Mechanism of electroacupuncture penetration needling for relieving synovial inflammation of knee osteoarthritis through TLR4/MyD88/NF-κB signal pathway
|更新时间:2023-08-11
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Mechanism of electroacupuncture penetration needling for relieving synovial inflammation of knee osteoarthritis through TLR4/MyD88/NF-κB signal pathway
ZHOU Zi-qi, YANG Yong-ju, MA Xian-de, et al. Mechanism of electroacupuncture penetration needling for relieving synovial inflammation of knee osteoarthritis through TLR4/MyD88/NF-κB signal pathway[J]. Acupuncture research, 2023, 48(4): 353-358.
DOI:
ZHOU Zi-qi, YANG Yong-ju, MA Xian-de, et al. Mechanism of electroacupuncture penetration needling for relieving synovial inflammation of knee osteoarthritis through TLR4/MyD88/NF-κB signal pathway[J]. Acupuncture research, 2023, 48(4): 353-358. DOI: 10.13702/j.1000-0607.20220418.
Mechanism of electroacupuncture penetration needling for relieving synovial inflammation of knee osteoarthritis through TLR4/MyD88/NF-κB signal pathway
目的:观察电针透刺法对大鼠滑膜Toll样受体4/髓样分化因子88/核转录因子-κB(TLR4/MyD88/NF-κB)信号通路及血清相关炎性因子的影响,探讨电针透刺法对膝关节骨关节炎(KOA)大鼠滑膜炎性反应的影响机制。方法:雄性SD大鼠随机分为假手术组、模型组、电针透刺组、普通电针组,每组16只。采用前交叉韧带离断术结合术后强迫运动制备KOA大鼠模型。电针透刺组于右侧“犊鼻”“内膝眼”予相互透刺5~8 mm
“血海”“梁丘”予相互透刺5~8 mm;普通电针组于右侧“犊鼻”“内膝眼”予向上与皮肤呈30°角斜刺3~5 mm
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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