Alpha-lipoic acid prevents endothelial dysfunction in obese rats via activation of AMP-activated protein kinase

Arterioscler Thromb Vasc Biol. 2005 Dec;25(12):2488-94. doi: 10.1161/01.ATV.0000190667.33224.4c. Epub 2005 Oct 13.

Abstract

Objective: Lipid accumulation in vascular endothelial cells may play an important role in the pathogenesis of atherosclerosis in obese subjects. We showed previously that alpha-lipoic acid (ALA) activates AMP-activated protein kinase (AMPK) and reduces lipid accumulation in skeletal muscle of obese rats. Here, we investigated whether ALA improves endothelial dysfunction in obese rats by activating AMPK in endothelial cells.

Methods and results: Endothelium-dependent vascular relaxation was impaired, and the number of apoptotic endothelial cells was higher in the aorta of obese rats compared with control rats. In addition, triglyceride and lipid peroxide levels were higher, and NO synthesis was lower. Administration of ALA improved all of these abnormalities. AMPK activity was lower in aortic endothelium of obese rats, and ALA normalized it. Incubation of human aortic endothelial cells with ALA activated AMPK and protected cells from linoleic acid-induced apoptosis. Dominant-negative AMPK inhibited the antiapoptotic effects of ALA.

Conclusions: Reduced AMPK activation may play an important role in the genesis of endothelial dysfunction in obese rats. ALA improves vascular dysfunction by normalizing lipid metabolism and activating AMPK in endothelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Adenoviridae / genetics
  • Animals
  • Aorta / metabolism
  • Aorta / pathology
  • Aorta / physiopathology
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Atherosclerosis / metabolism*
  • Atherosclerosis / pathology
  • Atherosclerosis / physiopathology
  • Cells, Cultured
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism*
  • Endothelium, Vascular / pathology
  • Gene Transfer Techniques
  • Genes, Dominant
  • Humans
  • Male
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Mitochondria / physiology
  • NADPH Oxidases / metabolism
  • Nitric Oxide Synthase / metabolism
  • Obesity / metabolism*
  • Obesity / pathology
  • Obesity / physiopathology
  • Phosphorylation
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Rats
  • Rats, Inbred OLETF
  • Thioctic Acid / metabolism*
  • Thioctic Acid / pharmacology
  • Triglycerides / metabolism
  • Vasodilation / drug effects
  • Vasodilation / physiology

Substances

  • Triglycerides
  • Thioctic Acid
  • Nitric Oxide Synthase
  • NADPH Oxidases
  • Protein Kinases
  • AMP-Activated Protein Kinase Kinases