Electroacupuncture may alleviate diabetic neuropathic pain by inhibiting the microglia P2X4R and neuroinflammation

被引:9
作者
Qu, Si-ying [1 ]
Wang, Han-zhi [1 ,2 ]
Hu, Qun-qi [1 ]
Ma, Yi-qi [1 ]
Kang, Yu-rong [1 ]
Ma, Li-qian [1 ]
Li, Xiang [1 ]
Chen, Lu-hang [1 ]
Liu, Bo-yu [1 ,3 ]
Shao, Xiao-mei [1 ,3 ]
Liu, Bo-yi [1 ,3 ]
Du, Jun-ying [1 ,3 ]
Liang, Yi [1 ,3 ]
Zhao, Hong-li [2 ]
Jiang, Yong-liang [1 ,3 ]
Fang, Jian-qiao [1 ,3 ]
He, Xiao-fen [1 ,3 ]
机构
[1] Zhejiang Chinese Med Univ, Hangzhou 310053, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Hangzhou Hosp Tradit Chinese Med, Dept TCM Gynecol, Hangzhou 310000, Peoples R China
[3] Zhejiang Chinese Med Univ, Clin Med Coll 3, Dept Neurobiol & Acupuncture Res, Key Lab Acupuncture & Neurol Zhejiang Prov, Hangzhou 310053, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Electroacupuncture; Diabetic neuropathic pain; Spinal cord; Microglia; PERIPHERAL-NERVE INJURY; SPINAL MICROGLIA; UP-REGULATION; MECHANICAL ALLODYNIA; P2X(4) RECEPTORS; RAT MODEL; STREPTOZOTOCIN; ACTIVATION; CORD; EXPRESSION;
D O I
10.1007/s11302-023-09972-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic neuropathic pain (DNP) is a common and destructive complication of diabetes mellitus. The discovery of effective therapeutic methods for DNP is vitally imperative because of the lack of effective treatments. Although 2 Hz electroacupuncture (EA) was a successful approach for relieving DNP, the mechanism underlying the effect of EA on DNP is still poorly understood. Here, we established a rat model of DNP that was induced by streptozotocin (STZ) injection. P2X4R was upregulated in the spinal cord after STZ-injection. The upregulation of P2X4R was mainly expressed on activated microglia. Intrathecal injection of a P2X4R antagonist or microglia inhibitor attenuated STZ-induced nociceptive thermal hyperalgesia and reduced the overexpression of brain-derived neurotrophic factor (BDNF), interleukin-1 beta (IL-1 beta) and tumor necrosis factor-alpha (TNF-alpha) in the spinal cord. We also assessed the effects of EA treatment on the pain hypersensitivities of DNP rats, and further investigated the possible mechanism underlying the analgesic effect of EA. EA relieved the hyperalgesia of DNP. In terms of mechanism, EA reduced the upregulation of P2X4R on activated microglia and decreased BDNF, IL-1 beta and TNF-alpha in the spinal cord. Mechanistic research of EA's analgesic impact would be beneficial in ensuring its prospective therapeutic effect on DNP as well as in extending EA's applicability.
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页数:15
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