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Reduced ex vivo interleukin-6 production by dietary fish oil is not modified by linoleic acid intake in healthy men.

Reduced ex vivo interleukin-6 production by dietary fish oil is not modified by linoleic acid intake in healthy men.
Reduced ex vivo interleukin-6 production by dietary fish oil is not modified by linoleic acid intake in healthy men.
Fish oil (FO) is considered antiinflammatory, but evidence regarding its effect on human cytokine production is conflicting. High linoleic acid (LA) intake may impair any effects of FO. The aim of this study was to investigate how FO combined with high or low LA intake affected ex vivo cytokine production from cultures of whole blood, peripheral blood mononuclear cells (PBMC), and monocytes in healthy men. The study was a double-blinded, controlled, 2 x 2 factorial 8-wk intervention. Sixty-four healthy men were randomized to 5 mL/d FO or olive oil (OO) provided in capsules and to spreads and oils with high or low LA content, resulting in LA intakes of 7 ± 2% and 4 ± 1% energy, respectively. We measured eicosapentaenoic acid (EPA) in PBMC and stimulated cytokine production in whole blood and PBMC 24-h cultures before and immediately after intervention and after an 8-wk wash-out period, and in monocyte cultures immediately after intervention. PBMC-EPA was markedly increased by FO (P < 0.001). LA intake did not modify the incorporation of FO and tended to have only a slight effect on PBMC-EPA by itself (P = 0.06). Lipopolysaccharide (LPS)-stimulated whole-blood interleukin (IL)-6 production immediately after intervention was lower with FO than OO (P = 0.02) but did not correlate with PBMC-EPA in the FO groups (r = –0.12; P = 0.53; n = 31). The LA intake did not modify IL-6 production or the effect of FO. Neither FO nor LA intake affected the production of tumor necrosis factor-{alpha}, IL-10, or interferon-{gamma} in any of the cultures. In conclusion, FO intake reduced IL-6 production from LPS-stimulated whole blood in healthy men compared with OO, but the effect was not modified by the LA intake.
0022-3166
1410-1414
Damsgaard, C.T.
d14da9a1-7f01-475a-bb56-1f063611e3e1
Lauritzen, L.
927e0097-2d74-47f5-b819-052d500d8ae0
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Kjaer, T.R.
0bfbdb64-ef4b-4eb1-b2b7-ae2fcded56be
Frokiaer, H.
13e4d97d-9100-465f-9a80-34fd53aee6a8
Damsgaard, C.T.
d14da9a1-7f01-475a-bb56-1f063611e3e1
Lauritzen, L.
927e0097-2d74-47f5-b819-052d500d8ae0
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Kjaer, T.R.
0bfbdb64-ef4b-4eb1-b2b7-ae2fcded56be
Frokiaer, H.
13e4d97d-9100-465f-9a80-34fd53aee6a8

Damsgaard, C.T., Lauritzen, L., Calder, P.C., Kjaer, T.R. and Frokiaer, H. (2009) Reduced ex vivo interleukin-6 production by dietary fish oil is not modified by linoleic acid intake in healthy men. Journal of Nutrition, 139, 1410-1414. (doi:10.3945/jn.108.102269).

Record type: Article

Abstract

Fish oil (FO) is considered antiinflammatory, but evidence regarding its effect on human cytokine production is conflicting. High linoleic acid (LA) intake may impair any effects of FO. The aim of this study was to investigate how FO combined with high or low LA intake affected ex vivo cytokine production from cultures of whole blood, peripheral blood mononuclear cells (PBMC), and monocytes in healthy men. The study was a double-blinded, controlled, 2 x 2 factorial 8-wk intervention. Sixty-four healthy men were randomized to 5 mL/d FO or olive oil (OO) provided in capsules and to spreads and oils with high or low LA content, resulting in LA intakes of 7 ± 2% and 4 ± 1% energy, respectively. We measured eicosapentaenoic acid (EPA) in PBMC and stimulated cytokine production in whole blood and PBMC 24-h cultures before and immediately after intervention and after an 8-wk wash-out period, and in monocyte cultures immediately after intervention. PBMC-EPA was markedly increased by FO (P < 0.001). LA intake did not modify the incorporation of FO and tended to have only a slight effect on PBMC-EPA by itself (P = 0.06). Lipopolysaccharide (LPS)-stimulated whole-blood interleukin (IL)-6 production immediately after intervention was lower with FO than OO (P = 0.02) but did not correlate with PBMC-EPA in the FO groups (r = –0.12; P = 0.53; n = 31). The LA intake did not modify IL-6 production or the effect of FO. Neither FO nor LA intake affected the production of tumor necrosis factor-{alpha}, IL-10, or interferon-{gamma} in any of the cultures. In conclusion, FO intake reduced IL-6 production from LPS-stimulated whole blood in healthy men compared with OO, but the effect was not modified by the LA intake.

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Published date: 3 July 2009

Identifiers

Local EPrints ID: 147715
URI: http://eprints.soton.ac.uk/id/eprint/147715
ISSN: 0022-3166
PURE UUID: ae227f67-69e7-480e-b23c-d82dbe6d28e7
ORCID for P.C. Calder: ORCID iD orcid.org/0000-0002-6038-710X

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Date deposited: 26 Apr 2010 12:26
Last modified: 14 Mar 2024 02:39

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Contributors

Author: C.T. Damsgaard
Author: L. Lauritzen
Author: P.C. Calder ORCID iD
Author: T.R. Kjaer
Author: H. Frokiaer

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