Effect of vitamin E supplementation on antioxidant defense systems and humoral immune responses in young, middle-aged and elderly Korean women
Summary Free radical-mediated oxidative stress has been implicated in the pathogenesis of numerous chronic diseases. Vitamin E is known to play an important role in the free-radical quenching process. However, clinical trials with vitamin E have yielded contrasting results in the prevention of sever...
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Published in | Journal of Nutritional Science and Vitaminology Vol. 49; no. 2; pp. 94 - 99 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Tokyo
Center for Academic Publications Japan
01.04.2003
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Subjects | |
Online Access | Get full text |
ISSN | 0301-4800 1881-7742 |
DOI | 10.3177/jnsv.49.94 |
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Summary: | Summary Free radical-mediated oxidative stress has been implicated in the pathogenesis of numerous chronic diseases. Vitamin E is known to play an important role in the free-radical quenching process. However, clinical trials with vitamin E have yielded contrasting results in the prevention of several diseases related to oxidative stress. This study was undertaken to investigate the antioxidative and humoral immunologic effects of vitamin E supplementation in three different age groups: young (mean age 32.7 =+- 5.7y), middle-aged (mean age 47.0 =+- 5.0y) and elderly (67.6 =+- 4.7y) women. Volunteer subjects were given a supplement of 400 IU dl-a-tocopherol acetate for 6 wk. Thiobarbituric acid reacting substances (TBARS) in the plasma significantly decreased with vitamin E supplementation. In addition, the radical scavenger activities (RSA) of red blood cells significantly increased with vitamin E supplementation in all age groups. However, humoral immune response modulation was not observed following vitamin E supplementation. Even though there is no clear indication that vitamin E supplementation is necessary to improve the humoral immune functions, vitamin E supplementation may be beneficial to all adult age groups as a preventive measure for complications related to oxidative damage. |
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Bibliography: | S20 2004003479 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0301-4800 1881-7742 |
DOI: | 10.3177/jnsv.49.94 |