Expression and function of PPARγ in rat and human vascular smooth muscle cells
RE Law, S Goetze, XP Xi, S Jackson, Y Kawano… - Circulation, 2000 - Am Heart Assoc
RE Law, S Goetze, XP Xi, S Jackson, Y Kawano, L Demer, MC Fishbein, WP Meehan…
Circulation, 2000•Am Heart AssocBackground—Peroxisome proliferator–activated receptor-γ (PPARγ) is activated by fatty
acids, eicosanoids, and insulin-sensitizing thiazolidinediones (TZDs). The TZD troglitazone
(TRO) inhibits vascular smooth muscle cell (VSMC) proliferation and migration in vitro and in
postinjury intimal hyperplasia. Methods and Results—Rat and human VSMCs express
mRNA and nuclear receptors for PPARγ1. Three PPARγ ligands, the TZDs TRO and
rosiglitazone and the prostanoid 15-deoxy-Δ12, 14-prostaglandin J2 (15d-PGJ2), all …
acids, eicosanoids, and insulin-sensitizing thiazolidinediones (TZDs). The TZD troglitazone
(TRO) inhibits vascular smooth muscle cell (VSMC) proliferation and migration in vitro and in
postinjury intimal hyperplasia. Methods and Results—Rat and human VSMCs express
mRNA and nuclear receptors for PPARγ1. Three PPARγ ligands, the TZDs TRO and
rosiglitazone and the prostanoid 15-deoxy-Δ12, 14-prostaglandin J2 (15d-PGJ2), all …
Background—Peroxisome proliferator–activated receptor-γ (PPARγ) is activated by fatty acids, eicosanoids, and insulin-sensitizing thiazolidinediones (TZDs). The TZD troglitazone (TRO) inhibits vascular smooth muscle cell (VSMC) proliferation and migration in vitro and in postinjury intimal hyperplasia.
Methods and Results—Rat and human VSMCs express mRNA and nuclear receptors for PPARγ1. Three PPARγ ligands, the TZDs TRO and rosiglitazone and the prostanoid 15-deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2), all inhibited VSMC proliferation and migration. PPARγ is upregulated in rat neointima at 7 days and 14 days after balloon injury and is also present in early human atheroma and precursor lesions.
Conclusions—Pharmacological activation of PPARγ expressed in VSMCs inhibits their proliferation and migration, potentially limiting restenosis and atherosclerosis. These receptors are upregulated during vascular injury.
Am Heart Assoc
