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炎性疼痛:激肽与拮抗剂

Inflammatory pain: kinins and antagonists.

作者信息

Calixto J B, Cabrini D A, Ferreira J, Campos M M

机构信息

Department of Pharmacology, Center of Biological Sciences, Universidade Federal de Santa Catarina, 88015-420 Florianópolis, Santa Catarina, Brazil.

出版信息

Curr Opin Anaesthesiol. 2001 Oct;14(5):519-26. doi: 10.1097/00001503-200110000-00010.

Abstract

This short review focuses on the most recent findings in the rapidly expanding field of kinin research. Through a series of recent publications, the crucial relevance of this group of peptides as mediators of inflammatory pain is becoming increasingly evident. On the strength of this idea, kinins have been implicated as algogen peptides produced in response to noxious stimuli. The importance of kinins has been elucidated by different pharmacological and molecular approaches. Special attention has been given to studies with selective kinin antagonists, as well as to the use of receptor gene deletion technology. The gathering of results has demonstrated that both B(1) and B(2) receptors seem to exert a meaningful role during nociceptive responses, the B(1) receptor being most relevant in the chronic stages of inflammatory pain. It is hoped that new effective and useful therapeutic agents, mainly B(1) kinin selective receptor antagonists, might soon be available.

摘要

这篇简短的综述聚焦于激肽研究这个迅速发展领域的最新发现。通过一系列近期的出版物,这组肽作为炎性疼痛介质的关键相关性正变得越来越明显。基于这一观点,激肽被认为是对有害刺激作出反应而产生的致痛肽。激肽的重要性已通过不同的药理学和分子学方法得以阐明。人们特别关注了选择性激肽拮抗剂的研究以及受体基因缺失技术的应用。结果的汇总表明,B(1)和B(2)受体在伤害性反应过程中似乎都发挥着重要作用,其中B(1)受体在炎性疼痛的慢性阶段最为相关。希望新的有效且实用的治疗药物,主要是B(1)激肽选择性受体拮抗剂,可能很快就会出现。

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