Cav3.2 T-Type Calcium Channels Are Physiologically Mandatory for the Auditory System

被引:11
|
作者
Lundt, Andreas [1 ]
Seidel, Robin [2 ]
Soos, Julien [1 ]
Henseler, Christina [1 ]
Mueller, Ralf [3 ,4 ]
Bakki, Maheshwar [1 ]
Arshaad, Muhammad Imran [1 ]
Ehninger, Dan [5 ]
Hescheler, Juergen [6 ]
Sachinidis, Agapios [6 ]
Broich, Karl [2 ]
Wormuth, Carola [1 ]
Papazoglou, Anna [1 ]
Weiergraeber, Marco [1 ]
机构
[1] Fed Inst Drugs & Med Devices, Expt Neuropsychopharmacol, Kurt Georg Kiesinger Allee 3, D-53175 Bonn, Germany
[2] Fed Inst Drugs & Med Devices, Kurt Georg Kiesinger Allee 3, D-53175 Bonn, Germany
[3] Univ Cologne, Fac Med, Dept Psychiat & Psychotherapy, Cognit Neurophysiol, Kerpener Str 62, D-50937 Cologne, Germany
[4] Univ Cologne, Fac Med, Univ Hosp Cologne, Kerpener Str 62, D-50937 Cologne, Germany
[5] German Ctr Neurodegenerat Dis, Mol & Cellular Cognit, Sigmund Freud Str 27, D-53127 Bonn, Germany
[6] Univ Cologne, Fac Med, Inst Neurophysiol, Robert Koch Str 39, D-50931 Cologne, Germany
关键词
auditory brainstem response; calcium channel; hair cells; spiral ganglion neuron; T-type; sensorineural hearing loss; SPIRAL GANGLION NEURONS; SENSORINEURAL HEARING-LOSS; CA(V)1.3 CA2+ CHANNELS; BRAIN-STEM RESPONSES; CARDIOVASCULAR-DISEASE; THERAPEUTIC FUNCTIONS; MOUSE MODELS; MICE; DYSFUNCTION; EXPRESSION;
D O I
10.1016/j.neuroscience.2019.04.024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Voltage-gated Ca2+ channels (VGCCs) play key roles in auditory perception and information processing within the inner ear and brainstem. Pharmacological inhibition of low voltage-activated (LVA) T-type Ca2+ channels is related to both age- and noise induced hearing loss in experimental animals and may represent a promising approach to the treatment of auditory impairment of various etiologies. Within the LVA Ca2+ channel subgroup, Ca(v)3.2 is the most prominently expressed T-type channel entity in the cochlea and auditory brainstem. Thus, we performed a complete gender specific click and tone burst based auditory brainstem response (ABR) analysis of Ca(v)3.2(+/-) and Ca(v)3.2(-/-) mice, including i.a. temporal progression in hearing loss, amplitude growth function and wave latency analysis as well as a cochlear qPCR based evaluation of other VGCCs transcripts. Our results, based on a self-programmed automated wavelet approach, demonstrate that both heterozygous and Ca(v)3.2 null mutant mice exhibit age-dependent increases in hearing thresholds at 5 months of age. In addition, complex alterations in WI-IV amplitudes and latencies were detected that were not attributable to alterations in the expression of other VGCCs in the auditory tract. Our results clearly demonstrate the important physiological role of Ca(v)3.2 VGCCs in the spatiotemporal organization of auditory processing in young adult mice and suggest potential pharmacological targets for interventions in the future. (C) 2019 The Author(s). Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:81 / 100
页数:20
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