艾灸对RA大鼠关节滑膜组织TRPV1通道及TLR4信号通路介导的炎症反应的影响OA
Effects of moxibustion on TRPV1 channel and TLR4 signaling pathway-mediated inflammatory network in articular synovial tissue of RA rats
目的:观察艾灸肾俞和足三里穴区对类风湿性关节炎(RA)大鼠模型关节滑膜组织瞬时电位感受器香草醛受体1(TRPV1)通道和Toll样受体4(TLR4)信号通路介导的炎症网络的影响,探究TRPV1通道在艾灸干预RA滑膜炎症疼痛中的靶点作用.方法:将56只健康雄性Sprague-Dawley大鼠按随机数字表法分为正常组、模型组、艾灸组、TRPV1激动剂组(辣椒素组)、艾灸+TRPV1激动剂组(艾灸+辣椒素组)、TRPV1拮抗剂组(辣椒平组)和艾灸+TRPV1拮抗剂组(艾灸+辣椒平组),每组8只.除正常组外,其余6组采用风、寒、湿环境因素+弗氏完全佐剂复合造模方法建立RA模型.造模成功后,艾灸组采用直径0.9 cm的艾条温和灸双侧肾俞和足三里穴区,30 min/次,每日1次,连续施灸14 d;TRPV1激动剂组与TRPV1拮抗剂组分别在大鼠双侧肾俞和足三里穴区皮下注射辣椒素和辣椒平,1次/d,连续干预14 d;艾灸+TRPV1激动剂组与艾灸+TRPV1拮抗剂组分别于双侧肾俞和足三里穴区皮下注射辣椒素和辣椒平30 min后进行艾灸干预,艾灸干预方式同艾灸组,连续干预14 d.干预结束后,苏木素-伊红染色与透射电镜观察滑膜组织和细胞病理变化;免疫组织化学法观察滑膜组织中白细胞介素(IL)-1β、IL-6、IL-17和肿瘤坏死因子(TNF)-α含量;免疫印迹法及逆转录聚合酶链反应检测滑膜组织中TLR4、髓样分化因子88(Myd88)、TRPV1蛋白及mRNA的相对表达量;酶联免疫吸附测定检测血清IL-1β、IL-2、IL-6、IL-17A和TNF-α含量.结果:与正常组比较,模型组大鼠滑膜组织病理损伤明显,滑膜组织中IL-1β、IL-6、IL-17及TNF-α含量明显升高(P<0.01或P<0.05),TLR4、Myd88及TRPV1蛋白表达显著升高(P<0.01),TLR4 mRNA、Myd88 mRNA及TRPV1 mRNA相对表达量显著升高(P<0.01),血清中IL-1β、IL-2、IL-6、IL-17A及TNF-α含量显著升高(P<0.01).与辣椒平组比较,辣椒素组大鼠滑膜组织病理损伤明显,滑膜组织中IL-1β、IL-6、IL-17及TNF-α含量明显升高(P<0.01),TLR4、Myd88及TRPV1蛋白表达显著升高(P<0.01),TLR4 mRNA、Myd88 mRNA及TRPV1 mRNA相对表达量显著升高(P<0.01),血清中IL-1β、IL-2、IL-6、IL-17A及TNF-α含量显著升高(P<0.01).与模型组比较,艾灸组大鼠滑膜组织病理损伤明显减轻,滑膜组织中IL-1β、IL-17及TNF-α含量明显降低(P<0.01),IL-6含量降低不显著(P>0.05),TLR4、Myd88及TRPV1蛋白表达显著降低(P<0.01),TLR4 mRNA、Myd88 mRNA及TRPV1 mRNA相对表达量显著减少(P<0.01),血清中IL-1β、IL-2、IL-6、IL-17A及TNF-α含量显著降低(P<0.01);辣椒素组大鼠滑膜组织病理损伤加重,滑膜组织中IL-6含量明显升高(P<0.01),IL-1β、IL-17及TNF-α含量升高不显著,滑膜组织中TLR4、Myd88及TRPV1蛋白表达显著升高(P<0.01),TLR4 mRNA、Myd88 mRNA及TRPV1 mRNA相对表达量显著升高(P<0.01),血清中IL-1β、IL-2、IL-6、IL-17A及TNF-α含量显著升高(P<0.01).与辣椒素组比较,艾灸+辣椒素组大鼠滑膜组织病理损伤明显减轻,滑膜组织中IL-1β及IL-6含量明显降低(P<0.01),IL-17及TNF-α含量降低不显著(P>0.05),TLR4、Myd88及TRPV1蛋白表达显著降低(P<0.01),TLR4 mRNA、Myd88 mRNA及TRPV1 mRNA相对表达量显著减少(P<0.01),血清中IL-1β、IL-2、IL-6、IL-17A及TNF-α含量显著降低(P<0.01).与辣椒平组比较,艾灸+辣椒平组大鼠滑膜组织病理损伤减轻,滑膜组织中IL-1β、IL-6、IL-17及TNF-α含量降低,但差异无统计学意义(P>0.05).TLR4蛋白表达显著降低(P<0.01),Myd88及TRPV1蛋白表达降低,但差异无统计学意义(P>0.05).TLR4 mRNA及Myd88 mRNA相对表达量显著减少(P<0.05,P<0.01),TRPV1 mRNA相对表达量减少,但差异无统计学意义(P>0.05),血清中IL-1β、IL-2、IL-6、IL-17A及TNF-α含量显著降低(P<0.01).结论:TRPV1通道激活会加剧RA模型大鼠TLR4通路介导的炎症反应,而艾灸可通过调控"穴位-滑膜"双重TRPV1通道,抑制TLR4信号通路介导的炎症反应,发挥抗炎镇痛效应,改善RA滑膜炎症损伤;位于穴位感受器与靶器官滑膜上的TRPV1通道可能是艾灸干预RA滑膜炎症的潜在空间特异性靶点.
Objective:To observe the effects of moxibustion at Shenshu(BL23)and Zusanli(ST36)point areas on the transient receptor potential vanilloid type 1(TRPV1)channel and the inflammatory network mediated by the Toll-like receptor 4(TLR4)signaling pathway in the articular synovial tissue of rheumatoid arthritis(RA)rat models,and to explore the target role of the TRPV1 channel in moxibustion intervention for synovial inflammatory pain in RA. Methods:A total of 56 healthy male Sprague-Dawley rats were divided into 7 groups using the random number table method,namely a normal group,a model group,a moxibustion group,a TRPV1 agonist group(capsaicin group),a moxibustion+TRPV1 agonist group(moxibustion+capsaicin group),a TRPV1 antagonist group(capsazepine group),and a