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本文引用的文献

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Opioid receptor subtypes: fact or artifact?阿片受体亚型:事实还是人为?
Br J Anaesth. 2011 Jul;107(1):8-18. doi: 10.1093/bja/aer115. Epub 2011 May 24.
2
Long-term opioid management for chronic noncancer pain.慢性非癌性疼痛的长期阿片类药物管理
Cochrane Database Syst Rev. 2010 Jan 20;2010(1):CD006605. doi: 10.1002/14651858.CD006605.pub2.
3
Oral or transdermal opioids for osteoarthritis of the knee or hip.用于膝或髋关节骨关节炎的口服或透皮阿片类药物。
Cochrane Database Syst Rev. 2009 Oct 7(4):CD003115. doi: 10.1002/14651858.CD003115.pub3.
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Opioids for chronic low-back pain.用于慢性下腰痛的阿片类药物。
Cochrane Database Syst Rev. 2007 Jul 18(3):CD004959. doi: 10.1002/14651858.CD004959.pub3.
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Oxycodone and morphine have distinctly different pharmacological profiles: radioligand binding and behavioural studies in two rat models of neuropathic pain.羟考酮和吗啡具有截然不同的药理学特征:在两种神经性疼痛大鼠模型中的放射性配体结合及行为学研究
Pain. 2007 Dec 5;132(3):289-300. doi: 10.1016/j.pain.2007.03.022. Epub 2007 Apr 30.
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Opioids for neuropathic pain.用于神经性疼痛的阿片类药物。
Cochrane Database Syst Rev. 2006 Jul 19(3):CD006146. doi: 10.1002/14651858.CD006146.
7
75 years of opioid research: the exciting but vain quest for the Holy Grail.75年的阿片类药物研究:对圣杯的追寻令人兴奋却徒劳无功。
Br J Pharmacol. 2006 Jan;147 Suppl 1(Suppl 1):S153-62. doi: 10.1038/sj.bjp.0706435.
8
Buprenorphine antinociception is abolished, but naloxone-sensitive reward is retained, in mu-opioid receptor knockout mice.在μ-阿片受体基因敲除小鼠中,丁丙诺啡的镇痛作用消失,但对纳洛酮敏感的奖赏效应仍保留。
Neuropsychopharmacology. 2004 Sep;29(9):1656-63. doi: 10.1038/sj.npp.1300463.
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Attacking pain at its source: new perspectives on opioids.从根源上攻克疼痛:阿片类药物的新视角
Nat Med. 2003 Aug;9(8):1003-8. doi: 10.1038/nm908.
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Morphine, the Proteus of organic molecules.吗啡,有机分子中的“千面怪”。
Chem Commun (Camb). 2002 Jun 7(11):1159-68. doi: 10.1039/b111551k.

基础阿片类药物药理学:最新进展

Basic opioid pharmacology: an update.

作者信息

Pathan Hasan, Williams John

机构信息

Royal Derby Hospital, Derby, UK.

Royal Derby Hospital, Derby, UK ; University of Nottingham, Derby, UK.

出版信息

Br J Pain. 2012 Feb;6(1):11-6. doi: 10.1177/2049463712438493.

DOI:10.1177/2049463712438493
PMID:26516461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4590096/
Abstract

Opioids are a group of analgesic agents commonly used in clinical practice. There are three classical opioid receptors (DOP, KOP and MOP), while the novel NOP receptor is considered to be a non-opioid branch of the opioid receptor family. Opioids can act at these receptors as agonists, antagonists or partial agonists. Opioid agonists bind to G-protein coupled receptors to cause cellular hyperpolarisation. Most clinically relevant opioid analgesics bind to MOP receptors in the central and peripheral nervous system in an agonist manner to elicit analgesia. Opioids may also be classified according to their mode of synthesis into alkaloids, semi-synthetic and synthetic compounds.

摘要

阿片类药物是临床实践中常用的一类镇痛药。存在三种经典的阿片受体(DOP、KOP和MOP),而新型的NOP受体被认为是阿片受体家族的非阿片类分支。阿片类药物可作为激动剂、拮抗剂或部分激动剂作用于这些受体。阿片类激动剂与G蛋白偶联受体结合,导致细胞超极化。大多数具有临床相关性的阿片类镇痛药以激动剂的方式与中枢和外周神经系统中的MOP受体结合,从而产生镇痛作用。阿片类药物也可根据其合成方式分为生物碱、半合成和合成化合物。