卡压性神经病束(ENU)药物穿刺治疗小鼠坐骨神经结扎所致神经性疼痛的疗效评价。

IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY
Journal of Pain Research Pub Date : 2025-05-12 eCollection Date: 2025-01-01 DOI:10.2147/JPR.S519298
Bitna Kweon, Dong-Uk Kim, Kyoungsu Park, Sangho Lee, Yousuk Youn, Hyeok Ju Park, Hyun Soo Shim, Junsang Yoo, Yong Kyu Lee, Gi-Sang Bae, Youngjin Choi
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引用次数: 0

摘要

背景:周围神经损伤引起的神经性疼痛是神经系统信号或加工异常引起的。药物穿刺与卡压性神经病变Unties (ENUs),一个多草药配方,可能提供一个补充的治疗策略。然而,其有效性尚未得到科学的体内验证。方法:采用小鼠坐骨神经结扎(SNL)致神经性疼痛模型。行为评估采用Von Frey细丝测量机械异常性痛。免疫荧光染色检测脊髓背角C-FOS和GFAP的表达。采用定量PCR (qPCR)评估炎症标志物Gfap、Iba1、Tnf-α、Il-1β的表达。结果:损伤部位局部给药ENUs可显著减轻SNL引起的机械异常痛(*p < 0.05, **p < 0.01, ***p < 0.001)。ENUs治疗组C-FOS、GFAP、促炎细胞因子的表达也有统计学意义的降低(*p < 0.05, **p < 0.01, ***p < 0.001)。在各治疗组中,ENU v2 -中、高剂量组与盐水治疗对照组相比,疗效最显著。结论:本研究首次提供了支持ENUs对神经性疼痛的镇痛和抗炎作用的体内证据。ENUs可能通过抑制神经胶质活化和神经元致敏来发挥这些作用。其临床应用及其分子机制有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Therapeutic Efficacy of Entrapment Neuropathy Unties (ENU) Pharmacopuncture in Neuropathic Pain Caused by Sciatic Nerve Ligation in Mice.

Background: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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来源期刊
Journal of Pain Research
Journal of Pain Research CLINICAL NEUROLOGY-
CiteScore
4.50
自引率
3.70%
发文量
411
审稿时长
16 weeks
期刊介绍: Journal of Pain Research is an international, peer-reviewed, open access journal that welcomes laboratory and clinical findings in the fields of pain research and the prevention and management of pain. Original research, reviews, symposium reports, hypothesis formation and commentaries are all considered for publication. Additionally, the journal now welcomes the submission of pain-policy-related editorials and commentaries, particularly in regard to ethical, regulatory, forensic, and other legal issues in pain medicine, and to the education of pain practitioners and researchers.
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