引用本文:程旭韬(综述),华 震(审校).瞬时受体电位香草酸亚型1受体介导疼痛的机制和治疗应用研究进展[J].中国临床新医学,2022,15(2):171-175.
【打印本页】   【下载PDF全文】   查看/发表评论  【EndNote】   【RefMan】   【BibTex】
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 1718次   下载 1156 本文二维码信息
码上扫一扫!
分享到: 微信 更多
瞬时受体电位香草酸亚型1受体介导疼痛的机制和治疗应用研究进展
程旭韬(综述),华 震(审校)
100005 北京,北京医院麻醉科,北京协和医学院研究生院
摘要:
[摘要] 瞬时受体电位香草酸亚型1(TRPV1)自首次成功克隆以来作为与疼痛密切相关的伤害性感受器而备受关注,其分子结构与生理功能、分布特征、激活与抑制等得到广泛研究。TRPV1受体参与炎症、脂质氧化等生物过程也与疼痛息息相关。多种内、外源性增敏剂或抑制剂可调节TRPV1通道敏感性,从而介导疼痛信号传导。TRPV1还可能通过细胞内钙超载等机制导致伤害性感受器的消融,这可能是镇痛治疗的一种潜在有效途径。该文旨在对TRPV1受体介导疼痛的相关机制及其应用研究进展作一综述。
关键词:  瞬时受体电位香草酸亚型1  辣椒素受体  慢性疼痛  伤害性感受器
DOI:10.3969/j.issn.1674-3806.2022.02.18
分类号:
基金项目:北京医院临床研究“121工程”项目(编号:BJ-2020-168)
Research progress on the mechanism of transient receptor potential vanilloid 1 receptor mediating pain and the therapeutic application
CHENG Xu-tao, HUA Zhen
Graduate School of Peking Union Medical College, Department of Anesthesiology, Beijing Hospital, Beijing 100005, China
Abstract:
[Abstract] Transient receptor potential vanilloid 1(TRPV1) has attracted much attention as a nociceptor closely related to pain since its first successful cloning, and its molecular structure, physiological function, distribution characteristics, activation and inhibition have been widely studied. TRPV1 receptor is also closely related to pain in terms of its involvement in biological processes such as inflammation and lipid oxidation. A variety of endogenous and exogenous sensitizers or inhibitors can modulate the sensitivity of TRPV1 channel, thus mediating pain signal transmission. TRPV1 may also lead to the ablation of nociceptors through intracellular calcium overload and other mechanisms, which may be a potential effective approach in the treatment of pain. The aim of this paper is to review the research progress on the related mechanisms and the applications of TRPV1 receptor in mediating pain.
Key words:  Transient receptor potential vanilloid 1(TRPV1)  Capsaicin receptor  Chronic pain  Nociceptors