• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

神经病理性疼痛中的瞬时受体电位通道

Transient Receptor Potential Channels in neuropathic pain.

作者信息

Basso Lilian, Altier Christophe

机构信息

Department of Physiology and Pharmacology, Inflammation Research Network, University of Calgary, Calgary, Alberta, Canada.

Department of Physiology and Pharmacology, Inflammation Research Network, University of Calgary, Calgary, Alberta, Canada.

出版信息

Curr Opin Pharmacol. 2017 Feb;32:9-15. doi: 10.1016/j.coph.2016.10.002. Epub 2016 Oct 27.

DOI:10.1016/j.coph.2016.10.002
PMID:27835802
Abstract

Neuropathic pain caused by disease or dysfunction of the nervous system is one of the most difficult pain conditions to treat. Symptoms include a hypersensitivity to mechanical and thermal stimuli, processed by specialized nociceptors that constitute the first line of defence of the somatosensory system. The detection of these stimuli depends on the TRP ion channel family, which activates upon damaging pressure, extreme temperature, or toxic endogenous and exogenous chemicals. This review will summarize the current knowledge of the contribution of TRP channels, particularly the thermosensitive TRP, including TRPV1, TRPA1 and TRPM8 channels that play a central role in the sensitization of nociceptive transduction. We will discuss the pharmacology of these receptors and their relative success in preclinical and clinical studies.

摘要

由神经系统疾病或功能障碍引起的神经性疼痛是最难治疗的疼痛病症之一。症状包括对机械和热刺激的超敏反应,这些刺激由构成躯体感觉系统第一道防线的特殊伤害感受器进行处理。这些刺激的检测取决于TRP离子通道家族,该家族在受到损伤性压力、极端温度或有毒内源性和外源性化学物质刺激时被激活。本综述将总结目前关于TRP通道,特别是热敏TRP通道(包括在伤害性转导敏化中起核心作用的TRPV1、TRPA1和TRPM8通道)作用的认识。我们将讨论这些受体的药理学及其在临床前和临床研究中的相对成效。

相似文献

1
Transient Receptor Potential Channels in neuropathic pain.神经病理性疼痛中的瞬时受体电位通道
Curr Opin Pharmacol. 2017 Feb;32:9-15. doi: 10.1016/j.coph.2016.10.002. Epub 2016 Oct 27.
2
TRP channels: targets for the relief of pain.瞬时受体电位通道:缓解疼痛的靶点。
Biochim Biophys Acta. 2007 Aug;1772(8):989-1003. doi: 10.1016/j.bbadis.2007.01.008. Epub 2007 Jan 23.
3
Antinociceptive activity of transient receptor potential channel TRPV1, TRPA1, and TRPM8 antagonists in neurogenic and neuropathic pain models in mice.瞬时受体电位通道TRPV1、TRPA1和TRPM8拮抗剂在小鼠神经源性和神经性疼痛模型中的抗伤害感受活性。
J Zhejiang Univ Sci B. 2015 Mar;16(3):167-78. doi: 10.1631/jzus.B1400189.
4
The TRPM8 channel forms a complex with the 5-HT(1B) receptor and phospholipase D that amplifies its reversal of pain hypersensitivity.瞬时受体电位M8通道与5-羟色胺(1B)受体及磷脂酶D形成复合物,该复合物可增强其对疼痛超敏反应的逆转作用。
Neuropharmacology. 2014 Apr;79:136-51. doi: 10.1016/j.neuropharm.2013.11.006. Epub 2013 Nov 20.
5
Temperature-sensitive transient receptor potential channels in corneal tissue layers and cells.角膜组织层和细胞中的温度敏感型瞬时受体电位通道
Ophthalmic Res. 2014;52(3):151-9. doi: 10.1159/000365334. Epub 2014 Oct 8.
6
Thermosensitive TRP ion channels mediate cytosolic calcium response in human synoviocytes.热敏性瞬时受体电位(TRP)离子通道介导人类滑膜细胞中的胞质钙反应。
Am J Physiol Cell Physiol. 2006 Sep;291(3):C424-32. doi: 10.1152/ajpcell.00553.2005. Epub 2006 Apr 5.
7
TRP channels: potential drug target for neuropathic pain.瞬时受体电位通道:神经性疼痛的潜在药物靶点。
Inflammopharmacology. 2016 Dec;24(6):305-317. doi: 10.1007/s10787-016-0288-x. Epub 2016 Oct 18.
8
Menthol derivative WS-12 selectively activates transient receptor potential melastatin-8 (TRPM8) ion channels.薄荷醇衍生物WS-12可选择性激活瞬时受体电位香草酸亚型8(TRPM8)离子通道。
Pak J Pharm Sci. 2008 Oct;21(4):370-8.
9
Stimulation of human TRPA1 channels by clinical concentrations of the antirheumatic drug auranofin.临床浓度的抗风湿药物金诺芬对人 TRPA1 通道的刺激作用。
Am J Physiol Cell Physiol. 2013 Feb 15;304(4):C354-61. doi: 10.1152/ajpcell.00096.2012. Epub 2012 Dec 5.
10
[Thermosensitive TRP channels and brain function].[热敏性瞬时受体电位通道与脑功能]
Nihon Shinkei Seishin Yakurigaku Zasshi. 2016 Apr;36(2):37-41.