moxibustion+TRPV1 antagonist group(moxibustion+capsazepine group),with 8 rats in each group.Except for the normal group,the other 6 groups were established as RA models using a composite modeling method combining wind-cold-damp environmental factors with Freund's complete adjuvant.After successful modeling,the moxibustion group received mild moxibustion with moxa sticks of 0.9 cm in diameter at bilateral Shenshu(BL23)and Zusanli(ST36)point areas,30 min per time,once daily for 14 consecutive days.The TRPV1 agonist group and TRPV1 antagonist group were subcutaneously injected with capsaicin and capsazepine,respectively,at bilateral Shenshu(BL23)and Zusanli(ST36)point areas,once daily for 14 consecutive days.The moxibustion+TRPV1 agonist group and moxibustion+TRPV1 antagonist group received moxibustion intervention 30 min after subcutaneous injection of capsaicin or capsazepine at the above point areas,with the same moxibustion protocol as in the moxibustion group,for 14 consecutive days.After the intervention,hematoxylin-eosin staining and transmission electron microscopy were used to observe the pathological changes of synovial tissue and cells.Immunohistochemistry was applied to detect the contents of interleukin(IL)-1β,IL-6,IL-17,and tumor necrosis factor(TNF)-α in the synovial tissue.Western blotting and reverse transcription-polymerase chain reaction were performed to measure the relative expression levels of TLR4,myeloid differentiation factor 88(Myd88),TRPV1 proteins and mRNAs in the synovial tissue.Enzyme-linked immunosorbent assay was used to determine the contents of IL-1β,IL-2,IL-6,IL-17,and TNF-α in the serum. Results:Compared with the normal group,the model group showed obvious pathological damage in rat synovial tissue,with significantly increased contents of IL-1β,IL-6,IL-17,and TNF-α(P<0.01 or P<0.05)in the synovial tissue,significantly upregulated protein expression of TLR4,Myd88,and TRPV1(P<0.01),significantly increased relative mRNA expression levels of TLR4,Myd88,and TRPV1(P<0.01),and significantly elevated serum contents of IL-1β,IL-2,IL-6,IL-17A,and TNF-α(P<0.01).Compared with the capsazepine group,the capsaicin group exhibited marked pathological damage in the synovial tissue,with significantly higher contents of IL-1β,IL-6,IL-17,and TNF-α in the synovial tissue(P<0.01),significantly increased protein expression of TLR4,Myd88,and TRPV1(P<0.01),significantly elevated relative mRNA expression levels of TLR4,Myd88,and TRPV1(P<0.01),and significantly higher serum contents of the above inflammatory cytokines(P<0.01).Compared with the model group,the moxibustion group had significantly alleviated pathological damage in the synovial tissue,with markedly decreased contents of IL-1β,IL-17,and TNF-α in the synovial tissue(P<0.01),no significant decrease in the IL-6 content(P>0.05),significantly downregulated protein expression of TLR4,Myd88,and TRPV1(P<0.01),significantly reduced relative mRNA expression levels of TLR4,Myd88,and TRPV1(P<0.01),and significantly lower serum contents of the above inflammatory