首页|期刊导航|针灸推拿医学(英文版)|基于小胶质细胞极化探讨按法对激痛点大鼠脊髓背角痛觉敏化的影响

基于小胶质细胞极化探讨按法对激痛点大鼠脊髓背角痛觉敏化的影响OA

Investigating the effect of pressing manipulation on pain sensitization of spinal cord dorsal horn in trigger point rats based on microglial polarization

中文摘要英文摘要

目的:观察推拿按法对肌筋膜激痛点大鼠脊髓背角(SCDH)痛觉敏化的影响.方法:将32只雄性Sprague-Dawley大鼠采用随机数字表法分成空白组10只和造模组22只.造模组大鼠采用钝性击打加离心运动进行造模,将造模成功的20只大鼠随机分为模型组和按法组,每组10只.空白组和模型组大鼠正常饲养;按法组大鼠进行按法干预,每分钟10 次,连续干预7.5 min,隔天1次,共7次.各组大鼠进行压力疼痛阈值(PPT)和软组织张力(STT)的D0.2值检测后,观察激痛点组织形态学变化;免疫组织化学检测腰膨大SCDH中囊泡谷氨酸转运蛋白1(VGluT1)、M1型小胶质细胞标志物(CD86)和M2型小胶质细胞标志物(CD206)的表达;免疫印迹法观察腰膨大SCDH中磷酸化细胞外信号调节激酶1/2(p-ERK1/2)、N-甲基-D-天冬氨酸受体亚基2B(NR2B)、磷酸化核因子κB p65亚基(p-p65)、白细胞介素(IL)-6和肿瘤坏死因子(TNF)-α的表达水平.结果:与空白组比较,模型组大鼠PPT和STT的D0.2值均显著降低(P<0.05);肌细胞形态结构改变,大小不一,细胞核内移,细胞间炎细胞浸润且成纤维细胞增多.与模型组比较,按法组大鼠PPT和STT的D0.2值均显著升高(P<0.05);肌细胞形态结构有所改善,细胞核内移现象、炎细胞浸润以及成纤维细胞增多情况均减轻.与空白组相比,模型组大鼠腰膨大SCDH中VGluT1、CD86、p-ERK1/2、NR2B、IL-6、TNF-α和p-p65的表达均显著升高(P<0.05),CD206的表达降低(P<0.05).按法干预后,按法组大鼠腰膨大SCDH中上述蛋白的表达均显著降低(P<0.05),CD206的表达升高(P<0.05).结论:推拿按法可能通过促进激痛点大鼠腰膨大SCDH小胶质细胞从M1向M2极化,减少炎症因子释放,抑制谷氨酸神经元及其突触活动,从而抑制痛觉敏化,缓解疼痛.

Objective:To observe the effect of pressing manipulation on pain sensitization of spinal cord dorsal horn(SCDH)in rats with myofascial trigger points. Methods:Thirty-two male Sprague-Dawley rats were divided into a blank group(n=10)and a group for modeling(n=22)using the random number table method.Rats in the group for modeling were subjected to blunt blow plus centrifugal motion,and 20 rats successfully modeled were randomly divided into a model group and a pressing manipulation group,with 10 rats in each group.Rats in the blank group and the model group were reared routinely.Rats in the pressing manipulation group were subjected to pressing manipulation for 7.5 min continuously at 10 times/min,once every other day for a total of 7 times.After the values of pressure pain threshold(PPT)and soft tissue tension(STT)D0.2 were measured in each group,the histomorphological changes at trigger points were observed.The expression levels of vesicular glutamate transporter 1(VGluT1),M1 microglia marker(CD86),and M2 microglia marker(CD206)in lumbar enlargement's SCDH were detected by immunohistochemistry.Western blotting was used to observe the expression levels of phosphorylated extracellular signal-regulated kinase 1/2(p-ERK1/2),N-methyl-D-aspartic acid receptor 2B(NR2B),phosphorylated nuclear factor-kappa B p65 subunit(p-p65),interleukin(IL)-6,and tumor necrosis factor(TNF)-α. Results:Compared with the blank group,the values of PPT and STT D0.2 were significantly decreased(P<0.05),and the morphological structure of muscle cells was changed with different sizes;the nucleus moved inward,inflammatory cells infiltrated between cells,and fibroblasts were increased in the model group.Compared with the model group,the values of PPT and STT D0.2 were significantly higher(P<0.05),the morphological structure of muscle cells showed improvement,and the phenomena of nuclear migration,inflammatory cell infiltration,and fibroblast proliferation were all reduced in the pressing manipulation group.Compared with the blank group,the expression levels of VGluT1,CD86,p-ERK1/2,NR2B,IL-6,TNF-α,and p-p65 were significantly increased(P<0.05),and the expression level of CD206 was decreased(P<0.05)in the lumbar enlargement's SCDH in the model group.Following pressing manipulation intervention,the expression levels of the aforementioned proteins were significantly reduced(P<0.05),while the expression level of CD206 was elevated(P<0.05)in the lumbar enlargement's SCDH in the pressing manipulation group. Conclusion:The pressing manipulation in Tuina(Chinese therapeutic massage)may promote microglial polarization from M1 to M2 in lumbar enlargement's SCDH in trigger point rats,reduce the release of inflammatory factors,and inhibit the activity of glutamate neurons and their synapses,thereby inhibiting pain sensitization and relieving pain.

唐丽亚;蒋全睿;潘杰灵;张玉乔;冯祥;艾坤;李武;李江山;杨燕萍

医药卫生

推拿按摩按法激痛点脊髓背角小胶质细胞极化痛觉敏化大鼠

TuinaMassagePressing ManipulationTrigger PointsSpinal Cord Dorsal HornMicroglial PolarizationPain SensitizationRats

《针灸推拿医学(英文版)》 2026 (3)

229-239,11

This work was supported by the Projects of National Natural Science Foundation of China(国家自然科学基金项目,No.82474669,No.82405597,No.82274676)Hunan Provincial Natural Science Foundation of China(湖南省自然科学基金,No.2023JJ30458)Graduate Research Innovation Project in Hunan Province(湖南省研究生创新项目,No.CX20240733).

10.1007/s11726-026-1573-x

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