千赫兹频率信号的斜坡产生神经传导阻滞,但无起始反应。

Edgar Peña, Nicole A Pelot, Warren M Grill
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摘要

目标。利用千赫兹频率(KHF)电信号可逆阻断周围神经传导在治疗疾病方面具有巨大的潜力。然而,发作反应,即khf诱导的兴奋在产生神经阻滞的过程中,是神经阻滞方案的一个不希望的结果。先前对KHF神经阻滞的研究发现,当KHF信号幅度在高达30khz的频率下线性上升长达60秒时,发作反应增加。在这里,我们评估了在广泛的斜坡持续时间和频率范围内的起始反应。在大鼠胫骨神经和生物物理轴突模型的实验中,我们量化了神经对持续时间为16至512秒、频率为10至83.3 kHz的线性倾斜KHF信号的反应。我们还通过使用拉科沙胺在药理学上增强缓慢失活,并在计算模型中引入缓慢失活门控变量,研究了线性斜坡期间缓慢失活对发病反应的作用。主要的结果。在实验中,足够高的频率(小于或等于20.8 kHz),其振幅斜坡足够慢(4.4-570μA s-1),产生没有开始反应的传导阻滞,并且增加的频率使更短的斜坡能够在没有开始反应的情况下阻断。实验中使用拉科沙胺增强缓慢失活也消除了发病反应。在计算模型中,匝道持续时间/匝道速率对起始反应的影响仅在引入慢速失活门控制变量后发生,并且模型没有考虑频率效应。结果首次揭示了使用电荷平衡线性斜坡KHF信号来阻断无启动响应的能力。这种新方法提高了神经阻断方案的精度,并使协调的神经控制能够恢复器官功能,例如脊髓损伤后的尿控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ramped kilohertz-frequency signals produce nerve conduction block without onset response.

Objective.Reversible block of peripheral nerve conduction using kilohertz-frequency (KHF) electrical signals has substantial potential for treating diseases. However, onset response, i.e. KHF-induced excitation en route to producing nerve block, is an undesired outcome of neural block protocols. Previous studies of KHF nerve block observed increased onset responses when KHF signal amplitude was linearly ramped for up to 60 s at frequencies up to 30 kHz. Here, we evaluated the onset response across a broad range of ramp durations and frequencies.Approach. In experiments on the rat tibial nerve and biophysical axon models, we quantified nerve responses to linearly ramped KHF signals applied for durations from 16 to 512 s and at frequencies from 10 to 83.3 kHz. We also investigated the role of slow inactivation on onset response during linear ramps by using lacosamide to enhance slow inactivation pharmacologically and by introducing a slow inactivation gating variable in computational models.Main results. In experiments, sufficiently high frequencies (⩾20.8 kHz) with amplitudes that were ramped sufficiently slowly (4.4-570μA s-1) generated conduction block without onset response, and increasing frequency enabled shorter ramps to block without onset response. Experimental use of lacosamide to enhance slow inactivation also eliminated onset response. In computational models, the effects of ramp duration/ramp rate on onset response only occurred after introducing a slow inactivation gating variable, and the models did not account for frequency effects.Significance. The results reveal, for the first time, the ability to use charge-balanced linearly ramped KHF signals to block without onset response. This novel approach enhances the precision of neural blocking protocols and enables coordinated neural control to restore organ function, such as in urinary control after spinal cord injury.

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