Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/2922
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dc.contributor.authorKennedy, Sean Roberten_UK
dc.contributor.authorLeaver, Michaelen_UK
dc.contributor.authorCampbell, Patricken_UK
dc.contributor.authorZheng, Xiaozhongen_UK
dc.contributor.authorDick, James Ren_UK
dc.contributor.authorTocher, Douglas Ren_UK
dc.date.accessioned2012-09-03T12:19:15Z-
dc.date.available2012-09-03T12:19:15Z-
dc.date.issued2006-05en_UK
dc.identifier.urihttp://hdl.handle.net/1893/2922-
dc.description.abstractThe overall objective is to test the hypothesis that conjugated linoleic acid (CLA) has beneficial effects in Atlantic salmon through affecting lipid and fatty acid metabolism. The specific aims of the present study were to determine the effects of CLA on some key pathways of fatty acid metabolism including fatty acid oxidation and highly unsaturated fatty acid (HUFA) synthesis. Salmon smolts were fed diets containing two levels of fish oil (low, ~18% and high, ~34%) containing three levels of CLA (a 1:1 mixture of 9-cis,trans-11 and trans-10,cis-12 at 0, 1 and 2% of diet) for 3 months. The effects of dietary CLA on HUFA synthesis and β-oxidation were measured and the expression of key genes in the fatty acid oxidation and HUFA synthesis pathways, and potentially important transcription factors, peroxisome proliferators activated receptors (PPARs), determined in selected tissues. Liver HUFA synthesis and desaturase gene expression was increased by dietary CLA and decreased by high dietary oil content. Carnitine palmitoyltransferase-I (CPT-I) activity and gene expression were generally increased by CLA in muscle tissues although dietary oil content had relatively little effect. In general CPT-I activity or gene expression was not correlated with β-oxidation. Dietary CLA tended to increase PPARα and β gene expression in both liver and muscle tissues, and PPARγ in liver. In summary, gene expression and activity of the fatty acid pathways were altered in response to dietary CLA and/or oil content, with data suggesting that PPARs are also regulated in response to CLA. Correlations were observed between dietary CLA, liver HUFA synthesis and desaturase gene expression, and liver PPARα expression, and also between dietary CLA, CPT-I expression and activity, and PPARα expression in muscle tissues. In conclusion, this study suggests that dietary CLA has effects on fatty acid metabolism in Atlantic salmon and on PPAR transcription factors. However, further work is required to assess the potential of CLA as a dietary supplement, and the role of PPARs in the regulation of lipid metabolism in fish.en_UK
dc.language.isoenen_UK
dc.publisherSpringer / American Oil Chemists' Society (AOCS)en_UK
dc.relationKennedy SR, Leaver M, Campbell P, Zheng X, Dick JR & Tocher DR (2006) Influence of Dietary Oil Content and Conjugated Linoleic Acid (CLA) on Lipid Metabolism Enzyme Activities and Gene Expression in Tissues of Atlantic Salmon (Salmo salar L.). Lipids, 41 (5), pp. 423-436. http://www.springerlink.com/content/0024-4201/; https://doi.org/10.1007/s11745-006-5116-4en_UK
dc.rightsPublished in Lipids by Springer / American Oil Chemists' Society (AOCS).; The final publication is available at www.springerlink.comen_UK
dc.subjectCLAen_UK
dc.subjectAtlantic salmonen_UK
dc.subjectLipiden_UK
dc.subjectFatty aciden_UK
dc.subjectMetabolismen_UK
dc.subjectGene expressionen_UK
dc.subjectLiveren_UK
dc.subjectMuscleen_UK
dc.subjectAtlantic salmonen_UK
dc.subjectDietary supplementsen_UK
dc.subjectFishes Feeding and feedsen_UK
dc.subjectLinoleic aciden_UK
dc.titleInfluence of Dietary Oil Content and Conjugated Linoleic Acid (CLA) on Lipid Metabolism Enzyme Activities and Gene Expression in Tissues of Atlantic Salmon (Salmo salar L.)en_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1007/s11745-006-5116-4en_UK
dc.citation.jtitleLipidsen_UK
dc.citation.issn1558-9307en_UK
dc.citation.issn0024-4201en_UK
dc.citation.volume41en_UK
dc.citation.issue5en_UK
dc.citation.spage423en_UK
dc.citation.epage436en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusAM - Accepted Manuscripten_UK
dc.identifier.urlhttp://www.springerlink.com/content/0024-4201/en_UK
dc.author.emaildrt1@stir.ac.uken_UK
dc.citation.date18/02/2007en_UK
dc.contributor.affiliationUniversity of Stirlingen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationBioMar U.K.en_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.identifier.isiWOS:000239575600003en_UK
dc.identifier.scopusid2-s2.0-33746944990en_UK
dc.identifier.wtid837015en_UK
dc.contributor.orcid0000-0002-3155-0844en_UK
dc.contributor.orcid0000-0002-8603-9410en_UK
dcterms.dateAccepted2007-02-18en_UK
dc.date.filedepositdate2011-04-14en_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionAMen_UK
local.rioxx.authorKennedy, Sean Robert|en_UK
local.rioxx.authorLeaver, Michael|0000-0002-3155-0844en_UK
local.rioxx.authorCampbell, Patrick|en_UK
local.rioxx.authorZheng, Xiaozhong|en_UK
local.rioxx.authorDick, James R|en_UK
local.rioxx.authorTocher, Douglas R|0000-0002-8603-9410en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2011-04-14en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/all-rights-reserved|2011-04-14|en_UK
local.rioxx.filenameL9915RevisedMS.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0024-4201en_UK
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