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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Hepatoprotective effect of 10% ethanolic extract from Curdrania tricuspidata leaves against ethanol-induced oxidative stress through suppression of CYP2E1
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Hepatoprotective effect of 10% ethanolic extract from Curdrania tricuspidata leaves against ethanol-induced oxidative stress through suppression of CYP2E1

机译:10%乙醇提取物从CYP2E1抑制CYP2E1抗乙醇诱导的乙醇诱导氧化胁迫的肝脏保护作用

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The hepatoprotective effect of 10% ethanolic extract of Curdrania tricuspidata (CTE) was investigated in HepG2/2E1 cells and C57BL/6 J mice. When compared ethanol-only treated HepG2/2E1 cells, pretreatment of LIE prevented increased intra-cellular reactive oxygen species levels and decreased antioxidant activities by ethanol-induced oxidative stress. In C57BL/6 J mice, CTE at a dose of 250 mg/kg/day was administered for 10 days, with ethanol (5 g/kg/day) administered for the final 3 days. Pretreatment with LIE prevented the elevated activities of serum aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase caused by ethanol-induced hepatic damage. CTE-treated mice displayed a reduced level of malondialdehyde and increased antioxidant activities of catalase, glutathione S-transferase, glutathione peroxidase, and superoxide dismutase, as well as a reduced level of glutathione as compared with ethanol-only-treated mice. CTE-treated mice exhibited significant inhibition of CYP2E1 activities and expression. These results suggest that CTE could be a useful agent for the prevention of ethanol-induced oxidative damage in the liver, elevating antioxidative potentials and alleviating oxidative stress by suppressing CYP2E1. (C) 2017 Elsevier Ltd. All rights reserved.
机译:在HepG2 / 2E1细胞和C57BL / 6 J小鼠中研究了10%乙醇提取物(CTICUSPIDATA(CTE)的肝脏保护作用。当比较仅乙醇处理的HEPG2 / 2E1细胞时,术语预处理可通过乙醇诱导的氧化应激预防细胞内反应性氧物质水平并降低抗氧化活性。在C57BL / 6 J小鼠中,给予250mg / kg /天的CTE 10天,用乙醇(5g / kg /天)给予最后3天。用沉默的预处理防止了由乙醇诱导的肝损伤引起的血清天冬氨酸氨基转移酶,丙氨酸氨基转移酶和碱性磷酸酶的活性。与乙醇处理的小鼠相比,CTE处理的小鼠显示出降低的丙二醛,谷胱甘肽S-转移酶,谷胱甘肽过氧化物酶和超氧化酶的抗氧化活性增加,以及减少的谷胱甘肽水平。 CTE处理的小鼠表现出CYP2E1活性和表达的显着抑制。这些结果表明,CTE可以是预防乙醇诱导肝脏氧化损伤的有用试剂,通过抑制CYP2E1升高抗氧化电位并减轻氧化应激。 (c)2017 Elsevier Ltd.保留所有权利。

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