Changes in microRNA Expression in the Cochlear Nucleus and Inferior Colliculus after Acute Noise-Induced Hearing Loss

Int J Mol Sci. 2020 Nov 20;21(22):8792. doi: 10.3390/ijms21228792.

Abstract

Noise-induced hearing loss (NIHL) can lead to secondary changes that induce neural plasticity in the central auditory pathway. These changes include decreases in the number of synapses, the degeneration of auditory nerve fibers, and reorganization of the cochlear nucleus (CN) and inferior colliculus (IC) in the brain. This study investigated the role of microRNAs (miRNAs) in the neural plasticity of the central auditory pathway after acute NIHL. Male Sprague-Dawley rats were exposed to white band noise at 115 dB for 2 h, and the auditory brainstem response (ABR) and morphology of the organ of Corti were evaluated on days 1 and 3. Following noise exposure, the ABR threshold shift was significantly smaller in the day 3 group, while wave II amplitudes were significantly larger in the day 3 group compared to the day 1 group. The organ of Corti on the basal turn showed evidence of damage and the number of surviving outer hair cells was significantly lower in the basal and middle turn areas of the hearing loss groups relative to controls. Five and three candidate miRNAs for each CN and IC were selected based on microarray analysis and quantitative reverse transcription PCR (RT-qPCR). The data confirmed that even short-term acoustic stimulation can lead to changes in neuroplasticity. Further studies are needed to validate the role of these candidate miRNAs. Such miRNAs may be used in the early diagnosis and treatment of neural plasticity of the central auditory pathway after acute NIHL.

Keywords: cochlear nucleus; inferior colliculus; microRNAs; neuroplasticity; noise-induced hearing loss.

MeSH terms

  • Animals
  • Cochlear Nucleus* / metabolism
  • Cochlear Nucleus* / pathology
  • Evoked Potentials, Auditory, Brain Stem
  • Hearing Loss, Noise-Induced / metabolism*
  • Inferior Colliculi* / metabolism
  • Inferior Colliculi* / pathology
  • Male
  • MicroRNAs / metabolism*
  • Neuronal Plasticity*
  • Organ of Corti / pathology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • MicroRNAs