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Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments
Age-related impairments in the primary auditory cortex (A1) include poor tuning selectivity, neural desynchronization, and degraded responses to low-probability sounds. These changes have been largely attributed to reduced inhibition in the aged brain, and are thought to contribute to substantial he...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775538/ https://www.ncbi.nlm.nih.gov/pubmed/24062649 http://dx.doi.org/10.3389/fnsys.2013.00052 |
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author | Kamal, Brishna Holman, Constance de Villers-Sidani, Etienne |
author_facet | Kamal, Brishna Holman, Constance de Villers-Sidani, Etienne |
author_sort | Kamal, Brishna |
collection | PubMed |
description | Age-related impairments in the primary auditory cortex (A1) include poor tuning selectivity, neural desynchronization, and degraded responses to low-probability sounds. These changes have been largely attributed to reduced inhibition in the aged brain, and are thought to contribute to substantial hearing impairment in both humans and animals. Since many of these changes can be partially reversed with auditory training, it has been speculated that they might not be purely degenerative, but might rather represent negative plastic adjustments to noisy or distorted auditory signals reaching the brain. To test this hypothesis, we examined the impact of exposing young adult rats to 8 weeks of low-grade broadband noise on several aspects of A1 function and structure. We then characterized the same A1 elements in aging rats for comparison. We found that the impact of noise exposure on A1 tuning selectivity, temporal processing of auditory signal and responses to oddball tones was almost indistinguishable from the effect of natural aging. Moreover, noise exposure resulted in a reduction in the population of parvalbumin inhibitory interneurons and cortical myelin as previously documented in the aged group. Most of these changes reversed after returning the rats to a quiet environment. These results support the hypothesis that age-related changes in A1 have a strong activity-dependent component and indicate that the presence or absence of clear auditory input patterns might be a key factor in sustaining adult A1 function. |
format | Online Article Text |
id | pubmed-3775538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37755382013-09-23 Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments Kamal, Brishna Holman, Constance de Villers-Sidani, Etienne Front Syst Neurosci Neuroscience Age-related impairments in the primary auditory cortex (A1) include poor tuning selectivity, neural desynchronization, and degraded responses to low-probability sounds. These changes have been largely attributed to reduced inhibition in the aged brain, and are thought to contribute to substantial hearing impairment in both humans and animals. Since many of these changes can be partially reversed with auditory training, it has been speculated that they might not be purely degenerative, but might rather represent negative plastic adjustments to noisy or distorted auditory signals reaching the brain. To test this hypothesis, we examined the impact of exposing young adult rats to 8 weeks of low-grade broadband noise on several aspects of A1 function and structure. We then characterized the same A1 elements in aging rats for comparison. We found that the impact of noise exposure on A1 tuning selectivity, temporal processing of auditory signal and responses to oddball tones was almost indistinguishable from the effect of natural aging. Moreover, noise exposure resulted in a reduction in the population of parvalbumin inhibitory interneurons and cortical myelin as previously documented in the aged group. Most of these changes reversed after returning the rats to a quiet environment. These results support the hypothesis that age-related changes in A1 have a strong activity-dependent component and indicate that the presence or absence of clear auditory input patterns might be a key factor in sustaining adult A1 function. Frontiers Media S.A. 2013-09-17 /pmc/articles/PMC3775538/ /pubmed/24062649 http://dx.doi.org/10.3389/fnsys.2013.00052 Text en Copyright © 2013 Kamal, Holman and de Villers-Sidani. 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 Kamal, Brishna Holman, Constance de Villers-Sidani, Etienne Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
title | Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
title_full | Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
title_fullStr | Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
title_full_unstemmed | Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
title_short | Shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
title_sort | shaping the aging brain: role of auditory input patterns in the emergence of auditory cortical impairments |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775538/ https://www.ncbi.nlm.nih.gov/pubmed/24062649 http://dx.doi.org/10.3389/fnsys.2013.00052 |
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