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Time Course of Activity-Dependent Changes in Auditory Nerve Synapses Reveals Multiple Underlying Cellular Mechanisms. | LitMetric

Time Course of Activity-Dependent Changes in Auditory Nerve Synapses Reveals Multiple Underlying Cellular Mechanisms.

J Neurosci

Department of Biological Sciences, University at Buffalo, State University of New York, Buffalo, New York 14260

Published: March 2022

AI Article Synopsis

  • Abnormal acoustic activity can lead to hearing issues like tinnitus and language processing disorders, but the cellular and synaptic changes underlying these problems are not well understood.
  • This study investigates how auditory nerve synapses in mice respond over time to noise exposure and conductive hearing loss, revealing complex changes in synaptic behavior.
  • Key findings include initial decreases in neurotransmitter release followed by gradual recovery, highlighting different mechanisms that adjust synaptic strength in response to varying levels of sound.

Article Abstract

Abnormal levels of acoustic activity can result in hearing problems such as tinnitus and language processing disorders, but the underlying cellular and synaptic changes triggered by abnormal activity are not well understood. To address this issue, we studied the time course of activity-dependent changes that occur at auditory nerve synapses in mice of both sexes after noise exposure and conductive hearing loss. We found that EPSC amplitude and synaptic depression decreased within 2 d of noise exposure through a decrease in the probability of vesicle release (). This was followed by a gradual increase in EPSC amplitude through a larger pool of releasable vesicles (). Occlusion of the ear canal led to a rapid decrease in EPSC amplitude through a decrease in , which was followed by an increase in EPSC amplitude and synaptic depression through an increase in After returning to normal sound levels, synaptic depression recovered to control levels within 1-2 d. However, repeated exposure to noise for as little as 8 h/d caused synaptic changes after 7 d, suggesting recovery did not fully offset changes. Thus, there appear to be three activity-dependent mechanisms in auditory nerve synapses-bidirectional changes in in 1-2 d, slower bidirectional changes in through synaptic growth or retraction, and rapid downregulation of with low activity. The dynamic changes indicate that multiple mechanisms are present to fine-tune synaptic fidelity across different acoustic conditions in a simple relay. Hearing impairments can arise from exposure to noise or conductive hearing loss. This appears to result from changes in the brain, but the mechanisms are not well understood. We study this issue by studying the synapses made by auditory nerve fibers called endbulbs of Held. These synapses undergo bidirectional changes in size and release probability of neurotransmitter in response to increased or decreased activity. Here, we made a close examination of how quickly these synaptic characteristics change, which indicates there are at least three cellular mechanisms underlying changes. Furthermore, repeated exposure to brief periods of noise can produce cumulative effects. These changes could significantly affect hearing, especially because they occur at the start of the central auditory pathway.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944231PMC
http://dx.doi.org/10.1523/JNEUROSCI.1583-21.2022DOI Listing

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