Leukocyte function in vitro after adding vitamins A, E, and Beta-Carotene

dc.citation.epage26en_US
dc.citation.spage23en_US
dc.contributor.authorEicher, S.D.
dc.contributor.authorMorrill, J.L.
dc.contributor.authorBlecha, Frank
dc.date.accessioned2011-05-12T18:12:53Z
dc.date.available2011-05-12T18:12:53Z
dc.date.issued2011-05-12
dc.date.published1992en_US
dc.description.abstractBlood neutrophils and pulmonary alveolar macrophages isolated from calves at 3 and 6 wk of age were cultured in medium without added vitamins or supplemented with vitamin A, vitamin E, vitamin A and vitamin E, or ßcarotene and vitamin E. Macrophage bactericidal activity improved with A-E supplementation compared to ß-carotene-E supplementation at wk 3. Neutrophil bactericidal activity decreased with all vitamin E treatments at wk 3 and with vitamins E and A-E at wk 6. Neutrophil phagocytosis improved at wk 3 with A, E, and A-E supplementations. The chemotactic index improved at wk 3 with ß-carotene- E compared to vitamin E alone and at wk 6 with vitamin E compared to vitamin A and control treatments. The retinol content of neutrophils at wk 3 was variable, but by wk 6, cells supplemented with A, E, or A-E had higher retinol concentrations than control cells. Neutrophil a-tocopherol concentrations at 3 wk increased over controls with vitamin E or ßcarotene- E supplementation, but at wk 6, vitamin E-supplemented cells were different only from vitamin A-supplemented cells. These data suggest that there are optimum plasma concentrations of vitamins A and E for leukocyte functions.en_US
dc.description.conferenceDairy Day, 1992, Kansas State University, Manhattan, KS, 1992
dc.identifier.urihttp://hdl.handle.net/2097/9148
dc.publisherKansas Agricultural Experiment Stationen_US
dc.relation.isPartOfDairy Day, 1992en_US
dc.relation.isPartOfKansas Agricultural Experiment Station contribution; no. 93-131-Sen_US
dc.subjectRetinolen_US
dc.subjectAlpha-Caroteneen_US
dc.subjectNeutrophilsen_US
dc.subjectMacrophagesen_US
dc.subjectCalvesen_US
dc.titleLeukocyte function in vitro after adding vitamins A, E, and Beta-Caroteneen_US
dc.typeConference paperen_US

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