Literature DB >> 9387987

Evidence that inner hair cells are the major source of cochlear summating potentials.

X Y Zheng1, D L Ding, S L McFadden, D Henderson.   

Abstract

The role of the inner hair cells (IHCs) in generating the cochlear summating potentials (SP) was assessed by measuring SP, cochlear nerve action potentials (CAP), cochlear microphonics (CM) and 2f1-f2 distortion product otoacoustic emissions (DPOAEs) in 15 chinchillas with either acute chemical de-afferentation, accomplished by applying kainic acid to the round window, or surgical de-afferentation and basal IHC loss, which developed within two months after sectioning the auditory nerve. In the auditory nerve sectioned ears, type I ganglion cells disappeared whereas most, if not all, type II ganglion cells were still present. Histological analysis of surface preparations and sections through the modiolus verified the de-afferentation in both models and showed a large IHC loss at the base of the cochlea in the ears with the auditory nerve sectioned while other structures of the cochlea remained intact. Unoperated (left) ears of 9 animals served as controls. CM and DPOAEs were normal in all ears whereas the CAP was substantially depressed in de-afferented ears. Comparisons among the SP input-output functions suggest that (1) the IHCs are the major generator of SP recorded from the round window in chinchilla, in particular at low to moderate stimulus levels, (2) the SP recorded from the round window largely reflects the responses from hair cells at the base of the cochlea, and (3) kainic acid results in an increase of SP amplitude to high-level stimuli whereas the SP to low- to moderate-level stimuli remains in the normal range.

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Year:  1997        PMID: 9387987     DOI: 10.1016/s0378-5955(97)00127-5

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


  27 in total

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Journal:  Hear Res       Date:  2018-10-29       Impact factor: 3.208

2.  Prolonged low-level noise-induced plasticity in the peripheral and central auditory system of rats.

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3.  An analytic approach to identifying the sources of the low-frequency round window cochlear response.

Authors:  Aryn M Kamerer; Mark E Chertoff
Journal:  Hear Res       Date:  2019-02-15       Impact factor: 3.208

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Authors:  Michael S Harris; William J Riggs; Christopher K Giardina; Brendan P O'Connell; Jourdan T Holder; Robert T Dwyer; Kanthaiah Koka; Robert F Labadie; Douglas C Fitzpatrick; Oliver F Adunka
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6.  Hair cell and neural contributions to the cochlear summating potential.

Authors:  Andrew K Pappa; Kendall A Hutson; William C Scott; J David Wilson; Kevin E Fox; Maheer M Masood; Christopher K Giardina; Stephen H Pulver; Gilberto D Grana; Charles Askew; Douglas C Fitzpatrick
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7.  Can auditory brain stem response accurately reflect the cochlear function?

Authors:  Dalian Ding; Jianhui Zhang; Wenjuan Li; Dong Li; Jintao Yu; Xuewen Wu; Weidong Qi; Fang Liu; Haiyan Jiang; Haibo Shi; Hong Sun; Peng Li; Weiluo Huang; Richard Salvi
Journal:  J Neurophysiol       Date:  2020-10-07       Impact factor: 2.714

8.  Electrophysiological correlates of progressive sensorineural pathology in carboplatin-treated chinchillas.

Authors:  Mohamed M El-Badry; Sandra L McFadden
Journal:  Brain Res       Date:  2007-01-02       Impact factor: 3.252

9.  Evaluation of inner hair cell and nerve fiber loss as sufficient pathologies underlying auditory neuropathy.

Authors:  Mohamed M El-Badry; Sandra L McFadden
Journal:  Hear Res       Date:  2009-06-14       Impact factor: 3.208

10.  Abnormal cochlear potentials from deaf patients with mutations in the otoferlin gene.

Authors:  Rosamaria Santarelli; Ignacio Del Castillo; Montserrat Rodríguez-Ballesteros; Pietro Scimemi; Elona Cama; Edoardo Arslan; Arnold Starr
Journal:  J Assoc Res Otolaryngol       Date:  2009-07-28
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