TY - JOUR T1 - Peroxisome Proliferator-Activated Receptor γ Down-Regulates Receptor for Advanced Glycation End Products and Inhibits Smooth Muscle Cell Proliferation in a Diabetic and Nondiabetic Rat Carotid Artery Injury Model JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 37 LP - 43 DO - 10.1124/jpet.105.095125 VL - 317 IS - 1 AU - Kai Wang AU - Zhongmin Zhou AU - Ming Zhang AU - Liming Fan AU - Farhad Forudi AU - Xiaorong Zhou AU - Wu Qu AU - A. Michael Lincoff AU - Ann Marie Schmidt AU - Eric J. Topol AU - Marc S. Penn Y1 - 2006/04/01 UR - http://jpet.aspetjournals.org/content/317/1/37.abstract N2 - Diabetes is associated with an increase in circulating advanced glycosylation end products (AGEs) and the increased expression of the receptor for AGEs (RAGE). Inhibition of AGE/RAGE binding through the administration of soluble RAGE (sRAGE) has been shown to decrease neointimal hyperplasia. Peroxisome proliferator-activated receptor γ (PPARγ), which inhibits neointimal hyperplasia, has been shown to decrease RAGE expression in cultured endothelial cells. We hypothesized that PPARγ agonists inhibit neointimal hyperplasia via down-regulation of RAGE in vivo. Pretreatment of rat aortic smooth muscle cells (SMCs) with PPARγ agonist rosiglitazone significantly down-regulated RAGE expression and inhibited SMC proliferation in response to the RAGE agonist S100/calgranulins. In vivo studies showed that rosiglitazone decreased RAGE expression and SMC proliferation at 7 days following carotid arterial injury in both diabetic and nondiabetic rats. At 21 days following injury, neointimal formation was significantly decreased in both diabetic and nondiabetic animals that received rosiglitazone. To determine whether inhibition of neointimal formation by PPARγ activation could fully be accounted for by its down-regulation of RAGE, we compared the results obtained in animals treated with sRAGE, PPARγ activator, and sRAGE + PPARγ activator. Consistent with PPARγ working through its effects on RAGE, we found that the addition of PPARγ activator to sRAGE did not result in any further decrease in neointimal formation. These data demonstrate for the first time that PPARγ agonists inhibit RAGE expression at sites of arterial injury and suggest that down-regulation of RAGE by the PPARγ activation inhibits neointimal formation in response to arterial injury. The American Society for Pharmacology and Experimental Therapeutics ER -