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

Objectives Voltage-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. Data description Information presented here includes ABR data from age-matched female and male Cav3.2+/+, Cav3.2+/− and Cav3.2−/− mice and technical aspects of the auditory recording protocol. Data were recorded using a commercially available ABR setup from Tucker Davis Technologies Inc. (TDT). Raw data files (arf.-file format) were exported as txt.-files with free access for analysis.


Objective
Voltage-gated Ca 2+ channels are key players in regulating cellular Ca 2+ homeostasis. Only few Ca 2+ channels have been functionally related to auditory information processing including Ca v 1.3 L-type Ca 2+ channels, the ablation of which results in congenital deafness. Recent animal studies suggested that Ca v 3.2 T-type Ca 2+ channels might play a role in age-and noise-induced hearing loss as ablation of the channel seemed to protect from sensorineural hearing loss. On the other hand, Ca v 3.2 Ca 2+ channels were reported to exhibit increased expression with age in the inner ear/spiral ganglion neurons pointing to an important functional role in the auditory system. Interestingly, no auditory profiling of Ca v 3.2 +/− and Ca v 3.2 −/− mice had been performed to unravel the physiological involvement of Ca v 3.2 in the peripheral and ascending auditor tract. To do so, we carried out click and tone burst evoked auditory brainstem response (ABR) recordings from Ca v 3.2 +/+ , Ca v 3.2 +/− and Ca v 3.2 −/− mice from both genders. Monaural recording results in all three lines were analyzed for threshold alterations and differences in peak amplitudes and peak latencies and submitted elsewhere. Raw ABR data were exported as txt.-files to provide free access and to enable researchers to carry out their own ABR data analysis, including further investigation of binaural recordings or application of additional manual and/ or automatic analytical tools (Table 1).

Experimental animals
Ca v 3. All ABR recordings were performed under free field conditions using a single loudspeaker (MF1 Multi-Function Speaker, TDT, USA) which was positioned 10 cm opposite to the rostrum of the animals.
The SigGenRZ software (TDT) was used to program stimulus protocols for click and tone bursts. The bioelectrical ABR signals recorded from the subdermal electrodes were transferred to a head stage (RA4LI, TDT) and forwarded to the preamplifier (RA4PA, TDT) with 20-fold amplification.
ABR data acquisition was carried out at a sampling rate of 24.4 kHz and signals were bandpass filtered (high pass 300 Hz, low pass 5 kHz) using a 6-pole Butterworth filter. The individual ABR data acquisition time was 25 ms starting with a 5 ms baseline period prior to the individual acoustic stimulus onset (pre ABR baseline) and exceeding the 10 ms ABR section by another 10 ms baseline (post ABR baseline) [Lundt et al., unpublished].
Two types of acoustic stimuli were applied for ABR recordings using the SigGenRZ software (TDT) and applied via the TDT BioSigRZ platform. The first stimulus entity was a click of 100 µs duration, with alternating polarity (switching between condensation and rarefaction).
The second stimulus entity was a 4.5 ms tone burst (transient sinusoidal plus) of alternating polarity with Hann envelope rise and fall times of 1.5 ms duration. The frequency range covers 1-42 kHz in 6 kHz steps. All acoustic stimuli were applied 300 times at a rate of 20 Hz for averaging. Sound pressure levels (SPL) were increased in 5 dB steps for clicks and 10 dB steps for tone bursts, starting from 0 dB up to 90 dB (increasing SPL mode). Sound pressure levels for tone bursts within the range of 1-42 kHz were calibrated each day prior to recording [Lundt et al., unpublished].

Limitations
ABR data presented here were performed under standard free field conditions. Data were recorded from agematched animals of ~ 20 weeks. We did not record from animals of different age.
Authors' contributions AL, data acquisition; CH, animal housing and genotyping; CW, data management; JS, data acquisition; RS, data management; RM, data management; IMA, data management; KB, drafting manuscript; JH, drafting manuscript; AS, drafting manuscript; DE, drafting manuscript; AP, data acquisition, drafting manuscript; MW, project management, project planning, data acquisition, writing manuscript. All authors read and approved the final manuscript.