Reduced alpha-lipoic acid synthase gene expression exacerbates atherosclerosis in diabetic apolipoprotein E-deficient mice

Atherosclerosis. 2012 Jul;223(1):137-43. doi: 10.1016/j.atherosclerosis.2012.04.025. Epub 2012 May 16.

Abstract

Objectives: To study the effects of reduced lipoic acid gene expression on diabetic atherosclerosis in apolipoprotein E null mice (Apoe(-/-)).

Methods and results: Heterozygous lipoic acid synthase gene knockout mice (Lias(+/-)) crossed with Apoe(-/-) mice were used to evaluate the diabetic effect induced by streptozotocin on atherosclerosis in the aortic sinus of the heart. While diabetes markedly increased atherosclerotic plaque size in Apoe(-/-) mice, a small but significant effect of reduced expression of lipoic acid gene was observed in diabetic Lias(+/-)Apoe(-/-) mice. In the aortic lesion area, the Lias(+/-)Apoe(-/-) mice exhibited significantly increased macrophage accumulation and cellular apoptosis than diabetic Lias(+/+)Apoe(-/-) littermates. Plasma glucose, cholesterol, and interleukin-6 were also higher. These abnormalities were accompanied with increased oxidative stress including a decreased ratio of reduced glutathione/oxidized glutathione in erythrocytes, increased systemic lipid peroxidation, and increased Gpx1 and MCP1 gene expression in the aorta.

Conclusions: Decreased endogenous lipoic acid gene expression plays a role in development of diabetic atherosclerosis. These findings extend our understanding of the role of antioxidant in diabetic atherosclerosis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Aortic Diseases / blood
  • Aortic Diseases / enzymology
  • Aortic Diseases / etiology*
  • Aortic Diseases / genetics
  • Aortic Diseases / pathology
  • Apolipoproteins E / deficiency*
  • Apolipoproteins E / genetics
  • Apoptosis
  • Atherosclerosis / blood
  • Atherosclerosis / enzymology
  • Atherosclerosis / etiology*
  • Atherosclerosis / genetics
  • Atherosclerosis / pathology
  • Blood Glucose / metabolism
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism
  • Cholesterol / blood
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / complications*
  • Disease Models, Animal
  • Gene Expression Regulation
  • Glutathione / blood
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Glutathione Peroxidase GPX1
  • Interleukin-6 / blood
  • Kidney / metabolism
  • Kidney / pathology
  • Liver / metabolism
  • Liver / pathology
  • Macrophages / metabolism
  • Macrophages / pathology
  • Male
  • Mice
  • Mice, 129 Strain
  • Mice, Knockout
  • Oxidative Stress
  • Sinus of Valsalva / enzymology*
  • Sinus of Valsalva / pathology
  • Sulfurtransferases / deficiency*
  • Sulfurtransferases / genetics

Substances

  • Apolipoproteins E
  • Blood Glucose
  • Ccl2 protein, mouse
  • Chemokine CCL2
  • Interleukin-6
  • Cholesterol
  • Glutathione Peroxidase
  • Sulfurtransferases
  • lipoic acid synthase
  • Glutathione
  • Glutathione Peroxidase GPX1
  • Gpx1 protein, mouse