Interference with PPARγ function in smooth muscle causes vascular dysfunction and hypertension

被引:148
作者
Halabi, Carmen M. [2 ]
Beyer, Andreas M. [2 ]
De lange, Willem J. [1 ]
Keen, Henry L. [1 ]
Baumbach, Gary L. [4 ]
Faraci, Frank M. [1 ,3 ]
Sigmund, Curt D. [1 ,5 ,6 ]
机构
[1] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Roy J & Lucille A Carver Coll Med, Genet Program, Iowa City, IA 52242 USA
[3] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Pharmacol, Iowa City, IA 52242 USA
[4] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Pathol, Iowa City, IA 52242 USA
[5] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
[6] Univ Iowa, Roy J & Lucille A Carver Coll Med, Ctr Funct Genom & Hypertens, Iowa City, IA 52242 USA
关键词
D O I
10.1016/j.cmet.2007.12.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Peroxisome proliferator-activated receptor gamma (PPAR gamma) is a ligand-activated transcription factor that plays a critical role in metabolism. Thiazolidinediones, high-affinity PPAR gamma ligands used clinically to treat type II diabetes, have been reported to lower blood pressure and provide other cardiovascular benefits. Some mutations in PPAR gamma (PPARG) cause type II diabetes and severe hypertension. Here we tested the hypothesis that PPAR gamma in vascular muscle plays a role in the regulation of vascular tone and blood pressure. Transgenic mice expressing dominant-negative mutations in PPAR gamma under the control of a smooth-muscle-specific promoter exhibit a loss of responsiveness to nitric oxide and striking alterations in contractility in the aorta, hypertrophy and inward remodeling in the cerebral microcirculation, and systolic hypertension. These results identify PPAR gamma as pivotal in vascular muscle as a regulator of vascular structure, vascular function, and blood pressure, potentially explaining some of the cardioprotective effects of thiazolidinediones.
引用
收藏
页码:215 / 226
页数:12
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