Department of Integrative Physiology, National Institute for Physiological Sciences, Okazaki 444-8585, Japan; Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto 390-8621, Japan.
Department of Integrative Physiology, National Institute for Physiological Sciences, Okazaki 444-8585, Japan.
Clin Neurophysiol. 2014 Sep;125(9):1870-7. doi: 10.1016/j.clinph.2014.01.009. Epub 2014 Jan 28.
To investigate whether intraepidermal electrical stimulation (IES) can evaluate nociceptive Aδ- and C-fiber dysfunctions of an experimental model of small-fiber neuropathy (SFN) with transdermal lidocaine.
Lidocaine tape or placebo was applied to the dorsum of the feet in 14 healthy subjects. Reaction time (RT), sensory threshold, and evoked potentials (EPs) were measured using IES before, and 30 and 60 min after lidocaine/placebo application.
All subjects felt pricking sensations following Aδ-fiber stimulation, and light painful sensations such as pricking, tingling, or burning following C-fiber stimulation using IES. RT was divided bimodally between Aδ- and C-fiber stimulations. At 30 min, lidocaine increased the sensory threshold and decreased the amplitude of EPs in both fiber stimulations. At 60 min, lidocaine's effects were greater for C fibers than for Aδ fibers. The sensory threshold and amplitude of EPs were unchanged among placebo sessions.
IES demonstrated differential effects of transdermal lidocaine on nociceptive Aδ and C fibers, and elucidated the pathophysiology of the experimental model of SFN.
IES has advantages in terms of cost, convenience, and invasiveness. It may have potential for a clinical tool to elucidate the pathophysiology of patients with SFN, including the differences between Aδ and C fibers.
研究经皮利多卡因是否可通过表皮内电刺激(IES)来评估小纤维神经病(SFN)实验模型中伤害性 Aδ 和 C 纤维功能障碍。
将利多卡因贴剂或安慰剂贴敷于 14 名健康受试者的足部背侧。在贴敷利多卡因/安慰剂前、后 30 和 60 分钟,使用 IES 测量反应时间(RT)、感觉阈值和诱发电位(EP)。
所有受试者在 Aδ 纤维刺激后均感觉到刺痛感,在 C 纤维刺激后感觉到刺痛、刺痛或烧灼感等轻痛感。RT 在 Aδ 和 C 纤维刺激之间呈双峰分布。30 分钟时,利多卡因增加了两种纤维刺激的感觉阈值并降低了 EP 的振幅。60 分钟时,利多卡因对 C 纤维的作用大于 Aδ 纤维。安慰剂治疗期间,感觉阈值和 EP 振幅均无变化。
IES 显示经皮利多卡因对伤害性 Aδ 和 C 纤维有不同的影响,并阐明了 SFN 实验模型的病理生理学。
IES 在成本、便利性和侵入性方面具有优势。它可能具有成为一种临床工具的潜力,用于阐明包括 Aδ 和 C 纤维差异在内的 SFN 患者的病理生理学。