Literature DB >> 2051201

Effect of contralateral acoustic stimulation on active cochlear micromechanical properties in human subjects: dependence on stimulus variables.

E Veuillet1, L Collet, R Duclaux.   

Abstract

1. Outer hair cells (OHCs) have active micromechanical properties that are thought to be the origin of evoked otoacoustic emissions (EOAEs). In the present study, click-evoked otoacoustic emissions were recorded in humans with or without various contralateral acoustic stimulations. A previous study, concentrating on contralateral stimulation with broadband noise, had shown a decrease of the EOAE amplitude in humans. Results support a role for the efferent system in cochlear mechanics; indeed, medial efferent neurons of the olivocochlear bundle terminate on the OHCs. To obtain a better understanding of the medial efferent system functioning in humans, the present study looked at the contralateral suppressive effect as a function of stimulus parameters. 2. The study of the input-output function of the EOAE amplitude with and without a 50-dB SPL contralateral broadband noise showed that the suppressive effect was equivalent to a mean reduction of 3.77 dB. 3. For the EOAEs to tone pips, the contralateral suppressive effect was strongest when the contralateral ear stimuli were narrow bands that were centered around the central EOAE frequency. This frequency specificity disappeared for contralateral narrow band noise levels greater than 50 dB SPL. 4. The contralateral suppressive effect was also observed with transient contralateral sounds (nonfiltered clicks). Significant reductions of the EOAE amplitude were seen with contralateral click levels as low as 17.5 dB SL. Above this level, the EOAE amplitude decreased as the contralateral stimulus level increased. This effect was still present in subjects without any stapedial reflex, but absent in total unilateral hearing-loss subjects. Therefore this suppressive effect is unlikely to be due to alteration of the middle ear function or to transcranially conducted sound. 5. When the contralateral interclick interval exceeded 14.2 ms. the suppressive effect was smaller. With contralateral stimulus level maintained subjectively constant, the effect was found to disappear when the interclick interval was greater than 49.9 ms. A saturation of the contralateral suppressive effect was observed for click rates greater than 70/s (interclick interval less than 14.2 ms). 6. Our study confirms and specifies the contralateral sound suppression effect on cochlear mechanisms in humans, assessing the equivalent reduction, showing a frequency specificity and extending these findings to contralateral transient sounds. Any influence of the acoustic crosstalk was eliminated. A role played by middle ear muscles cannot be absolutely ruled out but is not necessary to produce such a contralateral suppressive effect (the effect being found in subjects after surgical removal of the stapedius muscle) and could not explain the frequency specificity.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 2051201     DOI: 10.1152/jn.1991.65.3.724

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  39 in total

1.  Variation in inter-animal susceptibility to noise damage is associated with alpha 9 acetylcholine receptor subunit expression level.

Authors:  Anne E Luebke; Paul K Foster
Journal:  J Neurosci       Date:  2002-05-15       Impact factor: 6.167

2.  Frequency tuning of the contralateral medial olivocochlear reflex in humans.

Authors:  Wei Zhao; Sumitrajit Dhar
Journal:  J Neurophysiol       Date:  2012-03-28       Impact factor: 2.714

3.  Recording and labeling at a site along the cochlea shows alignment of medial olivocochlear and auditory nerve tonotopic mappings.

Authors:  M Christian Brown
Journal:  J Neurophysiol       Date:  2016-01-28       Impact factor: 2.714

4.  Click-Evoked Auditory Efferent Activity: Rate and Level Effects.

Authors:  Sriram Boothalingam; Julianne Kurke; Sumitrajit Dhar
Journal:  J Assoc Res Otolaryngol       Date:  2018-05-07

5.  Simultaneous measurement of noise-activated middle-ear muscle reflex and stimulus frequency otoacoustic emissions.

Authors:  Shawn S Goodman; Douglas H Keefe
Journal:  J Assoc Res Otolaryngol       Date:  2006-03-28

6.  Measurement of the distribution of medial olivocochlear acoustic reflex strengths across normal-hearing individuals via otoacoustic emissions.

Authors:  Bradford C Backus; John J Guinan
Journal:  J Assoc Res Otolaryngol       Date:  2007-10-12

7.  Medial olivocochlear efferent reflex in humans: otoacoustic emission (OAE) measurement issues and the advantages of stimulus frequency OAEs.

Authors:  John J Guinan; Bradford C Backus; Watjana Lilaonitkul; Vered Aharonson
Journal:  J Assoc Res Otolaryngol       Date:  2003-06-13

8.  Medial olivocochlear-induced transient-evoked otoacoustic emission amplitude shifts in individual subjects.

Authors:  Shawn S Goodman; Ian B Mertes; James D Lewis; Diana K Weissbeck
Journal:  J Assoc Res Otolaryngol       Date:  2013-08-28

9.  Otoacoustic-emission-based medial-olivocochlear reflex assays for humans.

Authors:  Lynne Marshall; Judi A Lapsley Miller; John J Guinan; Christopher A Shera; Charlotte M Reed; Zachary D Perez; Lorraine A Delhorne; Paul Boege
Journal:  J Acoust Soc Am       Date:  2014-11       Impact factor: 1.840

10.  Exploring the role of feedback-based auditory reflexes in forward masking by schroeder-phase complexes.

Authors:  Magdalena Wojtczak; Jordan A Beim; Andrew J Oxenham
Journal:  J Assoc Res Otolaryngol       Date:  2014-10-22
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