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Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation
To determine whether responses during infrared neural stimulation (INS) result from the direct interaction with spiral ganglion neurons (SGNs), we tested three genetically modified deaf mouse models: Atoh1-cre; Atoh1 (f/f) (Atoh1 conditional knockout, CKO), Atoh1-cre; Atoh1 (f/kiNeurog1) (Neurog1 kn...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762820/ https://www.ncbi.nlm.nih.gov/pubmed/29321651 http://dx.doi.org/10.1038/s41598-017-18814-9 |
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author | Tan, Xiaodong Jahan, Israt Xu, Yingyue Stock, Stuart Kwan, Changyow Claire Soriano, Carmen Xiao, Xianghui García-Añoveros, Jaime Fritzsch, Bernd Richter, Claus-Peter |
author_facet | Tan, Xiaodong Jahan, Israt Xu, Yingyue Stock, Stuart Kwan, Changyow Claire Soriano, Carmen Xiao, Xianghui García-Añoveros, Jaime Fritzsch, Bernd Richter, Claus-Peter |
author_sort | Tan, Xiaodong |
collection | PubMed |
description | To determine whether responses during infrared neural stimulation (INS) result from the direct interaction with spiral ganglion neurons (SGNs), we tested three genetically modified deaf mouse models: Atoh1-cre; Atoh1 (f/f) (Atoh1 conditional knockout, CKO), Atoh1-cre; Atoh1 (f/kiNeurog1) (Neurog1 knockin, KI), and the Vglut3 knockout (Vglut3 (−/−)) mice. All animals were exposed to tone bursts and clicks up to 107 dB (re 20 µPa) and to INS, delivered with a 200 µm optical fiber. The wavelength (λ) was 1860 nm, the radiant energy (Q) 0-800 µJ/pulse, and the pulse width (PW) 100–500 µs. No auditory responses to acoustic stimuli could be evoked in any of these animals. INS could not evoke auditory brainstem responses in Atoh1 CKO mice but could in Neurog1 KI and Vglut3 (−/−) mice. X-ray micro-computed tomography of the cochleae showed that responses correlated with the presence of SGNs and hair cells. Results in Neurog1 KI mice do not support a mechanical stimulation through the vibration of the basilar membrane, but cannot rule out the direct activation of the inner hair cells. Results in Vglut3 (−/−) mice, which have no synaptic transmission between inner hair cells and SGNs, suggested that hair cells are not required. |
format | Online Article Text |
id | pubmed-5762820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57628202018-01-17 Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation Tan, Xiaodong Jahan, Israt Xu, Yingyue Stock, Stuart Kwan, Changyow Claire Soriano, Carmen Xiao, Xianghui García-Añoveros, Jaime Fritzsch, Bernd Richter, Claus-Peter Sci Rep Article To determine whether responses during infrared neural stimulation (INS) result from the direct interaction with spiral ganglion neurons (SGNs), we tested three genetically modified deaf mouse models: Atoh1-cre; Atoh1 (f/f) (Atoh1 conditional knockout, CKO), Atoh1-cre; Atoh1 (f/kiNeurog1) (Neurog1 knockin, KI), and the Vglut3 knockout (Vglut3 (−/−)) mice. All animals were exposed to tone bursts and clicks up to 107 dB (re 20 µPa) and to INS, delivered with a 200 µm optical fiber. The wavelength (λ) was 1860 nm, the radiant energy (Q) 0-800 µJ/pulse, and the pulse width (PW) 100–500 µs. No auditory responses to acoustic stimuli could be evoked in any of these animals. INS could not evoke auditory brainstem responses in Atoh1 CKO mice but could in Neurog1 KI and Vglut3 (−/−) mice. X-ray micro-computed tomography of the cochleae showed that responses correlated with the presence of SGNs and hair cells. Results in Neurog1 KI mice do not support a mechanical stimulation through the vibration of the basilar membrane, but cannot rule out the direct activation of the inner hair cells. Results in Vglut3 (−/−) mice, which have no synaptic transmission between inner hair cells and SGNs, suggested that hair cells are not required. Nature Publishing Group UK 2018-01-10 /pmc/articles/PMC5762820/ /pubmed/29321651 http://dx.doi.org/10.1038/s41598-017-18814-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tan, Xiaodong Jahan, Israt Xu, Yingyue Stock, Stuart Kwan, Changyow Claire Soriano, Carmen Xiao, Xianghui García-Añoveros, Jaime Fritzsch, Bernd Richter, Claus-Peter Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation |
title | Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation |
title_full | Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation |
title_fullStr | Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation |
title_full_unstemmed | Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation |
title_short | Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation |
title_sort | auditory neural activity in congenitally deaf mice induced by infrared neural stimulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762820/ https://www.ncbi.nlm.nih.gov/pubmed/29321651 http://dx.doi.org/10.1038/s41598-017-18814-9 |
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