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Tinnitus Correlates with Downregulation of Cortical Glutamate Decarboxylase 65 Expression But Not Auditory Cortical Map Reorganization.
Miyakawa, Asako; Wang, Weihua; Cho, Sung-Jin; Li, Delia; Yang, Sungchil; Bao, Shaowen.
Afiliación
  • Miyakawa A; Helen Wills Neuroscience Institute, University of California, Berkeley, California 94720.
  • Wang W; Department of Physiology, University of Arizona, Tucson, Arizona 85724.
  • Cho SJ; Department of Biology, College of Natural Sciences, Chungbuk National University, Cheongju, Chungbuk 361-763, Republic of Korea, and.
  • Li D; Helen Wills Neuroscience Institute, University of California, Berkeley, California 94720.
  • Yang S; Department of Biomedical Science, City University of Hong Kong, Kowloon, Hong Kong. sbao@email.arizona.edu Sungchil.Yang@cityu.edu.hk.
  • Bao S; Helen Wills Neuroscience Institute, University of California, Berkeley, California 94720, sbao@email.arizona.edu Sungchil.Yang@cityu.edu.hk.
J Neurosci ; 39(50): 9989-10001, 2019 12 11.
Article en En | MEDLINE | ID: mdl-31704784
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, knock-down of glutamate decarboxylase 65 (GAD65) expression in auditory cortex (AI) by RNA interference gave rise to tinnitus in normal-hearing FVB mice. We found that tinnitus was significantly correlated with downregulation of GAD65 in the AI. 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.SIGNIFICANCE STATEMENT Hearing loss is the biggest risk factor for tinnitus in humans. Most animal models of tinnitus also exhibit comorbid hearing loss, making it difficult to dissociate the mechanisms underlying tinnitus from mere consequences of hearing loss. Here we show that, although both C57BL/6 and FVB mice exhibited similar noise-induced hearing threshold increase, only C57BL/6, but not FVB, mice developed tinnitus following noise exposure. Although both strains showed frequency map reorganization following noise-induced hearing loss, only C57BL/6 mice had reduced glutamate decarboxylase 65 (GAD65) expression in the auditory cortex (AI). Knocking down GAD65 expression in the AI resulted in tinnitus in normal-hearing FVB mice. Our results suggest that reduced inhibitory neuronal function, but not sensory map reorganization, underlies noise-induced tinnitus.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Corteza Auditiva / Vías Auditivas / Acúfeno / Regulación hacia Abajo / Glutamato Descarboxilasa / Pérdida Auditiva Provocada por Ruido / Plasticidad Neuronal Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: J Neurosci Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Corteza Auditiva / Vías Auditivas / Acúfeno / Regulación hacia Abajo / Glutamato Descarboxilasa / Pérdida Auditiva Provocada por Ruido / Plasticidad Neuronal Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: J Neurosci Año: 2019 Tipo del documento: Article