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dc.contributor.authorWibrand, Karinen_US
dc.contributor.authorBerge, Kjetilen_US
dc.contributor.authorMessaoudi, Michaëlen_US
dc.contributor.authorDuffaud, Anaïsen_US
dc.contributor.authorPanja, Debabrataen_US
dc.contributor.authorBramham, Clive R.en_US
dc.contributor.authorBurri, Lenaen_US
dc.date.accessioned2014-09-16T09:35:44Z
dc.date.available2014-09-16T09:35:44Z
dc.date.issued2013-01-25eng
dc.identifier.issn1476-511X
dc.identifier.urihttps://hdl.handle.net/1956/8483
dc.description.abstractBackground: The purpose of the study was to evaluate the effects of krill oil (KO) on cognition and depression-like behaviour in rats. Methods: Cognition was assessed using the Aversive Light Stimulus Avoidance Test (ALSAT). The Unavoidable Aversive Light Stimulus (UALST) and the Forced Swimming Test (FST) were used to evaluate the antidepressant-like effects of KO. Imipramine (IMIP) was used as the antidepressant reference substance. Results: After 7 weeks of KO intake, both males and females treated with KO were significantly better in discriminating between the active and the inactive levers in the ALSAT from day 1 of training (p<0.01). Both KO and IMIP prevented resignation/depression on the third day in the UALST. Similarly, a shorter immobility time was observed for the KO and IMIP groups compared to the control in the FST (p<0.001). These data support a robust antidepressant-like potential and beneficial cognitive effect of KO. Changes in expression of synaptic plasticity-related genes in the prefrontal cortex and hippocampus were also investigated. mRNA for brain-derived neurotrophic factor (Bdnf) was specifically upregulated in the hippocampus of female rats receiving 7 weeks of KO supplementation (p=0.04) and a similar trend was observed in males (p=0.08). Males also exhibited an increase in prefrontal cortex expression of Arc mRNA, a key protein in long-term synaptic plasticity (p=0.05). IMIP induced clear effects on several plasticity related genes including Bdnf and Arc. Conclusions: These results indicate that active components (eicosapentaenoic acid, docosahexaenoic acid and astaxanthin) in KO facilitate learning processes and provide antidepressant-like effects. Our findings also suggest that KO might work through different physiological mechanisms than IMIP.en_US
dc.language.isoengeng
dc.publisherBioMed Centraleng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0eng
dc.subjectBDNFeng
dc.subjectCognitioneng
dc.subjectDepressioneng
dc.subjectImipramineeng
dc.subjectKrill oileng
dc.subjectOmega-3eng
dc.subjectFatty acidseng
dc.subjectPhospholipidseng
dc.titleEnhanced cognitive function and antidepressant-like effects after krill oil supplementation in ratsen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2013-08-23T08:55:03Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2014 Wibrand et al.; licensee BioMed Central Ltd.
dc.rights.holderKarin Wibrand et al.; licensee BioMed Central Ltd.
dc.source.articlenumber6
dc.identifier.doihttps://doi.org/10.1186/1476-511x-12-6
dc.identifier.cristin1038448
dc.source.journalLipids in Health and Disease
dc.source.4012


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Except where otherwise noted, this item's license is described as Attribution CC BY