Hyperexcitability and seizures in the THY-Tau22 mouse model of tauopathy.


Journal

Neurobiology of aging
ISSN: 1558-1497
Titre abrégé: Neurobiol Aging
Pays: United States
ID NLM: 8100437

Informations de publication

Date de publication:
10 2020
Historique:
received: 01 04 2020
revised: 20 05 2020
accepted: 05 06 2020
pubmed: 18 7 2020
medline: 30 6 2021
entrez: 18 7 2020
Statut: ppublish

Résumé

Epileptic seizures constitute a significant comorbidity of Alzheimer's disease (AD), which are recapitulated in transgenic mouse models of amyloidogenesis. Here, we sought to evaluate the potential role of tau pathology regarding seizure occurrence. To this end, we performed intra-hippocampal electroencephalogram (EEG) recordings and PTZ (pentylenetetrazol) seizure threshold tests in THY-Tau22 transgenic mice of AD-like tau pathology. We demonstrate that despite a lack of spontaneous epileptiform activity in Tau22 mice, the animals display increased PTZ-induced seizure susceptibility and mortality. The increased propensity for induced seizures in THY-Tau22 mutants correlates with astrogliosis and increased expression of adenosine kinase, consistent with increased network excitability. These data support an impact of tau pathology toward AD-associated seizures and suggest that tau pathology may contribute to seizure generation in AD independent of Aβ pathology.

Identifiants

pubmed: 32679397
pii: S0197-4580(20)30195-0
doi: 10.1016/j.neurobiolaging.2020.06.004
pmc: PMC7483348
mid: NIHMS1605843
pii:
doi:

Substances chimiques

tau Proteins 0
Pentylenetetrazole WM5Z385K7T

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-270

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS065957
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS103740
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

Victoria Gomez-Murcia (V)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France; Alzheimer & Tauopathies, LabEx DISTALZ, LiCEND, Lille, France.

Ursula Sandau (U)

Department of Anesthesiology and Perioperative Medicine, Oregon Health and Sciences University, Portland, OR, USA.

Barbara Ferry (B)

Centre of Research in Neuroscience Lyon, CNRS UMR 5292 - INSERM U 1028 - Université Claude Bernard Lyon 1, Bron, France.

Sandrine Parrot (S)

Centre of Research in Neuroscience Lyon, CNRS UMR 5292 - INSERM U 1028 - Université Claude Bernard Lyon 1, Bron, France.

Cyril Laurent (C)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.

Marie Basquin (M)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.

Luc Buée (L)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France.

Detlev Boison (D)

Department of Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ, USA. Electronic address: detlev.boison@rutgers.edu.

David Blum (D)

University of Lille, Inserm, CHU Lille, U1172 - LilNCog - Lille Neuroscience & Cognition, Lille, France. Electronic address: david.blum@inserm.fr.

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