Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease

Soluble amyloid-beta oligomers (Aβo) start to accumulate in the human brain one to two decades before any clinical symptoms of Alzheimer's disease (AD) and are implicated in synapse loss, one of the best predictors of memory decline that characterize the illness. Cognitive impairment in AD was...

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Main Authors: Audrey Hector, Jonathan Brouillette
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Molecular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnmol.2020.600084/full
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spelling doaj-de6c79add7ca4f33aa2485f2bddab86d2021-01-07T06:24:08ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992021-01-011310.3389/fnmol.2020.600084600084Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's DiseaseAudrey HectorJonathan BrouilletteSoluble amyloid-beta oligomers (Aβo) start to accumulate in the human brain one to two decades before any clinical symptoms of Alzheimer's disease (AD) and are implicated in synapse loss, one of the best predictors of memory decline that characterize the illness. Cognitive impairment in AD was traditionally thought to result from a reduction in synaptic activity which ultimately induces neurodegeneration. More recent evidence indicates that in the early stages of AD synaptic failure is, at least partly, induced by neuronal hyperactivity rather than hypoactivity. Here, we review the growing body of evidence supporting the implication of soluble Aβo on the induction of neuronal hyperactivity in AD animal models, in vitro, and in humans. We then discuss the impact of Aβo-induced hyperactivity on memory performance, cell death, epileptiform activity, gamma oscillations, and slow wave activity. We provide an overview of the cellular and molecular mechanisms that are emerging to explain how Aβo induce neuronal hyperactivity. We conclude by providing an outlook on the impact of hyperactivity for the development of disease-modifying interventions at the onset of AD.https://www.frontiersin.org/articles/10.3389/fnmol.2020.600084/fullamyloid-beta oligomershyperactivityneurodegenerationmemoryepileptiform activitygamma oscillations
collection DOAJ
language English
format Article
sources DOAJ
author Audrey Hector
Jonathan Brouillette
spellingShingle Audrey Hector
Jonathan Brouillette
Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease
Frontiers in Molecular Neuroscience
amyloid-beta oligomers
hyperactivity
neurodegeneration
memory
epileptiform activity
gamma oscillations
author_facet Audrey Hector
Jonathan Brouillette
author_sort Audrey Hector
title Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease
title_short Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease
title_full Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease
title_fullStr Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease
title_full_unstemmed Hyperactivity Induced by Soluble Amyloid-β Oligomers in the Early Stages of Alzheimer's Disease
title_sort hyperactivity induced by soluble amyloid-β oligomers in the early stages of alzheimer's disease
publisher Frontiers Media S.A.
series Frontiers in Molecular Neuroscience
issn 1662-5099
publishDate 2021-01-01
description Soluble amyloid-beta oligomers (Aβo) start to accumulate in the human brain one to two decades before any clinical symptoms of Alzheimer's disease (AD) and are implicated in synapse loss, one of the best predictors of memory decline that characterize the illness. Cognitive impairment in AD was traditionally thought to result from a reduction in synaptic activity which ultimately induces neurodegeneration. More recent evidence indicates that in the early stages of AD synaptic failure is, at least partly, induced by neuronal hyperactivity rather than hypoactivity. Here, we review the growing body of evidence supporting the implication of soluble Aβo on the induction of neuronal hyperactivity in AD animal models, in vitro, and in humans. We then discuss the impact of Aβo-induced hyperactivity on memory performance, cell death, epileptiform activity, gamma oscillations, and slow wave activity. We provide an overview of the cellular and molecular mechanisms that are emerging to explain how Aβo induce neuronal hyperactivity. We conclude by providing an outlook on the impact of hyperactivity for the development of disease-modifying interventions at the onset of AD.
topic amyloid-beta oligomers
hyperactivity
neurodegeneration
memory
epileptiform activity
gamma oscillations
url https://www.frontiersin.org/articles/10.3389/fnmol.2020.600084/full
work_keys_str_mv AT audreyhector hyperactivityinducedbysolubleamyloidboligomersintheearlystagesofalzheimersdisease
AT jonathanbrouillette hyperactivityinducedbysolubleamyloidboligomersintheearlystagesofalzheimersdisease
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