Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/20004
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dc.contributor.authorHampel, Miriamen_UK
dc.contributor.authorBron, Jamesen_UK
dc.contributor.authorTaggart, Johnen_UK
dc.contributor.authorLeaver, Michaelen_UK
dc.date.accessioned2014-06-20T23:11:40Z-
dc.date.available2014-06-20T23:11:40Z-
dc.date.issued2014-06en_UK
dc.identifier.urihttp://hdl.handle.net/1893/20004-
dc.description.abstractConcerns are being expressed recently over possible environmental effects of human pharmaceuticals. Although the likelihood of acute toxicity is low, the continuous discharge of pharmaceuticals into the aquatic environment means that sublethal effects on non-target organisms need to be seriously considered. One-year-old Atlantic salmon parr were exposed to 7.85 ± 0.13 μg L-1 of the antidepressant drug Carbamazepine (CBZ) for five days to investigate changes of mRNA expression in the brain by means of a custom 17k Atlantic salmon cDNA microarray. The selected concentration is similar to upper levels that can be found in hospital and sewage treatment plant effluents. After treatment, 373 features were differently expressed with 26 showing up- or down-regulation of ≥2-fold (p ≤ 0.05). Among the mRNAs showing the highest change were the pituitary hormones encoding features somatolactin, prolactin and somatotropin, or growth hormone. Functional enrichment and network analyses of up- and down-regulated genes showed that CBZ induced a highly different gene expression profile in comparison to untreated organisms. CBZ induced expression of essential genes of the focal adhesion and extracellular matrix - receptor interaction pathways most likely through integrin alpha-6 (itga6) activation. Negative regulation of apoptotic process, extracellular matrix organization and heme biosynthesis were the most enriched biological process related GO-terms, with the simultaneous enrichment of collagen and extracellular region related cellular component GO-terms, and extracellular matrix structural constituent, hormone activity and chromatin binding molecular function related GO-terms. These results show that relatively low doses of CBZ may affect brain physiology in exposed salmon parr, targeting similar processes as in human, indicating a high degree of conservation of targets of CBZ action. However, and since the mRNAs showing most changes in expression are critical for adaptation to different stressors and life history transitions in Atlantic salmon, more research should be undertaken to assess CBZ effects to avoid impairment of normal development and maintenance of natural populations.en_UK
dc.language.isoenen_UK
dc.publisherElsevieren_UK
dc.relationHampel M, Bron J, Taggart J & Leaver M (2014) The antidepressant drug Carbamazepine induces differential transcriptome expression in the brain of Atlantic salmon, Salmo salar. Aquatic Toxicology, 151, pp. 114-123. https://doi.org/10.1016/j.aquatox.2013.12.018en_UK
dc.rightsThe publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.en_UK
dc.rights.urihttp://www.rioxx.net/licenses/under-embargo-all-rights-reserveden_UK
dc.subjectCarbamazepineen_UK
dc.subjectAtlantic salmonen_UK
dc.subjectcDNAen_UK
dc.subjectTranscriptome expressionen_UK
dc.subjectPituitary hormonesen_UK
dc.subjectFunctional enrichment and network analysisen_UK
dc.titleThe antidepressant drug Carbamazepine induces differential transcriptome expression in the brain of Atlantic salmon, Salmo salaren_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2999-12-31en_UK
dc.rights.embargoreason[Aquatic Toxicology 2014.pdf] The publisher does not allow this work to be made publicly available in this Repository therefore there is an embargo on the full text of the work.en_UK
dc.identifier.doi10.1016/j.aquatox.2013.12.018en_UK
dc.citation.jtitleAquatic Toxicologyen_UK
dc.citation.issn0166-445Xen_UK
dc.citation.volume151en_UK
dc.citation.spage114en_UK
dc.citation.epage123en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailm.j.leaver@stir.ac.uken_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.contributor.affiliationInstitute of Aquacultureen_UK
dc.identifier.isiWOS:000336188000015en_UK
dc.identifier.scopusid2-s2.0-84892170972en_UK
dc.identifier.wtid647588en_UK
dc.contributor.orcid0000-0003-3544-0519en_UK
dc.contributor.orcid0000-0002-3843-9663en_UK
dc.contributor.orcid0000-0002-3155-0844en_UK
dc.date.accepted2013-12-17en_UK
dcterms.dateAccepted2013-12-17en_UK
dc.date.filedepositdate2014-05-01en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorHampel, Miriam|en_UK
local.rioxx.authorBron, James|0000-0003-3544-0519en_UK
local.rioxx.authorTaggart, John|0000-0002-3843-9663en_UK
local.rioxx.authorLeaver, Michael|0000-0002-3155-0844en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2999-12-31en_UK
local.rioxx.licencehttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved||en_UK
local.rioxx.filenameAquatic Toxicology 2014.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source0166-445Xen_UK
Appears in Collections:Aquaculture Journal Articles

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