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Marine omega-3 fatty acids and inflammation

Marine omega-3 fatty acids and inflammation
Marine omega-3 fatty acids and inflammation
Marine n-3 polyunsaturated fatty acids (PUFAs) may influence inflammation through a variety of mechanisms; many of these are mediated by, or at least associated with, changes in fatty acid composition of inflammatory cell membranes. Changes in fatty acid composition can modify membrane fluidity, cell signaling mechanisms leading to altered gene expression, and the pattern of lipid mediator production. Human inflammatory cells are typically rich in the n-6 fatty acid arachidonic acid, but the contents of arachidonic acid and of the n-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) can be altered through oral administration of EPA and DHA. Eicosanoids produced from arachidonic acid (e.g. prostaglandin E2) have roles in inflammation. EPA also gives rise to eicosanoids and these may have differing properties from those of arachidonic acid-derived eicosanoids, often being less potent. EPA and DHA give rise to resolvins which are anti-inflammatory and inflammation resolving. Increased membrane content of EPA and DHA (and decreased arachidonic acid content) results in a changed pattern of production of eicosanoids and probably also of resolvins. Changing the fatty acid composition of inflammatory cells also affects the production of peptide mediators of inflammation (cytokines, adhesion molecules etc.). Thus, the fatty acid composition of human inflammatory cells influences their function; the contents of arachidonic acid, EPA and DHA appear to be especially important. The anti-inflammatory actions of marine n-3 PUFAs suggest that they may be of therapeutic use in diseases involving chronic inflammation
arachidonic acid, eicosapentaenoic acid, docosahexaenoic acid, eicosanoid, cytokine
1343-4594
233-244
Calder, Philip C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Calder, Philip C.
1797e54f-378e-4dcb-80a4-3e30018f07a6

Calder, Philip C. (2010) Marine omega-3 fatty acids and inflammation. Journal of Lipid Nutrition, 19 (2), 233-244.

Record type: Review

Abstract

Marine n-3 polyunsaturated fatty acids (PUFAs) may influence inflammation through a variety of mechanisms; many of these are mediated by, or at least associated with, changes in fatty acid composition of inflammatory cell membranes. Changes in fatty acid composition can modify membrane fluidity, cell signaling mechanisms leading to altered gene expression, and the pattern of lipid mediator production. Human inflammatory cells are typically rich in the n-6 fatty acid arachidonic acid, but the contents of arachidonic acid and of the n-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) can be altered through oral administration of EPA and DHA. Eicosanoids produced from arachidonic acid (e.g. prostaglandin E2) have roles in inflammation. EPA also gives rise to eicosanoids and these may have differing properties from those of arachidonic acid-derived eicosanoids, often being less potent. EPA and DHA give rise to resolvins which are anti-inflammatory and inflammation resolving. Increased membrane content of EPA and DHA (and decreased arachidonic acid content) results in a changed pattern of production of eicosanoids and probably also of resolvins. Changing the fatty acid composition of inflammatory cells also affects the production of peptide mediators of inflammation (cytokines, adhesion molecules etc.). Thus, the fatty acid composition of human inflammatory cells influences their function; the contents of arachidonic acid, EPA and DHA appear to be especially important. The anti-inflammatory actions of marine n-3 PUFAs suggest that they may be of therapeutic use in diseases involving chronic inflammation

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More information

Published date: 2010
Keywords: arachidonic acid, eicosapentaenoic acid, docosahexaenoic acid, eicosanoid, cytokine

Identifiers

Local EPrints ID: 190911
URI: http://eprints.soton.ac.uk/id/eprint/190911
ISSN: 1343-4594
PURE UUID: f2a38097-8d1c-4cbf-a272-786bc798ff01
ORCID for Philip C. Calder: ORCID iD orcid.org/0000-0002-6038-710X

Catalogue record

Date deposited: 16 Jun 2011 10:53
Last modified: 31 May 2023 01:33

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