cytokines(P<0.01);the capsaicin group showed aggravated pathological damage in the synovial tissue,with a significantly increased IL-6 content(P<0.01),but no significant elevation in the contents of IL-1β,IL-17,or TNF-α in the synovial tissue;meanwhile,the protein and mRNA expression levels of TLR4,Myd88,and TRPV1 in the synovial tissue and serum inflammatory cytokine contents were all significantly increased(P<0.01).Compared with the capsaicin group,the moxibustion+capsaicin group had significantly relieved pathological damage in the synovial tissue,with markedly decreased contents of IL-1β and IL-6 in the synovial tissue(P<0.01),but no significant reduction in the IL-17 or TNF-α content(P>0.05),significantly downregulated protein expression of TLR4,Myd88,and TRPV1(P<0.01),significantly reduced relative mRNA expression levels of TLR4,Myd88,and TRPV1(P<0.01),and significantly lower serum contents of the above inflammatory cytokines(P<0.01).Compared with the capsazepine group,the moxibustion+capsazepine group showed alleviated pathological damage in the synovial tissue,with insignificantly decreased contents of IL-1β,IL-6,IL-17,or TNF-α in the synovial tissue(P>0.05);the TLR4 protein expression was significantly decreased(P<0.01),while the protein expression of Myd88 and TRPV1 was reduced without statistical significance(P>0.05);the relative mRNA expression levels of TLR4 and Myd88 were significantly decreased(P<0.05,P<0.01),while that of TRPV1 was reduced without statistical significance(P>0.05);the serum contents of the above inflammatory cytokines were all significantly decreased(P<0.01). Conclusion:Activation of the TRPV1 channel exacerbates the inflammatory response mediated by the TLR4 signaling pathway in RA model rats.Moxibustion can exert anti-inflammatory and analgesic effects and ameliorate RA synovial inflammatory injury by regulating the dual"point-synovium"TRPV1 channels and inhibiting the inflammatory response mediated by the TLR4 signaling pathway.The TRPV1 channel located on point receptors and the targeted synovium may be potential spatially specific therapeutic targets for moxibustion intervention for RA synovial inflammation.
杨军;张传英;江帆;王晓妹;丛瑾;袁娟;彭传玉;吴子建;胡玲;胡倩倩
医药卫生
针灸疗法艾条灸关节炎,实验性关节炎,类风湿Toll样受体4髓样分化因子88TRPV阳离子通道大鼠
Acupuncture-moxibustion TherapyMoxa Stick MoxibustionArthritis,ExperimentalArthritis,RheumatoidToll-like Receptor 4Myeloid Differentiation Factor 88TRPV Cation ChannelsRats
《针灸推拿医学(英文版)》 2026 (4)
339-350,12
This work was supported by the Project of National Natural Science Foundation of China(国家自然科学基金资助项目,No.82205289)Key Projects of Natural Science Research in Higher Education Institutions in Anhui Province(安徽省高等学校自然科学研究重点项目,No.2022AH050526,No.2023AH050768,No.2022AH050454,No.2023AH050811,No.2024AH050915)Youth Project of Natural Science Foundation of Anhui Province(安徽省自然科学基金青年项目,No.2208085QH265)Key Project of Philosophy and Social Science Research of Colleges and Universities in Anhui Province(安徽省高校哲学社会科学研究重点项目,No.2023AH050710).
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