4.5 Article

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

Journal

NEUROBIOLOGY OF AGING
Volume 94, Issue -, Pages 265-270

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2020.06.004

Keywords

Alzheimer's disease; THY-Tau22; Tau; EEG; Epilepsy; Seizures

Funding

  1. Hauts-de-France (PARTEN-AIRR, COGNADORA)
  2. ANR (ADORASTrAU)
  3. CoEN [5008]
  4. Programs d'Investissements d'Avenir LabEx (excellence laboratory) DISTALZ (Development of Innovative Strategies for a Transdisciplinary approach to ALZheimer's disease)
  5. Fondation pour la Recherche Medicale
  6. France Alzheimer/Fondation de France
  7. FHU VasCog research network (Lille, France)
  8. Fondation Vaincre Alzheimer
  9. Fondation Plan Alzheimer
  10. Inserm, CNRS, Universite Lille, Lille Metropole Communaute Urbaine, DN2M
  11. Fondation pour la Recherche Medicale [SPF20160936000]
  12. US National Institutes of Health (NIH) [NS103740, NS065957]
  13. CURE foundation (CURE Catalyst Award)
  14. New Jersey Commission for Brain Injury Research

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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 A beta pathology. (C) 2020 Elsevier Inc. All rights reserved.

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