Abstract

The occurrence of tinnitus can be linked to hearing loss in the majority of cases, but there is nevertheless a large degree of unexplained heterogeneity in the relation between hearing loss and tinnitus. Part of the problem might be that hearing loss is usually quantified in terms of increased hearing thresholds, which only provides limited information about the underlying cochlear damage. Moreover, noise exposure that does not cause hearing threshold loss can still lead to “hidden hearing loss” (HHL), i.e., functional deafferentation of auditory nerve fibers (ANFs) through loss of synaptic ribbons in inner hair cells. While it is known that increased hearing thresholds can trigger increases in spontaneous neural activity in the central auditory system, i.e., a putative neural correlate of tinnitus, the central effects of HHL have not yet been investigated. Here, we exposed mice to octave-band noise at 100 and 105 dB SPL to generate HHL and permanent increases of hearing thresholds, respectively. Deafferentation of ANFs was confirmed through measurement of auditory brainstem responses and cochlear immunohistochemistry. Acute extracellular recordings from the auditory midbrain (inferior colliculus) demonstrated increases in spontaneous neuronal activity (a putative neural correlate of tinnitus) in both groups. Surprisingly, the increase in spontaneous activity was most pronounced in the mice with HHL, suggesting that the relation between hearing loss and neuronal hyperactivity might be more complex than currently understood. Our computational model indicated that these differences in neuronal hyperactivity could arise from different degrees of deafferentation of low-threshold ANFs in the two exposure groups. Our results demonstrate that HHL is sufficient to induce changes in central auditory processing, and they also indicate a non-monotonic relationship between cochlear damage and neuronal hyperactivity, suggesting an explanation for why tinnitus might occur without obvious hearing loss and conversely why hearing loss does not always lead to tinnitus.

Highlights

  • Epidemiological data suggest a close relation between hearing loss and tinnitus

  • We investigated the effects of two different levels of noise exposure – 100 dB SPL and 105 dB SPL – on young adult male CBA/Ca mice, using auditory brainstem response (ABR) measurements, cochlear immunohistochemistry, and multiunit recordings from the IC

  • We examined peripheral and central auditory function in mice exposed to different levels of noise; 100 dB SPL to elicit temporary shifts in hearing thresholds but long-term deafferentation of inner hair cells (IHCs) synapses, and 105 dB SPL to elicit both permanent threshold shifts and deafferentation

Read more

Summary

Introduction

Epidemiological data suggest a close relation between hearing loss and tinnitus. Most tinnitus patients have a certain degree of hearing loss [1, 2], tinnitus prevalence rises with hearing loss [3], 75–90% of patients with otosclerosis experience tinnitus [4, 5], as do 80% of patients with idiopathic sudden sensorineural hearing loss [6]. The degree of outer hair cell loss, for example, only shows a moderate correlation to hearing threshold shifts [14], and cochlear dead regions, i.e., cochlear regions with severe loss of inner hair cells (IHCs), cannot be reliably detected through audiometry alone [15]. Hearing thresholds are poor predictors of listening performance [16], and some hearing problems might not be detected by audiometry at all

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call