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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">MRP</journal-id><journal-title-group><journal-title>Medical Research and Practice</journal-title></journal-title-group><issn>2993-9690</issn><eissn>2993-9704</eissn><publisher><publisher-name>Art and Technology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.61369/MRP.2026060025</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>TRPV1、TRPA1 及TRPM8 在疼痛中的作用机制及研究进展</title><url>https://artdesignp.com/journal/MRP/4/6/10.61369/MRP.2026060025</url><author>莫洁红,赵雷</author><pub-date pub-type="publication-year"><year>2026</year></pub-date><volume>4</volume><issue>6</issue><history><date date-type="pub"><published-time>2026-06-20</published-time></date></history><abstract>瞬时受体电位（TRP）通道是参与健康及疼痛、炎症、代谢紊乱等疾病过程的多功能信号分子。其中，TRPA1 和TRPM8 感知冷觉温度，而 TRPV1 感知热觉温度，三者均对温度伤害感受及神经病理性疼痛至关重要。阿片类镇痛药疗效有限，且会导致严重的依赖性和成瘾性。因此，研究 TRP 通道可为开发新型非成瘾性镇痛靶点提供新思路。本综述总结了与疼痛相关的关键 TRP 通道（TRPV1、TRPA1、TRPM8）的研究现状、致痛机制及抑制剂研究进展，阐述了其生物学特性及在不同疼痛类型中的作用，并对其作为非成瘾性镇痛靶点的临床转化前景进行了展望。</abstract><keywords>TRP 离子通道,疼痛,镇痛分子靶点</keywords></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>[1]ZHANG M, MA Y, YE X, et al. 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