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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...

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Autores principales: Gratias, Paul, Nasr, Jamal, Affortit, Corentin, Ceccato, Jean-Charles, François, Florence, Casas, François, Pujol, Rémy, Pucheu, Sylvie, Puel, Jean-Luc, Wang, Jing
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
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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.
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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
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