Kweon Bitna, Kim Dong-Uk, Park Kyoungsu, Lee Sangho, Youn Yousuk, Park Hyeok Ju, Shim Hyun Soo, Yoo Junsang, Lee Yong Kyu, Bae Gi-Sang, Choi Youngjin
Department of Pharmacology, School of Korean Medicine, Wonkwang University, Iksan, 54538, Republic of Korea.
Hanbang Cardio-Renal Syndrome Research Center, Wonkwang University, Iksan, 54538, Republic of Korea.
J Pain Res. 2025 May 12;18:2393-2405. doi: 10.2147/JPR.S519298. eCollection 2025.
Neuropathic pain caused by peripheral nerve injury results from abnormal signaling or processing in the nervous system. Pharmacopuncture with Entrapment Neuropathy Unties (ENUs), a multi-herbal formulation, may offer a complementary therapeutic strategy. However, its efficacy has not been scientifically validated in vivo.
A mouse model of sciatic nerve ligation (SNL)-induced neuropathic pain was used. Behavioral assessments were performed using Von Frey filaments to measure mechanical allodynia. Immunofluorescence staining was conducted to detect C-FOS and GFAP expression in the spinal dorsal horn. Quantitative PCR (qPCR) was used to evaluate the expression of inflammatory markers, including Gfap, Iba1, Tnf-α, and Il-1β.
Local administration of ENUs at the injury site significantly alleviated mechanical allodynia induced by SNL (*p < 0.05, **p < 0.01, ***p < 0.001). Treatment with ENUs also led to statistically significant reductions in the expression of C-FOS, GFAP, and pro-inflammatory cytokines (*p < 0.05, **p < 0.01, ***p < 0.001). Among the treatment groups, the ENU V2-middle and V2-high dose groups demonstrated the most pronounced therapeutic effects compared to the saline-treated control group.
This study provides the first in vivo evidence supporting the analgesic and anti-inflammatory effects of ENUs in neuropathic pain. ENUs may exert these effects by suppressing glial activation and neuronal sensitization. Further research is warranted to explore its clinical applications and underlying molecular mechanisms.
外周神经损伤引起的神经性疼痛是由神经系统中异常信号传导或处理导致的。采用多草药配方的夹闭性神经病松解术(ENU)进行药物针灸可能提供一种辅助治疗策略。然而,其疗效尚未在体内得到科学验证。
使用坐骨神经结扎(SNL)诱导的神经性疼痛小鼠模型。使用von Frey细丝进行行为评估以测量机械性异常性疼痛。进行免疫荧光染色以检测脊髓背角中C-FOS和GFAP的表达。采用定量PCR(qPCR)评估包括Gfap、Iba1、Tnf-α和Il-1β在内的炎症标志物的表达。
在损伤部位局部施用ENU可显著减轻SNL诱导的机械性异常性疼痛(*p<0.05,**p<0.01,***p<0.001)。ENU治疗还导致C-FOS、GFAP和促炎细胞因子的表达在统计学上显著降低(*p<0.05,**p<0.01,***p<0.001)。在各治疗组中,与生理盐水处理的对照组相比,ENU V2-中剂量组和V2-高剂量组表现出最显著的治疗效果。
本研究提供了首个体内证据,支持ENU对神经性疼痛具有镇痛和抗炎作用。ENU可能通过抑制神经胶质细胞活化和神经元敏化发挥这些作用。有必要进一步研究以探索其临床应用和潜在的分子机制。