Experimental Neuropsychopharmacology, Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM), Bonn, Germany.
Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM), Bonn, Germany.
Eur J Neurosci. 2020 Apr;51(7):1583-1604. doi: 10.1111/ejn.14591. Epub 2019 Nov 3.
Voltage-gated Ca channels (VGCCs) are considered to play a key role in auditory perception and information processing within the murine inner ear and brainstem. In the past, Ca 1.3 L-type VGCCs gathered most attention as their ablation causes congenital deafness. However, isolated patch-clamp investigation and localization studies repetitively suggested that Ca 2.3 R-type VGCCs are also expressed in the cochlea and further components of the ascending auditory tract, pointing to a potential functional role of Ca 2.3 in hearing physiology. Thus, we performed auditory profiling of Ca 2.3 controls, heterozygous Ca 2.3 mice and Ca 2.3 null mutants (Ca 2.3 ) using brainstem-evoked response audiometry. Interestingly, click-evoked auditory brainstem responses (ABRs) revealed increased hearing thresholds in Ca 2.3 mice from both genders, whereas no alterations were observed in Ca 2.3 mice. Similar observations were made for tone burst-related ABRs in both genders. However, Ca 2.3 ablation seemed to prevent mutant mice from total hearing loss particularly in the higher frequency range (36-42 kHz). Amplitude growth function analysis revealed, i.a., significant reduction in ABR wave W and W amplitude in mutant animals. In addition, alterations in W -W interwave interval were observed in female Ca 2.3 mice whereas absolute latencies remained unchanged. In summary, our results demonstrate that Ca 2.3 VGCCs are mandatory for physiological auditory information processing in the ascending auditory tract.
电压门控钙通道(VGCCs)被认为在内耳和脑干的听觉感知和信息处理中发挥关键作用。过去,钙通道 1.3 型 L 型 VGCCs 受到最多关注,因为它们的缺失会导致先天性耳聋。然而,孤立的膜片钳研究和定位研究反复表明,钙通道 2.3 型 R 型 VGCCs 也在内耳和听觉上行通路的其他部分表达,这表明钙通道 2.3 在听觉生理学中具有潜在的功能作用。因此,我们使用脑干诱发反应听力测试对钙通道 2.3 对照组、杂合子钙通道 2.3 小鼠和钙通道 2.3 缺失突变体(钙通道 2.3 )进行了听觉分析。有趣的是,在两性中,钙通道 2.3 缺失突变体的 click 诱发听觉脑干反应(ABR)显示出听力阈值增加,而钙通道 2.3 缺失突变体的听力阈值没有变化。两性的 tone burst 相关 ABR 也观察到类似的变化。然而,钙通道 2.3 的缺失似乎阻止了突变体小鼠完全失聪,特别是在较高的频率范围(36-42 kHz)。振幅增长函数分析表明,突变动物的 ABR 波 W 和 W 振幅显著降低。此外,在雌性钙通道 2.3 小鼠中观察到 W-W 间隔的变化,而绝对潜伏期保持不变。总之,我们的结果表明,钙通道 2.3 VGCCs 是听觉上行通路中生理听觉信息处理所必需的。