Literature DB >> 29276975

Non-tip auditory-nerve responses that are suppressed by low-frequency bias tones originate from reticular lamina motion.

Hui Nam1, John J Guinan2.   

Abstract

Recent cochlear mechanical measurements show that active processes increase the motion response of the reticular lamina (RL) at frequencies more than an octave below the local characteristic frequency (CF) for CFs above 5 kHz. A possible correlate is that in high-CF (>5 kHz) auditory-nerve (AN) fibers, responses to frequencies 1-3 octaves below CF ("tail" frequencies) can be inhibited by medial olivocochlear (MOC) efferents. These results indicate that active processes enhance the sensitivity of tail-frequency RL and AN responses. Perhaps related is that some apical low-CF AN fibers have tuning-curve (TC) "side-lobe" response areas at frequencies above and below the TC-tip that are MOC inhibited. We hypothesized that the tail and side-lobe responses are enhanced by the same active mechanisms as CF cochlear amplification. If responses to CF, tail-frequency, and TC-side-lobe tones are all enhanced by prestin motility controlled by outer-hair-cell (OHC) transmembrane voltage, then they should depend on OHC stereocilia position in the same way. To test this, we cyclically changed the OHC-stereocilia mechano-electric-transduction (MET) operating point with low-frequency "bias" tones (BTs) and increased the BT level until the BT caused quasi-static OHC MET saturation that reduced or "suppressed" the gain of OHC active processes. While measuring cat AN-fiber responses, 50 Hz BT level series, 70-120 dB SPL, were run alone and with CF tones, or 2.5 kHz tail-frequency tones, or side-lobe tones. BT-tone-alone responses were used to exclude BT sound levels that produced AN responses that might obscure BT suppression. Data were analyzed to show the BT phase that suppressed the tone responses at the lowest sound level. We found that AN responses to CF, tail-frequency, and side-lobe tones were suppressed at the same BT phase in almost all cases. The data are consistent with the enhancement of responses to CF, tail-frequency, and side-lobe tones all being due to the same OHC-stereocilia MET-dependent active process. Thus, OHC active processes enhance AN responses at frequencies outside of the cochlear-amplified TC-tip region in both high- and low-frequency cochlear regions. The data are consistent with the AN response enhancements being due to enhanced RL motion that drives IHC-stereocilia deflection by traditional RL-TM shear and/or by changing the RL-TM gap. Since tail-frequency basilar membrane (BM) motion is not actively enhanced, the tail-frequency IHC drive is from a vibrational mode little present on the BM, not a "second filter" of BM motion.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Auditory nerve; Cochlear mechanics; Micromechanics

Mesh:

Year:  2017        PMID: 29276975      PMCID: PMC6002897          DOI: 10.1016/j.heares.2017.12.008

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  10 in total

1.  Organ of Corti vibration within the intact gerbil cochlea measured by volumetric optical coherence tomography and vibrometry.

Authors:  Wei Dong; Anping Xia; Patrick D Raphael; Sunil Puria; Brian Applegate; John S Oghalai
Journal:  J Neurophysiol       Date:  2018-10-03       Impact factor: 2.714

2.  Amplification and Suppression of Traveling Waves along the Mouse Organ of Corti: Evidence for Spatial Variation in the Longitudinal Coupling of Outer Hair Cell-Generated Forces.

Authors:  James B Dewey; Brian E Applegate; John S Oghalai
Journal:  J Neurosci       Date:  2019-01-16       Impact factor: 6.167

3.  Intrinsic mechanical sensitivity of mammalian auditory neurons as a contributor to sound-driven neural activity.

Authors:  Maria C Perez-Flores; Eric Verschooten; Jeong Han Lee; Hyo Jeong Kim; Philip X Joris; Ebenezer N Yamoah
Journal:  Elife       Date:  2022-03-10       Impact factor: 8.140

4.  Cochlear outer hair cell electromotility enhances organ of Corti motion on a cycle-by-cycle basis at high frequencies in vivo.

Authors:  James B Dewey; Alessandro Altoè; Christopher A Shera; Brian E Applegate; John S Oghalai
Journal:  Proc Natl Acad Sci U S A       Date:  2021-10-26       Impact factor: 11.205

5.  The Elusive Cochlear Filter: Wave Origin of Cochlear Cross-Frequency Masking.

Authors:  Alessandro Altoè; Karolina K Charaziak; James B Dewey; Arturo Moleti; Renata Sisto; John S Oghalai; Christopher A Shera
Journal:  J Assoc Res Otolaryngol       Date:  2021-10-22

6.  An outer hair cell-powered global hydromechanical mechanism for cochlear amplification.

Authors:  Wenxuan He; George Burwood; Anders Fridberger; Alfred L Nuttall; Tianying Ren
Journal:  Hear Res       Date:  2021-12-01       Impact factor: 3.672

7.  Unified cochlear model for low- and high-frequency mammalian hearing.

Authors:  Aritra Sasmal; Karl Grosh
Journal:  Proc Natl Acad Sci U S A       Date:  2019-06-20       Impact factor: 11.205

Review 8.  The interplay of organ-of-Corti vibrational modes, not tectorial- membrane resonance, sets outer-hair-cell stereocilia phase to produce cochlear amplification.

Authors:  John J Guinan
Journal:  Hear Res       Date:  2020-07-30       Impact factor: 3.208

9.  Timing of the reticular lamina and basilar membrane vibration in living gerbil cochleae.

Authors:  Wenxuan He; David Kemp; Tianying Ren
Journal:  Elife       Date:  2018-09-05       Impact factor: 8.140

10.  Behaviorally relevant frequency selectivity in single- and double-on neurons in the inferior colliculus of the Pratt's roundleaf bat, Hipposideros pratti.

Authors:  Ziying Fu; Guimin Zhang; Qing Shi; Dandan Zhou; Jia Tang; Long Liu; Qicai Chen
Journal:  PLoS One       Date:  2019-01-02       Impact factor: 3.240

  10 in total

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