Medical Journals

Sorting out the Roles of Ppar Alpha in Energy Metabolism and Vascular Homeostasis.

Authors:
  • Lefebvre Philippe
  • Chinetti Giulia
  • Fruchart Jean-Charles
  • Staels Bart

From: Département d’Athérosclérose, Institut Pasteur de Lille, INSERM U545, and Université de Lille 2, Lille, France.

The Journal of clinical investigation

  • Publish Date: Mar 2006
  • ISSN: 0021-9738
  • Volume: 116
  • Issue: 3
  • Pages: 571-80
  • Medium: Print
  • Language: English
  • Citation (JAMA): Lefebvre Philippe, Chinetti Giulia, Fruchart Jean-Charles, et al. Sorting out the Roles of Ppar Alpha in Energy Metabolism and Vascular Homeostasis.. J. Clin. Invest. Mar 2006;116:571-80

Abstract

PPARalpha is a nuclear receptor that regulates liver and skeletal muscle lipid metabolism as well as glucose homeostasis. Acting as a molecular sensor of endogenous fatty acids (FAs) and their derivatives, this ligand-activated transcription factor regulates the expression of genes encoding enzymes and transport proteins controlling lipid homeostasis, thereby stimulating FA oxidation and improving lipoprotein metabolism. PPARalpha also exerts pleiotropic antiinflammatory and antiproliferative effects and prevents the proatherogenic effects of cholesterol accumulation in macrophages by stimulating cholesterol efflux. Cellular and animal models of PPARalpha help explain the clinical actions of fibrates, synthetic PPARalpha agonists used to treat dyslipidemia and reduce cardiovascular disease and its complications in patients with the metabolic syndrome. Although these preclinical studies cannot predict all of the effects of PPARalpha in humans, recent findings have revealed potential adverse effects of PPARalpha action, underlining the need for further study. This Review will focus on the mechanisms of action of PPARalpha in metabolic diseases and their associated vascular pathologies.

Mesh Headings (Keywords): Animals, Blood Circulation, Energy Metabolism, Homeostasis, Humans, Metabolic Diseases, PPAR alpha


Check for Full Text / PubMed Unique Identifier (PMID): 16511589


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