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Auditory nerve synapses persist in ventral cochlear nucleus long after loss of acoustic input in mice with early-onset progressive hearing loss

机译:听觉神经突触在早期发作性进行性听力丧失的小鼠中失去听觉输入后很长一段时间仍在腹侧耳蜗核中存在

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摘要

Perceptual performance in persons with hearing loss, especially those using devices to restore hearing, is not fully predicted by traditional audiometric measurements designed to evaluate the status of peripheral function. The integrity of auditory brainstem synapses may vary with different forms of hearing loss, and differential effects on the auditory nerve-brain interface may have particularly profound consequences for the transfer of sound from ear to brain. Loss of auditory nerve synapses in ventral cochlear nucleus (VCN) has been reported after acoustic trauma, ablation of the organ of Corti, and administration of ototoxic compounds. The effects of gradually acquired forms deafness on these synapses are less well understood. We investigated VCN gross morphology and auditory nerve synapse integrity in DBA/2J mice with early-onset progressive sensorineural hearing loss. Hearing status was confirmed using auditory brainstem response audiometry and acoustic startle responses. We found no change in VCN volume, number of macroneurons, or number of VGLUT1-positive auditory nerve terminals between young adult and older, deaf DBA/2J. Cell-type specific analysis revealed no difference in the number of VGLUT1 puncta contacting bushy and multipolar cell body profiles, but the terminals were smaller in deaf DBA/2J mice. Transmission electron microscopy confirmed the presence of numerous healthy, vesicle-filled auditory nerve synapses in older, deaf DBA/2J mice. The present results suggest that synapses can be preserved over a relatively long time-course in gradually acquired deafness. Elucidating the mechanisms supporting survival of central auditory nerve synapses in models of acquired deafness may reveal new opportunities for therapeutic intervention.
机译:传统的听力测量旨在评估周围功能的状态,无法完全预测听力丧失者(尤其是使用设备恢复听力的人)的感知性能。听觉脑干突触的完整性可能随听力损失的不同形式而变化,并且对听觉神经脑接口的不同影响可能会对声音从耳朵到大脑的传递产生特别深远的影响。在听觉创伤,Corti器官消融和给予耳毒性化合物后,腹侧耳蜗核(VCN)的听觉神经突触丧失已有报道。逐渐获得性耳聋对这些突触的影响了解得很少。我们调查了早期发作的进行性感觉神经性听力损失的DBA / 2J小鼠的VCN总体形态和听觉神经突触完整性。使用听觉脑干反应测听法和听觉惊吓反应确认了听力状态。我们发现,聋人和成年聋人DBA / 2J之间的VCN体积,大神经元数量或VGLUT1阳性听觉神经末梢数量没有变化。细胞类型的特异性分析显示,接触丛状和多极细胞体轮廓的VGLUT1点的数量没有差异,但在聋的DBA / 2J小鼠中末端较小。透射电子显微镜证实,老年聋的DBA / 2J小鼠存在大量健康的囊泡性听神经突触。目前的结果表明,突触可以在相对较长的时间范围内保持在逐渐获得性耳聋中。在获得性耳聋模型中阐明支持中枢听觉神经突触存活的机制可能揭示治疗干预的新机会。

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