Department of Experimental Pain Research, Medical Faculty Mannheim, University of Heidelberg, Heidelberg, Germany.
Eur J Pain. 2021 Feb;25(2):385-397. doi: 10.1002/ejp.1678. Epub 2020 Nov 10.
Intradermal injection of 1 µg nerve growth factor (NGF) causes sustained nociceptor sensitization. Slowly depolarizing electrical current preferentially activates C-nociceptors.
We explored the differential contribution of A-delta and C-nociceptors in NGF-sensitized skin using slowly depolarizing transcutaneous electrical current stimuli, CO2 laser heat, mechanical impact, and A-fibre compression block. In 14 healthy volunteers, pain rating was recorded on a numeric scale at days 1-14 after NGF treatment. Ratings during A-fibre conduction block were investigated at days 3 and 7 post-NGF.
Pain ratings to electrical, CO2 heat and mechanical impact stimuli were enhanced (>30%, p < .0005, ANOVA) at NGF-injection sites. Axon reflex erythema evoked by electrical stimulation was also larger at NGF-injection sites (p < .02, ANOVA). Diminution of pain during continuous (1 min) sinusoidal current stimulation at 4 Hz was less pronounced after NGF (p < .05, ANOVA). Pain ratings to electrical sinusoidal and mechanical impact stimuli during A-fibre conduction block were significantly elevated at the NGF sites compared to NaCl-treated skin (p < .05, ANOVA).
NGF-induced sensitization of human skin to electrical and mechanical stimuli is primarily driven by C-nociceptors with little contribution from A-delta fibres. Less-pronounced accommodation during ongoing sinusoidal stimulation suggests that NGF could facilitate axonal spike generation and conduction in primary afferent nociceptors in humans. Further studies using this sinusoidal electrical stimulation profile to investigate patients with chronic inflammatory pain may allow localized assessment of skin C-nociceptors and their putative excitability changes under pathologic conditions.
The application of novel slowly depolarizing electrical stimuli demonstrated a predominant C-nociceptor sensitization in NGF-treated skin. Increased pain ratings, larger axon reflex erythema and less accommodation of C-fibres to ongoing sinusoidal stimulation all indicated an enhanced nociceptor discharge after NGF. A-fibre conduction block had little effect on electrical and mechanical hyperalgesia skin in NGF-treated compared to NaCl-treated skin. This electrical stimulus profile may be applicable for patients with chronic inflammatory pain, allowing localized assessment of skin C-nociceptors and their putative excitability changes under pathologic conditions.
皮内注射 1μg 神经生长因子(NGF)可导致持续性伤害感受器敏化。缓慢去极化电流优先激活 C 型伤害感受器。
我们使用缓慢去极化经皮电流刺激、CO2 激光热、机械冲击和 A 纤维压缩阻断,在 NGF 敏化皮肤中探索 Aδ 和 C 型伤害感受器的差异贡献。在 14 名健康志愿者中,在 NGF 治疗后第 1-14 天记录数字量表上的疼痛评分。在 NGF 后第 3 和 7 天研究 A 纤维传导阻断期间的评分。
电、CO2 热和机械冲击刺激的疼痛评分在 NGF 注射部位增强(>30%,p<0.0005,ANOVA)。电刺激引起的轴突反射红斑也在 NGF 注射部位更大(p<0.02,ANOVA)。NGF 后,4Hz 持续(1 分钟)正弦电流刺激时的疼痛减轻不那么明显(p<0.05,ANOVA)。与 NaCl 处理皮肤相比,NGF 部位电正弦和机械冲击刺激的疼痛评分显著升高(p<0.05,ANOVA)。
NGF 诱导的人皮肤对电和机械刺激的敏化主要由 C 型伤害感受器驱动,而 Aδ 纤维的贡献很小。在持续正弦刺激期间,适应性降低表明 NGF 可促进初级传入伤害感受器中的轴突尖峰产生和传导。使用这种正弦电刺激模式进一步研究慢性炎症性疼痛患者可能允许在病理条件下局部评估皮肤 C 型伤害感受器及其潜在的兴奋性变化。
新型缓慢去极化电刺激的应用显示 NGF 处理皮肤中 C 型伤害感受器敏化为主。疼痛评分增加、更大的轴突反射红斑和 C 纤维对持续正弦刺激的适应性降低均表明 NGF 后伤害感受器放电增加。与 NaCl 处理皮肤相比,A 纤维传导阻断对 NGF 处理皮肤的电和机械性痛觉过敏影响不大。这种电刺激模式可能适用于慢性炎症性疼痛患者,允许在病理条件下局部评估皮肤 C 型伤害感受器及其潜在的兴奋性变化。