Fox Susan, Silverdale Montague, Kellett Mark, Davies Rhys, Steiger Malcolm, Fletcher Nicholas, Crossman Alan, Brotchie Jonathan
The Walton Centre for Neurology and Neurosurgery, Liverpool, United Kingdom.
Mov Disord. 2004 May;19(5):554-60. doi: 10.1002/mds.10693.
Opioid peptide transmission is enhanced in the striatum of animal models and Parkinson's disease (PD) patients with levodopa-induced motor complications. Opioid receptor antagonists reduce levodopa-induced dyskinesia in primate models of PD; however, clinical trials to date have been inconclusive. A double-blind, placebo controlled, crossover design study in 14 patients with PD experiencing motor fluctuations was carried out, using the non-subtype-selective opioid receptor antagonist naloxone. Naloxone did not reduce levodopa-induced dyskinesia. The duration of action of levodopa was increased significantly by 17.5%. Non-subtype-selective opioid receptor antagonism may prove useful in the treatment of levodopa-related wearing-off in PD but not in dyskinesia.
在动物模型以及患有左旋多巴诱导运动并发症的帕金森病(PD)患者的纹状体中,阿片肽传递增强。阿片受体拮抗剂可减少PD灵长类动物模型中左旋多巴诱导的异动症;然而,迄今为止的临床试验尚无定论。对14名有运动波动的PD患者进行了一项双盲、安慰剂对照、交叉设计研究,使用非亚型选择性阿片受体拮抗剂纳洛酮。纳洛酮并未减少左旋多巴诱导的异动症。左旋多巴的作用持续时间显著增加了17.5%。非亚型选择性阿片受体拮抗作用可能被证明对治疗PD中与左旋多巴相关的疗效减退有用,但对异动症无效。