Monocyte chemoattractant protein-1 involvement in the alpha-tocopherol-induced reduction of atherosclerotic lesions in apolipoprotein E knockout mice

Br J Nutr. 2003 Jul;90(1):3-11. doi: 10.1079/bjn2003870.

Abstract

We studied the effects of alpha-tocopheryl acetate supplementation on the development of fatty streaks and its ability to modulate the expression of monocyte chemoattractant protein (MCP)-1 in aortic lesions of apolipoprotein E knockout mice. For this purpose, 16-week-old apolipoprotein E knockout mice received alpha-tocopherol supplementation (800 mg)/kg diet) for 6 weeks. After this time, total and lipoprotein cholesterol in the serum, hepatic tocopherol, aortic lesion area and MCP-1 (protein and mRNA) expression were analysed. Our present results showed that the dietary supplementation with alpha-tocopherol did not reduce serum cholesterol nor change lipoprotein profile, but it reduced the area of the aortic lesion by 55 %. The reduction in the lesion size was correlated with the reduced expression of MCP-1 mRNA and protein, as detected by real-time quantitative polymerase chain reaction and immunohistochemistry respectively. In conclusion, the results obtained here are relevant to the study of atherosclerosis, as they correlate the effectiveness of vitamin E supplementation in inhibiting the plaque formation with diminished expression of MCP-1 at the aortic lesion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aortic Diseases / drug therapy
  • Aortic Diseases / metabolism
  • Aortic Diseases / pathology
  • Apolipoproteins E / genetics*
  • Apolipoproteins E / metabolism
  • Arteriosclerosis / drug therapy*
  • Arteriosclerosis / metabolism
  • Arteriosclerosis / pathology
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism*
  • Cholesterol / blood
  • Immunohistochemistry
  • Lipoproteins / analysis
  • Liver / chemistry
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Models, Animal
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • alpha-Tocopherol / metabolism
  • alpha-Tocopherol / therapeutic use*

Substances

  • Apolipoproteins E
  • Chemokine CCL2
  • Lipoproteins
  • RNA, Messenger
  • Cholesterol
  • alpha-Tocopherol