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Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid

A common feature in the Alzheimer’s disease (AD) brain is the presence of acetylcholinesterase (AChE) which is commonly associated with β-amyloid plaques and neurofibrillary tangles (NFT). Although our understanding of the relationship between AChE and the pathological features of AD is incomplete,...

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Autores principales: García-Ayllón, María-Salud, Small, David H., Avila, Jesús, Sáez-Valero, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171929/
https://www.ncbi.nlm.nih.gov/pubmed/21949503
http://dx.doi.org/10.3389/fnmol.2011.00022
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author García-Ayllón, María-Salud
Small, David H.
Avila, Jesús
Sáez-Valero, Javier
author_facet García-Ayllón, María-Salud
Small, David H.
Avila, Jesús
Sáez-Valero, Javier
author_sort García-Ayllón, María-Salud
collection PubMed
description A common feature in the Alzheimer’s disease (AD) brain is the presence of acetylcholinesterase (AChE) which is commonly associated with β-amyloid plaques and neurofibrillary tangles (NFT). Although our understanding of the relationship between AChE and the pathological features of AD is incomplete, increasing evidence suggests that both β-amyloid protein (Aβ) and abnormally hyperphosphorylated tau (P-tau) can influence AChE expression. We also review recent findings which suggest the possible role of AChE in the development of a vicious cycle of Aβ and P-tau dysregulation and discuss the limited and temporary effect of therapeutic intervention with AChE inhibitors.
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spelling pubmed-31719292011-09-23 Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid García-Ayllón, María-Salud Small, David H. Avila, Jesús Sáez-Valero, Javier Front Mol Neurosci Neuroscience A common feature in the Alzheimer’s disease (AD) brain is the presence of acetylcholinesterase (AChE) which is commonly associated with β-amyloid plaques and neurofibrillary tangles (NFT). Although our understanding of the relationship between AChE and the pathological features of AD is incomplete, increasing evidence suggests that both β-amyloid protein (Aβ) and abnormally hyperphosphorylated tau (P-tau) can influence AChE expression. We also review recent findings which suggest the possible role of AChE in the development of a vicious cycle of Aβ and P-tau dysregulation and discuss the limited and temporary effect of therapeutic intervention with AChE inhibitors. Frontiers Research Foundation 2011-09-13 /pmc/articles/PMC3171929/ /pubmed/21949503 http://dx.doi.org/10.3389/fnmol.2011.00022 Text en Copyright © 2011 García-Ayllón, Small, Avila and Sáez-Valero. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Neuroscience
García-Ayllón, María-Salud
Small, David H.
Avila, Jesús
Sáez-Valero, Javier
Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid
title Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid
title_full Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid
title_fullStr Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid
title_full_unstemmed Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid
title_short Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid
title_sort revisiting the role of acetylcholinesterase in alzheimer’s disease: cross-talk with p-tau and β-amyloid
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171929/
https://www.ncbi.nlm.nih.gov/pubmed/21949503
http://dx.doi.org/10.3389/fnmol.2011.00022
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