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Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning
An increasing number of studies show that listeners often have difficulty hearing in situations with background noise, despite normal tuning curves in quiet. One potential source of this difficulty could be sensorineural changes in the auditory periphery (the ear). Signal in noise detection deficits...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890061/ https://www.ncbi.nlm.nih.gov/pubmed/33597563 http://dx.doi.org/10.1038/s41598-021-83115-1 |
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author | Ye, Yi Ihlefeld, Antje Rosen, Merri J. |
author_facet | Ye, Yi Ihlefeld, Antje Rosen, Merri J. |
author_sort | Ye, Yi |
collection | PubMed |
description | An increasing number of studies show that listeners often have difficulty hearing in situations with background noise, despite normal tuning curves in quiet. One potential source of this difficulty could be sensorineural changes in the auditory periphery (the ear). Signal in noise detection deficits also arise in animals raised with developmental conductive hearing loss (CHL), a manipulation that induces acoustic attenuation to model how sound deprivation changes the central auditory system. This model attributes perceptual deficits to central changes by assuming that CHL does not affect sensorineural elements in the periphery that could raise masked thresholds. However, because of efferent feedback, altering the auditory system could affect cochlear elements. Indeed, recent studies show that adult-onset CHL can cause cochlear synapse loss, potentially calling into question the assumption of an intact periphery in early-onset CHL. To resolve this issue, we tested the long-term peripheral effects of CHL via developmental bilateral malleus displacement. Using forward masking tuning curves, we compared peripheral tuning in animals raised with CHL vs age-matched controls. Using compound action potential measurements from the round window, we assessed inner hair cell synapse integrity. Results indicate that developmental CHL can cause minor synaptopathy. However, developmental CHL does not appreciably alter peripheral frequency tuning. |
format | Online Article Text |
id | pubmed-7890061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78900612021-02-22 Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning Ye, Yi Ihlefeld, Antje Rosen, Merri J. Sci Rep Article An increasing number of studies show that listeners often have difficulty hearing in situations with background noise, despite normal tuning curves in quiet. One potential source of this difficulty could be sensorineural changes in the auditory periphery (the ear). Signal in noise detection deficits also arise in animals raised with developmental conductive hearing loss (CHL), a manipulation that induces acoustic attenuation to model how sound deprivation changes the central auditory system. This model attributes perceptual deficits to central changes by assuming that CHL does not affect sensorineural elements in the periphery that could raise masked thresholds. However, because of efferent feedback, altering the auditory system could affect cochlear elements. Indeed, recent studies show that adult-onset CHL can cause cochlear synapse loss, potentially calling into question the assumption of an intact periphery in early-onset CHL. To resolve this issue, we tested the long-term peripheral effects of CHL via developmental bilateral malleus displacement. Using forward masking tuning curves, we compared peripheral tuning in animals raised with CHL vs age-matched controls. Using compound action potential measurements from the round window, we assessed inner hair cell synapse integrity. Results indicate that developmental CHL can cause minor synaptopathy. However, developmental CHL does not appreciably alter peripheral frequency tuning. Nature Publishing Group UK 2021-02-17 /pmc/articles/PMC7890061/ /pubmed/33597563 http://dx.doi.org/10.1038/s41598-021-83115-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ye, Yi Ihlefeld, Antje Rosen, Merri J. Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
title | Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
title_full | Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
title_fullStr | Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
title_full_unstemmed | Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
title_short | Conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
title_sort | conductive hearing loss during development does not appreciably alter the sharpness of cochlear tuning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890061/ https://www.ncbi.nlm.nih.gov/pubmed/33597563 http://dx.doi.org/10.1038/s41598-021-83115-1 |
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