Blast-induced cochlear synaptopathy in chinchillas

Abstract When exposed to continuous high-level noise, cochlear neurons are more susceptible to damage than hair cells (HCs): exposures causing temporary threshold shifts (TTS) without permanent HC damage can destroy ribbon synapses, permanently silencing the cochlear neurons they formerly activated....

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Autores principales: T. T. Hickman, C. Smalt, J. Bobrow, T. Quatieri, M. C. Liberman
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/bfa059d400cd4dcc99674651cda9b1a1
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spelling oai:doaj.org-article:bfa059d400cd4dcc99674651cda9b1a12021-12-02T11:40:25ZBlast-induced cochlear synaptopathy in chinchillas10.1038/s41598-018-28924-72045-2322https://doaj.org/article/bfa059d400cd4dcc99674651cda9b1a12018-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-28924-7https://doaj.org/toc/2045-2322Abstract When exposed to continuous high-level noise, cochlear neurons are more susceptible to damage than hair cells (HCs): exposures causing temporary threshold shifts (TTS) without permanent HC damage can destroy ribbon synapses, permanently silencing the cochlear neurons they formerly activated. While this “hidden hearing loss” has little effect on thresholds in quiet, the neural degeneration degrades hearing in noise and may be an important elicitor of tinnitus. Similar sensory pathologies are seen after blast injury, even if permanent threshold shift (PTS) is minimal. We hypothesized that, as for continuous-noise, blasts causing only TTS can also produce cochlear synaptopathy with minimal HC loss. To test this, we customized a shock tube design to generate explosive-like impulses, exposed anesthetized chinchillas to blasts with peak pressures from 160–175 dB SPL, and examined the resultant cochlear dysfunction and histopathology. We found exposures that cause large >40 dB TTS with minimal PTS or HC loss often cause synapse loss of 20–45%. While synaptopathic continuous-noise exposures can affect large areas of the cochlea, blast-induced synaptopathy was more focal, with localized damage foci in midcochlear and basal regions. These results clarify the pathology underlying blast-induced sensory dysfunction, and suggest possible links between blast injury, hidden hearing loss, and tinnitus.T. T. HickmanC. SmaltJ. BobrowT. QuatieriM. C. LibermanNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
T. T. Hickman
C. Smalt
J. Bobrow
T. Quatieri
M. C. Liberman
Blast-induced cochlear synaptopathy in chinchillas
description Abstract When exposed to continuous high-level noise, cochlear neurons are more susceptible to damage than hair cells (HCs): exposures causing temporary threshold shifts (TTS) without permanent HC damage can destroy ribbon synapses, permanently silencing the cochlear neurons they formerly activated. While this “hidden hearing loss” has little effect on thresholds in quiet, the neural degeneration degrades hearing in noise and may be an important elicitor of tinnitus. Similar sensory pathologies are seen after blast injury, even if permanent threshold shift (PTS) is minimal. We hypothesized that, as for continuous-noise, blasts causing only TTS can also produce cochlear synaptopathy with minimal HC loss. To test this, we customized a shock tube design to generate explosive-like impulses, exposed anesthetized chinchillas to blasts with peak pressures from 160–175 dB SPL, and examined the resultant cochlear dysfunction and histopathology. We found exposures that cause large >40 dB TTS with minimal PTS or HC loss often cause synapse loss of 20–45%. While synaptopathic continuous-noise exposures can affect large areas of the cochlea, blast-induced synaptopathy was more focal, with localized damage foci in midcochlear and basal regions. These results clarify the pathology underlying blast-induced sensory dysfunction, and suggest possible links between blast injury, hidden hearing loss, and tinnitus.
format article
author T. T. Hickman
C. Smalt
J. Bobrow
T. Quatieri
M. C. Liberman
author_facet T. T. Hickman
C. Smalt
J. Bobrow
T. Quatieri
M. C. Liberman
author_sort T. T. Hickman
title Blast-induced cochlear synaptopathy in chinchillas
title_short Blast-induced cochlear synaptopathy in chinchillas
title_full Blast-induced cochlear synaptopathy in chinchillas
title_fullStr Blast-induced cochlear synaptopathy in chinchillas
title_full_unstemmed Blast-induced cochlear synaptopathy in chinchillas
title_sort blast-induced cochlear synaptopathy in chinchillas
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/bfa059d400cd4dcc99674651cda9b1a1
work_keys_str_mv AT tthickman blastinducedcochlearsynaptopathyinchinchillas
AT csmalt blastinducedcochlearsynaptopathyinchinchillas
AT jbobrow blastinducedcochlearsynaptopathyinchinchillas
AT tquatieri blastinducedcochlearsynaptopathyinchinchillas
AT mcliberman blastinducedcochlearsynaptopathyinchinchillas
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