Biomedicine · 2015 · 35 citations · 22 references
PharmacyBiochemistryPharmacologyBiochemical PharmacologyHepatotoxicologyNutritional ToxicologyChemical-induced HepatotoxicityHepatic ToxicityHepatotoxicity MechanismsMechanisms Of Toxic InjuryPharmacokinetics In Liver DiseaseAcetaminophen-induced Liver NecrosisAspartate Aminotransferase ElevationCytochrome P450 OxidationHepatocellular Liver InjuryHepatotoxic MechanismsLiver Injury MechanismsSerum Alanine AminotransferaseSerum Aspartate Aminotransferase
(-)-Epigallocatechin-3-gallate (EGCG) is the most abundant catechin with various biological activities found in tea. In this study, the effects of EGCG on the metabolism and toxicity of acetaminophen in rat liver were investigated. Male Sprague-Dawley rats were fed a controlled diet without or with EGCG (0.54 %, w/w) for 1 week and were then intraperitoneally injected with acetaminophen (1 g/kg body weight) and killed after 12 h. Concentrations of acetaminophen and its conjugates in plasma and liver were then determined. The cytochrome P450 (CYP) and phase II enzymes activities were also evaluated. Rats fed the EGCG diet had lower plasma alanine aminotransferase and aspartate aminotransferase activities, as indices of hepatotoxicity, after acetaminophen treatment. Morphological damage by acetaminophen was lower in rats fed the EGCG diet. In addition, EGCG significantly reduced hepatic activities of midazolam 1-hydroxylation (CYP3A), nitrophenol 6-hydroxylase (CYP2E1), UDP-glucurosyltransferase, and sulfotransferase. Finally, EGCG feeding reduced acetaminophen-glucuronate and acetaminophen-glutathione contents in plasma and liver. These results indicate that EGCG feeding may reduce the metabolism and toxicity of acetaminophen in rats.
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