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Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model
Damage to cochlear outer hair cells (OHCs) usually affects frequency selectivity in proportion to hearing threshold increase. However, the current clinical heuristics that attributes poor hearing performance despite near-normal auditory sensitivity to auditory neuropathy or “hidden” synaptopathy ove...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832037/ https://www.ncbi.nlm.nih.gov/pubmed/29662891 http://dx.doi.org/10.1155/2018/6280969 |
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author | Souchal, Marion Labanca, Ludimila Alves da Silva Carvalho, Sirley Macedo de Resende, Luciana Blavignac, Christelle Avan, Paul Giraudet, Fabrice |
author_facet | Souchal, Marion Labanca, Ludimila Alves da Silva Carvalho, Sirley Macedo de Resende, Luciana Blavignac, Christelle Avan, Paul Giraudet, Fabrice |
author_sort | Souchal, Marion |
collection | PubMed |
description | Damage to cochlear outer hair cells (OHCs) usually affects frequency selectivity in proportion to hearing threshold increase. However, the current clinical heuristics that attributes poor hearing performance despite near-normal auditory sensitivity to auditory neuropathy or “hidden” synaptopathy overlooks possible underlying OHC impairment. Here, we document the part played by OHCs in influencing suprathreshold auditory performance in the presence of noise in a mouse model of progressive hair cell degeneration, the CD1 strain, at postnatal day 18–30 stages when high-frequency auditory thresholds remained near-normal. Nonetheless, total loss of high-frequency distortion product otoacoustic emissions pointed to nonfunctioning basal OHCs. This “discordant profile” came with a huge low-frequency shift of masking tuning curves that plot the level of interfering sound necessary to mask the response to a probe tone, against interfering frequency. Histology revealed intense OHC hair bundle abnormalities in the basal cochlea uncharacteristically associated with OHC survival and preserved coupling with the tectorial membrane. This pattern dismisses the superficial diagnosis of “hidden” neuropathy while underpinning a disorganization of cochlear frequency mapping with optimistic high-frequency auditory thresholds perhaps because responses to high frequencies are apically shifted. The audiometric advantage of frequency transposition is offset by enhanced masking by low-frequency sounds, a finding essential for guiding rehabilitation. |
format | Online Article Text |
id | pubmed-5832037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-58320372018-04-16 Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model Souchal, Marion Labanca, Ludimila Alves da Silva Carvalho, Sirley Macedo de Resende, Luciana Blavignac, Christelle Avan, Paul Giraudet, Fabrice Biomed Res Int Research Article Damage to cochlear outer hair cells (OHCs) usually affects frequency selectivity in proportion to hearing threshold increase. However, the current clinical heuristics that attributes poor hearing performance despite near-normal auditory sensitivity to auditory neuropathy or “hidden” synaptopathy overlooks possible underlying OHC impairment. Here, we document the part played by OHCs in influencing suprathreshold auditory performance in the presence of noise in a mouse model of progressive hair cell degeneration, the CD1 strain, at postnatal day 18–30 stages when high-frequency auditory thresholds remained near-normal. Nonetheless, total loss of high-frequency distortion product otoacoustic emissions pointed to nonfunctioning basal OHCs. This “discordant profile” came with a huge low-frequency shift of masking tuning curves that plot the level of interfering sound necessary to mask the response to a probe tone, against interfering frequency. Histology revealed intense OHC hair bundle abnormalities in the basal cochlea uncharacteristically associated with OHC survival and preserved coupling with the tectorial membrane. This pattern dismisses the superficial diagnosis of “hidden” neuropathy while underpinning a disorganization of cochlear frequency mapping with optimistic high-frequency auditory thresholds perhaps because responses to high frequencies are apically shifted. The audiometric advantage of frequency transposition is offset by enhanced masking by low-frequency sounds, a finding essential for guiding rehabilitation. Hindawi 2018-02-13 /pmc/articles/PMC5832037/ /pubmed/29662891 http://dx.doi.org/10.1155/2018/6280969 Text en Copyright © 2018 Marion Souchal et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Souchal, Marion Labanca, Ludimila Alves da Silva Carvalho, Sirley Macedo de Resende, Luciana Blavignac, Christelle Avan, Paul Giraudet, Fabrice Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model |
title | Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model |
title_full | Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model |
title_fullStr | Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model |
title_full_unstemmed | Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model |
title_short | Transient Abnormalities in Masking Tuning Curve in Early Progressive Hearing Loss Mouse Model |
title_sort | transient abnormalities in masking tuning curve in early progressive hearing loss mouse model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832037/ https://www.ncbi.nlm.nih.gov/pubmed/29662891 http://dx.doi.org/10.1155/2018/6280969 |
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