Peroxidative damage of mitochondrial respiration is substrate-dependent
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19093725
DOI
10.33549/physiolres.931635
PII: 1635
Knihovny.cz E-zdroje
- MeSH
- buněčné dýchání MeSH
- jaterní mitochondrie metabolismus MeSH
- krysa rodu Rattus MeSH
- kyselina glutamová metabolismus MeSH
- kyselina jantarová metabolismus MeSH
- kyselina pyrohroznová metabolismus MeSH
- kyseliny ketoglutarové metabolismus MeSH
- membránový potenciál mitochondrií MeSH
- oxidační stres * MeSH
- palmitoyl karnitin metabolismus MeSH
- potkani Wistar MeSH
- spotřeba kyslíku MeSH
- terc-butylhydroperoxid farmakologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- kyselina glutamová MeSH
- kyselina jantarová MeSH
- kyselina pyrohroznová MeSH
- kyseliny ketoglutarové MeSH
- palmitoyl karnitin MeSH
- terc-butylhydroperoxid MeSH
The concentration-dependence of tert-butyl hydroperoxide (BHP) inhibitory effect on oxygen consumption in isolated rat liver mitochondria was measured in the presence of various respiratory substrates. Strong inhibitory effect at low concentrations of BHP (15-30 microM) was found for oxoglutarate and palmitoyl carnitine oxidation. Pyruvate and glutamate oxidation was inhibited at higher concentrations of BHP (100-200 microM). Succinate oxidation was not affected even at 3.3 mM BHP. Determination of mitochondrial membrane potential has shown that in the presence of NADH-dependent substrates the membrane potential was dissipated by BHP but was completely restored after addition of succinate. Our data thus indicate that beside peroxidative damage of complex I also various mitochondrial NADH-dependent dehydrogenases are inhibited, but to a different extent and with different kinetics. Our data also show that succinate could be an important nutritional substrate protecting hepatocytes during peroxidative damage.
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