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Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery
A growing number of research publications have illustrated the remarkable ability of the brain to reorganize itself in response to various sensory experiences. A traditional view of this plastic nature of the brain is that it is predominantly limited to short epochs during early development. Althoug...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649212/ https://www.ncbi.nlm.nih.gov/pubmed/29085312 http://dx.doi.org/10.3389/fpsyg.2017.01657 |
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author | Voss, Patrice Thomas, Maryse E. Cisneros-Franco, J. Miguel de Villers-Sidani, Étienne |
author_facet | Voss, Patrice Thomas, Maryse E. Cisneros-Franco, J. Miguel de Villers-Sidani, Étienne |
author_sort | Voss, Patrice |
collection | PubMed |
description | A growing number of research publications have illustrated the remarkable ability of the brain to reorganize itself in response to various sensory experiences. A traditional view of this plastic nature of the brain is that it is predominantly limited to short epochs during early development. Although examples showing that neuroplasticity exists outside of these finite time-windows have existed for some time, it is only recently that we have started to develop a fuller understanding of the different regulators that modulate and underlie plasticity. In this article, we will provide several lines of evidence indicating that mechanisms of neuroplasticity are extremely variable across individuals and throughout the lifetime. This variability is attributable to several factors including inhibitory network function, neuromodulator systems, age, sex, brain disease, and psychological traits. We will also provide evidence of how neuroplasticity can be manipulated in both the healthy and diseased brain, including recent data in both young and aged rats demonstrating how plasticity within auditory cortex can be manipulated pharmacologically and by varying the quality of sensory inputs. We propose that a better understanding of the individual differences that exist within the various mechanisms that govern experience-dependent neuroplasticity will improve our ability to harness brain plasticity for the development of personalized translational strategies for learning and recovery following brain injury or disease. |
format | Online Article Text |
id | pubmed-5649212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56492122017-10-30 Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery Voss, Patrice Thomas, Maryse E. Cisneros-Franco, J. Miguel de Villers-Sidani, Étienne Front Psychol Psychology A growing number of research publications have illustrated the remarkable ability of the brain to reorganize itself in response to various sensory experiences. A traditional view of this plastic nature of the brain is that it is predominantly limited to short epochs during early development. Although examples showing that neuroplasticity exists outside of these finite time-windows have existed for some time, it is only recently that we have started to develop a fuller understanding of the different regulators that modulate and underlie plasticity. In this article, we will provide several lines of evidence indicating that mechanisms of neuroplasticity are extremely variable across individuals and throughout the lifetime. This variability is attributable to several factors including inhibitory network function, neuromodulator systems, age, sex, brain disease, and psychological traits. We will also provide evidence of how neuroplasticity can be manipulated in both the healthy and diseased brain, including recent data in both young and aged rats demonstrating how plasticity within auditory cortex can be manipulated pharmacologically and by varying the quality of sensory inputs. We propose that a better understanding of the individual differences that exist within the various mechanisms that govern experience-dependent neuroplasticity will improve our ability to harness brain plasticity for the development of personalized translational strategies for learning and recovery following brain injury or disease. Frontiers Media S.A. 2017-10-04 /pmc/articles/PMC5649212/ /pubmed/29085312 http://dx.doi.org/10.3389/fpsyg.2017.01657 Text en Copyright © 2017 Voss, Thomas, Cisneros-Franco and de Villers-Sidani. 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 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 | Psychology Voss, Patrice Thomas, Maryse E. Cisneros-Franco, J. Miguel de Villers-Sidani, Étienne Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery |
title | Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery |
title_full | Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery |
title_fullStr | Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery |
title_full_unstemmed | Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery |
title_short | Dynamic Brains and the Changing Rules of Neuroplasticity: Implications for Learning and Recovery |
title_sort | dynamic brains and the changing rules of neuroplasticity: implications for learning and recovery |
topic | Psychology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649212/ https://www.ncbi.nlm.nih.gov/pubmed/29085312 http://dx.doi.org/10.3389/fpsyg.2017.01657 |
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