Int J Angiol 2009; 18(2): 89-95
DOI: 10.1055/s-0031-1278333
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Vitamin E does not slow the progression of hypercholesterolemic atherosclerosis

Kailash Prasad
  • Department of Physiology, College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan
Further Information

Publication History

Publication Date:
28 April 2011 (online)

Abstract

BACKGROUND: Vitamin E suppresses the development of atherosclerosis but does not regress established hypercholesterolemic atherosclerosis.

OBJECTIVES: To investigate whether vitamin E slows the progression of established atherosclerosis, and whether this effect is associated with reductions in serum lipids and oxidative stress.

METHODS: The present study was performed in four groups of rabbits: group I, regular diet (control); group II, 0.25% cholesterol diet (two months); group III, 0.25% cholesterol diet (four months); and group IV, 0.25% cholesterol diet (two months) followed by 0.25% cholesterol and vitamin E (two months). Serum lipids and the chemi- luminescent activity of white blood cells (WBC-CL), a measure of oxygen radical production by white blood cells, were measured before and at monthly intervals for the duration of the study. Aortas were removed at the end of the protocol for assessment of atherosclerosis and the chemi-luminescent activity of aortic tissue (aortic-CL), a measure of antioxidant reserve.

RESULTS: Atherosclerosis was associated with hyperlipidemia and increased oxidative stress, indicated by increased nonactivated WBC-CL and alteration of the aortic-CL. Significant areas of the intimal surfaces of the aortas from group II (26.54%±4.11%), group III (69.37%±5.34%) and group IV (65.96%±7.86%) were covered with atherosclerotic lesions. Vitamin E did not alter serum lipids, aortic antioxidant reserve or WBC-CL. Vitamin E was ineffective in slowing the progression of hypercholesterolemic atherosclerosis.

CONCLUSION: Vitamin E did not slow the progression of hypercho- lesterolemic atherosclerosis, and this effect was associated with its ineffectiveness in reducing serum lipids and oxidative stress.