首页> 外文期刊>Journal of Pain Research >Prolonged-duration pulsed radiofrequency is associated with increased neuronal damage without further antiallodynic effects in neuropathic pain model rats
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Prolonged-duration pulsed radiofrequency is associated with increased neuronal damage without further antiallodynic effects in neuropathic pain model rats

机译:在神经性疼痛模型大鼠中,长时间脉冲射频与神经元损伤增加相关,而没有进一步的抗痛觉异常作用

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Aim of investigation: Pulsed radiofrequency (PRF) is a safe and effective approach for treating neuropathic pain. However, the optimal treatment conditions and analgesic mechanisms of PRF remain unclear. The aim of our study was to assess the beneficial and adverse effects of prolonged-duration PRF and the analgesic mechanisms of PRF treatment with neuropathic pain rats. Methods: Male Sprague Dawley rats received L5 spinal nerve ligation (SNL) for developing neuropathic pain. Fourteen days after L5 SNL surgery, they were divided into three groups according to duration of PRF current for 6?minutes, 12?minutes, and none. PRF current was delivered via direct visualization adjacent to the L5 dorsal root ganglion (DRG). Pain behavior was evaluated every week after L5 SNL surgery, until day 28. Seven days after PRF treatment, L5 DRG tissue was harvested to detect levels of activating translation factor 3 (ATF3; a marker of neuronal damage) and hyperpolarization-activated cyclic nucleotide (HCN)-gated cation channels (key factors in neuropathic pain) using quantitative PCR. Results: Before PRF application, withdrawal thresholds were significantly lower than at baseline and did not differ significantly between the three groups. After PRF application, withdrawal thresholds in the PRF6 and PRF12 groups were significantly increased compared to those in the sham group. However, those in the PRF6 and PRF12 groups did not differ significantly. The expression level of ATF3 mRNA in the PRF12 group was significantly higher than that in the sham group ( P 0.01), but the expression of HCN1 and HCN2 channels did not differ significantly between the three groups. Conclusion: Prolonged PRF exposure, from 6 to 12?minutes, was not only ineffective but also associated with increased neuronal damage. These findings do not support prolonged PRF exposure as a helpful treatment for neuropathic pain. In this study, the involvement of HCN channels in the antiallodynic effects of PRF was uncertain.
机译:研究目的:脉冲射频(PRF)是治疗神经性疼痛的一种安全有效的方法。但是,PRF的最佳治疗条件和止痛机制仍不清楚。我们研究的目的是评估持续时间的PRF的利弊以及神经性疼痛大鼠PRF的镇痛机制。方法:雄性Sprague Dawley大鼠接受L5脊神经结扎(SNL),以发展为神经性疼痛。 L5 SNL手术后第14天,根据PRF电流持续时间分别为6分钟,12分钟和3分钟的时间分为三组。 PRF电流通过与L5背根神经节(DRG)相邻的直接可视化传递。在L5 SNL手术后每周(直到第28天)评估疼痛行为。在PRF治疗后的7天,收集L5 DRG组织以检测激活翻译因子3(ATF3;神经元损伤的标志物)和超极化激活的环状核苷酸( HCN)门控的阳离子通道(神经性疼痛的关键因素),采用定量PCR技术。结果:在应用PRF之前,戒断阈值明显低于基线,并且三组之间没有显着差异。与假手术组相比,PRF施用后,PRF6和PRF12组的戒断阈值显着增加。但是,PRF6和PRF12组中的那些无显着差异。 PRF12组的ATF3 mRNA表达水平明显高于假手术组(P <0.01),但三组间HCN1和HCN2通道的表达无明显差异。结论:长时间暴露于PRF(6至12分钟)不仅无效,而且与神经元损伤增加有关。这些发现不支持延长PRF暴露作为神经性疼痛的有效治疗方法。在这项研究中,尚不确定HCN通道是否参与PRF的抗痛觉过敏作用。

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