Literature DB >> 12461165

Longitudinal pattern of basilar membrane vibration in the sensitive cochlea.

Tianying Ren1.   

Abstract

In the normal mammalian ear, sound vibrates the eardrum, causing the tiny bones of the middle ear to vibrate, transferring the vibration to the inner ear fluids. The vibration propagates from the base of the cochlea to its apex along the cochlear partition. As essential as this concept is to the theory of hearing, the waveform of cochlear partition vibration has yet to be measured in vivo. Here I report a "snapshot" (the instantaneous waveform of cochlear partition vibration) measured in the basal turn of the sensitive gerbil cochlea using a scanning laser interferometer. For 16-kHz tones, the phase delay is up to 6pi radians over the observed cochlear length (<1,000 microm), and instantaneous waveforms show sound propagation along the cochlear partition, supporting the existence of the cochlear traveling wave. The detectable basilar membrane response to a low-level 16-kHz tone occurs over a very restricted ( approximately equal 600 microm) range. The observed vibration shows compressive nonlinear growth, a shorter wavelength, and a slower propagation velocity along the cochlear length than previously reported. Data obtained at different frequencies show the relationship between the longitudinal pattern and frequency tuning, demonstrating that the observed localized traveling wave in this study is indeed the spatial representation of the sharp tuning observed in the frequency domain.

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Year:  2002        PMID: 12461165      PMCID: PMC139276          DOI: 10.1073/pnas.262663699

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  28 in total

1.  Direct measurement of intra-cochlear pressure waves.

Authors:  E S Olson
Journal:  Nature       Date:  1999-12-02       Impact factor: 49.962

2.  The spatial and temporal representation of a tone on the guinea pig basilar membrane.

Authors:  K E Nilsen; I J Russell
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

Review 3.  Amplification in the apical turn of the cochlea with negative feedback.

Authors:  S M Khanna; L F Hao
Journal:  Hear Res       Date:  2000-11       Impact factor: 3.208

4.  Study of mechanical motions in the basal region of the chinchilla cochlea.

Authors:  W S Rhode; A Recio
Journal:  J Acoust Soc Am       Date:  2000-06       Impact factor: 1.840

5.  Frequency tuning of basilar membrane and auditory nerve fibers in the same cochleae.

Authors:  S S Narayan; A N Temchin; A Recio; M A Ruggero
Journal:  Science       Date:  1998-12-04       Impact factor: 47.728

6.  Intensity-dependent peak shift in cochlear transfer functions at the cellular level, its elimination by sound exposure, and its possible underlying mechanisms.

Authors:  M Zhang; J J Zwislocki
Journal:  Hear Res       Date:  1996-07       Impact factor: 3.208

7.  Steady-state sinusoidal velocity responses of the basilar membrane in guinea pig.

Authors:  A L Nuttall; D F Dolan
Journal:  J Acoust Soc Am       Date:  1996-03       Impact factor: 1.840

8.  Observing middle and inner ear mechanics with novel intracochlear pressure sensors.

Authors:  E S Olson
Journal:  J Acoust Soc Am       Date:  1998-06       Impact factor: 1.840

9.  Cochlear mechanisms of frequency and intensity coding. I. The place code for pitch.

Authors:  M Chatterjee; J J Zwislocki
Journal:  Hear Res       Date:  1997-09       Impact factor: 3.208

10.  Basilar-membrane responses to tones at the base of the chinchilla cochlea.

Authors:  M A Ruggero; N C Rich; A Recio; S S Narayan; L Robles
Journal:  J Acoust Soc Am       Date:  1997-04       Impact factor: 1.840

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  86 in total

1.  Otoacoustic emissions from residual oscillations of the cochlear basilar membrane in a human ear model.

Authors:  Renato Nobili; Ales Vetesnik; Lorenzo Turicchia; Fabio Mammano
Journal:  J Assoc Res Otolaryngol       Date:  2003-07-10

2.  Limiting frequency of the cochlear amplifier based on electromotility of outer hair cells.

Authors:  Mark Ospeck; Xiao-xia Dong; Kuni H Iwasa
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

3.  Evidence of tectorial membrane radial motion in a propagating mode of a complex cochlear model.

Authors:  Hongxue Cai; Brett Shoelson; Richard S Chadwick
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-05       Impact factor: 11.205

4.  Reply to "on cochlear impedances and the miscomputation of power gain" by Shera et Al. J. Assoc. Re. Otolaryngol.

Authors:  Tianying Ren; Wenxuan He; Peter G Gillespie
Journal:  J Assoc Res Otolaryngol       Date:  2011-10-21

5.  Outer hair cell somatic electromotility in vivo and power transfer to the organ of Corti.

Authors:  Sripriya Ramamoorthy; Alfred L Nuttall
Journal:  Biophys J       Date:  2012-02-07       Impact factor: 4.033

6.  The biophysical origin of traveling-wave dispersion in the cochlea.

Authors:  Sripriya Ramamoorthy; Ding-Jun Zha; Alfred L Nuttall
Journal:  Biophys J       Date:  2010-09-22       Impact factor: 4.033

7.  Fast reverse propagation of sound in the living cochlea.

Authors:  Wenxuan He; Anders Fridberger; Edward Porsov; Tianying Ren
Journal:  Biophys J       Date:  2010-06-02       Impact factor: 4.033

Review 8.  Do forward- and backward-traveling waves occur within the cochlea? Countering the critique of Nobili et al.

Authors:  Christopher A Shera; Arnold Tubis; Carrick L Talmadge
Journal:  J Assoc Res Otolaryngol       Date:  2004-12

9.  Two-tone distortion at different longitudinal locations on the basilar membrane.

Authors:  Wenxuan He; Alfred L Nuttall; Tianying Ren
Journal:  Hear Res       Date:  2007-02-12       Impact factor: 3.208

10.  The role of organ of Corti mass in passive cochlear tuning.

Authors:  Ombeline de La Rochefoucauld; Elizabeth S Olson
Journal:  Biophys J       Date:  2007-09-28       Impact factor: 4.033

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