Suppr超能文献

阿片类药物。

Opioids.

作者信息

Zöllner C, Stein C

机构信息

Klinik für Anaesthesiologie und operative Intensivmedizin, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12200 Berlin, Germany.

出版信息

Handb Exp Pharmacol. 2007(177):31-63. doi: 10.1007/978-3-540-33823-9_2.

Abstract

Opioids are the most effective and widely used drugs in the treatment of severe pain. They act through G protein-coupled receptors. Four families of endogenous ligands (opioid peptides) are known. The standard exogenous opioid analgesic is morphine. Opioid agonists can activate central and peripheral opioid receptors. Three classes of opioid receptors (mu, delta, kappa) have been identified. Multiple pathways ofopioid receptor signaling (e.g., G(i/o) coupling, cAMP inhibition, Ca++ channel inhibition) have been described. The differential regulation of effectors, preclinical pharmacology, clinical applications, and side effects will be reviewed in this chapter.

摘要

阿片类药物是治疗重度疼痛最有效且应用最广泛的药物。它们通过G蛋白偶联受体发挥作用。已知有四类内源性配体(阿片肽)。标准的外源性阿片类镇痛药是吗啡。阿片类激动剂可激活中枢和外周阿片受体。已鉴定出三类阿片受体(μ、δ、κ)。已描述了阿片受体信号传导的多种途径(例如,G(i/o)偶联、cAMP抑制、Ca++通道抑制)。本章将综述效应器的差异调节、临床前药理学、临床应用及副作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验