Power efficiency of outer hair cell somatic electromotility.

Cochlear outer hair cells (OHCs) are fast biological motors that serve to enhance the vibration of the organ of Corti and increase the sensitivity of the inner ear to sound. Exactly how OHCs produce useful mechanical power at auditory frequencies, given their intrinsic biophysical properties, has be...

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Main Authors: Richard D Rabbitt, Sarah Clifford, Kathryn D Breneman, Brenda Farrell, William E Brownell
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-07-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC2705677?pdf=render
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spelling doaj-a9930b898a3a49488895efd190577e3b2020-11-25T01:32:25ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582009-07-0157e100044410.1371/journal.pcbi.1000444Power efficiency of outer hair cell somatic electromotility.Richard D RabbittSarah CliffordKathryn D BrenemanBrenda FarrellWilliam E BrownellCochlear outer hair cells (OHCs) are fast biological motors that serve to enhance the vibration of the organ of Corti and increase the sensitivity of the inner ear to sound. Exactly how OHCs produce useful mechanical power at auditory frequencies, given their intrinsic biophysical properties, has been a subject of considerable debate. To address this we formulated a mathematical model of the OHC based on first principles and analyzed the power conversion efficiency in the frequency domain. The model includes a mixture-composite constitutive model of the active lateral wall and spatially distributed electro-mechanical fields. The analysis predicts that: 1) the peak power efficiency is likely to be tuned to a specific frequency, dependent upon OHC length, and this tuning may contribute to the place principle and frequency selectivity in the cochlea; 2) the OHC power output can be detuned and attenuated by increasing the basal conductance of the cell, a parameter likely controlled by the brain via the efferent system; and 3) power output efficiency is limited by mechanical properties of the load, thus suggesting that impedance of the organ of Corti may be matched regionally to the OHC. The high power efficiency, tuning, and efferent control of outer hair cells are the direct result of biophysical properties of the cells, thus providing the physical basis for the remarkable sensitivity and selectivity of hearing.http://europepmc.org/articles/PMC2705677?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Richard D Rabbitt
Sarah Clifford
Kathryn D Breneman
Brenda Farrell
William E Brownell
spellingShingle Richard D Rabbitt
Sarah Clifford
Kathryn D Breneman
Brenda Farrell
William E Brownell
Power efficiency of outer hair cell somatic electromotility.
PLoS Computational Biology
author_facet Richard D Rabbitt
Sarah Clifford
Kathryn D Breneman
Brenda Farrell
William E Brownell
author_sort Richard D Rabbitt
title Power efficiency of outer hair cell somatic electromotility.
title_short Power efficiency of outer hair cell somatic electromotility.
title_full Power efficiency of outer hair cell somatic electromotility.
title_fullStr Power efficiency of outer hair cell somatic electromotility.
title_full_unstemmed Power efficiency of outer hair cell somatic electromotility.
title_sort power efficiency of outer hair cell somatic electromotility.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2009-07-01
description Cochlear outer hair cells (OHCs) are fast biological motors that serve to enhance the vibration of the organ of Corti and increase the sensitivity of the inner ear to sound. Exactly how OHCs produce useful mechanical power at auditory frequencies, given their intrinsic biophysical properties, has been a subject of considerable debate. To address this we formulated a mathematical model of the OHC based on first principles and analyzed the power conversion efficiency in the frequency domain. The model includes a mixture-composite constitutive model of the active lateral wall and spatially distributed electro-mechanical fields. The analysis predicts that: 1) the peak power efficiency is likely to be tuned to a specific frequency, dependent upon OHC length, and this tuning may contribute to the place principle and frequency selectivity in the cochlea; 2) the OHC power output can be detuned and attenuated by increasing the basal conductance of the cell, a parameter likely controlled by the brain via the efferent system; and 3) power output efficiency is limited by mechanical properties of the load, thus suggesting that impedance of the organ of Corti may be matched regionally to the OHC. The high power efficiency, tuning, and efferent control of outer hair cells are the direct result of biophysical properties of the cells, thus providing the physical basis for the remarkable sensitivity and selectivity of hearing.
url http://europepmc.org/articles/PMC2705677?pdf=render
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