Jing Wei-Yao, Du Xiao-Zheng, Su Cheng-Hong, Liu Li-Mei, Liu Cui, Yuan Bo, Zhang Xing-Hua, Chen Ping, Zhang Feng-Fan
College of Acupuncture-Moxibustion and Tuina, Gansu University of Chinese Medicine, Lanzhou 730000, China.
Department of Acupuncture and Pain, Affiliated Hospital of Gansu University of Chinese Medicine, Lanzhou 730000.
Zhen Ci Yan Jiu. 2023 Feb 25;48(2):125-32. doi: 10.13702/j.1000-0607.20220800.
To observe the effects of heat-reinforcing needling on synovial inflammation and microRNA-155 (miR-155)/Toll-like receptor 4 (TLR4)/nuclear transcription factor-κB (NF-κB) signaling axis, so as to investigate its anti-inflammatory mechanism in rabbits with cold syndrome of rheumatoid arthritis (RA).
A total of 36 rabbits were randomly divided into normal, model, agonist, inhibitor, heat-reinforcing needling (HRN) and agonist+heat-reinforcing needling (A+HRN) groups, with 6 rabbits in each group. The RA with cold syndrome model was induced by injecting ovalbumin dry powder and Freund's complete adjuvant combined with cold freezing. Rabbits in agonist group were intraperitoneally injected with miR-155 agomir 4.5 OD; rabbits in the inhibitor group were intraperitoneally injected with miR-155 antagomir 6.1 OD; rabbits in HRN group received heat-reinforcing needling at bilateral "Zusanli" (ST36) for 30 min;rabbits in A+HRN group received the same treatment as agonist group, and 30 min later, received the same treatment as the HRN group; rabbits in the normal and model groups were grasped and fixed in the same way, all groups received continuous treatment once a day for 7 d. After modeling, the knee joints of rabbits were examined by ultrasound, the pain threshold and the circumference were determined. After the interventions, the pain threshold and knee circumference were measured; the pathological morphology of synovial tissue of the knee joints were observed by HE staining; the mRNA levels of miR-155 and suppressor of cytokine signaling protein 1 (SOCS1), the expression levels of SOCS1, TLR4, NF-κB p65, interleukin (IL)-1β and IL-17A proteins in synovial tissue of knee joints were detected by real-time PCR and Western blot respectively.
Compared with the normal group, the pain threshold was significantly decreased (<0.05), and the knee circumference was significantly increased (<0.05); the synovial tissue of knee joints showed significant hyperplasia, abundant blood flow signal, joint cavity effusion and obvious inflammatory invasion, the pathological score was significantly increased (<0.05), the expressions of miR-155 mRNA and IL-1β, IL-17A, TLR4, NF-κB p65 proteins were significantly increased (<0.05), the expressions of SOCS1 mRNA and protein were significantly decreased (<0.05) in the model group. Compared with model group, the pain threshold was significantly increased (<0.05), the circumference of knee joint was significantly decreased (<0.05); in synovial tissue, the pathological score was decreased (<0.05), the expression levels of miR-155 mRNA and IL-1β, IL-17A, TLR4, NF-κB p65 proteins were significantly decreased (<0.05), and the expressions of SOCS1 mRNA and protein were significantly increased (<0.05) in inhibitor group and HRN group, while the above changes in agonist group were reversed (<0.05). Compared with the agonist group, the pain threshold was significantly increased (<0.05), the knee circumference was significantly decreased (<0.05), the synovial pathological score was significantly decreased (<0.05), the expressions of miR-155 mRNA and IL-1β, IL-17A, TLR4, NF-κB proteins in synovial tissue were significantly decreased (<0.05), and the expression levels of SOCS1 mRNA and protein were significantly increased (<0.05) in A+HRN group.
The heat-reinforcing needling can increase the pain threshold, reduce the knee circumference and inhibit the inflammatory response in rabbits with RA cold syndrome. The possible mechanism is related to the regulation of miR-155/TLR4/NF-κB signaling axis.
观察温针治疗对类风湿关节炎(RA)寒证模型兔滑膜炎症及微小RNA-155(miR-155)/Toll样受体4(TLR4)/核转录因子-κB(NF-κB)信号轴的影响,探讨其抗炎机制。
将36只家兔随机分为正常组、模型组、激动剂组、抑制剂组、温针组和激动剂+温针组,每组6只。采用卵白蛋白干粉与弗氏完全佐剂联合冷冻法制备RA寒证模型。激动剂组腹腔注射miR-155激动剂4.5 OD;抑制剂组腹腔注射miR-155拮抗剂6.1 OD;温针组针刺双侧“足三里”(ST36)30 min;激动剂+温针组先腹腔注射miR-155激动剂4.5 OD,30 min后针刺双侧“足三里”(ST36)30 min;正常组与模型组仅抓取固定,不做其他处理。各组均连续治疗7 d,每日1次。造模后行膝关节超声检查,测量疼痛阈值及膝关节周径。干预后再次测量疼痛阈值及膝关节周径;取膝关节滑膜组织行HE染色观察病理形态;采用实时荧光定量PCR法检测滑膜组织中miR-155及细胞因子信号转导抑制蛋白1(SOCS1)mRNA水平,采用蛋白质免疫印迹法检测滑膜组织中SOCS1、TLR4、NF-κB p65、白细胞介素(IL)-1β及IL-17A蛋白表达水平。
与正常组比较,模型组疼痛阈值明显降低(<0.05),膝关节周径明显增大(<0.05);膝关节滑膜组织明显增生,血流信号丰富,关节腔积液,炎症浸润明显,病理评分明显升高(<0.05),miR-155 mRNA及IL-1β、IL-17A、TLR4、NF-κB p65蛋白表达明显升高(<0.05),SOCS1 mRNA及蛋白表达明显降低(<0.05)。与模型组比较,抑制剂组、温针组疼痛阈值明显升高(<0.05),膝关节周径明显减小(<0.05);滑膜组织病理评分降低(<0.05),miR-155 mRNA及IL-1β、IL-