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Sirtuins in neurodegenerative diseases: an update on potential mechanisms

Silent information regulator 2 proteins (sirtuins or SIRTs) are a group of deacetylases (or deacylases) whose activities are dependent on and regulated by nicotinamide adenine dinucleotide (NAD(+)). Compelling evidence supports that sirtuins play major roles in many aspects of physiology, especially...

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Autores principales: Min, Sang-Won, Sohn, Peter D., Cho, Seo-Hyun, Swanson, Raymond A., Gan, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782645/
https://www.ncbi.nlm.nih.gov/pubmed/24093018
http://dx.doi.org/10.3389/fnagi.2013.00053
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author Min, Sang-Won
Sohn, Peter D.
Cho, Seo-Hyun
Swanson, Raymond A.
Gan, Li
author_facet Min, Sang-Won
Sohn, Peter D.
Cho, Seo-Hyun
Swanson, Raymond A.
Gan, Li
author_sort Min, Sang-Won
collection PubMed
description Silent information regulator 2 proteins (sirtuins or SIRTs) are a group of deacetylases (or deacylases) whose activities are dependent on and regulated by nicotinamide adenine dinucleotide (NAD(+)). Compelling evidence supports that sirtuins play major roles in many aspects of physiology, especially in pathways related to aging – the predominant and unifying risk factor for neurodegenerative diseases. In this review, we highlight the molecular mechanisms underlying the protective effects of sirtuins in neurodegenerative diseases, focusing on protein homeostasis, neural plasticity, mitochondrial function, and sustained chronic inflammation. We will also examine the potential and challenges of targeting sirtuin pathways to block these pathogenic pathways.
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spelling pubmed-37826452013-10-03 Sirtuins in neurodegenerative diseases: an update on potential mechanisms Min, Sang-Won Sohn, Peter D. Cho, Seo-Hyun Swanson, Raymond A. Gan, Li Front Aging Neurosci Neuroscience Silent information regulator 2 proteins (sirtuins or SIRTs) are a group of deacetylases (or deacylases) whose activities are dependent on and regulated by nicotinamide adenine dinucleotide (NAD(+)). Compelling evidence supports that sirtuins play major roles in many aspects of physiology, especially in pathways related to aging – the predominant and unifying risk factor for neurodegenerative diseases. In this review, we highlight the molecular mechanisms underlying the protective effects of sirtuins in neurodegenerative diseases, focusing on protein homeostasis, neural plasticity, mitochondrial function, and sustained chronic inflammation. We will also examine the potential and challenges of targeting sirtuin pathways to block these pathogenic pathways. Frontiers Media S.A. 2013-09-25 /pmc/articles/PMC3782645/ /pubmed/24093018 http://dx.doi.org/10.3389/fnagi.2013.00053 Text en Copyright © Min, Sohn, Cho, Swanson and Gan. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or 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
Min, Sang-Won
Sohn, Peter D.
Cho, Seo-Hyun
Swanson, Raymond A.
Gan, Li
Sirtuins in neurodegenerative diseases: an update on potential mechanisms
title Sirtuins in neurodegenerative diseases: an update on potential mechanisms
title_full Sirtuins in neurodegenerative diseases: an update on potential mechanisms
title_fullStr Sirtuins in neurodegenerative diseases: an update on potential mechanisms
title_full_unstemmed Sirtuins in neurodegenerative diseases: an update on potential mechanisms
title_short Sirtuins in neurodegenerative diseases: an update on potential mechanisms
title_sort sirtuins in neurodegenerative diseases: an update on potential mechanisms
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782645/
https://www.ncbi.nlm.nih.gov/pubmed/24093018
http://dx.doi.org/10.3389/fnagi.2013.00053
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