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首页> 外文期刊>Journal of Translational Medicine >Activation of axonal Kv7 channels in human peripheral nerve by flupirtine but not placebo - therapeutic potential for peripheral neuropathies: results of a randomised controlled trial
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Activation of axonal Kv7 channels in human peripheral nerve by flupirtine but not placebo - therapeutic potential for peripheral neuropathies: results of a randomised controlled trial

机译:氟吡汀而非安慰剂激活人周围神经轴突Kv7通道-周围神经病变的治疗潜力:一项随机对照试验的结果

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Background Flupirtine is an analgesic with muscle-relaxing properties that activates Kv7 potassium channels. Kv7 channels are expressed along myelinated and unmyelinated peripheral axons where their activation is expected to reduce axonal excitability and potentially contribute to flupirtine’s clinical profile. Trial design To investigate the electrical excitability of peripheral myelinated axons following orally administered flupirtine, in-vitro experiments on isolated peripheral nerve segments were combined with a randomised, double-blind, placebo-controlled, phase I clinical trial (RCT). Methods Threshold tracking was used to assess the electrical excitability of myelinated axons in isolated segments of human sural nerve in vitro and motoneurones to abductor pollicis brevis (APB) in situ in healthy subjects. In addition, the effect of flupirtine on ectopic action potential generation in myelinated axons was examined using ischemia of the lower arm. Results Flupirtine (3-30 μM) shortened the relative refractory period and increased post-conditioned superexcitability in human myelinated axons in vitro. Similarly, in healthy subjects the relative refractory period of motoneurones to APB was reduced 2 hours after oral flupirtine but not following placebo. Whether this effect was due to a direct action of flupirtine on peripheral axons or temperature could not be resolved. Flupirtine (200 mg p.o.) also reduced ectopic axonal activity induced by 10 minutes of lower arm ischemia. In particular, high frequency (ca. 200 Hz) components of EMG were reduced in the post-ischemic period. Finally, visual analogue scale ratings of sensations perceived during the post-ischemic period were reduced following flupirtine (200 mg p.o.). Conclusions Clinical doses of flupirtine reduce the excitability of peripheral myelinated axons. Trial registration ClinicalTrials registration is NCT01450865 .
机译:背景氟吡汀是一种具有松弛肌肉特性的镇痛药,可激活Kv7钾通道。 Kv7通道沿有髓和无髓外周轴突表达,它们的活化预计会降低轴突兴奋性,并可能有助于氟吡汀的临床表现。试验设计为了研究口服氟吡汀后外周髓鞘轴突的电兴奋性,将离体外周神经节段的体外实验与一项随机,双盲,安慰剂对照的I期临床试验(RCT)相结合。方法采用阈值跟踪法评估人腓肠神经离体段中髓鞘轴突的电兴奋性,以及运动神经元对健康受试者中短距外展短肌(APB)的电兴奋性。另外,使用下臂缺血检查了氟吡汀对有髓轴突中异位动作电位产生的影响。结果氟吡汀(3-30μM)缩短了人髓鞘轴突的相对不应期并增加了条件后超兴奋性。同样,在健康受试者中,口服氟吡汀后2小时,运动神经元对APB的相对不应期减少了,但在安慰剂之后没有减少。这种作用是否是由于氟吡汀对外周轴突的直接作用还是温度尚不清楚。氟吡汀(200 mg p.o.)还降低了下臂缺血10分钟引起的异位轴突活性。特别是,在缺血后时期,EMG的高频(约200 Hz)成分减少了。最后,氟吡汀(200 mg p.o.)降低了缺血后阶段感觉到的视觉模拟量表评分。结论临床剂量的氟吡汀可降低外周髓鞘轴突的兴奋性。试验注册临床试验注册为NCT01450865。

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