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dc.contributor.authorWalker, R.E.
dc.contributor.authorRichter, C.K.
dc.contributor.authorSkulas-Ray, A.C.
dc.contributor.authorFlock, M.R.
dc.contributor.authorHarsch, B.A.
dc.contributor.authorAnnevelink, C.E.
dc.contributor.authorKris-Etherton, P.M.
dc.contributor.authorJensen, G.L.
dc.contributor.authorShearer, G.C.
dc.date.accessioned2024-08-18T05:33:23Z
dc.date.available2024-08-18T05:33:23Z
dc.date.issued2023-05
dc.identifier.citationWalker, R. E., Richter, C. K., Skulas-Ray, A. C., Flock, M. R., Harsch, B. A., Annevelink, C. E., ... & Shearer, G. C. (2023). Effect of omega-3 ethyl esters on the triglyceride-rich lipoprotein response to endotoxin challenge in healthy young men. Journal of Lipid Research, 64(5).
dc.identifier.issn0022-2275
dc.identifier.pmid36907552
dc.identifier.doi10.1016/j.jlr.2023.100353
dc.identifier.urihttp://hdl.handle.net/10150/674549
dc.description.abstractOxylipins are produced enzymatically from polyunsaturated fatty acids, are abundant in triglyceride-rich lipoproteins (TGRLs), and mediate inflammatory processes. Inflammation elevates TGRL concentrations, but it is unknown if the fatty acid and oxylipin compositions change. In this study, we investigated the effect of prescription ω-3 acid ethyl esters (P-OM3; 3.4 g/d EPA þ DHA) on the lipid response to an endotoxin challenge (lipopolysaccharide; 0.6 ng/kg body weight). Healthy young men (N = 17) were assigned 8-12 weeks of P-OM3 and olive oil control in a randomized order crossover study. Following each treatment period, subjects received endotoxin challenge, and the time-dependent TGRL composition was observed. Postchallenge, arachidonic acid was 16% [95% CI: 4%, 28%] lower than baseline at 8 h with control. P-OM3 increased TGRL ω-3 fatty acids (EPA 24% [15%, 34%]; DHA 14% [5%, 24%]). The timing of ω-6 oxylipin responses differed by class; arachidonic acid-derived alcohols peaked at 2 h, while linoleic acid-derived alcohols peaked at 4 h (pint = 0.006). P-OM3 increased EPA alcohols by 161% [68%, 305%] and DHA epoxides by 178% [47%, 427%] at 4 h compared to control. In conclusion, this study shows that TGRL fatty acid and oxylipin composition changes following endotoxin challenge. P-OM3 alters the TGRL response to endotoxin challenge by increasing availability of ω-3 oxylipins for resolution of the inflammatory response. © 2023 THE AUTHORS. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
dc.language.isoen
dc.publisherAmerican Society for Biochemistry and Molecular Biology Inc.
dc.rights© 2023 The Authors. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology. This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/).
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectchylomicrons
dc.subjectfatty acids
dc.subjectinflammation
dc.subjectlipopolysaccharide
dc.subjectlipoprotein kinetics
dc.subjectomega-3 acid ethyl esters
dc.subjectoxylipins
dc.subjectpolyunsaturated fatty acids
dc.subjecttriglycerides
dc.subjectVLDL
dc.titleEffect of omega-3 ethyl esters on the triglyceride-rich lipoprotein response to endotoxin challenge in healthy young men
dc.typeArticle
dc.typetext
dc.contributor.departmentDepartment of Nutritional Sciences, University of Arizona
dc.identifier.journalJournal of Lipid Research
dc.description.noteOpen access article
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitleJournal of Lipid Research
refterms.dateFOA2024-08-18T05:33:23Z


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© 2023 The Authors. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology. This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as © 2023 The Authors. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology. This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/).