Chen Ping, He Wen-Jie, Du Xiao-Zheng, Zhang Xing-Hua, Li Xiang-Jun, Ren Chao-Zhan, Zhang Feng-Fan, Jing Wei-Yao
College of Acupuncture and Massage, Gansu University of Chinese Medicine, Lanzhou 730000, China.
Gansu Health Vocational College, Lanzhou 730207.
Zhen Ci Yan Jiu. 2022 Nov 25;47(11):1012-8. doi: 10.13702/j.1000-0607.20220302.
To observe the effects of heat-reinforcing needling on the expression of purinergic ligand-gated ion channel 7 receptor(P2X7R),Nodlike receptor protein 3(NLRP3) and Caspase-1 in synovium tissues of knee joint of rabbits with cold syndrome rheumatoid arthritis(RA),so as to explore the anti-inflammatory mechanism of heat reinforcing needling in the treatment of RA.
Thirty male New Zealand white rabbits were randomly divided into normal group, model group, reinforcing-reducing needling group(RRG), heat-reinforcing needling group(HRG), and antagonist group(AG), with 6 rabbits in each group.The model of cold syndrome RA was established by ovalbumin combined with Freund's adjuvant and cryogenic freezing. Rabbits of RRG and HRG were treated with corresponding acupuncture techniques on both sides of "Zusanli"(ST36) for 30 min, once a day for 7 days; Rabbits of the AG was intraperitoneally injected with A438079(2.5 mg/kg), once a day for 7 days. After intervention, color Doppler ultrasound was used to observe the joint cavity effusion, synovial thickness and internal blood flow signal.The histomorphological changes of synovial tissues were observed by HE staining. Quantitative real-time PCR method was used to detect the mRNA expression levels of P2X7R, NLRP3, and Caspase-1 in synovial tissues. Western blot was used to detect the protein expression of interleukin(IL)-1β, IL-6 and tumor necrosis factor(TNF)-α in synovial tissues.
Compared with the normal group, the synovial tissues in the model group was thickened, linear and punctate blood flow signals were increased, joint effusion was obvious, synovial coating cells were enlarged, the synovial matrix was severely hyperplasia, inflammatory cells infiltration was obvious.The mRNAs expression levels of P2X7R, NLRP3, Caspase-1 and IL-1β, IL-6, TNF-α proteins in synovial tissues were significantly increased(<0.01). Compared with model group, abnormal blood flow signals, synovial thickness, joint effusion, proliferation of synovial matrix, inflammatory cell infiltration and synovial coating cells in the RRG, HRG and AG were improved. The mRNAs expression levels of P2X7R, NLRP3, Caspase-1 and IL-1β, IL-6, TNF-α proteins in synovial tissues were decreased in the RRG, HRG and AG (<0.05, <0.01). Compared with the RRG, the above indexes were lower in the HRG and AG (<0.05, <0.01).There was no significant difference in all indexes above between the HRG and AG (<0.01, <0.05).
Heat reinforcing needling can improve synovial inflammation of RA, which may be related to regulating the expressions of P2X7R/NLRP3/Caspase-1 signaling pathway.
观察温针治疗寒证类风湿关节炎(RA)家兔膝关节滑膜组织中嘌呤能配体门控离子通道7受体(P2X7R)、Nod样受体蛋白3(NLRP3)及半胱天冬酶-1(Caspase-1)的表达情况,探讨温针治疗RA的抗炎机制。
将30只雄性新西兰白兔随机分为正常组、模型组、提插补泻针法组(RRG)、温针组(HRG)和拮抗剂组(AG),每组6只。采用卵白蛋白联合弗氏佐剂及低温冷冻法制备寒证RA模型。RRG组和HRG组家兔双侧“足三里”(ST36)采用相应针刺手法治疗30分钟,每日1次,连续7天;AG组家兔腹腔注射A438079(2.5mg/kg),每日1次,连续7天。干预后,采用彩色多普勒超声观察关节腔积液、滑膜厚度及内部血流信号。通过HE染色观察滑膜组织的组织形态学变化。采用定量实时PCR法检测滑膜组织中P2X7R、NLRP3和Caspase-1的mRNA表达水平。采用蛋白质印迹法检测滑膜组织中白细胞介素(IL)-1β、IL-6和肿瘤坏死因子(TNF)-α的蛋白表达。
与正常组比较,模型组滑膜组织增厚明显,线状及点状血流信号增多,关节积液明显,滑膜衬里细胞肿大,滑膜基质重度增生,炎症细胞浸润明显。滑膜组织中P2X7R、NLRP3、Caspase-1的mRNA表达水平及IL-1β、IL-6、TNF-α蛋白表达水平均显著升高(<0.01)。与模型组比较,RRG组、HRG组和AG组异常血流信号、滑膜厚度、关节积液、滑膜基质增生、炎症细胞浸润及滑膜衬里细胞均有所改善。RRG组、HRG组和AG组滑膜组织中P2X7R、NLRP3、Caspase-1的mRNA表达水平及IL-1β、IL-6、TNF-α蛋白表达水平均降低(<0.05,<0.01)。与RRG组比较,HRG组和AG组上述指标更低(<0.05,<0.01)。HRG组与AG组上述各项指标比较,差异均无统计学意义(<0.01,<0.05)。
温针可改善RA的滑膜炎症,其机制可能与调节P2X7R/NLRP3/Caspase-1信号通路的表达有关。