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Tinnitus Correlates with Downregulation of Cortical Glutamate Decarboxylase 65 Expression But Not Auditory Cortical Map Reorganization

  • Asako Miyakawa
  • , Weihua Wang
  • , Sung-Jin Cho
  • , Delia Li
  • , Sungchil Yang*
  • , Shaowen Bao*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

55 Downloads (CityUHK Scholars)

Abstract

Hearing loss is the biggest risk factor for tinnitus and hearing loss-related pathological changes in the auditory pathway have been hypothesized as the mechanism underlying tinnitus. However, due to the comorbidity of tinnitus and hearing loss, it has been difficult to differentiate between neural correlates of tinnitus and consequences of hearing loss. In this study, we dissociated tinnitus and hearing loss in FVB mice, which exhibit robust resistance to tinnitus following monaural noise-induced hearing loss. Furthermore, knockdown of glutamate decarboxylase 65 (GAD65) expression in auditory cortex by RNA interference gave rise to tinnitus in normal-hearing FVB mice. We found that tinnitus was significantly correlated with down-regulation of GAD65 in the auditory cortex. By contrast, cortical map distortions, which have been hypothesized as a mechanism underlying tinnitus, were correlated with hearing loss but not tinnitus. Our findings suggest new strategies for the rehabilitation of tinnitus and other phantom sensation, such as phantom pain. 

© 2019 the authors
Original languageEnglish
Pages (from-to)9989-10001
Number of pages13
JournalThe Journal of Neuroscience
Volume39
Issue number50
Online published8 Nov 2019
DOIs
Publication statusPublished - 11 Dec 2019

Research Keywords

  • hearing loss
  • inhibition
  • noise trauma
  • sensory map plasticity
  • tinnitus

Publisher's Copyright Statement

  • COPYRIGHT TERMS OF DEPOSITED FINAL PUBLISHED VERSION FILE: This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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