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羧酸酯酶1g/酯酶-x在肝脏中的特异性表达可减轻肝脏脂肪变性,对抗血脂异常并改善胰岛素信号传导。

Liver-specific expression of carboxylesterase 1g/esterase-x reduces hepatic steatosis, counteracts dyslipidemia and improves insulin signaling.

作者信息

Bahitham Wesam, Watts Russell, Nelson Randal, Lian Jihong, Lehner Richard

机构信息

Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta T6G 2S2, Canada; Department of Pediatrics, University of Alberta, Edmonton, Alberta T6G 2S2, Canada; King Abdullah International Medical Research Center (KAIMRC), Jeddah, Saudi Arabia.

Group on Molecular and Cell Biology of Lipids, University of Alberta, Edmonton, Alberta T6G 2S2, Canada; Department of Pediatrics, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.

出版信息

Biochim Biophys Acta. 2016 May;1861(5):482-90. doi: 10.1016/j.bbalip.2016.03.009. Epub 2016 Mar 11.

Abstract

Ces1g/Es-x deficiency in mice results in weight gain, insulin resistance, fatty liver and hyperlipidemia through upregulation of de novo lipogenesis and oversecretion of triacylglycerol (TG)-rich lipoproteins. Here, we show that restoration of Ces1g/Es-x expression only in the liver significantly reduced hepatic TG concentration accompanied by decreased size of lipid droplets, reduced secretion of very low-density lipoproteins and improved insulin-mediated signal transduction in the liver. Collectively, these results demonstrate that hepatic Ces1g/Es-x plays a critical role in limiting hepatic steatosis, very low-density lipoprotein assembly and in augmenting insulin sensitivity.

摘要

小鼠体内Ces1g/Es-x缺乏会通过上调从头脂肪生成和富含三酰甘油(TG)的脂蛋白过度分泌,导致体重增加、胰岛素抵抗、脂肪肝和高脂血症。在此,我们表明仅在肝脏中恢复Ces1g/Es-x表达可显著降低肝脏TG浓度,同时伴随着脂滴大小减小、极低密度脂蛋白分泌减少以及肝脏中胰岛素介导的信号转导改善。总体而言,这些结果表明肝脏中的Ces1g/Es-x在限制肝脏脂肪变性、极低密度脂蛋白组装以及增强胰岛素敏感性方面发挥着关键作用。

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