1. Role of selenium in reducing hypoxia-induced oxidative stress: an in vivo study.
- Author
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Sarada SK, Sairam M, Dipti P, Anju B, Pauline T, Kain AK, Sharma SK, Bagawat S, Ilavazhagan G, and Kumar D
- Subjects
- Animals, Antioxidants pharmacology, Antioxidants therapeutic use, Glutathione metabolism, Hypoxia drug therapy, Lipid Peroxidation physiology, Male, Malondialdehyde metabolism, Oxidative Stress physiology, Rats, Rats, Sprague-Dawley, Selenium blood, Selenium therapeutic use, Hypoxia metabolism, Lipid Peroxidation drug effects, Oxidative Stress drug effects, Selenium pharmacology
- Abstract
At high altitudes, the reactive oxygen species are continuously generated as a consequence of low oxygen partial pressure (hypoxia), which causes tissue damage. The body's defence system to combat the oxidative stress (e.g., anti-oxidant enzymes, free radical scavengers such as vitamin C, vitamin E, beta-carotene, reduced glutathione and minerals such as selenium, etc.) may diminish. In the present study, the antioxidant effect of selenium (Se) in reducing the hypoxia-induced oxidative stress was evaluated by exposing male albino rats to hypoxic stress in a decompression chamber. Exposure to hypoxia resulted in an increase in malondialdehyde (MDA) levels in plasma and tissues and a concurrent decrease in blood glutathione (GSH), glutathione peroxidase (GPx), plasma protein and plasma selenium content when compared with controls. Haemoglobin concentration (Hb%), red blood corpuscles (RBC) and white blood corpuscles (WBC) count were also increased in the hypoxia-exposed group. Selenium supplementation to animals reversed the trend. There was a significant decrease (P < 0.001) in MDA and subsequent increase in plasma and tissue GSH levels. Similarly the blood and tissue GPx and plasma protein also increased significantly in the Se supplemented animals compared with control animals. The Hb%, RBC and WBC counts showed no significant difference between Se-fed and control rats. These results suggest that selenium may help in reducing the lipid peroxidation during hypoxia.
- Published
- 2002
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