首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Noise-induced Cochlear Synaptopathy with and Without Sensory Cell Loss
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Noise-induced Cochlear Synaptopathy with and Without Sensory Cell Loss

机译:噪声诱导的耳蜗突触术,没有感官细胞损失

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Prior work has provided extensive documentation of threshold sensitivity and sensory hair cell losses after noise exposure. It is now clear, however, that cochlear synaptic loss precedes such losses, at least at low-moderate noise doses, silencing affected neurons. To address questions of whether, and how, cochlear synaptopathy and underlying mechanisms change as noise dose is varied, we assessed cochlear physiologic and histologic consequences of a range of exposures varied in duration from 15 min to 8 h and in level from 85 to 112 dB SPL. Exposures delivered to adult CBA/CaJ mice produced acute elevations in hair cell- and neural-based response thresholds ranging from trivial (similar to 5 dB) to large (similar to 50 dB), followed by varying degrees of recovery. Males appeared more noise vulnerable for some conditions of exposure. There was little to no inner hair cell (IHC) loss, but outer hair cell (OHC) loss could be substantial at highest frequencies for highest noise doses. Synapse loss was an early manifestation of noise injury and did not scale directly with either temporary or permanent threshold shift. With increasing noise dose, synapse loss grew to similar to 50%, then declined for exposures yielding permanent hair cell injury/loss. All synaptopathic, but no non-synaptopathic exposures produced persistent neural response amplitude declines; those additionally yielding permanent OHC injury/loss also produced persistent reductions in OHC-based responses and exaggerated neural amplitude declines. Findings show that widespread cochlear synaptopathy can be present with and without noise-induced sensory cell loss and that differing patterns of cellular injury influence synaptopathic outcomes. (C) 2019 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:在噪声暴露后,事先工作提供了广泛的阈值敏感性和感觉毛细胞损失的文献。然而,现在是耳蜗突触损失在这种损失之前,至少在低于中度噪声剂量,沉默受影响的神经元。为了解决是否如何改变噪声剂量的耳蜗突触病变和潜在机制如何变化的问题,我们评估了一系列暴露的耳蜗生理和组织学后果,从15分钟到8小时,水平为85至112 dB。 SPL。递送给成人CBA / CAJ小鼠的曝光在毛细胞和神经基响应阈值中产生急性升高,从而从微不足道(类似于5 dB)到大(类似于50dB),然后改变恢复程度。男性出现了更多噪音易受某些曝光条件的噪音。几乎没有内部毛细胞(IHC)损失,但外毛细胞(OHC)损耗可能在最高噪声剂量上的最高频率上具有很大的基本。 Synapse损失是抗噪声的早期表现,并没有直接缩放临时或永久性阈值偏移。随着噪音剂量的增加,突触损失增长至50%,随后拒绝曝光,产生永久性毛细胞损伤/损失。所有突触病,但没有非突触病暴露产生持续的神经反应幅度下降;另外屈服于永久性OCC损伤/损失的那些也产生了基于OCC的反应和夸张的神经振幅下降的持续减少。结果表明,广泛的耳蜗突触术可以存在,并且没有噪声诱导的感官细胞损失,并且细胞损伤的不同模式影响突触疗法结果。 (c)2019年IBRO。 elsevier有限公司出版。保留所有权利。

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