Toxicity and oxidative stress of organic and inorganic selenium to rats was studied by orally administering them daily with sub-median lethal dose (3.2mg Se/kg body weight, 0.25-1.0 times of LD
50). Four groups of rats were respectively administered with water (A), aqueous suspension of selenium enriched yeast (B), sodium selenite solution suspended with baker's yeast (C), and aqueous selenite solution (D) for 38 days. Body weights of the rats were measured every day, and oxidative stresses of blood plasma, once a week during the survey by d-ROMs test (derivatives of Reactive Oxygen Metabolites), and plasma biochemical tests and Se deposition to serum and liver, at autopsy. Body weights of B-D groups decreased after a day of first administration, turned to increase after a week. The growth rates, however, were 0.4, 0.4, and 0.1 times the rate of A, for B, C, and D, respectively. The amounts of Se depositions were 9(B) and 5(C) times the value of D in serum, 2.1(B) and 1.4(C) times the value of D in liver, much larger differences between organic and inorganic Se than those reported for low concentrations of Se supplementation. ALT and AST activities in plasma were almost the same for A and B, but 2 and 5 times larger for C and D, suggesting that Se yeast has a little effect on the function of liver, but Na
2SeO
3 caused hepatic lesion. D showed malnutrition with low total protein and albumin content in their bloods. The d-ROMs value of A remained constant (280) but those of B-D increased with days reached a plateau (850) after 4-5 weeks, showing rapidly increasing oxidative stress with days. No differences in d-ROMs values existed with time among B-D despite the difference in toxicity between B and D.
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