Effects of MCP-1 in isometric exercise training promotes the collateral artery formation in mice with myocardial ischemia
10.3969/j.issn.1001-1242.2017.08.001
- VernacularTitle:单核细胞趋化因子-1在等长收缩运动促进大鼠缺血心肌侧支动脉生成中的作用
- Author:
Juntao GUAN
;
Canru GENG
;
Xiao LU
- Keywords:
isometric exercise training;
myocardial ischemia;
monocyte chemoattractant protein;
arteriogenesis;
artery density
- From:
Chinese Journal of Rehabilitation Medicine
2017;32(8):856-862
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To investigate the role of monocyte chemoattractant protein-1 in the progress that isometric exercise training improves arteriogenesis.Method:Twenty-four male Sprague-Dawley rats were used,weighing (200±20)g.The rats were randomized into control group (CG),myocardial ischemia group (MI),exercise training group (ET),MCP-1 inhibitor group (LG).There were 6 rats in each group.Rats were continuously administered 10mg/kg subcutaneously isoproterenol for successive 2 weeks to establish the myocardial ischemia model.Successfully modeled rats were in groups MI,ET and LG.Isometric exercise training were performed in group ET and LG.The rats in group LG were given MCP-1 inhibitor leflunomide by gavage.After 8 weeks of training,the left ventricular myocardium was extracted and relative collateral blood flow (RCBF) was measured by microspheres.Artery density (AD) and monocytes were measured by immunohistochemistry analysis.Western blot analysis and real-time quantitative PCR were performed to assay protein and mRNA of MCP-1.Result:RCBF and AD increased significantly in group ET as compared to the rest groups.RCBF and AD in group LG showed higher than that in group MI but not significant.The number of monocytes,MCP-1 mRNA and MCP-1 expression were significantly elevated in ischemic myocardium of group ET.Interestingly,the number of monocytes,MCP-1 mRNA and MCP-1 expression showed lower than that in group MI but also not significant.Conclusion:Eight weeks of isometric exercise training can increase the expression of MCP-1 in ischemic myocardium and promote the arteriogenesis.
