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Comorbidities of early-onset temporal epilepsy: Cognitive, social, emotional, and morphologic dimensions

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    SYSNO ASEP0508570
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleComorbidities of early-onset temporal epilepsy: Cognitive, social, emotional, and morphologic dimensions
    Author(s) Mikulecká, Anna (FGU-C) RID, ORCID
    Druga, Rastislav (FGU-C) RID, ORCID, SAI
    Stuchlík, Aleš (FGU-C) RID, ORCID
    Mareš, Pavel (FGU-C) RID, ORCID
    Kubová, Hana (FGU-C) RID, ORCID
    Article numberUNSP 113005
    Source TitleExperimental Neurology. - : Elsevier - ISSN 0014-4886
    Roč. 320, Oct (2019)
    Number of pages14 s.
    Languageeng - English
    CountryUS - United States
    Keywordsanxiety ; anxiety ; depression ; epilepsy ; exploratory behavior ; hippocampus ; pilocarpine ; rats ; spatial learning ; status epilepticus
    Subject RIVFH - Neurology
    OECD categoryNeurosciences (including psychophysiology
    R&D ProjectsGA16-04726S GA ČR - Czech Science Foundation (CSF)
    GA17-04047S GA ČR - Czech Science Foundation (CSF)
    NV16-29857A GA MZd - Ministry of Health (MZ)
    Method of publishingLimited access
    Institutional supportFGU-C - RVO:67985823
    UT WOS000483420200027
    EID SCOPUS85068505495
    DOI10.1016/j.expneurol.2019.113005
    AnnotationEpilepsy, the most common neurologic disorder in childhood, is associated with a subset of psychiatric dysfunctions, including cognitive deficits, and alterations in emotionality (e.g., anxiety and depression) and social functioning. In the present study, we evaluated an integrative set of behavioral responses, including cognitive/ socio-cognitive and emotional dimensions, using a number of behavioral paradigms in the LiCl/pilocarpine model of status epilepticus (SE) in rats. The aims of the study were to examine whether SE affects: 1) non-associative learning (habituation of exploratory behavior), 2) investigatory response to an indifferent stimulus object, 3) sociability/social novelty preference, 4) social recognition or discrimination, and 4) short- and long-term memory in the Morris water maze (MWM). Finally, we investigated the morphology of key brain structures involved in the examined behavioral dysfunctions. SE did not affect habituation to an open-field arena in juvenile (P25), adolescent (P32), or adult (P80) rats. SE rats spent less time in the central part of the arena. SE adolescent rats (P32) displayed a higher number of rearings with a shorter duration. SE rats displayed a markedly attenuated investigatory response to an indifferent stimulus object. SE rats in all age groups demonstrated pronounced deficits in sociability and the preference for social novelty. In addition, SE rats spent a reduced amount of time investigating a juvenile rat upon first exposure. After 30 min re-exposure together with an additional, novel juvenile, the SE rats spent equal time investigating both juveniles. In the MWM task, acquisition was unimpaired but there was a deficit in delayed memory retention after 10 days. SE did not affect cognitive flexibility expressed by reversal learning. Together, these findings suggest that early-life SE leads to alterations in emotional/anxiety-related behavior and affects sociability/preference for social novelty and social discrimination. Early-life SE did not alter acquisition of spatial learning, but it impaired delayed retention. Using Fluoro Jade B staining performed 24 h after SE revealed apparent neurodegeneration in the dorsal hippocampus, mediodorsal thalamic nucleus and medial amygdala, brain areas that are critically involved in network underlying emotional behavior and cognitive functions.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2020
    Electronic addresshttps://doi.org/10.1016/j.expneurol.2019.113005
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