首页|离子通道翻译后修饰在神经病理性疼痛中的研究进展

离子通道翻译后修饰在神经病理性疼痛中的研究进展

扫码查看
离子通道是细胞膜上的跨膜蛋白质分子,在神经病理性疼痛(neuropathic pain,NP)的发生和发展过程中发挥重要作用.目前,治疗NP的靶向离子通道药物在临床上被广泛应用,但药物在使用过程中通常会引发一系列不良反应.研究表明,离子通道的翻译后修饰系统可以有效调控疼痛行为,涉及离子电流调节的神经元兴奋性、突触可塑性和膜运输等功能.靶向伤害感受信号通路中的离子通道功能调控可能是潜在的镇痛研究方向.本文将对翻译后修饰的离子通道在调节NP中的作用进行综述,重点介绍泛素化、磷酸化和棕榈酰化等修饰调节,旨在系统阐明其在疼痛调控中的关键作用,为开发治疗慢性疼痛的新型镇痛药物提供新的靶标.
Research progress of post-translational modification of ion channels in neuropathic pain
Ion channels are transmembrane protein located on the cell membrane,playing an important role in the occurrence and development of neuropathic pain.Currently,drugs targeted ion channel for the treatment of NP are widely used in clinical practice,but they usually cause a series of adverse reactions.Studies have shown that post-translational modification systems of ion channels can effectively regulate pain by impacting neuronal excitability,synaptic plasticity and membrane transport.Targeting the function of nociceptive ion channels'functions may be a promising avenue for analgesia research.This article aims to review the role of post-translational modified ion channels in the regulation of NP,with a specific focus on ubiquitination,phos-phorylation,palmitoylation and other modifications.The goal is to systematically clarify their key role in pain regulation and provide new targets for the development of novel analgesic drugs for the treatment of chronic pain.

neuropathic painion channelspost-translational modificationsynaptic functionanalgesic targets

张艺佳、鄂思含、宋庆彪、张志宇、梁映霞

展开 >

山东第二医科大学麻醉学院,潍坊 261053

山东第二医科大学附属医院创伤骨科,潍坊 261035

神经病理性疼痛 离子通道 翻译后修饰 突触功能 镇痛靶点

国家自然科学基金山东省自然科学基金山东省卫生与医疗创新计划项目

81300969ZR2020MH130202004070430

2024

中国疼痛医学杂志
北京大学,中华医学会疼痛学分会

中国疼痛医学杂志

CSTPCD北大核心
影响因子:1.457
ISSN:1006-9852
年,卷(期):2024.30(10)
  • 1