a very low capacity). The maximum capacities can greatly exceed the actual rates observed in the absence of electron transport chain inhibitors, so maximum capacities are a poor guide to actual rates. Here, we use new approaches to measure the rates at which different mitochondrial sites produce superoxide/H2O2 using isolated muscle mitochondria incubated in media mimicking the cytoplasmic substrate and effector mix of skeletal muscle during rest and exercise. We find that four or five sites dominate during rest in this ex vivo system. Remarkably, the quinol site in complex I (site I-Q) and the flavin site in complex II (site IIF) each account for about a quarter of the total measured rate of H2O2 production. Site I-F, site IIIQo, and perhaps site E-F in the -oxidation pathway account for most of the remainder. Under conditions mimicking mild and intense aerobic exercise, total production is much less, and the low capacity site I-F dominates. These results give novel insights into which mitochondrial sites may produce superoxide/H(2)O(2)in vivo.

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