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In vitro multichannel single-unit recordings of action potentials from mouse sciatic nerve

机译:小鼠坐骨神经动作电位的体外多通道单单位记录

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摘要

Electrode arrays interfacing with peripheral nerves are essential for neuromodulation devices targeting peripheral organs to relieve symptoms. To modulate (i.e., single-unit recording and stimulating) individual peripheral nerve axons remains a technical challenge. Here, we report an in vitro setup to allow simultaneous single-unit recordings from multiple mouse sciatic nerve axons. The sciatic nerve (~30 mm) was harvested and transferred to a tissue chamber, the ~5mm distal end pulled into an adjacent recording chamber filled with paraffin oil. A custom-built multi-wire electrode array was used to interface with split fine nerve filaments. Single-unit action potentials were evoked by electrical stimulation and recorded from 186 axons, of which 49.5% were classed A-type with conduction velocities (CV) greater than 1 m/s and 50.5% were C-type (CV < 1 m/s). The single-unit recordings had no apparent bias towards A- or C-type axons, were robust and repeatable for over 60 minutes, and thus an ideal opportunity to assess different neuromodulation strategies targeting peripheral nerves. For instance, ultrasonic modulation of action potential transmission was assessed using the setup, indicating increased nerve conduction velocity following ultrasound stimulus. This setup can also be used to objectively assess the design of next-generation electrode arrays interfacing with peripheral nerves.
机译:与周围神经连接的电极阵列对于靶向周围器官以缓解症状的神经调节装置至关重要。调节(即单单位记录和刺激)单个周围神经轴突仍然是技术挑战。在这里,我们报告一个体外设置,以允许从多个小鼠坐骨神经轴突同时进行单单元记录。收集坐骨神经(〜30 mm)并转移至组织腔,将〜5mm远端拉入充满石蜡油的相邻记录腔中。使用定制的多线电极阵列与分裂的细神经丝连接。通过电刺激诱发单单位动作电位并从186个轴突中记录下来,其中49.5%的A型传导速度(CV)大于1 m / s,而50.5%的C型为C型(CV <1 m / s)。单个单位的录音对A型或C型轴突没有明显的偏见,在60分钟内具有强大的可重复性,因此是评估针对周围神经的不同神经调节策略的理想机会。例如,使用该设置评估了动作电位传递的超声调制,表明超声刺激后神经传导速度增加。此设置还可用于客观评估与周围神经接口的下一代电极阵列的设计。

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