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

IF 2.4 4区 医学 Q2 NEUROSCIENCES
Purinergic Signalling Pub Date : 2025-08-01 Epub Date: 2023-10-23 DOI:10.1007/s11302-023-09972-9
Si-Ying Qu, Han-Zhi Wang, Qun-Qi Hu, Yi-Qi Ma, Yu-Rong Kang, Li-Qian Ma, Xiang Li, Lu-Hang Chen, Bo-Yu Liu, Xiao-Mei Shao, Bo-Yi Liu, Jun-Ying Du, Yi Liang, Hong-Li Zhao, Yong-Liang Jiang, Jian-Qiao Fang, Xiao-Fen He
{"title":"Electroacupuncture may alleviate diabetic neuropathic pain by inhibiting the microglia P2X4R and neuroinflammation.","authors":"Si-Ying Qu, Han-Zhi Wang, Qun-Qi Hu, Yi-Qi Ma, Yu-Rong Kang, Li-Qian Ma, Xiang Li, Lu-Hang Chen, Bo-Yu Liu, Xiao-Mei Shao, Bo-Yi Liu, Jun-Ying Du, Yi Liang, Hong-Li Zhao, Yong-Liang Jiang, Jian-Qiao Fang, Xiao-Fen He","doi":"10.1007/s11302-023-09972-9","DOIUrl":null,"url":null,"abstract":"<p><p>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-1β (IL-1β) and tumor necrosis factor-α (TNF-α) 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-1β and TNF-α 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.</p>","PeriodicalId":20952,"journal":{"name":"Purinergic Signalling","volume":" ","pages":"533-547"},"PeriodicalIF":2.4000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12454746/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Purinergic Signalling","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11302-023-09972-9","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/23 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

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-1β (IL-1β) and tumor necrosis factor-α (TNF-α) 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-1β and TNF-α 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.

Abstract Image

电针可通过抑制小胶质细胞P2X4R和神经炎症来减轻糖尿病神经性疼痛。
糖尿病神经性疼痛(DNP)是糖尿病常见的破坏性并发症。由于缺乏有效的治疗方法,发现有效的DNP治疗方法至关重要。尽管2Hz电针(EA)是一种成功的缓解DNP的方法,但电针对DNP影响的机制仍知之甚少。在此,我们建立了链脲佐菌素(STZ)注射诱导的DNP大鼠模型。注射STZ后脊髓中P2X4R上调。P2X4R的上调主要在活化的小胶质细胞上表达。鞘内注射P2X4R拮抗剂或小胶质细胞抑制剂可减弱STZ诱导的伤害性热痛觉过敏,并减少脊髓中脑源性神经营养因子(BDNF)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的过表达。我们还评估了电针治疗对DNP大鼠疼痛超敏反应的影响,并进一步研究了电针镇痛作用的可能机制。电针可减轻DNP的痛觉过敏。从机制上讲,电针降低了激活的小胶质细胞P2X4R的上调,降低了脊髓中的BDNF、IL-1β和TNF-α。对电针镇痛作用的机制研究将有助于确保其对DNP的预期治疗效果以及扩大电针的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信