Publication:
Interval timing is disrupted in female 5xFAD mice: an indication of altered memory processes

dc.contributor.coauthorFertan, Emre
dc.contributor.coauthorAlkins, Kindree
dc.contributor.coauthorWong, Aimee A.
dc.contributor.coauthorBrown, Richard E.
dc.contributor.departmentN/A
dc.contributor.departmentDepartment of Psychology
dc.contributor.kuauthorGür, Ezgi
dc.contributor.kuauthorBalcı, Fuat
dc.contributor.kuprofilePhD Student
dc.contributor.kuprofileFaculty Member
dc.contributor.otherDepartment of Psychology
dc.contributor.schoolcollegeinstituteGraduate School of Social Sciences and Humanities
dc.contributor.schoolcollegeinstituteCollege of Social Sciences and Humanities
dc.contributor.yokidN/A
dc.contributor.yokid51269
dc.date.accessioned2024-11-10T00:09:38Z
dc.date.issued2019
dc.description.abstractTemporal information processing in the seconds-to-minutes range is disrupted in patients with Alzheimer's disease (AD). In this study, we investigated the timing behavior of the 5xFAD mouse model of AD in the peak interval (PI) procedure. Nine-month-old female mice were trained with sucrose solution reinforcement for their first response after a fixed-interval (FI) and tested in the inter-mixed non-reinforced PI trials that lasted longer than FI. Timing performance indices were estimated from steady-state timed anticipatory nose-poking responses in the PI trials. We found that the time of maximal reward expectancy (peak time) of the 5xFAD mice was significantly earlier than that of the wild-type (WT) controls with no differences in other indices of timing performance. These behavioral differences corroborate the findings of previous studies on the disruption of temporal associative memory abilities of 5xFAD mice and can be accounted for by the scalar timing theory based on altered long-term memory consolidation of temporal information in the 5xFAD mice. This is the first study to directly show an interval timing phenotype in a genetic mouse model of AD.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue7
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsorshipTurkiye Bilimsel ve Teknolojik Arastirma Kurumu [BIDEB 2211E, GEBIP-2015]
dc.description.sponsorshipNatural Sciences and Engineering Research Council of Canada [7441] Turkiye Bilimsel ve Teknolojik Arastirma Kurumu, Grant/Award Number: BIDEB 2211E
dc.description.sponsorshipTurkiye Bilimler Akademisi, Grant/Award Number: GEBIP-2015 award
dc.description.sponsorshipNatural Sciences and Engineering Research Council of Canada, Grant/Award Number: 7441
dc.description.volume97
dc.identifier.doi10.1002/jnr.24418
dc.identifier.eissn1097-4547
dc.identifier.issn0360-4012
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85064515299
dc.identifier.urihttp://dx.doi.org/10.1002/jnr.24418
dc.identifier.urihttps://hdl.handle.net/20.500.14288/17164
dc.identifier.wos476936600009
dc.keywordsAlzheimer's disease
dc.keywordsİnterval timing
dc.keywordsLong-term memory
dc.keywordsPeak interval
dc.keywordsPhenotyping
dc.keywordsTransgenic mice
dc.languageEnglish
dc.publisherWiley
dc.sourceJournal of Neuroscience Research
dc.subjectNeurosciences
dc.titleInterval timing is disrupted in female 5xFAD mice: an indication of altered memory processes
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0003-3103-2446
local.contributor.authorid0000-0003-3390-9352
local.contributor.kuauthorGür, Ezgi
local.contributor.kuauthorBalcı, Fuat
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relation.isOrgUnitOfPublication.latestForDiscoveryd5fc0361-3a0a-4b96-bf2e-5cd6b2b0b08c

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