Effect of peroxisome proliferator-activated receptor γ ligand.: Rosiglitazone on left ventricular remodeling in rats with myocardial infarction

被引:40
作者
Geng, Deng-feng
Wu, Wei
Jin, Dong-mei
Wang, Jing-feng
Wu, Yi-mei
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 2, Dept Cardiol, Guangzhou 510120, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 2, Dept Rehabil Med, Guangzhou 510120, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 2, Dept Rheumatol, Guangzhou 510120, Peoples R China
关键词
PPAR gamma; thiazolidinediones; myocardial infarction; ventricular remodeling; renin angiotensin system;
D O I
10.1016/j.ijcard.2006.03.060
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Recent studies have demonstrated that PPAR gamma ligands have anti-inflammatory effect which is involved in ventlicular remodeling. So we hypothesized that PPAR gamma ligand may have beneficial effects on post-infarct ventricular remodeling. Methods: Experimental myocardial infarction (MI) was induced in SD rats by ligation of the left coronary artery. Twenty-four hours after surgery, survival rats were randomly divided into MI group and Rosiglitazone (MI+Ros) group which would take rosiglitazone 3 mg/kg day for 8 weeks. After 8 weeks treatment, left ventricular hemodynamics were measured and organs were weighed. Myocardial collagen analysis was determined in Van Gieson staining by quantitative morphometry. Myocardial angiotensin II and aldosterone were detected by radioimmunoassay. Myocardial AT1 and AT2 mRNA expression were determined by RT-PCR. Results: Only 1 rat in MI group died of anesthesia at the 8th week. Rosiglitazone treatment could improve left ventricular +/- dp/dt(max), collagen volume fraction and perivascular circumferential area; reduce lung/body mass ratio and liver/body mass ratio; inhibit myocardial angiotensin II and aldosterone; and had no significant effects on myocardial AT1 and AT2 mRNA. Plasma insulin and blood glucose were comparable between two groups. Conclusions: PPAR gamma ligand has neutral effect on mortality and beneficial effect on post-infarct ventricular remodeling, partly by suppressing myocardial angiotensin II and aldosterone, irrespective of plasma insulin and blood glucose level. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:86 / 91
页数:6
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