Protection of Phagocytic Macrophages from Peroxidative Damage by Selenium and Vitamin E.
10.3349/ymj.1982.23.2.101
- Author:
Sang Hwan OH
1
;
Myung Ho LEE
;
Chang Jo CHUNG
Author Information
1. Department of Biochemistry, Yonsei University College of Medicine, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Selenium;
Vitamin E;
Peroxidation;
Macrophage;
Phagocytosis
- MeSH:
Animal;
Macrophages/drug effects;
Macrophages/physiology*;
Male;
Peroxides/metabolism*;
Phagocytosis/drug effects*;
Rats;
Selenium/pharmacology*;
Vitamin E/pharmacology*
- From:Yonsei Medical Journal
1982;23(2):101-109
- CountryRepublic of Korea
- Language:English
-
Abstract:
The Protective effect of vitamin E and selenium against peroxidative damage in white blood cells was studied. Forty-eight male rats (~100g BW) were divided into four groups and were fed with a torula yeast based diet deficient in Vit.E and Se. Vit.E (100IU/Kg diet) and Se (0.3ppm) supplementation increased the total peritoneal cell (P.C) population and cell survival rate. Selenium supplementation decreased the hydrogen peroxide generation (half of the control) significantly and Vit.E supplementation reduced the malonaldehyde production during phagocytosis in vitro. However, superoxide generation was not affected by the supplementation of Vit.E or Se. There were no significant differences in catalase activity between groups but glutathione peroxidase activity was increased about twofold by Se supplementation with no effect of Vit.E. In a separate experiment, activated alveolar macrophages were obtained from BCG infected rabbits fed a diet supplemented with Vit.E (100 IU/Kg diet) or Se (0.3 ppm). Se supplementation increased glutathione peroxidase in cells, and both Vit.E and Se increased the cell survival rate during phagocytosis as compared to the control. Both Vit.E and Se are necessary to protect host cells from peroxidative damage during phagocytosis.
