Do glial cells control pain?

Marc R Suter, Yeong-Ray Wen, Isabelle Decosterd, Ru-Rong Ji
{"title":"Do glial cells control pain?","authors":"Marc R Suter, Yeong-Ray Wen, Isabelle Decosterd, Ru-Rong Ji","doi":"10.1017/S1740925X08000100","DOIUrl":null,"url":null,"abstract":"<p><p>Management of chronic pain is a real challenge, and current treatments that focus on blocking neurotransmission in the pain pathway have resulted in limited success. Activation of glial cells has been widely implicated in neuroinflammation in the CNS, leading to neurodegeneration in conditions such as Alzheimer's disease and multiple sclerosis. The inflammatory mediators released by activated glial cells, such as tumor necrosis factor-a and interleukin-1b not only cause neurodegeneration in these disease conditions, but also cause abnormal pain by acting on spinal cord dorsal horn neurons in injury conditions. Pain can also be potentiated by growth factors such as brain-derived growth factor and basic fibroblast growth factor, which are produced by glia to protect neurons. Thus, glial cells can powerfully control pain when they are activated to produce various pain mediators. We review accumulating evidence that supports an important role for microglial cells in the spinal cord for pain control under injury conditions (e.g. nerve injury). We also discuss possible signaling mechanisms, in particular mitogen-activated protein kinase pathways that are crucial for glial-mediated control of pain.Investigating signaling mechanisms in microglia might lead to more effective management of devastating chronic pain.</p>","PeriodicalId":19153,"journal":{"name":"Neuron glia biology","volume":"3 3","pages":"255-68"},"PeriodicalIF":0.0000,"publicationDate":"2007-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394739/pdf/nihms49881.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuron glia biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1017/S1740925X08000100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Management of chronic pain is a real challenge, and current treatments that focus on blocking neurotransmission in the pain pathway have resulted in limited success. Activation of glial cells has been widely implicated in neuroinflammation in the CNS, leading to neurodegeneration in conditions such as Alzheimer's disease and multiple sclerosis. The inflammatory mediators released by activated glial cells, such as tumor necrosis factor-a and interleukin-1b not only cause neurodegeneration in these disease conditions, but also cause abnormal pain by acting on spinal cord dorsal horn neurons in injury conditions. Pain can also be potentiated by growth factors such as brain-derived growth factor and basic fibroblast growth factor, which are produced by glia to protect neurons. Thus, glial cells can powerfully control pain when they are activated to produce various pain mediators. We review accumulating evidence that supports an important role for microglial cells in the spinal cord for pain control under injury conditions (e.g. nerve injury). We also discuss possible signaling mechanisms, in particular mitogen-activated protein kinase pathways that are crucial for glial-mediated control of pain.Investigating signaling mechanisms in microglia might lead to more effective management of devastating chronic pain.

神经胶质细胞控制疼痛吗?
慢性疼痛的管理是一个真正的挑战,目前专注于阻断疼痛通路中神经传递的治疗方法收效甚微。神经胶质细胞的激活广泛涉及中枢神经系统的神经炎症,导致阿尔茨海默病和多发性硬化症等疾病的神经退行性变。活化的神经胶质细胞释放的炎症介质,如肿瘤坏死因子-a和白细胞介素-1b,不仅在这些疾病条件下引起神经退行性变,而且在损伤条件下通过作用于脊髓背角神经元而引起异常疼痛。神经胶质细胞产生的保护神经元的生长因子,如脑源性生长因子和碱性成纤维细胞生长因子,也会增强疼痛。因此,当神经胶质细胞被激活产生各种疼痛介质时,它们可以有力地控制疼痛。我们综述了越来越多的证据,这些证据支持脊髓中的小胶质细胞在损伤条件下(如神经损伤)对疼痛控制的重要作用。我们还讨论了可能的信号传导机制,特别是对神经胶质介导的疼痛控制至关重要的丝裂原活化蛋白激酶途径。研究小胶质细胞的信号机制可能会更有效地治疗破坏性慢性疼痛。
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
Neuron glia biology
Neuron glia biology 医学-神经科学
自引率
0.00%
发文量
0
×
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