| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1905196 | Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | 2011 | 8 Pages |
Recent studies demonstrated the beneficial role of atorvastatin in reducing the risk of cardiovascular morbidity and mortality in patients with diabetes mellitus and/or metabolic syndrome. To investigate the mechanisms underlying the anti-atheroscleroic action of atorvastatin, we examined the expression of the receptor for advanced glycation end products (RAGE) and its downstream target gene, monocyte chemoattractant protein-1 (MCP-1) using real-time PCR. In in vitro studies, exposure to high glucose or AGE induced oxidative stress and activation of the AGE/RAGE system in human umbilical vein endothelial cells. Treatment of the cells with atorvastatin significantly released the oxidative stress by restoring the levels of glutathione and inhibited the RAGE upregulation. In diabetic Goto Kakisaki (GK) rats fed with a high-fat diet for 12 weeks, RAGE and MCP-1 were upregulated in the aortas, and there was a significant correlation between RAGE and MCP-1 mRNA abundance (r = 0.482, P = 0.031). Treatment with atorvastatin (20 mg/kg qd) significantly downregulated the expression of RAGE and MCP-1. These data thus demonstrate a novel “pleiotropic” activity of atorvastatin in reducing the risk of cardiovascular diseases by targeting RAGE expression.
Research highlights► High glucose or AGE activates the AGE/RAGE system in HUVECs. ► Atorvastatin releases oxidative stress by restoring the level of glutathione. ► Suppression of the activated RAGE and MCP-1 by atorvastatin in HUVECs. ► Atorvastatin downregulats RAGE and MCP-1 in diabetic Goto Kakisaki rats. ► A novel “pleiotropic” activity of atorvastatin by targeting RAGE expression.
