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用于神经性疼痛的丁丙诺啡——针对痛觉过敏

Buprenorphine for neuropathic pain--targeting hyperalgesia.

作者信息

Induru Raghava R, Davis Mellar P

机构信息

Division of Solid Tumor, Harry R. Horvitz Center for Palliative Medicine, The Cleveland Clinic, Taussig Cancer Center, Cleveland, Ohio, USA.

出版信息

Am J Hosp Palliat Care. 2009;26(6):470-3. doi: 10.1177/1049909109341868. Epub 2009 Aug 7.

Abstract

Opioids are well known to relieve severe, acute, and chronic nociceptive pain, but neuropathic pain shows a relatively poor response to opioids. Buprenorphine, a partial mu and ORL-1-receptor agonist, kappa-delta receptor antagonist, interacts with different G proteins than potent mu agonists and hence is not cross-tolerant to standard opioids. Buprenorphine blocks central sensitization (hyperalgesia) that is commonly found with neuropathic pain. We present a patient with neuropathic pain and tactile allodynia in which buprenorphine alleviated the hyperalgesia to a greater extent than pain severity. We found buprenorphine to be effective in reducing hypersensitivity in neuropathic pain when pure mu agonists fail to produce a response or in individuals who are intolerant to pure mu agonists.

摘要

众所周知,阿片类药物可缓解严重的急性和慢性伤害性疼痛,但神经性疼痛对阿片类药物的反应相对较差。丁丙诺啡是一种μ和ORL-1受体部分激动剂、κ-δ受体拮抗剂,与强效μ激动剂与不同的G蛋白相互作用,因此与标准阿片类药物不存在交叉耐受性。丁丙诺啡可阻断神经性疼痛中常见的中枢敏化(痛觉过敏)。我们报告了一名患有神经性疼痛和触觉异常性疼痛的患者,丁丙诺啡在该患者中减轻痛觉过敏的程度大于减轻疼痛严重程度。我们发现当纯μ激动剂无效或个体对纯μ激动剂不耐受时,丁丙诺啡可有效减轻神经性疼痛中的超敏反应。

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