SIRT1: a novel target to prevent atherosclerosis

J Cell Biochem. 2009 Sep 1;108(1):10-3. doi: 10.1002/jcb.22240.

Abstract

Atherosclerosis is a chronic immuno-inflammatory disease associated with blood lipids disorder. Many studies have demonstrated that caloric restriction (CR) can prevent atherosclerosis and extend lifespan. Sir2 protein, mammal's SIRT1, has been reported to at least partly contribute to the protective effect of CR. Hence, we hypothesize that SIRT1 is a key regulator in the pathogenesis of atherosclerosis and that upregulation of SIRT1 in endothelial cells may mimic CR's beneficial effect on vascular health. The recent studies have demonstrated that endothelial SIRT1 is an anti-atherosclerosis factor and the possible mechanism may be related to inhibit oxidized low-density lipoprotein (oxLDL)-induced apoptosis, upregulate endothelial nitric oxide synthase (eNOS) expression, and improve endothelium relaxation function. We infer that SIRT1 may be a novel target for atherosclerosis prevention and treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atherosclerosis / etiology
  • Atherosclerosis / prevention & control*
  • Caloric Restriction
  • Endothelial Cells / enzymology
  • Endothelial Cells / metabolism
  • Humans
  • Lipoproteins, LDL / metabolism
  • Nitric Oxide Synthase Type III / metabolism
  • Sirtuin 1 / metabolism*

Substances

  • Lipoproteins, LDL
  • oxidized low density lipoprotein
  • Nitric Oxide Synthase Type III
  • Sirtuin 1