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Influence of dietary supplementation with long-chain n-3 or n-6 polyunsaturated fatty acids on blood inflammatory cell populations and functions and on plasma soluble adhesion molecules in healthy adults

Influence of dietary supplementation with long-chain n-3 or n-6 polyunsaturated fatty acids on blood inflammatory cell populations and functions and on plasma soluble adhesion molecules in healthy adults
Influence of dietary supplementation with long-chain n-3 or n-6 polyunsaturated fatty acids on blood inflammatory cell populations and functions and on plasma soluble adhesion molecules in healthy adults
Greatly increasing the amounts of flaxseed oil [rich in ?-linolenic acid (ALNA)] or fish oil (FO); [rich in eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)] in the diet can decrease inflammatory cell functions and so might impair host defense. The objective of this study was to determine the effect of dietary supplementation with moderate levels of ALNA, ?-linolenic acid (GLA), arachidonic acid (ARA), DHA, or FO on inflammatory cell numbers and functions and on circulating levels of soluble adhesion molecules. Healthy subjects aged 55 to 75 yr consumed nine capsules per day for 12 wk. The capsules contained placebo oil (an 80:20 mix of palm and sunflowerseed oils) or blends of placebo oil with oils rich in ALNA, GLA, ARA, or DHA or FO. Subjects in these groups consumed 2 g ALNA; approximately 700 mg GLA, ARA, or DHA; or 1 g EPA plus DHA (720 mg EPA + 280 mg DHA) daily from the capsules. Total fat intake from the capsules was 4 g per day. None of the treatments affected inflammatory cell numbers in the bloodstream; neutrophil and monocyte phagocytosis or respiratory burst in response to E. coli; production of tumor necrosis factor-?, interleukin-1?, and interleukin-6 in response to bacterial lipopolysaccharide; or plasma concentrations of soluble intercellular adhesion molecule-1. In contrast, the ALNA and FO treatments decreased the plasma concentrations of soluble vascular cell adhesion molecule-1 (16 and 28% decrease, respectively) and soluble E-selectin (23 and 17% decrease, respectively). It is concluded that, in contrast to previous reports using higher amounts of these fatty acids, a moderate increase in consumption of long-chain n-6 or n-3 polyunsaturated fatty acids does not significantly affect inflammatory cell numbers or neutrophil and monocyte responses in humans and so would not be expected to cause immune impairment. Furthermore, we conclude that moderate levels of ALNA and FO, which could be incorporated into the diet, can decrease some markers of endothelial activation and that this mechanism of action may contribute to the reported health benefits of n-3 fatty acids.
0024-4201
1183-1193
Thies, F.
1e990f58-abab-4bbc-a83b-4d8b35002e23
Miles, E.A.
20332899-ecdb-4214-95bc-922dde36d416
Nebe-von-Caron, G.
23643830-7cc6-4988-b8a1-66e0c9b2ec12
Powell, J.R.
200c6083-6f7c-46ee-8c78-dc2405962895
Hurst, T.L.
874c7105-6bce-4720-aca2-36569a2ae003
Newsholme, E.A.
d85c20a1-ac67-4ec0-a0f4-ffa6ab3bb697
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Thies, F.
1e990f58-abab-4bbc-a83b-4d8b35002e23
Miles, E.A.
20332899-ecdb-4214-95bc-922dde36d416
Nebe-von-Caron, G.
23643830-7cc6-4988-b8a1-66e0c9b2ec12
Powell, J.R.
200c6083-6f7c-46ee-8c78-dc2405962895
Hurst, T.L.
874c7105-6bce-4720-aca2-36569a2ae003
Newsholme, E.A.
d85c20a1-ac67-4ec0-a0f4-ffa6ab3bb697
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6

Thies, F., Miles, E.A., Nebe-von-Caron, G., Powell, J.R., Hurst, T.L., Newsholme, E.A. and Calder, P.C. (2001) Influence of dietary supplementation with long-chain n-3 or n-6 polyunsaturated fatty acids on blood inflammatory cell populations and functions and on plasma soluble adhesion molecules in healthy adults. Lipids, 36 (11), 1183-1193.

Record type: Article

Abstract

Greatly increasing the amounts of flaxseed oil [rich in ?-linolenic acid (ALNA)] or fish oil (FO); [rich in eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA)] in the diet can decrease inflammatory cell functions and so might impair host defense. The objective of this study was to determine the effect of dietary supplementation with moderate levels of ALNA, ?-linolenic acid (GLA), arachidonic acid (ARA), DHA, or FO on inflammatory cell numbers and functions and on circulating levels of soluble adhesion molecules. Healthy subjects aged 55 to 75 yr consumed nine capsules per day for 12 wk. The capsules contained placebo oil (an 80:20 mix of palm and sunflowerseed oils) or blends of placebo oil with oils rich in ALNA, GLA, ARA, or DHA or FO. Subjects in these groups consumed 2 g ALNA; approximately 700 mg GLA, ARA, or DHA; or 1 g EPA plus DHA (720 mg EPA + 280 mg DHA) daily from the capsules. Total fat intake from the capsules was 4 g per day. None of the treatments affected inflammatory cell numbers in the bloodstream; neutrophil and monocyte phagocytosis or respiratory burst in response to E. coli; production of tumor necrosis factor-?, interleukin-1?, and interleukin-6 in response to bacterial lipopolysaccharide; or plasma concentrations of soluble intercellular adhesion molecule-1. In contrast, the ALNA and FO treatments decreased the plasma concentrations of soluble vascular cell adhesion molecule-1 (16 and 28% decrease, respectively) and soluble E-selectin (23 and 17% decrease, respectively). It is concluded that, in contrast to previous reports using higher amounts of these fatty acids, a moderate increase in consumption of long-chain n-6 or n-3 polyunsaturated fatty acids does not significantly affect inflammatory cell numbers or neutrophil and monocyte responses in humans and so would not be expected to cause immune impairment. Furthermore, we conclude that moderate levels of ALNA and FO, which could be incorporated into the diet, can decrease some markers of endothelial activation and that this mechanism of action may contribute to the reported health benefits of n-3 fatty acids.

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More information

Published date: 2001
Additional Information: Paper no. L8763

Identifiers

Local EPrints ID: 26028
URI: http://eprints.soton.ac.uk/id/eprint/26028
ISSN: 0024-4201
PURE UUID: f47349d6-8e6d-47a9-8a69-f06a393a2e5b
ORCID for E.A. Miles: ORCID iD orcid.org/0000-0002-8643-0655
ORCID for P.C. Calder: ORCID iD orcid.org/0000-0002-6038-710X

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Date deposited: 24 Apr 2006
Last modified: 08 Jan 2022 02:42

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Contributors

Author: F. Thies
Author: E.A. Miles ORCID iD
Author: G. Nebe-von-Caron
Author: J.R. Powell
Author: T.L. Hurst
Author: E.A. Newsholme
Author: P.C. Calder ORCID iD

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