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Near physiological spectral selectivity of cochlear optogenetics
Cochlear implants (CIs) electrically stimulate spiral ganglion neurons (SGNs) and partially restore hearing to half a million CI users. However, wide current spread from intracochlear electrodes limits spatial selectivity (i.e. spectral resolution) of electrical CIs. Optogenetic stimulation might be...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488702/ https://www.ncbi.nlm.nih.gov/pubmed/31036812 http://dx.doi.org/10.1038/s41467-019-09980-7 |
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author | Dieter, Alexander Duque-Afonso, Carlos J. Rankovic, Vladan Jeschke, Marcus Moser, Tobias |
author_facet | Dieter, Alexander Duque-Afonso, Carlos J. Rankovic, Vladan Jeschke, Marcus Moser, Tobias |
author_sort | Dieter, Alexander |
collection | PubMed |
description | Cochlear implants (CIs) electrically stimulate spiral ganglion neurons (SGNs) and partially restore hearing to half a million CI users. However, wide current spread from intracochlear electrodes limits spatial selectivity (i.e. spectral resolution) of electrical CIs. Optogenetic stimulation might become an alternative, since light can be confined in space, promising artificial sound encoding with increased spectral selectivity. Here we compare spectral selectivity of optogenetic, electric, and acoustic stimulation by multi-channel recordings in the inferior colliculus (IC) of gerbils. When projecting light onto tonotopically distinct SGNs, we observe corresponding tonotopically ordered IC activity. An activity-based comparison reveals that spectral selectivity of optogenetic stimulation is indistinguishable from acoustic stimulation for modest intensities. Moreover, optogenetic stimulation outperforms bipolar electric stimulation at medium and high intensities and monopolar electric stimulation at all intensities. In conclusion, we demonstrate better spectral selectivity of optogenetic over electric SGN stimulation, suggesting the potential for improved hearing restoration by optical CIs. |
format | Online Article Text |
id | pubmed-6488702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64887022019-05-01 Near physiological spectral selectivity of cochlear optogenetics Dieter, Alexander Duque-Afonso, Carlos J. Rankovic, Vladan Jeschke, Marcus Moser, Tobias Nat Commun Article Cochlear implants (CIs) electrically stimulate spiral ganglion neurons (SGNs) and partially restore hearing to half a million CI users. However, wide current spread from intracochlear electrodes limits spatial selectivity (i.e. spectral resolution) of electrical CIs. Optogenetic stimulation might become an alternative, since light can be confined in space, promising artificial sound encoding with increased spectral selectivity. Here we compare spectral selectivity of optogenetic, electric, and acoustic stimulation by multi-channel recordings in the inferior colliculus (IC) of gerbils. When projecting light onto tonotopically distinct SGNs, we observe corresponding tonotopically ordered IC activity. An activity-based comparison reveals that spectral selectivity of optogenetic stimulation is indistinguishable from acoustic stimulation for modest intensities. Moreover, optogenetic stimulation outperforms bipolar electric stimulation at medium and high intensities and monopolar electric stimulation at all intensities. In conclusion, we demonstrate better spectral selectivity of optogenetic over electric SGN stimulation, suggesting the potential for improved hearing restoration by optical CIs. Nature Publishing Group UK 2019-04-29 /pmc/articles/PMC6488702/ /pubmed/31036812 http://dx.doi.org/10.1038/s41467-019-09980-7 Text en © The Author(s) 2019 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 Dieter, Alexander Duque-Afonso, Carlos J. Rankovic, Vladan Jeschke, Marcus Moser, Tobias Near physiological spectral selectivity of cochlear optogenetics |
title | Near physiological spectral selectivity of cochlear optogenetics |
title_full | Near physiological spectral selectivity of cochlear optogenetics |
title_fullStr | Near physiological spectral selectivity of cochlear optogenetics |
title_full_unstemmed | Near physiological spectral selectivity of cochlear optogenetics |
title_short | Near physiological spectral selectivity of cochlear optogenetics |
title_sort | near physiological spectral selectivity of cochlear optogenetics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488702/ https://www.ncbi.nlm.nih.gov/pubmed/31036812 http://dx.doi.org/10.1038/s41467-019-09980-7 |
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