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DOI 10.1016/j.neuroscience.2025.08.053

Медицинская библиотека · Neuroscience · 2025

A multi-channel integrated auditory function test system.

Xiao Shijie, Zheng Yihang, Lin Guanting, Liu Jinxuan, Xiong Wei, Song Lei, Chen Fangyi

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The auditory brainstem response (ABR) remains the gold standard for evaluating hearing function in both animal models and humans. Features of ABR, including threshold, wave I amplitude and latency are critical for diagnosing and investigating the mechanisms of hearing loss. Critically, the rapid proliferation of genetically engineered mouse models in hearing research has created an imperative demand for high-throughput ABR testing capabilities. Currently, the Tucker-Davis Technologies (TDT) system serves as the standard, and nearly exclusive, platform for animal ABR assessment. However, the design of single-animal testing system, with low sampling rates, serves as limitation to certain applications such as large-scale screening and studies of high frequency distortion product otoacoustic emission (DPOAE) and cochlear microphonic (CM). We developed a four-channel ABR system enabling simultaneous testing of four subjects, coupled with a custom acoustic chamber providing > 50 dB noise attenuation across mouse hearing frequencies. The system's enhanced acoustic and electrical performance obtains high-frequency (>32 kHz) DPOAE and CM recordings beyond the capabilities of the TDT System3 and RZ6. In mouse ABR assessments, it consistently replicates TDT-measured thresholds, wave I latency, and amplitude while tripling test throughput. This comprehensive platform meets modern high-volume ABR demands, delivering superior efficiency and expanded functional assessment for scalable, high-fidelity auditory phenotyping in next-generation research.

Для цитирования: Xiao Shijie, Zheng Yihang, Lin Guanting, Liu Jinxuan, Xiong Wei, Song Lei, Chen Fangyi. A multi-channel integrated auditory function test system.. Neuroscience. 2025. DOI: 10.1016/j.neuroscience.2025.08.053.

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