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Studies on nifurtimox nitroreductase activity in liver and other rat tissues.
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1984
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Lipid PeroxidationNfx Nitroreductase ActivityNifurtimox Nitroreductase ActivityRedox BiologyOxidative StressReactive Nitrogen SpecieToxicologyHepatotoxicityNitroreductase ActivityHealth SciencesBiochemistryLiver PhysiologyOther Rat TissuesReactive Oxygen SpecieMetabolomicsPharmacologyRat LiverPhysiologyMetabolismMedicineNitrosative Stress
Rat liver microsomes exhibit nifurtimox (NFX) nitroreductase activity, which is mostly NADPH-dependent and is completely abolished by heating and under an atmosphere of air. Pure carbon monoxide inhibits for 28% microsomal NFX nitroreductase activity while FAD 1 mM significantly enhances it. Smaller activities than in liver were found in brain, small intestine, testes, lung and heart. Rat liver cytosol also showed NFX nitroreductase activity using either hypoxanthine or N-methylnicotinamide as substrates. These activities were inhibited by allopurinol or menadione respectively. Results suggest that cytochrome P-450, NADPH cytochrome c reductase, xanthinoxidase and aldehyde oxidase are able to reduce NFX nitrogroups in rat liver and other tissues.