Electroacupuncture Protects Against Cerebral Ischemia-Reperfusion Injury: Reducing Inflammatory Response and Cell Pyroptosis by Inhibiting P2X7/ NLRP3/GSDMD Pathway

被引:1
作者
Chen, Sifang
Hao, Panfu
Liang, Yueguang
Cao, Yu
Han, Wei
Sun, Shanbin [1 ]
机构
[1] Anhui Univ Tradit Chinese Med, Affiliated Hosp 2, Dept Rehabil Med, 300 Shouchun Rd, Hefei 230061, Peoples R China
关键词
Tongdu Tiaoshen; electroacupuncture; cerebral ischemia-reperfusion injury; inflammatory; pyroptosis; GLOBAL BURDEN; STROKE; MECHANISM;
D O I
10.2147/NDT.S485884
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: To investigate the mechanism underlying the effects of Tongdu Tiaoshen electroacupuncture in the treatment of cerebral ischemia-reperfusion (I/R) injury. Methods: Sixty adult male Sprague-Dawley (SD) rats were randomly allocated to five groups (n=12): Sham, I/R, electroacupuncture (EA), BBG (P2X7R inhibitor), and MCC950 (NLRP3 inhibitor). The EA group received acupuncture at Shenting (GV24), Baihui (GV20), and Dazhui (GV14) points with a stimulation frequency of 2/5 Hz, intensity of 2 mA, and a duration of 40 min. Neurologic deficit scoring was then performed, and cerebral infarction volume was determined using triphenyl tetrazolium chloride (TTC) staining. Morphological changes in neurons in cortical areas were observed using an electron microscope, interleukin-18 (IL-18) and interleukin-1(3 (IL-1(3) levels were assessed via the enzyme-linked immunosorbent assay (ELISA). Moreover, the expression of P2X7R/NLRP3/GSDMD pathway-related proteins and mRNAs was quantified by immunofluorescence staining, Western blot assay, and real-time fluorescence quantitative (RT-PCR) analysis. Results: Electroacupuncture improved neurologic deficit scores, cerebral infarct size, and cell pyroptosis, and reduced IL-1(3 and IL- 18 levels. Furthermore, electroacupuncture and inhibitor treatment significantly downregulated the expression of P2X7R, ASC, Caspase-1, NLRP3, and GSDMD involved in the P2X7/NLRP3/GSDMD signaling pathway. Conclusion: Tongdu Tiaoshen electroacupuncture may exert cerebral protection by inhibiting neuroinflammation through the P2X7/ NLRP3/GSDMD pathway and reducing cellular pyroptosis.
引用
收藏
页码:2335 / 2346
页数:12
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