Insights into incretin-based therapies for treatment of diabetic dyslipidemia

被引:29
作者
Stemmer, Kerstin [1 ,2 ,3 ,4 ]
Finan, Brian [5 ]
DiMarchi, Richard D. [6 ]
Tschoep, Matthias H. [1 ,2 ,3 ,7 ]
Mueller, Timo D. [1 ,2 ,3 ,8 ]
机构
[1] Helmholtz Zentrum Munchen, Inst Diabet & Obes, Ingolstadter Landstr 1, D-85764 Neuherberg, Germany
[2] Helmholtz Zentrum Munchen, Helmholtz Diabet Ctr, Neuherberg, Germany
[3] Helmholtz Zentrum Munchen, German Ctr Diabet Res DZD, Neuherberg, Germany
[4] Univ Konstanz, Dept Biol, Constance, Germany
[5] Novo Nordisk Res Ctr Indianapolis, Indianapolis, IN 46241 USA
[6] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[7] Tech Univ Munich, Dept Med, Div Metab Dis, Munich, Germany
[8] Karls Univ Hosp & Clin, Eberhard Inst Expt & Clin Pharmacol & Pharmacogen, Dept Pharmacol Expt Therapy & Toxicol, D-72076 Tubingen, Germany
基金
欧洲研究理事会;
关键词
Incretins; Lipoproteins; Dyslipidemia; Diabetes; Obesity; GLUCAGON-LIKE PEPTIDE-1; GASTRIC-INHIBITORY POLYPEPTIDE; DEPENDENT INSULINOTROPIC POLYPEPTIDE; LIPOPROTEIN-LIPASE ACTIVITY; LOW-DENSITY-LIPOPROTEIN; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; IMPAIRED GLUCOSE-TOLERANCE; BROWN ADIPOSE-TISSUE; HIGH-FAT; RECEPTOR AGONIST;
D O I
10.1016/j.addr.2020.05.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Derangements in triglyceride and cholesterol metabolism (dyslipidemia) are major risk factors for the development of cardiovascular diseases in obese and type-2 diabetic (T2D) patients. An emerging class of glucagon-like peptide-1 (GLP-1) analogues and next generation peptide dual-agonists such as GLP-1/glucagon or GLP-1/GIP could provide effective therapeutic options for T2D patients. In addition to their role in glucose and energy homeostasis, GLP-1, GIP and glucagon serve as regulators of lipid metabolism. This review summarizes the current knowledge in GLP-1, glucagon and GIP effects on lipid and lipoprotein metabolism and frames the emerging therapeutic benefits of GLP-1 analogs and GLP-1-based multiagonists as add-on treatment options for diabetes associated dyslipidemia. (C) 2020 Published by Elsevier B.V.
引用
收藏
页码:34 / 53
页数:20
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