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Gender specific click and tone burst evoked ABR datasets from mice lacking the Cav3.2 T-type voltage-gated calcium channel

机译:缺乏Cav3.2 T型电压门控钙通道的小鼠的性别特异性咔嗒声和音调诱发的ABR数据集

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摘要

ObjectivesVoltage-gated Ca2+ channels (VGCCs) are of central relevance in regulating Ca2+ influx into living cells. The low-voltage activated (LVA) Cav3 T-type Ca2+ channels are widely distributed throughout the brain including the peripheral auditory system and ascending auditory tract. Their exact role in auditory information processing is still not fully understood. Within the LVA subgroup, Cav3.2 T-type Ca2+ channels seem to be of special importance as qPCR revealed a steady increase in Cav3.2 transcript levels over age, e.g. in the cochlea and spiral ganglion neurons (SGN). Furthermore, pharmacological studies suggested an association between Cav3.2 expression and both age-related and noise-induced hearing loss. Given the potential functional relevance of Cav3.2 VGGCs in sensorineural hearing loss, we recorded gender specific auditory evoked brainstem responses (ABRs) upon both click and tone burst presentation. Here we present auditory brainstem response (ABR) data from Cav3.2+/+, Cav3.2+/− and Cav3.2−/− mice from both genders which are of value for researchers who want to evaluate how Cav3.2 loss affects basic auditory parameters, e.g. click and tone burst based hearing thresholds, amplitude growth function and peak latencies.
机译:目的电压门控Ca 2 + 通道(VGCC)在调节Ca 2 + 流入活细胞中具有重要意义。低压激活(LVA)Cav3 T型Ca 2 + 通道广泛分布于整个大脑,包括外周听觉系统和听觉通道。它们在听觉信息处理中的确切作用仍未被完全理解。在LVA亚组中,Cav3.2 T型Ca 2 + 通道似乎特别重要,因为qPCR显示随着年龄的增长,Cav3.2转录水平会随着年龄的增长而稳定增加。在耳蜗和螺旋神经节神经元(SGN)中。此外,药理学研究表明Cav3.2表达与年龄相关和噪音引起的听力损失之间存在关联。鉴于Cav3.2 VGGCs在感觉神经性听力损失中的潜在功能相关性,我们在点击和音调爆发时都记录了性别特定的听觉诱发性脑干反应(ABR)。在这里,我们介绍了来自Cav3.2 + / + ,Cav3.2 +/- 和Cav3.2 -/-的听觉脑干反应(ABR)数据。 sup>两种性别的小鼠,对于想要评估Cav3.2缺失如何影响基本听觉参数的研究人员来说非常有价值基于喀哒声和音调猝发的听力阈值,幅度增长函数和峰值延迟。

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