Exendin-4 Improves Thermogenic Capacity by Regulating Fat Metabolism on Brown Adipose Tissue in Mice with Diet-Induced Obesity

被引:0
作者
Wei, Qiong [1 ]
Li, Ling [1 ]
Chen, Ji-an [2 ]
Wang, Shao-hua [1 ]
Sun, Zi-lin [1 ]
机构
[1] Southeast Univ, Affiliated ZhongDa Hosp, Dept Endocrinol, Nanjing 210009, Peoples R China
[2] Third Mil Med Univ, Coll Mil Prevent Med, Dept Environm Hyg, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Thermogenesis; obesity; Glucagon-like Peptide-1 Receptor Agonist; GLUCAGON-LIKE PEPTIDE-1; GLP-1; RECEPTOR; UNCOUPLING PROTEIN-1; FOOD-INTAKE; GLUCOSE-UTILIZATION; ENERGY-EXPENDITURE; EXPRESSION; WEIGHT; HYPERGLYCEMIA; AGONIST;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective. This study aimed to investigate the benefits of exendin-4 treatment on brown adipose tissue (BAT) in C57BL/6J mice with high-fat diet (HFD)-induced obesity. Methods. We examined the effects of exendin-4 on body adiposity and the level of genes associated with adipogenesis, glucose/lipid uptake, lipolysis, and thermogenesis in mice with diet-induced obesity. Results. Exendin-4 treatment deceased body weight, serum-free fatty acid, and triglyceride levels in HFD-induced obese C57BL/6J mice. Exendin-4 treatment increased the expression of genes associated with adipogenesis, glucose/lipid uptake, lipolysis, and thermogenesis in BAT. Compared with HFD-fed mice, exendin-4 treatment also exhibited elevated energy expenditure and reduced respiratory quotient, but showed similar food intake and locomotor activity. Conclusions. Exendin-4 treatment reduced high-fat-induced obesity by decreasing adiposity and increasing thermogenesis. This result suggests that GLP-1 agonist may be a new approach to combat obesity by shifting the energy balance from obesogenesis to thermogenesis.
引用
收藏
页码:158 / 165
页数:8
相关论文
共 34 条
[1]   GLP-1 receptor agonists and DPP-4 inhibitors in the treatment of type 2 diabetes [J].
Ahrén, B ;
Schmitz, O .
HORMONE AND METABOLIC RESEARCH, 2004, 36 (11-12) :867-876
[2]   Brown adipose tissue: Function and physiological significance [J].
Cannon, B ;
Nedergaard, J .
PHYSIOLOGICAL REVIEWS, 2004, 84 (01) :277-359
[3]   Mitochondrial ion transport pathways: Role in metabolic diseases [J].
Cardoso, Ariel R. ;
Queliconi, Bruno B. ;
Kowaltowski, Alicia J. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2010, 1797 (6-7) :832-838
[4]   Brown fat as a therapy for obesity and diabetes [J].
Cypess, Aaron M. ;
Kahn, C. Ronald .
CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2010, 17 (02) :143-149
[5]   Exendin-4, a glucagon-like protein-1 (GLP-1) receptor agonist, reverses hepatic steatosis in ob/ob mice [J].
Ding, XK ;
Saxena, NK ;
Lin, SB ;
Gupta, N ;
Anania, FA .
HEPATOLOGY, 2006, 43 (01) :173-181
[6]   Short-Term Exenatide Treatment Leads to Significant Weight Loss in a Subset of Obese Women Without Diabetes [J].
Dushay, Jody ;
Gao, Chuanyun ;
Gopalakrishnan, Gosala S. ;
Crawley, Meghan ;
Mitten, Emilie K. ;
Wilker, Elissa ;
Mullington, Janet ;
Maratos-Flier, Eleftheria .
DIABETES CARE, 2012, 35 (01) :4-11
[7]   GLP-1: a new approach for type 2 diabetes therapy [J].
Giorgino, Francesco ;
Laviola, Luigi ;
Leonardini, Anna ;
Natalicchio, Annalisa .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2006, 74 :S152-S155
[8]   Glucagon-like peptide-1 promotes satiety and reduces food intake in patients with diabetes mellitus type 2 [J].
Gutzwiller, JP ;
Drewe, J ;
Göke, B ;
Schmidt, H ;
Rohrer, B ;
Lareida, J ;
Beglinger, C .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (05) :R1541-R1544
[9]   BROWN ADIPOSE-TISSUE THERMOGENESIS, ENERGY-BALANCE, AND OBESITY [J].
HIMMSHAGEN, J .
CANADIAN JOURNAL OF BIOCHEMISTRY AND CELL BIOLOGY, 1984, 62 (07) :610-617
[10]   GLUCOSE-UTILIZATION BY INTERSCAPULAR BROWN ADIPOSE-TISSUE INVIVO DURING NUTRITIONAL TRANSITIONS IN THE RAT [J].
HOLNESS, MJ ;
LIU, YL ;
BEECH, JS ;
SUGDEN, MC .
BIOCHEMICAL JOURNAL, 1991, 273 :233-235