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Depositordc.contributorOren, Iris
Funderdc.contributor.otherMRC - Medical Research Councilen_UK
Funderdc.contributor.otherAlzheimer's Societyen_UK
Spatial Coveragedc.coverage.spatialUKen_UK
Data Creatordc.creatorBrown, Rosalind
Data Creatordc.creatorGonzalez-Sulser, Alfredo
Data Creatordc.creatorJones, Mary
Data Creatordc.creatorChou, Robert Chang-Chih
Data Creatordc.creatorHemonnot, Anne-Laure
Data Creatordc.creatorRibchester, Richard R
Data Creatordc.creatorOren, Iris
Date Accessioneddc.date.accessioned2018-03-08T15:36:56Z
Date Availabledc.date.available2018-03-27T04:15:30Z
Citationdc.identifier.citationBrown, Rosalind; Gonzalez-Sulser, Alfredo; Jones, Mary; Chou, Robert Chang-Chih; Hemonnot, Anne-Laure; Ribchester, Richard R; Oren, Iris. (2018). Circadian and brain state modulation of network hyperexcitability in Alzheimer's disease - rodent datasets, [dataset]. University of Edinburgh. Edinburgh Medical School. Biomedical Sciences. https://doi.org/10.7488/ds/2319.en
Persistent Identifierdc.identifier.urihttps://hdl.handle.net/10283/3041
Persistent Identifierdc.identifier.urihttps://doi.org/10.7488/ds/2319
Dataset Description (abstract)dc.description.abstractNetwork hyperexcitability is a feature of Alzheimer's disease (AD) as well as numerous transgenic mouse models of AD. While hyperexcitability in AD patients and AD animal models share certain features, the mechanistic overlap remains to be established. We aimed to identify features of network hyperexcitability in AD models that can be related to epileptiform activity signatures in AD patients. We studied network hyperexcitability in mice expressing amyloid precursor protein (APP) with mutations that cause familial AD, and compared a transgenic model that overexpresses human APP (J20), to a knock-in model expressing APP at physiological levels (APPNL/F). We recorded continuous long-term electrocorticogram activity from mice, and studied modulation by circadian cycle, behavioural, and brain state. We report that while J20s exhibit frequent inter-ictal spikes (IIS), APPNL/F mice do not. In J20 mice, IIS were most prevalent during daylight hours and the circadian modulation was associated with sleep. Further analysis of brain state revealed that IIS in J20s are associated with features of rapid-eye movement (REM) sleep. We found no evidence of cholinergic changes that may contribute to IIS-circadian coupling in J20s. In contrast to J20s, intracranial recordings capturing IIS in AD patients demonstrated frequent IIS in non-REM sleep. The salient differences in sleep-stage coupling of IIS in APP overexpressing mice and AD patients suggests that different mechanisms may underlie network hyperexcitability in mice and humans. We posit that sleep-stage coupling of IIS should be an important consideration in identifying mouse AD models that most closely recapitulate network hyperexcitability in human AD. This repository contains the data relating to the rodent experiments.en_UK
Languagedc.language.isoengen_UK
Publisherdc.publisherUniversity of Edinburgh. Edinburgh Medical School. Biomedical Sciencesen_UK
Relation (Is Referenced By)dc.relation.isreferencedbyhttps://doi.org/10.1523/ENEURO.0426-17.2018
Relation (Is Referenced By)dc.relation.isreferencedbyBrown, R, Lam, AD, Gonzalez-sulser, A, Ying, A, Jones, M, Chou, RC, Tzioras, M, Jordan, CY, Jedrasiak-cape, I, Hemonnot, A, Abou Jaoude, M, Cole, AJ, Cash, SS, Saito, T, Saido, T, Ribchester, RR, Hashemi, K & Oren, I 2018, 'Circadian and Brain State Modulation of Network Hyperexcitability in Alzheimer’s Disease', eNeuro. https://doi.org/10.1523/ENEURO.0426-17.2018
Rightsdc.rightsCreative Commons Attribution 4.0 International Public Licenseen
Subjectdc.subjectAlzheimer's diseaseen_UK
Subjectdc.subjectEEGen_UK
Subjectdc.subjectEpilepsyen_UK
Subject Classificationdc.subject.classificationMedicine and Dentistry::Pre-clinical Medicineen_UK
Titledc.titleCircadian and brain state modulation of network hyperexcitability in Alzheimer's disease - rodent datasetsen_UK
Typedc.typedataseten_UK

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