| Literature DB >> 14333551 |
Abstract
1. alpha-3,4,5,6-Tetrachlorocyclohex-1-ene and gamma-2,3,4,5,6-pentachlorocyclohex-1-ene are conjugated with glutathione in vitro by a rat-liver enzyme that is probably glutathione S-aryltransferase. 2. Chlorocyclohexane and the alpha-, beta-, gamma- and delta-isomers of hexachlorocyclohexane were not substrates for rat-liver glutathione S-aryltransferase. 3. Glutathione-S-aryltransferase activity was present in tissue preparations of houseflies of insecticide-resistant and -susceptible strains. More activity was found in a dieldrin-resistant strain of houseflies fed on dieldrin than in either a dieldrin-resistant strain not fed on dieldrin or a control strain of dieldrin-susceptible houseflies. 4. Housefly soluble supernatant preparations converted S-(2-chloro-4-nitrophenyl)glutathione into the corresponding cysteine and mercapturic acid derivatives.Entities:
Keywords: BENZENE HEXACHLORIDE; CHROMATOGRAPHY; CYCLOPARAFFINS; DIELDRIN; EXPERIMENTAL LAB STUDY; GLUTATHIONE; HOUSEFLIES; LIVER ENZYMOLOGY; METABOLISM; RATS; TRANSFERASES
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Year: 1965 PMID: 14333551 PMCID: PMC1215189 DOI: 10.1042/bj0950156
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857