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pubmed-article:9015155pubmed:abstractTextIncubation of both rat and mouse hepatocytes with 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX) in vitro resulted in a dose-dependent increase in unscheduled DNA synthesis (UDS) at sub-cytotoxic concentrations (1-10 microM MX; 20 h incubation). Depletion of glutathione stores by pre-treatment of rat hepatocytes with buthionine sulfoximine did not result in a significant increase in UDS produced by MX. In contrast, MX did not induce UDS in mouse hepatocytes ex vivo either 3 or 16 h following administration of a single oral dose of 100 mg/kg MX. Despite the ability of MX to produce repairable DNA damage, restricted access of MX to the liver may prevent a measurable UDS response in vivo.lld:pubmed
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pubmed-article:9015155pubmed:articleTitleProduction of unscheduled DNA synthesis in rodent hepatocytes in vitro, but not in vivo, by 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX).lld:pubmed
pubmed-article:9015155pubmed:affiliationSchool of Biochemistry, University of Birmingham, Edgbaston, UK.lld:pubmed
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pubmed-article:9015155pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed