Cargando…
Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice
Recent studies demonstrated that reversible continuous noise exposure may induce a temporary threshold shift (TTS) with a permanent degeneration of auditory nerve fibers, although hair cells remain intact. To probe the impact of TTS-inducing impulse noise exposure on hearing, CBA/J Mice were exposed...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698479/ https://www.ncbi.nlm.nih.gov/pubmed/34942983 http://dx.doi.org/10.3390/antiox10121880 |
_version_ | 1784620289350434816 |
---|---|
author | Gratias, Paul Nasr, Jamal Affortit, Corentin Ceccato, Jean-Charles François, Florence Casas, François Pujol, Rémy Pucheu, Sylvie Puel, Jean-Luc Wang, Jing |
author_facet | Gratias, Paul Nasr, Jamal Affortit, Corentin Ceccato, Jean-Charles François, Florence Casas, François Pujol, Rémy Pucheu, Sylvie Puel, Jean-Luc Wang, Jing |
author_sort | Gratias, Paul |
collection | PubMed |
description | Recent studies demonstrated that reversible continuous noise exposure may induce a temporary threshold shift (TTS) with a permanent degeneration of auditory nerve fibers, although hair cells remain intact. To probe the impact of TTS-inducing impulse noise exposure on hearing, CBA/J Mice were exposed to noise impulses with peak pressures of 145 dB SPL. We found that 30 min after exposure, the noise caused a mean elevation of ABR thresholds of ~30 dB and a reduction in DPOAE amplitude. Four weeks later, ABR thresholds and DPOAE amplitude were back to normal in the higher frequency region (8–32 kHz). At lower frequencies, a small degree of PTS remained. Morphological evaluations revealed a disturbance of the stereociliary bundle of outer hair cells, mainly located in the apical regions. On the other hand, the reduced suprathreshold ABR amplitudes remained until 4 weeks later. A loss of synapse numbers was observed 24 h after exposure, with full recovery two weeks later. Transmission electron microscopy revealed morphological changes at the ribbon synapses by two weeks post exposure. In addition, increased levels of oxidative stress were observed immediately after exposure, and maintained for a further 2 weeks. These results clarify the pathology underlying impulse noise-induced sensory dysfunction, and suggest possible links between impulse-noise injury, cochlear cell morphology, metabolic changes, and hidden hearing loss. |
format | Online Article Text |
id | pubmed-8698479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86984792021-12-24 Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice Gratias, Paul Nasr, Jamal Affortit, Corentin Ceccato, Jean-Charles François, Florence Casas, François Pujol, Rémy Pucheu, Sylvie Puel, Jean-Luc Wang, Jing Antioxidants (Basel) Article Recent studies demonstrated that reversible continuous noise exposure may induce a temporary threshold shift (TTS) with a permanent degeneration of auditory nerve fibers, although hair cells remain intact. To probe the impact of TTS-inducing impulse noise exposure on hearing, CBA/J Mice were exposed to noise impulses with peak pressures of 145 dB SPL. We found that 30 min after exposure, the noise caused a mean elevation of ABR thresholds of ~30 dB and a reduction in DPOAE amplitude. Four weeks later, ABR thresholds and DPOAE amplitude were back to normal in the higher frequency region (8–32 kHz). At lower frequencies, a small degree of PTS remained. Morphological evaluations revealed a disturbance of the stereociliary bundle of outer hair cells, mainly located in the apical regions. On the other hand, the reduced suprathreshold ABR amplitudes remained until 4 weeks later. A loss of synapse numbers was observed 24 h after exposure, with full recovery two weeks later. Transmission electron microscopy revealed morphological changes at the ribbon synapses by two weeks post exposure. In addition, increased levels of oxidative stress were observed immediately after exposure, and maintained for a further 2 weeks. These results clarify the pathology underlying impulse noise-induced sensory dysfunction, and suggest possible links between impulse-noise injury, cochlear cell morphology, metabolic changes, and hidden hearing loss. MDPI 2021-11-25 /pmc/articles/PMC8698479/ /pubmed/34942983 http://dx.doi.org/10.3390/antiox10121880 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gratias, Paul Nasr, Jamal Affortit, Corentin Ceccato, Jean-Charles François, Florence Casas, François Pujol, Rémy Pucheu, Sylvie Puel, Jean-Luc Wang, Jing Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice |
title | Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice |
title_full | Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice |
title_fullStr | Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice |
title_full_unstemmed | Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice |
title_short | Impulse Noise Induced Hidden Hearing Loss, Hair Cell Ciliary Changes and Oxidative Stress in Mice |
title_sort | impulse noise induced hidden hearing loss, hair cell ciliary changes and oxidative stress in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698479/ https://www.ncbi.nlm.nih.gov/pubmed/34942983 http://dx.doi.org/10.3390/antiox10121880 |
work_keys_str_mv | AT gratiaspaul impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT nasrjamal impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT affortitcorentin impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT ceccatojeancharles impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT francoisflorence impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT casasfrancois impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT pujolremy impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT pucheusylvie impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT pueljeanluc impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice AT wangjing impulsenoiseinducedhiddenhearinglosshaircellciliarychangesandoxidativestressinmice |