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Neuronal epigenetics and the aging synapse

Two of the most salient phenotypes of aging are cognitive decline and loss of motor function, both of which are controlled by the nervous system. Cognition and muscle contraction require that neuronal synapses develop and maintain proper structure and function. We review the literature on how normal...

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Detalles Bibliográficos
Autores principales: Azpurua, Jorge, Eaton, Benjamin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444820/
https://www.ncbi.nlm.nih.gov/pubmed/26074775
http://dx.doi.org/10.3389/fncel.2015.00208
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author Azpurua, Jorge
Eaton, Benjamin A.
author_facet Azpurua, Jorge
Eaton, Benjamin A.
author_sort Azpurua, Jorge
collection PubMed
description Two of the most salient phenotypes of aging are cognitive decline and loss of motor function, both of which are controlled by the nervous system. Cognition and muscle contraction require that neuronal synapses develop and maintain proper structure and function. We review the literature on how normal physiological aging disrupts central and peripheral synapse function including the degradation of structure and/or control of neurotransmission. Here we also attempt to connect the work done on the epigenetics of aging to the growing literature of how epigenetic mechanisms control synapse structure and function. Lastly, we address possible roles of epigenetic mechanisms to explain why the basal rates of age-related dysfunction vary so widely across individuals.
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spelling pubmed-44448202015-06-12 Neuronal epigenetics and the aging synapse Azpurua, Jorge Eaton, Benjamin A. Front Cell Neurosci Neuroscience Two of the most salient phenotypes of aging are cognitive decline and loss of motor function, both of which are controlled by the nervous system. Cognition and muscle contraction require that neuronal synapses develop and maintain proper structure and function. We review the literature on how normal physiological aging disrupts central and peripheral synapse function including the degradation of structure and/or control of neurotransmission. Here we also attempt to connect the work done on the epigenetics of aging to the growing literature of how epigenetic mechanisms control synapse structure and function. Lastly, we address possible roles of epigenetic mechanisms to explain why the basal rates of age-related dysfunction vary so widely across individuals. Frontiers Media S.A. 2015-05-27 /pmc/articles/PMC4444820/ /pubmed/26074775 http://dx.doi.org/10.3389/fncel.2015.00208 Text en Copyright © 2015 Azpurua and Eaton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Azpurua, Jorge
Eaton, Benjamin A.
Neuronal epigenetics and the aging synapse
title Neuronal epigenetics and the aging synapse
title_full Neuronal epigenetics and the aging synapse
title_fullStr Neuronal epigenetics and the aging synapse
title_full_unstemmed Neuronal epigenetics and the aging synapse
title_short Neuronal epigenetics and the aging synapse
title_sort neuronal epigenetics and the aging synapse
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444820/
https://www.ncbi.nlm.nih.gov/pubmed/26074775
http://dx.doi.org/10.3389/fncel.2015.00208
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