Reduced prostaglandin F-2 alpha release from blood mononuclear leukocytes after oral supplementation of omega 3 fatty acids: the OmegAD studyShow others and affiliations
2010 (English)In: Journal of Lipid Research, ISSN 0022-2275, E-ISSN 1539-7262, Vol. 51, no 5, p. 1179-1185Article in journal (Refereed) Published
Abstract [en]
Omega-3 fatty acids, e. g., dokosahexaenoic acid (DHA) and eikosapentaenoic acid (EPA), ameliorate inflammatory reactions by various mechanisms, but the role of prostaglandins remains unclear. Our aim was to determine if dietary supplementation with a DHA-rich fish oil influenced the release of PGF(2 alpha) from peripheral blood mononuclear cells (PBMC). In the OmegAD study, 174 Alzheimer disease patients received either 1.7 g DHA plus 0.6 g EPA or a placebo daily for six months. PBMCs from the 21 ( 9 on fish oil and 12 on placebo) first-randomized patients were stimulated with either lipopolysaccharide (LPS) or phytohemagglutinin (PHA) before and after 6 months. Our results showed that plasma concentrations of DHA and EPA increased significantly at 6 months in the omega-3 group. PGF(2 alpha) release from LPS- ( but not from PHA-) stimulated PBMC was significantly diminished in this group; no change was noted in the placebo group. PGF(2 alpha) changes correlated inversely with changes in plasma DHA and EPA. Decreased IL-6 and IL-1(beta) levels correlated with decreased PGF(2 alpha) levels. The stimulus-specific PGF(2 alpha) release from PBMC after 6 months of oral supplementation with the DHA-rich fish oil might be one event related to reduced inflammatory reactions associated with omega-3 fatty acid intake.
Place, publisher, year, edition, pages
American Society for Biochemistry and Molecular Biology, 2010. Vol. 51, no 5, p. 1179-1185
Keywords [en]
DHA, EPA, LPS, Omega-3 fatty acid, PBMC, PGF, PHA, prostaglandin
National Category
Medical and Health Sciences Other Clinical Medicine
Identifiers
URN: urn:nbn:se:oru:diva-79168DOI: 10.1194/jlr.M002667ISI: 000276633100033PubMedID: 19965584Scopus ID: 2-s2.0-77951085015OAI: oai:DiVA.org:oru-79168DiVA, id: diva2:1385468
Note
This study was supported by Swedish Medical Research Council Grants 19X-05991 and 71XS-13135. This study was also supported by funding from the Swedish Association against Rheumatism; Karolinska Institutet; Huddinge University Hospital; the Funds of Å Wiberg; King Gustaf V:s 80-year; Uggla; N Svartz; Vårdal; Swedish Cancer Society; Cancer Society of Stockholm; Swedish Alzheimer Foundation; and the regional agreement on medical training and clinical research (ALF) between Stockholm County Council and the Karolinska Institutet. Clinical Trials. Gov Identifier: NCT00211159.
2020-01-142020-01-142020-01-21Bibliographically approved