The specific objectives of the proposed research are to determine the chemical compounds of selenium deposited in tissues as influenced by the administered forms using both tissue cultures and the live animal, to study the induction of selenoproteins by selenium, and to investigate the influence of selenium deficiency on immunity. Radioactive selenite, selcnomethionine and selenocystine will be administered to rats and lambs, and the chemical forms present in intestinal contents, intestinal mucosa, blood and liver determined. The metabolic changes occurring in these selenium compounds are planned to be determined by intestinal perfusion techniques, cannulation of the mesenteric and portal veins, and in vitro incubations of intestinal contents, mucosa cells and tissue cellular fractions. Tissue cultures are planned to determine selenium requirements of, the uptake and incorporation of, and the chemical forms when fibroblasts are grown with selenite, selenomethionine or selenocystine. Chromatography on ion exchange resin columns and gel filtration methods are planned techniques to determine the chemical forms of selenium. Since most of the selenium is present as organic compounds in plants, but selenite has been used to treat deficiencies it is important to obtain more information on metabolism of various selenium containing compounds. Selenium will be injected into selenium deficient rats and lambs, and the relative rates of synthesis of the selenoproteins measured by gel filtration of tissue cytosols at various times afterwards. The use of protein inhibitors is planned to determine whether protein synthesis is necessary for selenium incorporation into these proteins. In further studies, rats are planned to be fed various levels of dietary selenium and the deposition of selenium in cytosolic proteins determined by gel filtration. The immunity studies are planned with sheep using in vivo antibody response to bovine viral diarrhea virus vaccine, and with mitogen-induced lymphocyte blastogenesis in vitro, a test of the functional capacity of the immune system. An understanding of the metabolism of various selenium compounds will be valuable for assessing the implications of this element in human health.
Park, Yeong-Chul; Kim, Jong-Bong; Heo, Yong et al. (2004) Metabolism of subtoxic level of selenite by double-perfused small intestine in rats. Biol Trace Elem Res 98:143-57 |
Whanger, P D (2001) Selenium and the brain: a review. Nutr Neurosci 4:81-97 |
Alabi, N S; Beilstein, M A; Whanger, P D (2000) Chemical forms of selenium present in rat and ram spermatozoa. Biol Trace Elem Res 76:161-73 |
Gu, Q P; Sun, Y; Ream, L W et al. (2000) Selenoprotein W accumulates primarily in primate skeletal muscle, heart, brain and tongue. Mol Cell Biochem 204:49-56 |
Whanger, P D (2000) Selenoprotein W: a review. Cell Mol Life Sci 57:1846-52 |
Gu, Q P; Beilstein, M A; Barofsky, E et al. (1999) Purification, characterization, and glutathione binding to selenoprotein W from monkey muscle. Arch Biochem Biophys 361:25-33 |
Yeh, J Y; Vendeland, S C; Gu, Q et al. (1997) Dietary selenium increases selenoprotein W levels in rat tissues. J Nutr 127:2165-72 |
Whanger, P D; Vendeland, S C; Gu, Q P et al. (1997) Selenoprotein W cDNAs from five species of animals. Biomed Environ Sci 10:190-7 |
Gu, Q P; Beilstein, M A; Vendeland, S C et al. (1997) Conserved features of selenocysteine insertion sequence (SECIS) elements in selenoprotein W cDNAs from five species. Gene 193:187-96 |
Yeh, J Y; Gu, Q P; Beilstein, M A et al. (1997) Selenium influences tissue levels of selenoprotein W in sheep. J Nutr 127:394-402 |
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