引用本文的文献

1
Molecular Mechanisms of Chronic Pain and Therapeutic Interventions.慢性疼痛的分子机制与治疗干预
MedComm (2020). 2025 Aug 7;6(8):e70325. doi: 10.1002/mco2.70325. eCollection 2025 Aug.
2
Dual Roles of Prostaglandin E2 (PGE2) in Bone Remodeling and Pain Management: Bridging the Gap in Osteoarthritis Research.前列腺素E2(PGE2)在骨重塑和疼痛管理中的双重作用:弥合骨关节炎研究中的差距
Mediators Inflamm. 2025 Jul 26;2025:8882429. doi: 10.1155/mi/8882429. eCollection 2025.
3
Opiorphin and neuropathic pain: a promising treatment approach?
阿片样肽与神经性疼痛:一种有前景的治疗方法?
Inflammopharmacology. 2025 Jul 3. doi: 10.1007/s10787-025-01827-6.
4
Lysosomal ion channels and pain.溶酶体离子通道与疼痛。
Pain Rep. 2025 Jun 5;10(4):e1282. doi: 10.1097/PR9.0000000000001282. eCollection 2025 Aug.
5
NGF in Neuropathic Pain: Understanding Its Role and Therapeutic Opportunities.神经病理性疼痛中的神经生长因子:了解其作用及治疗机会
Curr Issues Mol Biol. 2025 Jan 31;47(2):93. doi: 10.3390/cimb47020093.
6
A comprehensive review of traditional Chinese medicine in treating neuropathic pain.中医治疗神经性疼痛的综合综述。
Heliyon. 2024 Sep 3;10(17):e37350. doi: 10.1016/j.heliyon.2024.e37350. eCollection 2024 Sep 15.
7
Exploring the Analgesic Initiation Mechanism of Tuina in the Dorsal Root Ganglion of Minor CCI Rats via the TRPV1/TRPA1-cGMP Pathway.探讨经皮穴位电刺激通过 TRPV1/TRPA1-cGMP 通路对小CCI 大鼠背根神经节中推拿镇痛起始机制的影响。
Pain Res Manag. 2024 Jul 24;2024:2437396. doi: 10.1155/2024/2437396. eCollection 2024.
8
Dysregulation of sphingolipid metabolism in pain.疼痛中鞘脂代谢的失调
Front Pharmacol. 2024 Mar 8;15:1337150. doi: 10.3389/fphar.2024.1337150. eCollection 2024.
9
The transmembrane channel-like 6 (TMC6) in primary sensory neurons involving thermal sensation via modulating M channels.初级感觉神经元中的跨膜通道样蛋白6(TMC6)通过调节M通道参与热感觉。
Front Pharmacol. 2024 Feb 19;15:1330167. doi: 10.3389/fphar.2024.1330167. eCollection 2024.
10
The Concise Guide to PHARMACOLOGY 2023/24: Ion channels.《药理学简明指南 2023/24 年版》:离子通道。
Br J Pharmacol. 2023 Oct;180 Suppl 2(Suppl 2):S145-S222. doi: 10.1111/bph.16178.