Inhibitory effect of t-butyl hydroperoxide on mitochondrial oxidative phosphorylation in isolated rat hepatocytes
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17381246
DOI
10.33549/physiolres.931006
PII: 1006
Knihovny.cz E-resources
- MeSH
- Potassium Chloride pharmacology MeSH
- Digitonin pharmacology MeSH
- Energy Metabolism drug effects MeSH
- Hepatocytes metabolism MeSH
- Mitochondria, Liver drug effects metabolism MeSH
- Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone pharmacology MeSH
- Rats MeSH
- Membrane Potentials drug effects MeSH
- Mitochondrial Membranes drug effects MeSH
- Oxidative Phosphorylation drug effects MeSH
- Rats, Wistar MeSH
- Uncoupling Agents pharmacology MeSH
- Cell Separation MeSH
- Oxygen Consumption drug effects MeSH
- In Vitro Techniques MeSH
- tert-Butylhydroperoxide pharmacology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Potassium Chloride MeSH
- Digitonin MeSH
- Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone MeSH
- Uncoupling Agents MeSH
- tert-Butylhydroperoxide MeSH
Using high-resolution oxygraphy, we tested the changes of various parameters characterizing the mitochondrial energy provision system that were induced by peroxidative damage. In the presence of succinate as respiratory substrate, 3 mM t-butyl hydroperoxide increased respiration in the absence of ADP, which indicated partial uncoupling of oxidative phosphorylation. Low activity of coupled respiration was still maintained as indicated by the ADP-activated and oligomycin-inhibited respiration. However, during the incubation the phosphorylative capacity decreased as indicated by the continuous decrease of the mitochondrial membrane potential. Under these experimental conditions the maximum capacity of the succinate oxidase system was inhibited by 50% in comparison with values obtained in the absence of t-butyl hydroperoxide. Our data thus indicate that the oxygraphic evaluation of mitochondrial function represents a useful tool for evaluation of changes participating in peroxidative damage of cell energy metabolism.
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