Article ID Journal Published Year Pages File Type
2597175 Toxicology 2008 4 Pages PDF
Abstract

We recently reported that para-nonylphenol, an environmental chemical, induced hydroxyl radical (OH) formation in rat striatum. In this study we examined the antioxidant effects of angiotensin-converting enzyme inhibitors (captopril or enalaprilat) on para-nonylphenol (nonylphenol) and 1-methyl-4-phenylpyridinium ion (MPP+)-induced hydroxyl radical (OH) formation and dopamine (DA) efflux in extracellular fluid of rat striatum, using a microdialysis technique. para-Nonylphenol clearly enhanced OH formation and DA efflux induced by MPP+. When captopril or enalaprilat was infused in nonylphenol and MPP+-treated rats, DA efflux and OH formation significantly decreased, as compared with that in the nonylphenol and MPP+-treated control. We compared the ability of non-SH-containing enalaprilat with a SH-containing captopril to scavenge OH and DA efflux. Both inhibitors were able to scavenge OH and DA efflux induced by para-nonylphenol and MPP+. The results suggest that angiotensin-converting enzyme inhibitors may protect against nonylphenol and MPP+-induced OH formation via suppressing DA efflux in the rat striatum.

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