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CEACAM1的肝脏强制过表达可减轻饮食诱导的胰岛素抵抗。

Forced Hepatic Overexpression of CEACAM1 Curtails Diet-Induced Insulin Resistance.

作者信息

Al-Share Qusai Y, DeAngelis Anthony M, Lester Sumona Ghosh, Bowman Thomas A, Ramakrishnan Sadeesh K, Abdallah Simon L, Russo Lucia, Patel Payal R, Kaw Meenakshi K, Raphael Christian K, Kim Andrea Jung, Heinrich Garrett, Lee Abraham D, Kim Jason K, Kulkarni Rohit N, Philbrick William M, Najjar Sonia M

机构信息

Center for Diabetes and Endocrine Research, College of Medicine and Life Sciences, The University of Toledo, Toledo, OH Department of Physiology and Pharmacology, College of Medicine and Life Sciences, The University of Toledo, Toledo, OH.

Center for Diabetes and Endocrine Research, College of Medicine and Life Sciences, The University of Toledo, Toledo, OH Department of Rehabilitation Sciences, College of Health Sciences, The University of Toledo, Toledo, OH.

出版信息

Diabetes. 2015 Aug;64(8):2780-90. doi: 10.2337/db14-1772. Epub 2015 May 13.

Abstract

Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) regulates insulin sensitivity by promoting hepatic insulin clearance. Liver-specific inactivation or global null-mutation of Ceacam1 impairs hepatic insulin extraction to cause chronic hyperinsulinemia, resulting in insulin resistance and visceral obesity. In this study we investigated whether diet-induced insulin resistance implicates changes in hepatic CEACAM1. We report that feeding C57/BL6J mice a high-fat diet reduced hepatic CEACAM1 levels by >50% beginning at 21 days, causing hyperinsulinemia, insulin resistance, and elevation in hepatic triacylglycerol content. Conversely, liver-specific inducible CEACAM1 expression prevented hyperinsulinemia and markedly limited insulin resistance and hepatic lipid accumulation that were induced by prolonged high-fat intake. This was partly mediated by increased hepatic β-fatty acid oxidation and energy expenditure. The data demonstrate that the high-fat diet reduced hepatic CEACAM1 expression and that overexpressing CEACAM1 in liver curtailed diet-induced metabolic abnormalities by protecting hepatic insulin clearance.

摘要

癌胚抗原相关细胞粘附分子1(CEACAM1)通过促进肝脏胰岛素清除来调节胰岛素敏感性。Ceacam1基因在肝脏中的特异性失活或整体无效突变会损害肝脏对胰岛素的摄取,导致慢性高胰岛素血症,进而引发胰岛素抵抗和内脏肥胖。在本研究中,我们调查了饮食诱导的胰岛素抵抗是否与肝脏CEACAM1的变化有关。我们发现,给C57/BL6J小鼠喂食高脂饮食21天后,肝脏CEACAM1水平降低了50%以上,导致高胰岛素血症、胰岛素抵抗以及肝脏三酰甘油含量升高。相反,肝脏特异性可诱导的CEACAM1表达可预防高胰岛素血症,并显著限制由长期高脂摄入诱导的胰岛素抵抗和肝脏脂质积累。这部分是由肝脏β-脂肪酸氧化增加和能量消耗介导的。数据表明,高脂饮食降低了肝脏CEACAM1的表达,而在肝脏中过表达CEACAM1可通过保护肝脏胰岛素清除来减少饮食诱导的代谢异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb96/4512217/8afccfbdc730/db141772f1.jpg

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