Combination benefit of amlodipine plus atorvastatin treatment on carotid atherosclerosis in Zucker metabolic rats

Neurol Res. 2013 Mar;35(2):181-6. doi: 10.1179/1743132812Y.0000000131. Epub 2012 Dec 17.

Abstract

Objectives: Obesity is the major risk factor for metabolic syndrome and atherosclerotic cardiocerebrovascular diseases.

Methods: We studied effects of amlodipine, atorvastatin, and their combination on carotid arteriosclerotic processes in a metabolic syndrome model of Zucker fatty rats. Zucker fatty rats were treated with vehicle, amlodipine, atorvastatin, or combination amlodipine plus atorvastatin for 28 days.

Results: Compared with the single treatment with amlodipine or atorvastatin, the combination of amlodipine plus atorvastatin treatment prevented arteriosclerotic processes, and induced a strong recovery of Sirtuin1 (Sirt1) expression and a marked reduction in p53, p21, and monocyte chemoattractant protein-1 (MCP-1).

Discussion: As Sirt1 is a longevity gene that prevents endothelial atherosclerotic processes, and p53, p21, and MCP-1 play pivotal roles in the initiation and development of atherosclerosis, these data suggest a strong synergistic benefit of combination therapy with amlodipine and atorvastatin for preventing atherosclerotic processes, and potentially reducing the clinical risk of cerebrovascular events in metabolic obesity patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amlodipine / administration & dosage*
  • Animals
  • Antihypertensive Agents / administration & dosage
  • Atorvastatin
  • Carotid Artery Diseases / drug therapy*
  • Carotid Artery Diseases / metabolism*
  • Carotid Artery, Common / drug effects*
  • Carotid Artery, Common / metabolism
  • Chemokine CCL2 / biosynthesis
  • Cyclin-Dependent Kinase Inhibitor p21 / biosynthesis
  • Drug Therapy, Combination
  • Endothelial Cells / metabolism
  • Heptanoic Acids / administration & dosage*
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage
  • Male
  • Pyrroles / administration & dosage*
  • Rats
  • Sirtuin 1 / biosynthesis
  • Tumor Suppressor Protein p53 / biosynthesis

Substances

  • Antihypertensive Agents
  • Chemokine CCL2
  • Cyclin-Dependent Kinase Inhibitor p21
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrroles
  • Tumor Suppressor Protein p53
  • Amlodipine
  • Atorvastatin
  • Sirtuin 1