Long-term effects of a PPAR-gamma agonist, pioglitazone, on neointimal hyperplasia and endothelial regrowth in insulin resistant rats

被引:12
作者
Desouza, Cyrus V. [1 ]
Gerety, Moira [1 ]
Hamel, Frederick G. [1 ]
机构
[1] Univ Nebraska Med Ctr, Omaha VA Med Ctr, Med Dept 111, Omaha, NE 68105 USA
关键词
PPAR-gamma; pioglitazone; neointimal hyperplasia; endothelial regrowth; insulin resistance;
D O I
10.1016/j.vph.2006.10.001
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Objective: Insulin resistance is an independent risk factor for cardiovascular disease. PPAR-gamma agonists like pioglitazone decrease insulin resistance and have been shown to reduce neointimal hyperplasia in the short-term. However long-term studies on endothelial regrowth and neointimal hyperplasia have not been done. Methods and results: We used hyperinsulinemic, normoglycemic Zucker fatty rats. Rats were treated with either 10 mg/kg body wt. pioglitazone or placebo till the end of the experiment. Rats underwent carotid angioplasty at age 12-14 weeks, I week after treatment was begun. In one set of experiments rats were sacrificed at 6 months and neointimal hyperplasia and VEGF expression was assessed. In another set of experiments rats were sacrificed at 3 and 6 months. Endothelial regrowth was determined. The rats were all normoglycemic and hyperinsulinemic. Pioglitazone treated rats had a significantly lesser degree of neointimal hyperplasia than control rats. Treated rats also had decreased VEGF expression. Endothelial regrowth was decreased in the treated rats at 6 months. Conclusion: We conclude that although pioglitazone decreases neointimal hyperplasia, even at 6 months, it retards endothelial regrowth, which could predispose the denuded vessel to thrombotic events. This may be modulated by a suppression of VEGF expression. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:188 / 194
页数:7
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