Shaopeng Zhang, Longtu Chen, Sajjad Rigi Ladez, Ahmet Seferge, Jia Liu, Bin Feng
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Action potentials were evoked on one end of the nerve and recorded on the other end from teased nerve filaments, i.e., single-fiber recordings. ePNS was delivered in the middle of the nerve trunk using a glass suction electrode at frequencies of 5, 10, 50, 100, 500, and 1000 Hz.Suprathreshold ePNS reversibly blocks axonal neural transmission of both thinly myelinated Aδ-fiber axons and unmyelinated C-fiber axons. ePNS leads to a progressive decrease in conduction velocity (CV) until transmission blockage, suggesting activity-dependent conduction slowing. The blocking efficiency is dependent on the axonal conduction velocity, with Aδ-fibers efficiently blocked by 50–1000 Hz stimulation and C-fibers blocked by 10–50 Hz. The corresponding NEURON simulation of action potential transmission indicates that the disrupted transmembrane sodium and potassium concentration gradients underly the transmission block by the ePNS.The current study provides direct evidence of reversible Aδ- and C-fiber transmission blockage by low-frequency (<100 Hz) electrical stimulation of the nerve trunk, a previously overlooked mechanism that can be harnessed to enhance the therapeutic effect of ePNS in treating neurological disorders.","PeriodicalId":509131,"journal":{"name":"Frontiers in Neuroscience","volume":"54 22","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Blocking Aδ- and C-fiber neural transmission by sub-kilohertz peripheral nerve stimulation\",\"authors\":\"Shaopeng Zhang, Longtu Chen, Sajjad Rigi Ladez, Ahmet Seferge, Jia Liu, Bin Feng\",\"doi\":\"10.3389/fnins.2024.1404903\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We recently showed that sub-kilohertz electrical stimulation of the afferent somata in the dorsal root ganglia (DRG) reversibly blocks afferent transmission. 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引用次数: 0
摘要
我们最近发现,对背根神经节(DRG)传入体的亚千赫电刺激可逆性地阻断传入传导。在此,我们进一步研究了通过外周神经电刺激(ePNS)刺激神经干是否能实现类似的传导阻滞。我们通过从小鼠身上采集的两条躯体神经(坐骨神经和隐神经)和一条自主神经(迷走神经)的体外单纤维记录,探索了 ePNS 传导阻滞的机制和参数。在神经的一端诱发动作电位,在另一端通过挑逗神经丝记录动作电位,即单纤记录、阈上 ePNS 可逆性地阻断髓鞘较薄的 Aδ 纤维轴突和无髓鞘的 C 纤维轴突的轴突神经传导。阻断效率取决于轴突传导速度,50-1000 赫兹的刺激可有效阻断 Aδ 纤维,10-50 赫兹的刺激可阻断 C 纤维。目前的研究提供了低频(<100 Hz)电刺激神经干可逆性阻断 Aδ 和 C 纤维传导的直接证据,这是一种以前被忽视的机制,可以利用它来增强 ePNS 在治疗神经系统疾病方面的疗效。
Blocking Aδ- and C-fiber neural transmission by sub-kilohertz peripheral nerve stimulation
We recently showed that sub-kilohertz electrical stimulation of the afferent somata in the dorsal root ganglia (DRG) reversibly blocks afferent transmission. Here, we further investigated whether similar conduction block can be achieved by stimulating the nerve trunk with electrical peripheral nerve stimulation (ePNS).We explored the mechanisms and parameters of conduction block by ePNS via ex vivo single-fiber recordings from two somatic (sciatic and saphenous) and one autonomic (vagal) nerves harvested from mice. Action potentials were evoked on one end of the nerve and recorded on the other end from teased nerve filaments, i.e., single-fiber recordings. ePNS was delivered in the middle of the nerve trunk using a glass suction electrode at frequencies of 5, 10, 50, 100, 500, and 1000 Hz.Suprathreshold ePNS reversibly blocks axonal neural transmission of both thinly myelinated Aδ-fiber axons and unmyelinated C-fiber axons. ePNS leads to a progressive decrease in conduction velocity (CV) until transmission blockage, suggesting activity-dependent conduction slowing. The blocking efficiency is dependent on the axonal conduction velocity, with Aδ-fibers efficiently blocked by 50–1000 Hz stimulation and C-fibers blocked by 10–50 Hz. The corresponding NEURON simulation of action potential transmission indicates that the disrupted transmembrane sodium and potassium concentration gradients underly the transmission block by the ePNS.The current study provides direct evidence of reversible Aδ- and C-fiber transmission blockage by low-frequency (<100 Hz) electrical stimulation of the nerve trunk, a previously overlooked mechanism that can be harnessed to enhance the therapeutic effect of ePNS in treating neurological disorders.