基于IL-17F/IL-17RC信号通路及M1小胶质细胞探讨"三法三穴"推拿手法即刻镇痛作用的机制OA北大核心CSTPCD
Mechanism of the immediate analgesic effect of the"three methods and three points"tuina technique based on the IL-17F/IL-17RC signaling pathway and M1 microglia
目的 通过观察"三法三穴"推拿手法对轻型慢性压迫性损伤(minor CCI)模型大鼠脊髓背角中白细胞介素-17F(IL-17F)、白细胞介素-17受体C(IL-17RC)、核转录因子-κB激活剂1(Act1)、肿瘤坏死因子受体相关因子6(TRAF6)及M1型小胶质细胞表达的影响,探讨推拿对周围神经病理性疼痛的即刻镇痛机制.方法 将36只SD大鼠按随机数字表法分为假手术组、模型组、推拿组,12只/组,结扎右侧坐骨神经复制minor CCI模型.推拿组使用按摩推拿手法模拟仪在大鼠患侧殷门、承山、阳陵泉依次进行点法、拨法、揉法,假手术组及模型组仅抓握束缚,干预1次.采用机械痛实验与冷板实验评价即刻干预后大鼠对机械刺激、冷刺激的反应情况;采用蛋白质印迹法检测各组大鼠脊髓背角中IL-17F、TRAF6的蛋白表达情况;采用实时荧光PCR(RT-PCR)法检测各组大鼠脊髓背角中IL-17F、IL-17RC、Act1、TRAF6的mRNA表达情况;采用免疫荧光法检测各组大鼠脊髓背角中M1型小胶质细胞平均荧光强度.结果 行为学结果显示,干预前,与假手术组比较,模型组、推拿组大鼠机械缩足反射阈值(PMWT)降低,冷敏阈值升高;推拿手法干预后,与模型组比较,推拿组大鼠PMWT升高,冷敏阈值降低;与干预前比较,干预后推拿组大鼠PMWT升高,冷敏阈值降低(均P<0.05).RT-PCR结果显示,与假手术组比较,模型组大鼠脊髓背角中IL-17F、IL-17RC、TRAF6、Act 1的mRNA表达均升高;与模型组比较,推拿组大鼠上述指标mRNA表达均降低(均P<0.05).蛋白质印迹法结果显示,与假手术组比较,模型组大鼠脊髓背角中IL-17F、TRAF6蛋白表达升高;与模型组比较,推拿组大鼠IL-17F、TRAF6蛋白表达降低(均P<0.05).免疫荧光结果显示,与假手术组比较,模型组大鼠脊髓背角分化簇40(CD40)平均荧光强度增强;与模型组比较,推拿组大鼠CD40平均荧光强度减弱(均P<0.05).结论 "三法三穴"推拿手法干预1次,其机制可能是通过抑制脊髓背角中IL-17F、IL-17RC、Act1、TRAF6的表达及M1型小胶质细胞的活化实现的,从而有即刻镇痛的作用.
Objective By observing the effects of"three methods and three points"tuina technique on the expression of interleukin-17F(IL-17F),interleukin-17 receptor C(IL-17RC),activator 1 of nuclear transcription factor-κB(Act1),tumour necrosis factor receptor-associated factor 6(TRAF6)and M1 microglial cell expression in the spinal dorsal horn of rats with mild chronic compressive injury(minor CCI)model,we explored the immediate analgesic mechanism of tuina on peripheral neuropathic pain(pNP).Methods Thirty-six SD rats were divided into the sham group,the model group and the tuina group according to the random number method,twelve rats in each group,and the minor CCI model was replicated by ligating the right sciatic nerve.The rats in the tuina group were subjected to pointing,plucking and kneading at the BL37,BL57 and GB34 points on the affected side using a tuina simulator,while the sham group and the model group were only grasped and restrained,and were intervened for one time.The mechanical pain test and cold plate test were used to evaluate the response of rats to mechanical stimulation and cold stimulation after immediate intervention.The protein expression of IL-17F and TRAF6 in the spinal dorsal horn of rats in each group was detected by Western blotting.The mRNA expression of IL-17F,IL-17RC,Act1 and TRAF6 in the spinal dorsal horn of rats in each group was detected by real-time PCR.The average fluorescence intensity of M1 microglia in the spinal dorsal horn of rats in each group was detected by immunofluorescence.Results Behavioral results showed that before intervention,compared with the sham group,paw mechanical withdraw threshold(PMWT)decreased and cold sensitivity threshold(CST)increased in the model group and the tuina group;after tuina intervention,PMWT in the tuina group was increased,and CST was decreased compared with the model group;after intervention,PMWT in the tuina group was increased,while CST was decreased(P<0.05).RT-PCR results showed that compared with the sham group,mRNA expression levels of IL-17F,IL-17RC,TRAF6 and Act1 in the spinal dorsal horn of the model group were increased;compared with model group,the mRNA expression levels of above indexes in the tuina group were decreased(P<0.05).Western boltting results showed that compared with the sham group,the expression levels of IL-17F and TRAF6 protein in the spinal dorsal horn of the model group were increased;compared with the model group,the expression levels of IL-17F and TRAF6 protein in the tuina group decreased(P<O.05).Immunofluorescence results showed that the mean fluorescence intensity of CD40 in the spinal dorsal horn of model group was enhanced compared with the sham group;compared with the model group,the mean fluorescence intensity of CD40 in the tuina group was decreased(P<0.05).Conclusion The"three methods and three points"tuina technique can produce immediate analgesia by inhibiting the expression of IL-17F,IL-17RC,Act1,TRAF6 and the activation of M1 microglia in the dorsal horn of the spinal cord after one intervention.
陈金平;张润龙;张汉钰;刘家玥;孙佳伟;刘志凤;于天源;王厚融;张英琦;官乾;徐亚静;杨震杰;萨出拉
北京中医药大学针灸推拿学院 北京 100029北京中医药大学东直门医院北京医院
中医学
推拿小胶质细胞殷门承山阳陵泉大鼠
tuinamicrogliaBL37BL57GB34rats
《北京中医药大学学报》 2024 (001)
以RNA-Seq技术为主探究三法三穴对CCI模型鼠镇痛的启动机制
116-123 / 8
国家自然科学基金项目(No.82074573,No.82274675);北京市自然科学基金项目(No.7232278)National Natural Science Foundation of China(Nos.82074573 and 82274675);Natural Science Foundation of Beijing(No.7232278)
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