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GLP-1 mimetics as a potential therapy for nonalcoholic steatohepatitis
GLP-1 模拟物作为非酒精性脂肪性肝炎的潜在疗法
非アルコール性脂肪性肝炎の潜在的な治療法としてのGLP-1模倣薬
비알코올성 지방간염에 대한 잠재적 치료제로서의 GLP-1 모방체
Miméticos de GLP-1 como terapia potencial para la esteatohepatitis no alcohólica
Les mimétiques du GLP-1 comme traitement potentiel de la stéatohépatite non alcoolique
Миметики GLP-1 как потенциальная терапия неалкогольного стеатогепатита
Yan Chen ¹, Ying-na Xu ¹, Chen-yu Ye ¹, Wen-bo Feng ¹, Qing-tong Zhou 周庆同 ¹, De-hua Yang 杨德华 ² ³, Ming-wei Wang 王明伟 ¹ ² ³ ⁴
¹ Department of Pharmacology, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China
中国 上海 复旦大学基础医学院药理学系
² The CAS Key Laboratory of Receptor Research and The National Center for Drug Screening, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China
中国 上海 中国科学院上海药物研究所 受体结构与功能重点实验室 国家新药筛选中心
³ Research Center for Deepsea Bioresources, Sanya, 572025, China
中国 三亚 深海生物学研究室
⁴ School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China
中国 上海 上海科技大学生命科学与技术学院
Acta Pharmacologica Sinica, 21 December 2021
Abstract

Nonalcoholic steatohepatitis (NASH), as a severe form of nonalcoholic fatty liver disease (NAFLD), is characterized by liver steatosis, inflammation, hepatocellular injury and different degrees of fibrosis. The pathogenesis of NASH is complex and multifactorial, obesity and type 2 diabetes mellitus (T2DM) have been implicated as major risk factors. Glucagon-like peptide-1 receptor (GLP-1R) is one of the most successful drug targets of T2DM and obesity, and its peptidic ligands have been proposed as potential therapeutic agents for NASH.

In this article we provide an overview of the pathophysiology and management of NASH, with a special focus on the pharmacological effects and possible mechanisms of GLP-1 mimetics in treating NAFLD/NASH, including dual and triple agonists at GLP-1R, glucose-dependent insulinotropic polypeptide receptor or glucagon receptor.
Acta Pharmacologica Sinica_1
Acta Pharmacologica Sinica_2
Acta Pharmacologica Sinica_3
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