A mouse model of cochlear implantation with chronic electric stimulation.

<h4>Objectives</h4>Cochlear implants provide an effective treatment option for those with severe hearing loss, including those with preserved low frequency hearing. However, certain issues can reduce implant efficacy including intracochlear tissue response and delayed loss of residual ac...

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Main Authors: Alexander D Claussen, René Vielman Quevedo, Brian Mostaert, Jonathon R Kirk, Wolfram F Dueck, Marlan R Hansen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0215407
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spelling doaj-95a712010ac14cbe83643776e83962b02021-03-04T11:54:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01144e021540710.1371/journal.pone.0215407A mouse model of cochlear implantation with chronic electric stimulation.Alexander D ClaussenRené Vielman QuevedoBrian MostaertJonathon R KirkWolfram F DueckMarlan R Hansen<h4>Objectives</h4>Cochlear implants provide an effective treatment option for those with severe hearing loss, including those with preserved low frequency hearing. However, certain issues can reduce implant efficacy including intracochlear tissue response and delayed loss of residual acoustic hearing. We describe a mouse model of cochlear implantation with chronic electric stimulation that can be used to study cochlear implant biology and related pathologies.<h4>Methods</h4>Twelve normal hearing adult CBA/J mice underwent unilateral cochlear implantation and were evenly divided into one group receiving electric stimulation and one not. Serial impedance and neural response telemetry (NRT) measurements were made to assess implant functionality. Functionality was defined as having at least one electrode with an impedance ≤ 35 kOhms. Mouse cochleae were harvested for histology and 3D x-ray microscopy 21 days post-operatively, or, in case the implant was still functional, at a later time point when the implant failed. A separate experiment measured the hearing preservation rate in 7 adult CBA/J mice undergoing unilateral cochlear implantation with serial auditory brainstem response (ABR) and distortion product otoacoustic emissions (DPOAE).<h4>Results</h4>Implants maintained functionality for a mean of 35 days in the non-stimulated group and 19.8 days in the stimulated group. Reliable NRT and behavioral responses to electric stimulation were recorded. A robust intracochlear peri-implant tissue response with neo-ossification was seen in all cochleae. Six of seven mice maintained intact low frequency hearing up to 6 weeks following cochlear implantation.<h4>Conclusions</h4>We demonstrate the feasibility of cochlear implantation and behaviorally significant electric stimulation in the mouse, with the potential for hearing preservation. This model may be combined with established mouse models of hearing loss and the large genetic and molecular research toolkit unique to the mouse for mechanistic and therapeutic investigations of cochlear implant biology.https://doi.org/10.1371/journal.pone.0215407
collection DOAJ
language English
format Article
sources DOAJ
author Alexander D Claussen
René Vielman Quevedo
Brian Mostaert
Jonathon R Kirk
Wolfram F Dueck
Marlan R Hansen
spellingShingle Alexander D Claussen
René Vielman Quevedo
Brian Mostaert
Jonathon R Kirk
Wolfram F Dueck
Marlan R Hansen
A mouse model of cochlear implantation with chronic electric stimulation.
PLoS ONE
author_facet Alexander D Claussen
René Vielman Quevedo
Brian Mostaert
Jonathon R Kirk
Wolfram F Dueck
Marlan R Hansen
author_sort Alexander D Claussen
title A mouse model of cochlear implantation with chronic electric stimulation.
title_short A mouse model of cochlear implantation with chronic electric stimulation.
title_full A mouse model of cochlear implantation with chronic electric stimulation.
title_fullStr A mouse model of cochlear implantation with chronic electric stimulation.
title_full_unstemmed A mouse model of cochlear implantation with chronic electric stimulation.
title_sort mouse model of cochlear implantation with chronic electric stimulation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description <h4>Objectives</h4>Cochlear implants provide an effective treatment option for those with severe hearing loss, including those with preserved low frequency hearing. However, certain issues can reduce implant efficacy including intracochlear tissue response and delayed loss of residual acoustic hearing. We describe a mouse model of cochlear implantation with chronic electric stimulation that can be used to study cochlear implant biology and related pathologies.<h4>Methods</h4>Twelve normal hearing adult CBA/J mice underwent unilateral cochlear implantation and were evenly divided into one group receiving electric stimulation and one not. Serial impedance and neural response telemetry (NRT) measurements were made to assess implant functionality. Functionality was defined as having at least one electrode with an impedance ≤ 35 kOhms. Mouse cochleae were harvested for histology and 3D x-ray microscopy 21 days post-operatively, or, in case the implant was still functional, at a later time point when the implant failed. A separate experiment measured the hearing preservation rate in 7 adult CBA/J mice undergoing unilateral cochlear implantation with serial auditory brainstem response (ABR) and distortion product otoacoustic emissions (DPOAE).<h4>Results</h4>Implants maintained functionality for a mean of 35 days in the non-stimulated group and 19.8 days in the stimulated group. Reliable NRT and behavioral responses to electric stimulation were recorded. A robust intracochlear peri-implant tissue response with neo-ossification was seen in all cochleae. Six of seven mice maintained intact low frequency hearing up to 6 weeks following cochlear implantation.<h4>Conclusions</h4>We demonstrate the feasibility of cochlear implantation and behaviorally significant electric stimulation in the mouse, with the potential for hearing preservation. This model may be combined with established mouse models of hearing loss and the large genetic and molecular research toolkit unique to the mouse for mechanistic and therapeutic investigations of cochlear implant biology.
url https://doi.org/10.1371/journal.pone.0215407
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