[Mechanism of electroacupuncture penetration needling for relieving synovial inflammation of knee osteoarthritis through TLR4/MyD88/NF-κB signal pathway].

Zi-Qi Zhou, Yong-Ju Yang, Xian-de Ma, Shi-Yao Zhang, Xue-Feng Guan
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Abstract

Objective: To observe the effects of electroacupuncture (EA) penetration needling on Toll-like receptors 4/myeloid differentiation factor 88/nuclear factor-kappa B (TLR4/MyD88/NF-κB) signaling pathway in rat synovium and the serum-related inflammatory factors, so as to explore the mechanism of EA penetration needling on synovial inflammation in rats with knee osteoarthritis (KOA).

Methods: SD male rats were randomly divided into sham-operation group, model group, EA+penetration needling group, and conventional EA group, with 16 rats in each group. The rats model was prepared by anterior cruciate ligment transection and these rats were forced to exercise for 8 weeks after operation. After successful modeling, in the EA+penetration needling group, the needles were inserted at "Dubi" (ST35) "Neixiyan" (EX-LE4), and at "Xuehai"(SP10) "Liangqiu"(ST34) on the right hind limb, towards each other, 5-8 mm in depth, respectively. In the conventional EA group, the needles were inserted at ST35 and EX-LE4 on the right hind limb, obliquely, at 30° angle to the skin, 3-5 mm in depth; and were inserted at SP10 and ST34 on the right hind limb perpendicularly, 3-5 mm in depth. In these two groups, electric stimulation was operated with dense-disperse wave, 2 Hz/10 Hz in frequency and 0.5-1.5 mA in intensity, retained for 20 min in each treatment. The treatment was given once daily, 10 days as 1 course of treatment, and 2 courses were required at the interval of 2 days. After the intervention, the knee joint effusion was observed by musculoskeletal ultrasound; the contents of IL-1β, IL-6 and TNF-α in serum were determined by ELISA; the morphological changes in the synovium were observed after H.E. staining; the positive expression of NF-κB p65 in the synovial membrane was detected by immunohistochemical method; the expression levels of TLR4, MyD88, TRAF-6 and NF-κB p65 proteins in the synovial membrane were determined by Western blot.

Results: Compared with the sham-operation group, in the model group, the knee joint effusion was obviously increased, the synovial lining cells were distributed irregularly, the cells were disarranged, the pannus was formed largely, and a great number of the inflammatory cells were infiltrated; the contents of serum IL-1β, IL-6 and TNF-α, the positive expression of NF-κB p65, the protein expression levels of TLR4, MyD88, TRAF-6 and NF-κB p65 in the synovial tissue were increased (P<0.05). Compared with the model group, the knee joint effusion was reduced, the synovial lining cells were proliferated, a small number of the inflammatory cells were infiltrated, and the pannus was formed lightly; the contents of serum IL-1β, IL-6 and TNF-α, the positive expression of NF-κB p65, the protein expression levels of TLR4, MyD88, TRAF-6 and NF-κB p65 in the synovial tissue were lower (P<0.05) in the EA+penetration needling group and the conventional EA group. In the conventional EA group, the knee joint effusion was increased, the synovial lining cells were proliferated, the inflammatory cells were infiltrated largely, and the pannus was formed increasingly; the contents of serum IL-1β, IL-6 and TNF-α, and the protein expression levels of TLR4, MyD88 and NF-κB p65 in the synovial tissue were increased when compared with the EA+penetration needling group (P<0.05).

Conclusion: The EA+penetration needling can significantly relieve the synovial inflammatory reaction and the knee joint effusion in KOA rats. The mechanism is probably related to down-regulating the downstream inflammatory cascade through inhibiting the transduction of TLR4/MyD88/NF-κB signaling pathway.

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[电针透刺通过TLR4/MyD88/NF-κB信号通路缓解膝骨性关节炎滑膜炎症的机制]。
目的:观察电针(EA)透刺对大鼠滑膜toll样受体4/髓样分化因子88/核因子κB (TLR4/MyD88/NF-κB)信号通路及血清相关炎症因子的影响,探讨电针(EA)透刺治疗膝骨关节炎(KOA)大鼠滑膜炎症的作用机制。方法:将SD雄性大鼠随机分为假手术组、模型组、电针+穿刺组和常规电针组,每组16只。采用前交叉韧带横断法制备大鼠模型,术后强制运动8周。造模成功后,EA+穿透针刺组在“Dubi”(ST35)处插入针。“内溪岩”(EX-LE4)和“雪海”(SP10)右后肢“良秋”(ST34),彼此朝向,深度分别为5- 8mm。常规EA组在右后肢ST35和EX-LE4处斜插针,与皮肤成30°角,深度3-5 mm;垂直插入右后肢SP10和ST34处,深度3-5 mm。两组电刺激均采用密集分散波,频率2 Hz/10 Hz,强度0.5 ~ 1.5 mA,每次治疗持续20 min。治疗方法为每日1次,10天为1个疗程,每隔2天需要2个疗程。干预后,通过肌肉骨骼超声观察膝关节积液情况;ELISA法测定血清中IL-1β、IL-6、TNF-α的含量;H.E.染色观察滑膜形态变化;免疫组化法检测滑膜中NF-κB p65的阳性表达;Western blot检测大鼠滑膜组织中TLR4、MyD88、TRAF-6、NF-κB p65蛋白的表达水平。结果:与假手术组比较,模型组膝关节积液明显增多,滑膜内膜细胞分布不规则,排列紊乱,形成大量鞘膜,炎性细胞大量浸润;血清IL-1β、IL-6、TNF-α含量升高,NF-κB p65阳性表达,TLR4、MyD88、TRAF-6、NF-κB p65蛋白表达水平升高(ppp)结论:EA+刺入能显著缓解KOA大鼠滑膜炎症反应及膝关节积液。其机制可能与通过抑制TLR4/MyD88/NF-κB信号通路的转导下调下游炎症级联有关。
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