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联合使用美他多辛和大蒜油治疗可有效消除大鼠肝脏中的酒精性脂肪变性并诱导CYP2E1,同时恢复AMPK活性。

Combined metadoxine and garlic oil treatment efficaciously abrogates alcoholic steatosis and CYP2E1 induction in rat liver with restoration of AMPK activity.

作者信息

Ki Sung Hwan, Choi Jae Hoon, Kim Choon Won, Kim Sang Geon

机构信息

College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, South Korea.

出版信息

Chem Biol Interact. 2007 Aug 30;169(2):80-90. doi: 10.1016/j.cbi.2007.05.008. Epub 2007 Jun 2.

Abstract

Alcoholic steatosis is the earliest and most common response to heavy alcohol intake, and may precede more severe forms of liver injury. Accumulation of fat, largely triglyceride, in hepatocytes results from the inhibition of fatty acid oxidation and excessive oxidative stress involving CYP2E1. This study evaluated the therapeutic effects of metadoxine, garlic oil or their combination on alcoholic steatosis. Feeding rats an alcohol-containing diet for 4 weeks elicited an increase in hepatic triglyceride content and induced CYP2E1. The concurrent administration of metadoxine and garlic oil (MG) to rats during the last week of the diet feeding efficaciously abrogated both fat accumulation and CYP2E1 induction as compared to the individual treatment at higher doses. Histopathology confirmed the ability of MG combination to inhibit lipid accumulation. Blood biochemistry verified improvement of liver function in rats treated with MG. Alcohol administration resulted in a decrease in AMP-activated protein kinase-alpha (AMPKalpha) phosphorylation, which was restored by MG treatments. Recovery of AMPK activity by MG was supported by an increase in acetyl-CoA carboxylase phosphorylation. Hepatic fatty acid synthase (FAS) expression was markedly decreased after alcohol consumption, which correlated with a decrease in AMPK activity and a commensurate increase in lipid content. Combined MG treatments caused restoration of the FAS level. These results demonstrate that the combination of MG effectively treats alcoholic steatosis with CYP2E1 inhibition, which may be associated with the recovery of AMPK activity, promising that the combination therapy may constitute an advance in the development of clinical candidates for alcoholic steatosis.

摘要

酒精性脂肪变性是对大量饮酒最早且最常见的反应,可能先于更严重的肝损伤形式出现。肝细胞内脂肪(主要是甘油三酯)的积累是由于脂肪酸氧化受到抑制以及涉及细胞色素P450 2E1(CYP2E1)的过度氧化应激所致。本研究评估了美他多辛、大蒜油或它们的组合对酒精性脂肪变性的治疗效果。给大鼠喂食含酒精的饮食4周会导致肝脏甘油三酯含量增加并诱导CYP2E1表达。在饮食喂养的最后一周同时给大鼠施用美他多辛和大蒜油(MG),与更高剂量的单独治疗相比,能有效消除脂肪积累和CYP2E1诱导。组织病理学证实了MG组合抑制脂质积累的能力。血液生化检测证实了用MG治疗的大鼠肝功能得到改善。给予酒精导致腺苷酸活化蛋白激酶α(AMPKα)磷酸化水平降低,而MG治疗可使其恢复。MG使AMPK活性恢复得到乙酰辅酶A羧化酶磷酸化增加的支持。饮酒后肝脏脂肪酸合酶(FAS)表达明显降低,这与AMPK活性降低和脂质含量相应增加相关。联合MG治疗可使FAS水平恢复。这些结果表明,MG组合通过抑制CYP2E1有效治疗酒精性脂肪变性,这可能与AMPK活性的恢复有关,有望使联合疗法在酒精性脂肪变性临床候选药物的开发方面取得进展。

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