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Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression
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 electroac...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934063/ https://www.ncbi.nlm.nih.gov/pubmed/33626989 http://dx.doi.org/10.1177/1744806921997654 |
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author | Wu, Qiaoyun Yue, Jingjing Lin, Li Yu, Xiaolan Zhou, Ye Ying, Xinwang Chen, Xiaolong Tu, Wenzhan Lou, Xinfa Yang, Guanhu Zhou, Kecheng Jiang, Songhe |
author_facet | Wu, Qiaoyun Yue, Jingjing Lin, Li Yu, Xiaolan Zhou, Ye Ying, Xinwang Chen, Xiaolong Tu, Wenzhan Lou, Xinfa Yang, Guanhu Zhou, Kecheng Jiang, Songhe |
author_sort | Wu, Qiaoyun |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7934063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79340632021-03-17 Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression Wu, Qiaoyun Yue, Jingjing Lin, Li Yu, Xiaolan Zhou, Ye Ying, Xinwang Chen, Xiaolong Tu, Wenzhan Lou, Xinfa Yang, Guanhu Zhou, Kecheng Jiang, Songhe Mol Pain Research Article 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. SAGE Publications 2021-02-24 /pmc/articles/PMC7934063/ /pubmed/33626989 http://dx.doi.org/10.1177/1744806921997654 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Wu, Qiaoyun Yue, Jingjing Lin, Li Yu, Xiaolan Zhou, Ye Ying, Xinwang Chen, Xiaolong Tu, Wenzhan Lou, Xinfa Yang, Guanhu Zhou, Kecheng Jiang, Songhe Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression |
title | Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression |
title_full | Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression |
title_fullStr | Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression |
title_full_unstemmed | Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression |
title_short | Electroacupuncture may alleviate neuropathic pain via suppressing P2X7R expression |
title_sort | electroacupuncture may alleviate neuropathic pain via suppressing p2x7r expression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934063/ https://www.ncbi.nlm.nih.gov/pubmed/33626989 http://dx.doi.org/10.1177/1744806921997654 |
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