Activities of conjugating and antioxidant enzymes following endmost exposure

Angela M. Watson, Graham Warren, Georgette Howard, Steven I. Shedlofsky, Robert A. Blouin

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

Endotoxin exposure elicits various responses in mammals including the acute phase response that has been shown to cause changes in the activity of several forms of cytochrome F450s and other enzymes. Therefore, the hepatic conjugating enzyme, glutathione S-transferase (GST), and UDP-glucuronosyltransferase (UDPGT), the antioxidant enzymes, glutathione peroxidase (GSHPx), catalase, and superoxide dismutase (SOD), as well as lipid peroxidation were investigated following the administration of endotoxin to male Sprague-Dawley rats (8 mg/kg body weight). Rats were euthanized at various times following endotoxin administration and the livers removed and processed to assess various enzyme activities. Glutathione S-transferase, UDPGT, and GSHPx activity showed statistically significant decreases after 24 hours and remained lower than controls for the duration of the study. Decreases in total SOD and catalase activities were seen at 24, 48, and 72 hours following endotoxin administration; however, only catalase activity showed statistically significant differences between control and treated samples at those time points, and total SOD activity showed a statistically significant decrease at 24 hours. No statistically significant changes were seen in the level of lipid peroxidation in the liver microsomes from endotoxin-treated animals. Changes in the conjugative enzymes and the free-radical scavenging enzymes following endotoxin exposure may alter the host's metabolism and response to free radicals.

Original languageEnglish
Pages (from-to)63-69
Number of pages7
JournalJournal of Biochemical and Molecular Toxicology
Volume13
Issue number2
DOIs
StatePublished - 1999

Funding

FundersFunder number
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilP01NS031220

    Keywords

    • Antioxidant Enzymes
    • Catalase
    • Conjugating Enzymes
    • Endotoxin
    • Glutathione
    • Glutathione Peroxidase
    • Glutathione S-Transferase
    • Superoxide Dismutase
    • UDP-Glucuronosyltransferase

    ASJC Scopus subject areas

    • Biochemistry
    • Molecular Medicine
    • Molecular Biology
    • Toxicology
    • Health, Toxicology and Mutagenesis

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