| Literature DB >> 33583024 |
Liudmila Sosulina1,2, Manuel Mittag3, Hans-Rüdiger Geis1, Kerstin Hoffmann3, Igor Klyubin4, Yingjie Qi4, Julia Steffen3, Detlef Friedrichs1, Niklas Henneberg1, Falko Fuhrmann1, Daniel Justus1, Kevin Keppler5, A Claudio Cuello6, Michael J Rowan4, Martin Fuhrmann3, Stefan Remy1,2.
Abstract
Neuronal network dysfunction is a hallmark of Alzheimer's disease (AD). However, the underlying pathomechanisms remain unknown. We analyzed the hippocampal micronetwork in transgenic McGill-R-Thy1-APP rats (APPtg) at the beginning of extracellular amyloid beta (Aβ) deposition. We established two-photon Ca2+ -imaging in vivo in the hippocampus of rats and found hyperactivity of CA1 neurons. Patch-clamp recordings in brain slices in vitro revealed increased neuronal input resistance and prolonged action potential width in CA1 pyramidal neurons. We did neither observe changes in synaptic inhibition, nor in excitation. Our data support the view that increased intrinsic excitability of CA1 neurons may precede inhibitory dysfunction at an early stage of Aβ-deposition and disease progression.Entities:
Keywords: Alzheimer's disease; Hippocampus; disease model; hyperexcitability; β-amyloidosis
Year: 2021 PMID: 33583024 DOI: 10.1111/jnc.15323
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372