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A role for tectorial membrane mechanics in activating the cochlear amplifier

The mechanical and electrical responses of the mammalian cochlea to acoustic stimuli are nonlinear and highly tuned in frequency. This is due to the electromechanical properties of cochlear outer hair cells (OHCs). At each location along the cochlear spiral, the OHCs mediate an active process in whi...

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Autores principales: Nankali, Amir, Wang, Yi, Strimbu, Clark Elliott, Olson, Elizabeth S., Grosh, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573614/
https://www.ncbi.nlm.nih.gov/pubmed/33077807
http://dx.doi.org/10.1038/s41598-020-73873-9
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author Nankali, Amir
Wang, Yi
Strimbu, Clark Elliott
Olson, Elizabeth S.
Grosh, Karl
author_facet Nankali, Amir
Wang, Yi
Strimbu, Clark Elliott
Olson, Elizabeth S.
Grosh, Karl
author_sort Nankali, Amir
collection PubMed
description The mechanical and electrical responses of the mammalian cochlea to acoustic stimuli are nonlinear and highly tuned in frequency. This is due to the electromechanical properties of cochlear outer hair cells (OHCs). At each location along the cochlear spiral, the OHCs mediate an active process in which the sensory tissue motion is enhanced at frequencies close to the most sensitive frequency (called the characteristic frequency, CF). Previous experimental results showed an approximate 0.3 cycle phase shift in the OHC-generated extracellular voltage relative the basilar membrane displacement, which was initiated at a frequency approximately one-half octave lower than the CF. Findings in the present paper reinforce that result. This shift is significant because it brings the phase of the OHC-derived electromotile force near to that of the basilar membrane velocity at frequencies above the shift, thereby enabling the transfer of electrical to mechanical power at the basilar membrane. In order to seek a candidate physical mechanism for this phenomenon, we used a comprehensive electromechanical mathematical model of the cochlear response to sound. The model predicts the phase shift in the extracellular voltage referenced to the basilar membrane at a frequency approximately one-half octave below CF, in accordance with the experimental data. In the model, this feature arises from a minimum in the radial impedance of the tectorial membrane and its limbal attachment. These experimental and theoretical results are consistent with the hypothesis that a tectorial membrane resonance introduces the correct phasing between mechanical and electrical responses for power generation, effectively turning on the cochlear amplifier.
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spelling pubmed-75736142020-10-21 A role for tectorial membrane mechanics in activating the cochlear amplifier Nankali, Amir Wang, Yi Strimbu, Clark Elliott Olson, Elizabeth S. Grosh, Karl Sci Rep Article The mechanical and electrical responses of the mammalian cochlea to acoustic stimuli are nonlinear and highly tuned in frequency. This is due to the electromechanical properties of cochlear outer hair cells (OHCs). At each location along the cochlear spiral, the OHCs mediate an active process in which the sensory tissue motion is enhanced at frequencies close to the most sensitive frequency (called the characteristic frequency, CF). Previous experimental results showed an approximate 0.3 cycle phase shift in the OHC-generated extracellular voltage relative the basilar membrane displacement, which was initiated at a frequency approximately one-half octave lower than the CF. Findings in the present paper reinforce that result. This shift is significant because it brings the phase of the OHC-derived electromotile force near to that of the basilar membrane velocity at frequencies above the shift, thereby enabling the transfer of electrical to mechanical power at the basilar membrane. In order to seek a candidate physical mechanism for this phenomenon, we used a comprehensive electromechanical mathematical model of the cochlear response to sound. The model predicts the phase shift in the extracellular voltage referenced to the basilar membrane at a frequency approximately one-half octave below CF, in accordance with the experimental data. In the model, this feature arises from a minimum in the radial impedance of the tectorial membrane and its limbal attachment. These experimental and theoretical results are consistent with the hypothesis that a tectorial membrane resonance introduces the correct phasing between mechanical and electrical responses for power generation, effectively turning on the cochlear amplifier. Nature Publishing Group UK 2020-10-19 /pmc/articles/PMC7573614/ /pubmed/33077807 http://dx.doi.org/10.1038/s41598-020-73873-9 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nankali, Amir
Wang, Yi
Strimbu, Clark Elliott
Olson, Elizabeth S.
Grosh, Karl
A role for tectorial membrane mechanics in activating the cochlear amplifier
title A role for tectorial membrane mechanics in activating the cochlear amplifier
title_full A role for tectorial membrane mechanics in activating the cochlear amplifier
title_fullStr A role for tectorial membrane mechanics in activating the cochlear amplifier
title_full_unstemmed A role for tectorial membrane mechanics in activating the cochlear amplifier
title_short A role for tectorial membrane mechanics in activating the cochlear amplifier
title_sort role for tectorial membrane mechanics in activating the cochlear amplifier
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573614/
https://www.ncbi.nlm.nih.gov/pubmed/33077807
http://dx.doi.org/10.1038/s41598-020-73873-9
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