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

Autor: Anna Papazoglou, Julien Soos, Muhammad Imran Arshaad, Carola Wormuth, Andreas Lundt, Robin Seidel, Marco Weiergräber, Jürgen Hescheler, Ralf Müller, Agapios Sachinidis, Christina Henseler, Karl Broich, Dan Ehninger
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
Male
lcsh:Medicine
Audiology
Monaural
physiology [Evoked Potentials
Auditory
Brain Stem]

Amplitude
methods [Audiometry
Evoked Response]

Mice
Calcium Channels
T-Type

0302 clinical medicine
genetics [Calcium Channels
T-Type]

030212 general & internal medicine
lcsh:QH301-705.5
Voltage-dependent calcium channel
General Medicine
Click
physiology [Calcium Channels
T-Type]

medicine.anatomical_structure
Sensorineural hearing loss
Female
medicine.symptom
medicine.medical_specialty
Hearing loss
Mice
Transgenic

Biology
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
Sex Factors
ddc:570
medicine
otorhinolaryngologic diseases
Auditory system
Animals
lcsh:Science (General)
Spiral ganglion
Cochlea
deficiency [Calcium Channels
T-Type]

lcsh:R
physiopathology [Hearing Loss
Sensorineural]

medicine.disease
Cacna1h protein
mouse

Auditory brainstem responses
Disease Models
Animal

Cav3.2
030104 developmental biology
Auditory brainstem response
lcsh:Biology (General)
Calcium channel
lcsh:Q1-390
Zdroj: BMC Research Notes, Vol 12, Iss 1, Pp 1-3 (2019)
BMC Research Notes 12(1), 157 (2019). doi:10.1186/s13104-019-4169-4
ISSN: 1756-0500
DOI: 10.1186/s13104-019-4169-4
Popis: 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.
Databáze: OpenAIRE