Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice

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Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice. / Jensen, Jane Bjerg; Lysaght, Andrew C; Liberman, M Charles; Qvortrup, Klaus; Stankovic, Konstantina M.

I: PLOS ONE, Bind 10, Nr. 5, e0125160, 2015, s. 1-17.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jensen, JB, Lysaght, AC, Liberman, MC, Qvortrup, K & Stankovic, KM 2015, 'Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice', PLOS ONE, bind 10, nr. 5, e0125160, s. 1-17. https://doi.org/10.1371/journal.pone.0125160

APA

Jensen, J. B., Lysaght, A. C., Liberman, M. C., Qvortrup, K., & Stankovic, K. M. (2015). Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice. PLOS ONE, 10(5), 1-17. [e0125160]. https://doi.org/10.1371/journal.pone.0125160

Vancouver

Jensen JB, Lysaght AC, Liberman MC, Qvortrup K, Stankovic KM. Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice. PLOS ONE. 2015;10(5):1-17. e0125160. https://doi.org/10.1371/journal.pone.0125160

Author

Jensen, Jane Bjerg ; Lysaght, Andrew C ; Liberman, M Charles ; Qvortrup, Klaus ; Stankovic, Konstantina M. / Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice. I: PLOS ONE. 2015 ; Bind 10, Nr. 5. s. 1-17.

Bibtex

@article{2d098b40b0a64b0ca83efdc33dee0e1c,
title = "Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice",
abstract = "Moderate acoustic overexposure in adult rodents is known to cause acute loss of synapses on sensory inner hair cells (IHCs) and delayed degeneration of the auditory nerve, despite the completely reversible temporary threshold shift (TTS) and morphologically intact hair cells. Our objective was to determine whether a cochlear synaptopathy followed by neuropathy occurs after noise exposure in pubescence, and to define neuropathic versus non-neuropathic noise levels for pubescent mice. While exposing 6 week old CBA/CaJ mice to 8-16 kHz bandpass noise for 2 hrs, we defined 97 dB sound pressure level (SPL) as the threshold for this particular type of neuropathic exposure associated with TTS, and 94 dB SPL as the highest non-neuropathic noise level associated with TTS. Exposure to 100 dB SPL caused permanent threshold shift although exposure of 16 week old mice to the same noise is reported to cause only TTS. Amplitude of wave I of the auditory brainstem response, which reflects the summed activity of the cochlear nerve, was complemented by synaptic ribbon counts in IHCs using confocal microscopy, and by stereological counts of peripheral axons and cell bodies of the cochlear nerve from 24 hours to 16 months post exposure. Mice exposed to neuropathic noise demonstrated immediate cochlear synaptopathy by 24 hours post exposure, and delayed neurodegeneration characterized by axonal retraction at 8 months, and spiral ganglion cell loss at 8-16 months post exposure. Although the damage was initially limited to the cochlear base, it progressed to also involve the cochlear apex by 8 months post exposure. Our data demonstrate a fine line between neuropathic and non-neuropathic noise levels associated with TTS in the pubescent cochlea.",
author = "Jensen, {Jane Bjerg} and Lysaght, {Andrew C} and Liberman, {M Charles} and Klaus Qvortrup and Stankovic, {Konstantina M}",
year = "2015",
doi = "10.1371/journal.pone.0125160",
language = "English",
volume = "10",
pages = "1--17",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "5",

}

RIS

TY - JOUR

T1 - Immediate and delayed cochlear neuropathy after noise exposure in pubescent mice

AU - Jensen, Jane Bjerg

AU - Lysaght, Andrew C

AU - Liberman, M Charles

AU - Qvortrup, Klaus

AU - Stankovic, Konstantina M

PY - 2015

Y1 - 2015

N2 - Moderate acoustic overexposure in adult rodents is known to cause acute loss of synapses on sensory inner hair cells (IHCs) and delayed degeneration of the auditory nerve, despite the completely reversible temporary threshold shift (TTS) and morphologically intact hair cells. Our objective was to determine whether a cochlear synaptopathy followed by neuropathy occurs after noise exposure in pubescence, and to define neuropathic versus non-neuropathic noise levels for pubescent mice. While exposing 6 week old CBA/CaJ mice to 8-16 kHz bandpass noise for 2 hrs, we defined 97 dB sound pressure level (SPL) as the threshold for this particular type of neuropathic exposure associated with TTS, and 94 dB SPL as the highest non-neuropathic noise level associated with TTS. Exposure to 100 dB SPL caused permanent threshold shift although exposure of 16 week old mice to the same noise is reported to cause only TTS. Amplitude of wave I of the auditory brainstem response, which reflects the summed activity of the cochlear nerve, was complemented by synaptic ribbon counts in IHCs using confocal microscopy, and by stereological counts of peripheral axons and cell bodies of the cochlear nerve from 24 hours to 16 months post exposure. Mice exposed to neuropathic noise demonstrated immediate cochlear synaptopathy by 24 hours post exposure, and delayed neurodegeneration characterized by axonal retraction at 8 months, and spiral ganglion cell loss at 8-16 months post exposure. Although the damage was initially limited to the cochlear base, it progressed to also involve the cochlear apex by 8 months post exposure. Our data demonstrate a fine line between neuropathic and non-neuropathic noise levels associated with TTS in the pubescent cochlea.

AB - Moderate acoustic overexposure in adult rodents is known to cause acute loss of synapses on sensory inner hair cells (IHCs) and delayed degeneration of the auditory nerve, despite the completely reversible temporary threshold shift (TTS) and morphologically intact hair cells. Our objective was to determine whether a cochlear synaptopathy followed by neuropathy occurs after noise exposure in pubescence, and to define neuropathic versus non-neuropathic noise levels for pubescent mice. While exposing 6 week old CBA/CaJ mice to 8-16 kHz bandpass noise for 2 hrs, we defined 97 dB sound pressure level (SPL) as the threshold for this particular type of neuropathic exposure associated with TTS, and 94 dB SPL as the highest non-neuropathic noise level associated with TTS. Exposure to 100 dB SPL caused permanent threshold shift although exposure of 16 week old mice to the same noise is reported to cause only TTS. Amplitude of wave I of the auditory brainstem response, which reflects the summed activity of the cochlear nerve, was complemented by synaptic ribbon counts in IHCs using confocal microscopy, and by stereological counts of peripheral axons and cell bodies of the cochlear nerve from 24 hours to 16 months post exposure. Mice exposed to neuropathic noise demonstrated immediate cochlear synaptopathy by 24 hours post exposure, and delayed neurodegeneration characterized by axonal retraction at 8 months, and spiral ganglion cell loss at 8-16 months post exposure. Although the damage was initially limited to the cochlear base, it progressed to also involve the cochlear apex by 8 months post exposure. Our data demonstrate a fine line between neuropathic and non-neuropathic noise levels associated with TTS in the pubescent cochlea.

U2 - 10.1371/journal.pone.0125160

DO - 10.1371/journal.pone.0125160

M3 - Journal article

C2 - 25955832

VL - 10

SP - 1

EP - 17

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 5

M1 - e0125160

ER -

ID: 137754407