Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression

被引:47
作者
Wu, Qiaoyun [1 ,2 ,3 ]
Yue, Jingjing [1 ,2 ,3 ]
Lin, Li [1 ,2 ,3 ]
Yu, Xiaolan [1 ,2 ,3 ]
Zhou, Ye [1 ,2 ,3 ]
Ying, Xinwang [1 ,2 ,3 ]
Chen, Xiaolong [1 ,2 ,3 ]
Tu, Wenzhan [1 ,2 ,3 ]
Lou, Xinfa [3 ]
Yang, Guanhu [1 ,2 ,3 ]
Zhou, Kecheng [1 ,2 ,3 ]
Jiang, Songhe [1 ,2 ,3 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Phys Med & Rehabil, 268 Xue Yuan Xi Rd, Wenzhou 325027, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Peoples R China
[3] Wenzhou Med Univ, China USA Inst Acupuncture & Rehabil, Integrat & Optimized Med Res Ctr, Wenzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Neuropathic pain; electroacupuncture; inflammation; dendritic spine; synaptic reconstruction; DORSAL-ROOT GANGLION; SYNAPTIC PLASTICITY; MICROGLIAL ACTIVATION; SPINAL MICROGLIA; RAT MODEL; RECEPTOR; INHIBITION; ERK; PATHWAYS; INJURY;
D O I
10.1177/1744806921997654
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuropathic pain is a severe problem that is difficult to treat clinically. Reducing abnormal remodeling of dendritic spines/synapses and increasing the anti-inflammatory effects in the spinal cord dorsal horn are potential methods to treat this disease. Previous studies have reported that electroacupuncture (EA) could increase the pain threshold after peripheral nerve injury. However, the underlying mechanism is unclear. P2X7 receptors (P2X7R) mediate the activation of microglia and participate in the occurrence and development of neuropathic pain. We hypothesized that the effects of EA on relieving pain may be related to the downregulation of the P2X7R. Spinal nerve ligation (SNL) rats were used as a model in this experiment, and 2'(3')-O-(4-benzoyl)benzoyl ATP (BzATP) was used as a P2X7R agonist. We found that EA treatment decreased dendritic spine density, inhibited synaptic reconstruction and reduced inflammatory response, which is consistent with the decrease in P2X7R expression as well as the improved neurobehavioral performance. In contrast to the beneficial effects of EA, BzATP enhanced abnormal remodeling of dendritic spines/synapses and inflammation. Furthermore, the EA-mediated positive effects were reversed by BzATP, which is consistent with the increased P2X7R expression. These findings indicated that EA improves neuropathic pain by reducing abnormal dendritic spine/synaptic reconstruction and inflammation via suppressing P2X7R expression.
引用
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页数:13
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