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Protective effects of (-)-epigallocatechin-3-gallate against acetaminophen-induced liver injury in rats)

机译:(-)-表没食子儿茶素-3-没食子酸酯对乙酰氨基酚引起的大鼠肝损伤的保护作用)

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摘要

(-)-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.
机译:(-)-Epigallocatechin-3-gallate(EGCG)是茶中含量最高的儿茶素,具有多种生物活性。在这项研究中,研究了EGCG对对乙酰氨基酚在大鼠肝脏中的代谢和毒性的影响。给雄性Sprague-Dawley大鼠喂食无或含EGCG(0.54%,w / w)的对照饮食1周,然后腹膜内注射对乙酰氨基酚(1 g / kg体重),并在12 h后处死。然后测定血浆和肝脏中对乙酰氨基酚及其结合物的浓度。还评估了细胞色素P450(CYP)和II期酶的活性。对乙酰氨基酚治疗后,饲喂EGCG饮食的大鼠血浆丙氨酸氨基转移酶和天冬氨酸氨基转移酶活性较低,这是肝毒性的指标。对乙酰氨基酚的形态学损害在喂食EGCG饮食的大鼠中较低。此外,EGCG显着降低了咪达唑仑1-羟基化(CYP3A),硝基酚6-羟化酶(CYP2E1),UDP-葡萄糖醛糖基转移酶和磺基转移酶的肝活性。最后,EGCG喂养降低了血浆和肝脏中对乙酰氨基酚-葡萄糖醛酸和对乙酰氨基酚-谷胱甘肽的含量。这些结果表明,EGCG喂养可能会降低大鼠对乙酰氨基酚的代谢和毒性。

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