Low dose ketamine: a therapeutic and research tool to explore N-methyt-Daspartate (NMDA) receptor-mediated plasticity in pain pathways

被引:82
作者
Chizh, Boris A. [1 ]
机构
[1] Addenbrookes Hosp, GlaxoSmithKline, Addenbrookes Ctr Clin Invest, Cambridge CB2 2GG, England
关键词
nMDA receptors; neuroplasticity; neuropathic pain; postoperative pain; fibromyalgia; hyperalgesia; allodynia; central senzitisation;
D O I
10.1177/0269881105062484
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Ketamine is a dissociative anaesthetic that has been used in the clinic for many years. At Low, subanaesthetic doses, it is a relatively selective and potent antagonist of the N-methyt-D-aspartate (NMDA) receptor. It belongs to the class of uncompetitive antagonists and blocks the receptor by binding to a specific site within the NMDA receptor channel when it is open. Like other compounds of this class, ketamine can cause hallucinations or other untoward central effects which limit its use in the clinic. Nevertheless, because of the evidence on the importance of NMDA receptor-mediated plasticity in chronic pain, tow doses of ketamine have been explored in a wide range of pain conditions. The majority of studies with ketamine have shown efficacy; however, it has not been possible to
引用
收藏
页码:259 / 271
页数:13
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