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非酒精性脂肪性肝病中肝胰高血糖素抵抗的恶性循环

The Vicious Circle of Hepatic Glucagon Resistance in Non-Alcoholic Fatty Liver Disease.

作者信息

Galsgaard Katrine D

机构信息

Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

出版信息

J Clin Med. 2020 Dec 15;9(12):4049. doi: 10.3390/jcm9124049.

Abstract

A key criterion for the most common chronic liver disease-non-alcoholic fatty liver disease (NAFLD)-is an intrahepatic fat content above 5% in individuals who are not using steatogenic agents or having significant alcohol intake. Subjects with NAFLD have increased plasma concentrations of glucagon, and emerging evidence indicates that subjects with NAFLD may show hepatic glucagon resistance. For many years, glucagon has been thought of as the counterregulatory hormone to insulin with a primary function of increasing blood glucose concentrations and protecting against hypoglycemia. However, in recent years, glucagon has re-emerged as an important regulator of other metabolic processes including lipid and amino acid/protein metabolism. This review discusses the evidence that in NAFLD, hepatic glucagon resistance may result in a dysregulated lipid and amino acid/protein metabolism, leading to excess accumulation of fat, hyperglucagonemia, and increased oxidative stress contributing to the worsening/progression of NAFLD.

摘要

最常见的慢性肝病——非酒精性脂肪性肝病(NAFLD)的一个关键标准是,在未使用致脂肪生成药物或未大量饮酒的个体中,肝内脂肪含量超过5%。NAFLD患者的胰高血糖素血浆浓度升高,新出现的证据表明,NAFLD患者可能存在肝胰高血糖素抵抗。多年来,胰高血糖素一直被认为是胰岛素的对抗调节激素,其主要功能是提高血糖浓度并预防低血糖。然而,近年来,胰高血糖素再次成为包括脂质和氨基酸/蛋白质代谢在内的其他代谢过程的重要调节因子。本综述讨论了相关证据,即在NAFLD中,肝胰高血糖素抵抗可能导致脂质和氨基酸/蛋白质代谢失调,导致脂肪过度蓄积、高胰高血糖素血症以及氧化应激增加,从而促使NAFLD恶化/进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18f1/7765287/02e36554d84c/jcm-09-04049-g001.jpg

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