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Hepatocyte‐Specific Expression of Human Carboxylesterase 1 Attenuates Diet‐Induced Steatohepatitis and Hyperlipidemia in Mice

机译:人羧酸酯酶1的肝细胞特异性表达衰减小鼠中的饮食诱导的脂肪肝炎和高脂血症

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摘要

Rodents have at least five carboxylesterase 1 ( Ces1 ) genes, whereas there is only one CES1 gene in humans, raising the question as to whether human CES1 and mouse Ces1 genes share the same functions. In this study, we investigate the role of human CES1 in the development of steatohepatitis or dyslipidemia in C57BL/6 mice. Hepatocyte‐specific expression of human CES1 prevented Western diet or alcohol‐induced steatohepatitis and hyperlipidemia. Mechanistically, human CES1 induced lipolysis and fatty acid oxidation, leading to a reduction in hepatic triglyceride and free fatty acid levels. Human CES1 also reduced hepatic‐free cholesterol levels and induced low‐density lipoprotein receptor. In addition, human CES1 induced hepatic lipoprotein lipase and apolipoprotein C‐II expression. Conclusion: Hepatocyte‐specific overexpression of human CES1 attenuates diet‐induced steatohepatitis and hyperlipidemia.
机译:啮齿动物具有至少五个羧酸酶1(CES1)基因,而人类只有一个CES1基因,提出了人类CES1和小鼠CES1基因是否共享相同功能的问题。在这项研究中,我们调查人CES1在C57BL / 6小鼠中脱脂缺血性或血脂血症的发展中的作用。人CES1的肝细胞特异性表达预防西方饮食或酒精诱导的脂肪肝炎和高脂血症。机械地,人CES1诱导脂解和脂肪酸氧化,导致肝甘油三酯和游离脂肪酸水平降低。人CES1还降低了无肝胆固醇水平并诱导低密度脂蛋白受体。此外,人CES1诱导肝脂蛋白脂肪酶和载脂蛋白C-II表达。结论:人CES1的肝细胞特异性过表达衰减饮食诱导的脱脂性肝炎和高脂血症。

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