Kazim Syed Faraz, Seo Joon Ho, Bianchi Riccardo, Larson Chloe S, Sharma Abhijeet, Wong Robert K S, Gorbachev Kirill Y, Pereira Ana C
Department of Neurology and Nash Family Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
The Robert F. Furchgott Center for Neural and Behavioral Science, and Department of Physiology and Pharmacology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, NY 11203.
eNeuro. 2021 Apr 23;8(2). doi: 10.1523/ENEURO.0418-20.2020. Print 2021 Mar-Apr.
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.
阿尔茨海默病(AD)是最常见的神经退行性疾病,通常导致老年人痴呆。最近的证据表明,包括过度同步、振荡节律活动改变、中间神经元功能障碍和突触抑制在内的网络异常可能是AD认知衰退的关键介质。在本综述中,我们讨论了AD中神经元网络兴奋性的特征,以及Aβ和tau在诱导网络过度兴奋中的作用。许多携带导致Aβ生成增加的基因突变的患者在斑块形成之前就患有癫痫发作和癫痫。同样,过度磷酸化tau的病理积累与海马体的过度兴奋有关。我们阐述了tau和Aβ在AD神经元过度兴奋中的共同和不同作用,以及可作为未来实验模板的假说。