中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
GLP-1 mimetics as a potential therapy for nonalcoholic steatohepatitis

文献类型:期刊论文

作者Chen, Yan2; Xu, Ying-na2; Ye, Chen-yu2; Feng, Wen-bo2; Zhou, Qing-tong2; Yang, De-hua1,3,4; Wang, Ming-wei1,2,3,4,5
刊名ACTA PHARMACOLOGICA SINICA
出版日期2021-12-21
页码11
ISSN号1671-4083
关键词NAFLD NASH GLP-1R GLP-1 mimetics dual agonists triple agonists GPCR
DOI10.1038/s41401-021-00836-9
通讯作者Yang, De-hua(dhyang@simm.ac.cn) ; Wang, Ming-wei(mwwang@simm.ac.cn)
英文摘要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.
WOS关键词GLUCAGON-LIKE PEPTIDE-1 ; FATTY LIVER-DISEASE ; GASTRIC-INHIBITORY POLYPEPTIDE ; INDUCED HEPATIC STEATOSIS ; INSULIN-RESISTANCE ; RECEPTOR AGONIST ; ADIPOSE-TISSUE ; GUT MICROBIOTA ; LONG-TERM ; MITOCHONDRIAL-FUNCTION
资助项目National Natural Science Foundation of China[81872915] ; National Natural Science Foundation of China[82073904] ; National Natural Science Foundation of China[81773792] ; National Natural Science Foundation of China[81973373] ; National Natural Science Foundation of China[21704064] ; National Science & Technology Major Project of China-Key New Drug Creation and Manufacturing Program[2018ZX09735-001] ; National Science & Technology Major Project of China-Key New Drug Creation and Manufacturing Program[2018ZX09711002-002-005] ; National Key Basic Research Program of China[2018YFA0507000] ; Science and Technology Commission of Shanghai Municipality[18431907100] ; Novo Nordisk-CAS Research Fund grant[NNCAS-2017-1-CC] ; SA-SIBS Scholarship Program
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
出版者NATURE PUBL GROUP
WOS记录号WOS:000732502400001
源URL[http://119.78.100.183/handle/2S10ELR8/300791]  
专题中国科学院上海药物研究所
通讯作者Yang, De-hua; Wang, Ming-wei
作者单位1.Res Ctr Deepsea Bioresources, Sanya 572025, Peoples R China
2.Fudan Univ, Sch Basic Med Sci, Dept Pharmacol, Shanghai 200032, Peoples R China
3.Chinese Acad Sci, CAS Key Lab Receptor Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
4.Chinese Acad Sci, Natl Ctr Drug Screening, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
5.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
推荐引用方式
GB/T 7714
Chen, Yan,Xu, Ying-na,Ye, Chen-yu,et al. GLP-1 mimetics as a potential therapy for nonalcoholic steatohepatitis[J]. ACTA PHARMACOLOGICA SINICA,2021:11.
APA Chen, Yan.,Xu, Ying-na.,Ye, Chen-yu.,Feng, Wen-bo.,Zhou, Qing-tong.,...&Wang, Ming-wei.(2021).GLP-1 mimetics as a potential therapy for nonalcoholic steatohepatitis.ACTA PHARMACOLOGICA SINICA,11.
MLA Chen, Yan,et al."GLP-1 mimetics as a potential therapy for nonalcoholic steatohepatitis".ACTA PHARMACOLOGICA SINICA (2021):11.

入库方式: OAI收割

来源:上海药物研究所

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