DIETARY POLYUNSATURATED FATTY-ACID EFFECTS ON IMMUNE CELLS OF THE PORCINE LUNG

Citation
Jj. Turek et al., DIETARY POLYUNSATURATED FATTY-ACID EFFECTS ON IMMUNE CELLS OF THE PORCINE LUNG, Journal of leukocyte biology, 56(5), 1994, pp. 599-604
Citations number
44
Categorie Soggetti
Immunology,Hematology
ISSN journal
07415400
Volume
56
Issue
5
Year of publication
1994
Pages
599 - 604
Database
ISI
SICI code
0741-5400(1994)56:5<599:DPFEOI>2.0.ZU;2-C
Abstract
The effects of various dietary polyunsaturated fatty acids (PUFAs) on the function of immune cells of the porcine lung was studied. Groups o f six pigs were fed diets containing 10.5 % corn oil [CO; enriched in linoleic acid (18:2, n-6)], linseed oil (LO; enriched in alpha-linolen ic acid (18:3, n-3)], menhaden oil (MO; enriched in eicosapentaenoic ( 20:5; n-3) and docosahexaenoic (22:6; n-3) acids], linseed + corn oil (1:1; LC), and menhaden + corn oil (1:1; MC) for 28-30 days. Basal lev els of alveolar macrophage (m phi) tumor necrosis factor-alpha (TNF-al pha) production were higher (P < .05) for LC- and MC-fed pigs than for CO- and LO-fed pigs. Lipopolysaccharide (LPS)-stimulated LC and MC m phi s produced more TNF than m phi s from pigs fed CO, LO, and MO diet s. Macrophages from pigs receiving the CO and LC diets had higher (P < .05) levels of leucine aminopeptidase than m phi s from the other die tary groups. Lipopolysaccharide did not increase m phi nitrite product ion over basal levels except in the MO diet group. However, LPS-stimul ated m phi s from the CO, MO, and LC dietary groups produced more nitr ite than m phi s from MC-fed pigs. Alveolar lymphocytes from pigs rece iving the MC diet produced more T cell growth factors than LO and MO m phi s. Alveolar m phi s from the different dietary groups did not dif fer in their capacity for non-immune-mediated phagocytosis of fluoresc ent latex beads. These results indicate that dietary PUFAs can modulat e some functions of porcine alveolar immune cells and that this may pr ove significant for host response to respiratory disease agents.