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膜联蛋白1:一种调节炎性疼痛的糖皮质激素诱导蛋白。

Annexin 1: a glucocorticoid-inducible protein that modulates inflammatory pain.

作者信息

Chen L, Lv F, Pei L

机构信息

Department of Neurology of the First People's Hospital of Jingzhou, The first affiliated hospital of Yangtze University, Jingzhou, China.

出版信息

Eur J Pain. 2014 Mar;18(3):338-47. doi: 10.1002/j.1532-2149.2013.00373.x. Epub 2013 Jul 31.

Abstract

Annexin 1, a glucocorticoid (GC)-inducible protein, can play an important role via formyl peptide receptor like 1 (FPR2/ALX, also known as FPRL1) in inflammatory pain modulation. The aim of this review is to analyze different lines of evidence for the role of ANXA1 with different mechanisms on inflammatory pain and describe the profile of ANXA1 as a potential analgesic. A Medline (PUBMED) search using the terms 'Annexin 1 distribution OR expression, FPR2/ALX distribution OR expression, Annexin 1 AND pain, Annexin 1 AND FPR2/ALX AND pain' was performed. Articles with a publication date up to Nov. 1st, 2012 were included. The antinociception of ANXA1 has been evaluated in diverse pain models. It has been suggested that ANXA1 may exerts its action via: (1) inhibiting vital cytokines involved in pain transmission, (2) inhibiting neutrophil accumulation through preventing transendothelial migration via an interaction with formyl peptide receptors, (3) facilitating tonic opioid release from neutrophil in inflammatory site, (4) interrupting the peripheral nociceptive transmission by suppressing neuronal excitability. In general, ANXA1 is a potential mediator for anti-nociception and the role with its receptor constitute attractive targets for developing anesthesia and analgesic drugs, and their interaction may prove to be a useful strategy to treat inflammatory pain.

摘要

膜联蛋白1是一种糖皮质激素(GC)诱导蛋白,可通过类甲酰肽受体1(FPR2/ALX,也称为FPRL1)在炎症性疼痛调节中发挥重要作用。本综述的目的是分析关于膜联蛋白1在炎症性疼痛中通过不同机制发挥作用的不同证据,并描述膜联蛋白1作为一种潜在镇痛药的特征。使用“膜联蛋白1分布或表达、FPR2/ALX分布或表达、膜联蛋白1与疼痛、膜联蛋白1与FPR2/ALX与疼痛”等术语在Medline(PUBMED)数据库中进行了检索。纳入了截至2012年11月1日发表的文章。膜联蛋白1的抗伤害感受作用已在多种疼痛模型中得到评估。有人提出,膜联蛋白1可能通过以下方式发挥作用:(1)抑制参与疼痛传递的重要细胞因子;(2)通过与甲酰肽受体相互作用阻止跨内皮迁移,从而抑制中性粒细胞聚集;(3)促进炎症部位中性粒细胞释放阿片类物质;(4)通过抑制神经元兴奋性中断外周伤害性信号传递。总体而言,膜联蛋白1是抗伤害感受的潜在介质,其与受体的作用构成了开发麻醉药和镇痛药的有吸引力的靶点,它们之间的相互作用可能是治疗炎症性疼痛的一种有用策略。

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