A Glucagon-Like Peptide-1 Analog Reverses the Molecular Pathology and Cardiac Dysfunction of a Mouse Model of Obesity

作者：Noyan Ashraf Mohammad Hossein; Shikatani Eric Akihiko; Schuiki Irmgard; Mukovozov Ilya; Wu Jun; Li Ren Ke; Volchuk Allen; Robinson Lisa Annette; Billia Filio; Drucker Daniel J; Husain Mansoor^*

来源：Circulation, 2013, 127(1): 74-+.

DOI：10.1161/CIRCULATIONAHA.112.091215

• obesity
• heart
• glucagon-like peptide-1
• inflammation
• connexin-43
• AMP-activated protein kinase

Background-Cardiac consequences of obesity include inflammation, hypertrophy, and compromised energy metabolism. Glucagon-like peptide-1 is an incretin hormone capable of cytoprotective actions that reduces inflammation and endoplasmic reticulum stress in other tissues. Here we examine the cardiac effects of the glucagon-like peptide-1 analog liraglutide in a model of obesity, independent of changes in body weight.
Methods and Results-C57Bl6 mice were placed on a 45% high-fat diet (HFD) or a regular chow diet. Mice on HFD developed 46 +/- 2% and 60 +/- 2% greater body weight relative to regular chow diet-fed mice at 16 and 32 weeks, respectively (both P<0.0001), manifesting impaired glucose tolerance, insulin resistance, and cardiac ceramide accumulation by 16 weeks. One-week treatment with liraglutide (30 mu g/kg twice daily) did not reduce body weight, but reversed insulin resistance, cardiac tumor necrosis factor-alpha expression, nuclear factor kappa B translocation, obesity-induced perturbations in cardiac endothelial nitric oxide synthase, connexin-43, and markers of hypertrophy and fibrosis, in comparison with placebo-treated HFD controls. Liraglutide improved the cardiac endoplasmic reticulum stress response and also improved cardiac function in animals on HFD by an AMP-activated protein kinase-dependent mechanism. Supporting a direct mechanism of action, liraglutide (100 nmol/L) prevented palmitate-induced lipotoxicity in isolated mouse cardiomyocytes and primary human coronary smooth muscle cells and prevented adhesion of human monocytes to tumor necrosis factor-alpha-activated human endothelial cells in vitro.
Conclusions-Weight-neutral treatment with a glucagon-like peptide-1 analog activates several cardioprotective pathways, prevents HFD-induced insulin resistance and inflammation, reduces monocyte vascular adhesion, and improves cardiac function in vivo by activating AMP-activated protein kinase. These data support a role for glucagon-like peptide-1 analogs in limiting the cardiovascular risks of obesity. (Circulation. 2013;127:74-85.)

• 出版日期2013-1-1