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자료유형
학술저널
저자정보
Son, Eun-Wha (Department of Pharmacognosy and Material Development, Kangwon National University) Lee, Sung-Ryul (Department of Food and Nutrition, Kangwon National University) Choi, Hye-Sook (Department of Food and Nutrition, Kangwon National University) Koo, Hyun-Jung (Department of Food and Nutrition, Kangwon National University) Huh, Jung-Eun (Department of Food and Nutrition, Kangwon National University) Kim, Mi-Hyun (Division of Immunopharmacology, College of Pharmacy, Sungkyunkwan University) Pyo, Suh-kneung (Department of Food and Nutrition, Kangwon National University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제30권 제6호
발행연도
2007.1
수록면
743 - 749 (7page)

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The magnesium (Mg) and manganese (Mn) were evaluated for its effectiveness as an immunomodulator in rats. The treatments were as follows: Group 1, AIN-93M diet (0.05% Mg, 0.001% Mn); Group 2, high-dose Mg (0.1% Mg, 0.001% Mn); and Group 3, high dose Mn(0.05% Mg 0.01% Mn) (n-12/group). After 12 weeks of supplementation, rats were sacrificed to assess the effect on a range of innate responses (tumoricidal activity, oxidative burst and nitric oxide) and the mitogen-stimulated lymphoproliferative response. Immune function was significantly affected in both the high dose Mg and the Mn group. Lymphocyte proliferative responses and NK cell activity were measured in pooled spleen from each group. The mitogen response of lymphocytes to LPS in the spleen was significantly reduced in high dose Mg-treated groups, whereas the response to ConA was not affected in both high dose minerals-treated groups. The reactive oxygen species level of macrophages was decreased in both groups. These effects were more pronounced in high dose Mg-treated group. Nitric oxide production was also decreased in high dose minerals-treated group. In addition, tumoricidal activities of splenic NK cell and peritoneal macrophage in mineral exposed rats were significantly increased. Moreover, percent death of macrophage was reduced in two groups receiving high dose mineral supplements. Taken together, the present data suggest that high dose trace minerals exert a differential effect on the function of immune cells.

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