Biophysics Program, University of Michigan, Ann Arbor, Michigan, United States of America.
Department of Mechanical Engineering, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS Comput Biol. 2021 Jan 22;17(1):e1008499. doi: 10.1371/journal.pcbi.1008499. eCollection 2021 Jan.
Hidden hearing loss (HHL) is an auditory neuropathy characterized by normal hearing thresholds but reduced amplitudes of the sound-evoked auditory nerve compound action potential (CAP). In animal models, HHL can be caused by moderate noise exposure or aging, which induces loss of inner hair cell (IHC) synapses. In contrast, recent evidence has shown that transient loss of cochlear Schwann cells also causes permanent auditory deficits in mice with similarities to HHL. Histological analysis of the cochlea after auditory nerve remyelination showed a permanent disruption of the myelination patterns at the heminode of type I spiral ganglion neuron (SGN) peripheral terminals, suggesting that this defect could be contributing to HHL. To shed light on the mechanisms of different HHL scenarios observed in animals and to test their impact on type I SGN activity, we constructed a reduced biophysical model for a population of SGN peripheral axons whose activity is driven by a well-accepted model of cochlear sound processing. We found that the amplitudes of simulated sound-evoked SGN CAPs are lower and have greater latencies when heminodes are disorganized, i.e. they occur at different distances from the hair cell rather than at the same distance as in the normal cochlea. These results confirm that disruption of heminode positions causes desynchronization of SGN spikes leading to a loss of temporal resolution and reduction of the sound-evoked SGN CAP. Another mechanism resulting in HHL is loss of IHC synapses, i.e., synaptopathy. For comparison, we simulated synaptopathy by removing high threshold IHC-SGN synapses and found that the amplitude of simulated sound-evoked SGN CAPs decreases while latencies remain unchanged, as has been observed in noise exposed animals. Thus, model results illuminate diverse disruptions caused by synaptopathy and demyelination on neural activity in auditory processing that contribute to HHL as observed in animal models and that can contribute to perceptual deficits induced by nerve damage in humans.
隐性听力损失(HHL)是一种听觉神经病,其特征为听力阈值正常,但声音诱发的听神经复合动作电位(CAP)的幅度降低。在动物模型中,HHL 可由中度噪声暴露或衰老引起,这会导致内毛细胞(IHC)突触丧失。相比之下,最近的证据表明,耳蜗施万细胞的短暂丧失也会导致具有 HHL 相似特征的小鼠出现永久性听觉缺陷。听觉神经再髓鞘后的耳蜗组织学分析显示,I 型螺旋神经节神经元(SGN)外周末梢的髓鞘模式发生永久性破坏,这表明这种缺陷可能是 HHL 的原因之一。为了阐明在动物中观察到的不同 HHL 情况的机制,并测试其对 I 型 SGN 活性的影响,我们构建了一个简化的生物物理模型,用于模拟 SGN 外周轴突的群体活动,其活动由公认的耳蜗声音处理模型驱动。我们发现,当半神经节紊乱时,模拟声音诱发的 SGN CAP 的幅度更低,潜伏期更长,即它们发生在与正常耳蜗不同的距离,而不是在相同的距离。这些结果证实,半神经节位置的破坏导致 SGN 尖峰失步,导致时间分辨率降低和声音诱发的 SGN CAP 减少。导致 HHL 的另一个机制是 IHC 突触丧失,即突触病。为了比较,我们通过去除高阈值 IHC-SGN 突触模拟突触病,发现模拟声音诱发的 SGN CAP 的幅度降低,而潜伏期保持不变,这与噪声暴露动物中观察到的情况一致。因此,模型结果阐明了突触病和脱髓鞘对听觉处理中神经活动的不同破坏,这些破坏导致了动物模型中观察到的 HHL,并可能导致人类神经损伤引起的感知缺陷。