| Literature DB >> 33741601 |
Syed Faraz Kazim1, Joon Ho Seo1, Riccardo Bianchi2, Chloe S Larson1, Abhijeet Sharma1, Robert K S Wong2, Kirill Y Gorbachev1, Ana C Pereira3,4.
Abstract
Alzheimer's disease (AD) is the most frequent neurodegenerative disorder that commonly causes dementia in the elderly. Recent evidence indicates that network abnormalities, including hypersynchrony, altered oscillatory rhythmic activity, interneuron dysfunction, and synaptic depression, may be key mediators of cognitive decline in AD. In this review, we discuss characteristics of neuronal network excitability in AD, and the role of Aβ and tau in the induction of network hyperexcitability. Many patients harboring genetic mutations that lead to increased Aβ production suffer from seizures and epilepsy before the development of plaques. Similarly, pathologic accumulation of hyperphosphorylated tau has been associated with hyperexcitability in the hippocampus. We present common and divergent roles of tau and Aβ on neuronal hyperexcitability in AD, and hypotheses that could serve as a template for future experiments.Entities:
Keywords: amyloid β; neuronal excitability; seizures; tau
Year: 2021 PMID: 33741601 PMCID: PMC8174042 DOI: 10.1523/ENEURO.0418-20.2020
Source DB: PubMed Journal: eNeuro ISSN: 2373-2822