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dc.contributor.authorWronikowska, Olga
dc.contributor.authorMichalak, Agnieszka
dc.contributor.authorSkalicka-Woźniak, Krystyna
dc.contributor.authorCrawford, Alexander Dettmar
dc.contributor.authorBudzynska, Barbara
dc.date.accessioned2020-11-11T10:52:35Z
dc.date.available2020-11-11T10:52:35Z
dc.date.created2020-04-26T12:40:40Z
dc.date.issued2020
dc.identifier.citationProgress in Neuro-psychopharmacology and Biological Psychiatry. 2020, 98, 109826, 1-10.en_US
dc.identifier.issn0278-5846
dc.identifier.urihttps://hdl.handle.net/11250/2687342
dc.description.abstractNicotine, the primary psychoactive component of tobacco, is the most widely used drug of abuse. Although the substance is well-known, there is still a lack of information concerning its long-term neurological and physiological effects and its mechanisms of action. In order to search for new, effective drugs in the therapy of nicotinism, as well as to design new drugs that exert positive nicotine-like effects, further experiments are needed, ideally also using new behavioural models and paradigms. A wide range of complex behaviours – including aggression, anxiety, long- and short-term memory, object discrimination and colour preference – have recently been comprehensively classified and characterized in the zebrafish model. Zebrafish offer an attractive experimental platform, based on a microscale in vivo bioassays, which can be used to investigate psychoactive drugs, their effects on the central nervous system and potential treatments of drug addictions. In this review, we present recent data revealing the potential of the zebrafish model to evaluate the effects and molecular mechanisms of nicotine by taking into consideration its impact on anxiety, learning and memory, addiction and social behaviours.en_US
dc.language.isoengen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleFishing for a deeper understanding of nicotine effects using zebrafish behavioural modelsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-10en_US
dc.source.volume98en_US
dc.source.journalProgress in Neuro-psychopharmacology and Biological Psychiatryen_US
dc.identifier.doi10.1016/j.pnpbp.2019.109826
dc.identifier.cristin1808077
dc.source.articlenumber109826en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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