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dc.contributor.authorParker, MOen_US
dc.contributor.authorAnnan, LVen_US
dc.contributor.authorKanellopoulos, AHen_US
dc.contributor.authorBrock, AJen_US
dc.contributor.authorCombe, FJen_US
dc.contributor.authorBaiamonte, Men_US
dc.contributor.authorTeh, MTen_US
dc.contributor.authorBrennan, CHen_US
dc.date.accessioned2016-07-04T12:05:57Z
dc.date.issued2014-12-03en_US
dc.date.submitted2016-07-04T11:31:04.196Z
dc.identifier.issn0278-5846en_US
dc.identifier.other10.1016/j.pnpbp.2014.03.011
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/13179
dc.description.abstract© 2014 Elsevier Inc. Exposure to moderate levels of ethanol during brain development has a number of effects on social behavior but the molecular mechanisms that mediate this are not well understood. Gaining a better understanding of these factors may help to develop therapeutic interventions in the future. Zebrafish offer a potentially useful model in this regard. Here, we introduce a zebrafish model of moderate prenatal ethanol exposure. Embryos were exposed to 20mM ethanol for seven days (48hpf-9dpf) and tested as adults for individual social behavior and shoaling. We also tested their basal anxiety with the novel tank diving test. We found that the ethanol-exposed fish displayed reductions in social approach and shoaling, and an increase in anxiety in the novel tank test. These behavioral differences corresponded to differences in hrt1aa, slc6a4 and oxtr expression. Namely, acute ethanol caused a spike in oxtr and ht1aa mRNA expression, which was followed by down-regulation at 7dpf, and an up-regulation in slc6a4 at 72hpf. This study confirms the utility of zebrafish as a model system for studying the molecular basis of developmental ethanol exposure. Furthermore, it proposes a putative developmental mechanism characterized by ethanol-induced OT inhibition leading to suppression of 5-HT and up-regulation of 5-HT1A, which leads, in turn, to possible homeostatic up-regulation of 5-HTT at 72hpf and subsequent imbalance of the 5-HT system.en_US
dc.description.sponsorshipMP was funded by project grant G1000053 from the National Centre for the Replacement, Reduction and Refinement of Animals in Research (NC3Rs; UK). CHB is a Royal Society (UK) Industrial Research Fellow.en_US
dc.format.extent94 - 100en_US
dc.language.isoenen_US
dc.relation.ispartofProgress in Neuro-Psychopharmacology and Biological Psychiatryen_US
dc.titleThe utility of zebrafish to study the mechanisms by which ethanol affects social behavior and anxiety during early brain developmenten_US
dc.typeArticle
dc.rights.holder2016 Elsevier B.V. or its licensors or contributors
dc.identifier.doi10.1016/j.pnpbp.2014.03.011en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume55en_US


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