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低剂量利培酮和吗啡相互作用可在大鼠中产生更强的镇痛作用和更大的锥体外系效应。

Low doses of risperidone and morphine interact to produce more analgesia and greater extrapyramidal effects in rats.

机构信息

Department of Psychology, Buffalo State College, Buffalo, NY 14222, USA.

出版信息

Neurosci Lett. 2011 Feb 18;490(1):21-6. doi: 10.1016/j.neulet.2010.12.018. Epub 2010 Dec 15.

DOI:10.1016/j.neulet.2010.12.018
PMID:21167255
Abstract

The search for non-narcotic drugs that will enhance the analgesic effects of opiates without enhancing their side effects has included the investigation of psychoactive drugs already approved for other uses. Some research has supported an analgesic effect of risperidone (RIS), an atypical neuroleptic. However, the analysis of the analgesic efficacy of RIS alone or as an adjuvant to morphine (MOR) has not considered the production of adverse motor effects that would limit its usefulness as a treatment for pain. We tested whether low doses of RIS would enhance the analgesic action of opiates without inducing untoward motor effects. The analgesia induced by a range of RIS doses (0.1-1.0 mg/kg, SC) was assessed alone and in combination with MOR (5 mg/kg, IP) in male Long-Evans (hooded) rats using two different algesiometric assays: hotplate and tail-flick test. The presence or absence of ptosis, vacuous chewing, and abnormal stationary postures was recorded to evaluate dyskinetic effects. No dose of RIS alone altered pain threshold. However, the highest dose of RIS, 1.0 mg/kg SC, significantly increased the analgesic effects of MOR. Dyskinetic effects of RIS were dose-dependent and enhanced in RIS+MOR treatment. These results do not support the hypothesis that RIS, alone or in combination with MOR, elevates pain threshold without also inducing motor side effects. These findings suggest caution in the use of RIS as either a primary treatment or opiate adjuvant treatment for pain.

摘要

寻找非麻醉性药物来增强阿片类药物的镇痛效果而不增强其副作用,包括调查已经批准用于其他用途的精神活性药物。一些研究支持利培酮(RIS)的镇痛作用,利培酮是一种非典型的神经安定药。然而,单独使用 RIS 或作为吗啡(MOR)的佐剂的镇痛效果分析并没有考虑到产生不良运动效应的可能性,这会限制其作为疼痛治疗的用途。我们测试了低剂量的 RIS 是否会增强阿片类药物的镇痛作用而不引起不良的运动效应。使用两种不同的痛觉测量法:热板和尾巴闪烁测试,在雄性 Long-Evans(带帽)大鼠中评估了一系列 RIS 剂量(0.1-1.0mg/kg,SC)单独使用和与 MOR(5mg/kg,IP)联合使用时的镇痛作用。评估了睑下垂、空咀嚼和异常静止姿势的存在或不存在,以评估运动障碍效应。单独使用 RIS 的任何剂量都没有改变疼痛阈值。然而,1.0mg/kg SC 的最高剂量 RIS 显著增强了 MOR 的镇痛作用。RIS 的运动障碍效应呈剂量依赖性,并在 RIS+MOR 治疗中增强。这些结果不支持 RIS 单独或与 MOR 联合使用可升高疼痛阈值而不引起运动副作用的假设。这些发现表明,在将 RIS 用作疼痛的主要治疗或阿片类药物佐剂治疗时应谨慎。

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