Journal of the American Society of Hypertension
Volume 2, Issue 4 , Pages 227-238, July 2008

Peroxisome proliferator-activated receptors and the vascular system: beyond their metabolic effects

  • Chiara Marchesi, MD
  • ,
  • Ernesto L. Schiffrin, MD, PhD, FRSC, FRCPC

      Affiliations

    • Corresponding Author InformationCorresponding author: Ernesto L. Schiffrin, MD, PhD, FRSC, FRCPC, Department of Medicine, Sir Mortimer B. Davis-Jewish General Hospital, #B-127, 3755 Côte Ste-Catherine Road, Montreal, Quebec, Canada H3T 1E2. Tel: 514-340-7538; fax: 514-340-7539.

Lady Davis Institute for Medical Research, Sir Mortimer B. Davis-Jewish General Hospital, McGill University, Montreal, Quebec, Canada

Received 21 November 2007; accepted 28 December 2007. published online 03 June 2008.

Abstract 

Peroxisome proliferator-activated receptors (PPARs) alpha and gamma are ligand-activated transcription factors belonging to the nuclear receptor superfamily. PPARα has effects on fatty acid metabolism and its activation by fibrates results in reduction of triglyceride concentrations in blood. PPARγ induces differentiation of adipocytes, and its activation by thiazolidinediones (TZDs) has insulin sensitizing effects, for which reason these agents are used for treating type 2 diabetes. PPARα and PPARγ are present in the vasculature, where they have been shown to exert antioxidant and anti-inflammatory effects and to blunt the development of fibrosis and remodeling in experimental models and in several cardiovascular clinical conditions. This review will discuss some of the evidence, both experimental and clinical, that suggests that activation of PPARα and PPARγ in hypertension may exert beneficial cardiovascular protective effects. However, a recent meta-analysis suggests an excess of myocardial infarction and borderline excess of cardiovascular death in type 2 diabetic patients treated with rosiglitazone. Thus the safety of use of PPARγ activators for cardiovascular prevention and whether they are protective or actually may be harmful remains to be established.

Keywords: Blood vessels, atherosclerosis, hypertension, inflammation

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 This work was supported by Canadian Institutes of Health Research Grants 37917 and 82790 and a Canada Research Chair on Hypertension and Vascular Research to Dr. Schiffrin.

PII: S1933-1711(08)00002-8

doi:10.1016/j.jash.2007.12.007

Journal of the American Society of Hypertension
Volume 2, Issue 4 , Pages 227-238, July 2008