Lateral superior olive function in congenital deafness

Detalhes bibliográficos
Autor(a) principal: Couchman, Kiri
Data de Publicação: 2011
Outros Autores: Garrett, Andrew, Deardorff, Adam S., Rattay, Frank, Resatz, Susanne, Fyffe, Robert, Walmsley, Bruce, Leão, Richardson Naves
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/23113
Resumo: The development of cochlear ilmplants for the treatment of patients with profound hearing loss has advanced considerably in the last few decades, particularly in the field of speech comprehension. However, attempts to provide not only sound decoding but also spatial hearing are limited by our understanding of circuit adaptations in the absence of auditory input. Here we investigate the lateral superior olive (LSO), a nucleus involved in interaural level difference (ILD) processing in the auditory brainstem using a mouse model of congenital deafness (the dn/dn mouse). An electrophysiological investigation of principal neurons of the LSO from the dn/dn mouse reveals a higher than normal proportion of single spiking (SS) neurons, and an increase in the hyperpolarisation-activated Ih current. However, inhibitory glycinergic input to the LSO appears to develop normally both pre and postsynaptically in dn/dn mice despite the absence of auditory nerve activity. In combination with previous electrophysiological findings from the dn/ dn mouse, we also compile a simple Hodgkin and Huxley circuit model in order to investigate possible computational deficits in ILD processing resulting from congenital hearing loss. We find that the predominance of SS neurons in the dn/dn LSO may compensate for upstream modifications and help to maintain a functioning ILD circuit in the dn/dn mouse. This could have clinical repercussions on the development of stimulation paradigms for spatial hearing with cochlear implants.
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spelling Couchman, KiriGarrett, AndrewDeardorff, Adam S.Rattay, FrankResatz, SusanneFyffe, RobertWalmsley, BruceLeão, Richardson Naves2017-05-26T14:01:02Z2017-05-26T14:01:02Z2011-01-270378-5955https://repositorio.ufrn.br/jspui/handle/123456789/23113engDevelopment of cochlear ilmplantsHearing lossSS neuronsLateral superior olive functionCongenital deafnessLateral superior olive function in congenital deafnessinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleThe development of cochlear ilmplants for the treatment of patients with profound hearing loss has advanced considerably in the last few decades, particularly in the field of speech comprehension. However, attempts to provide not only sound decoding but also spatial hearing are limited by our understanding of circuit adaptations in the absence of auditory input. Here we investigate the lateral superior olive (LSO), a nucleus involved in interaural level difference (ILD) processing in the auditory brainstem using a mouse model of congenital deafness (the dn/dn mouse). An electrophysiological investigation of principal neurons of the LSO from the dn/dn mouse reveals a higher than normal proportion of single spiking (SS) neurons, and an increase in the hyperpolarisation-activated Ih current. However, inhibitory glycinergic input to the LSO appears to develop normally both pre and postsynaptically in dn/dn mice despite the absence of auditory nerve activity. In combination with previous electrophysiological findings from the dn/ dn mouse, we also compile a simple Hodgkin and Huxley circuit model in order to investigate possible computational deficits in ILD processing resulting from congenital hearing loss. We find that the predominance of SS neurons in the dn/dn LSO may compensate for upstream modifications and help to maintain a functioning ILD circuit in the dn/dn mouse. 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dc.title.pt_BR.fl_str_mv Lateral superior olive function in congenital deafness
title Lateral superior olive function in congenital deafness
spellingShingle Lateral superior olive function in congenital deafness
Couchman, Kiri
Development of cochlear ilmplants
Hearing loss
SS neurons
Lateral superior olive function
Congenital deafness
title_short Lateral superior olive function in congenital deafness
title_full Lateral superior olive function in congenital deafness
title_fullStr Lateral superior olive function in congenital deafness
title_full_unstemmed Lateral superior olive function in congenital deafness
title_sort Lateral superior olive function in congenital deafness
author Couchman, Kiri
author_facet Couchman, Kiri
Garrett, Andrew
Deardorff, Adam S.
Rattay, Frank
Resatz, Susanne
Fyffe, Robert
Walmsley, Bruce
Leão, Richardson Naves
author_role author
author2 Garrett, Andrew
Deardorff, Adam S.
Rattay, Frank
Resatz, Susanne
Fyffe, Robert
Walmsley, Bruce
Leão, Richardson Naves
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Couchman, Kiri
Garrett, Andrew
Deardorff, Adam S.
Rattay, Frank
Resatz, Susanne
Fyffe, Robert
Walmsley, Bruce
Leão, Richardson Naves
dc.subject.por.fl_str_mv Development of cochlear ilmplants
Hearing loss
SS neurons
Lateral superior olive function
Congenital deafness
topic Development of cochlear ilmplants
Hearing loss
SS neurons
Lateral superior olive function
Congenital deafness
description The development of cochlear ilmplants for the treatment of patients with profound hearing loss has advanced considerably in the last few decades, particularly in the field of speech comprehension. However, attempts to provide not only sound decoding but also spatial hearing are limited by our understanding of circuit adaptations in the absence of auditory input. Here we investigate the lateral superior olive (LSO), a nucleus involved in interaural level difference (ILD) processing in the auditory brainstem using a mouse model of congenital deafness (the dn/dn mouse). An electrophysiological investigation of principal neurons of the LSO from the dn/dn mouse reveals a higher than normal proportion of single spiking (SS) neurons, and an increase in the hyperpolarisation-activated Ih current. However, inhibitory glycinergic input to the LSO appears to develop normally both pre and postsynaptically in dn/dn mice despite the absence of auditory nerve activity. In combination with previous electrophysiological findings from the dn/ dn mouse, we also compile a simple Hodgkin and Huxley circuit model in order to investigate possible computational deficits in ILD processing resulting from congenital hearing loss. We find that the predominance of SS neurons in the dn/dn LSO may compensate for upstream modifications and help to maintain a functioning ILD circuit in the dn/dn mouse. This could have clinical repercussions on the development of stimulation paradigms for spatial hearing with cochlear implants.
publishDate 2011
dc.date.issued.fl_str_mv 2011-01-27
dc.date.accessioned.fl_str_mv 2017-05-26T14:01:02Z
dc.date.available.fl_str_mv 2017-05-26T14:01:02Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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