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Vitamins C and E Prolong Time to Arterial Thrombosis in Rats

Manuscript received 24 July 1998. Initial reviews completed 10 September 1998. Revision accepted 23 October 1998.

Jason Mehta, Dayuan Li, and Jawahar L. Mehta

Department of Medicine, University of Florida College of Medicine and the VA Medical Center, Gainesville, FL

To examine the modulation of arterial thrombosis by vitamins C and E, Sprague-Dawley rats were fed nonpurified diet, or diet mixed with vitamin C [100 mg/(kg body weight·d)], vitamin E [100 mg/(kg·d)] or both vitamins C and E [each 100 mg/(kg·d)], for a period of 9-19 d (mean 15 d). An occlusive aortic thrombus was created by application of a Whatman filter soaked in 1 mol/L FeCl3. Both vitamins C and E and their combination decreased platelet aggregation and delayed time to occlusive thrombus formation (P < 0.05 vs. control). Vitamins C and E decreased arterial superoxide generation (P < 0.05 vs. control). Interestingly, vitamin E also increased endogenous superoxide dismutase activity (SOD) and protein expression in aortic tissues (P < 0.05 vs. control). The combination of vitamins C and E was not superior to each vitamin alone with regard to effect on time to thrombus formation, but it was more potent with regard to platelet inhibition. The increase in endogenous antioxidant activity by vitamin E is an intriguing observation. This study shows that the antioxidant vitamins C and E have important effects on platelet aggregation, SOD activity, superoxide generation and thrombus formation.

Key words: platelet aggregation, thrombosis, superoxide dismutase, vitamin C, vitamin E, rats.

The Journal of Nutrition Vol. 129 No. 1 January 1999, pp. 109-112
Copyright ©1999 by the American Society for Nutritional Sciences




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