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吗啡和丁丙诺啡诱导的人炎性疼痛模型中的镇痛和抗痛觉过敏:一项双盲、随机、安慰剂对照、五臂交叉研究。

Morphine- and buprenorphine-induced analgesia and antihyperalgesia in a human inflammatory pain model: a double-blind, randomized, placebo-controlled, five-arm crossover study.

机构信息

Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.

出版信息

J Pain Res. 2013;6:23-38. doi: 10.2147/JPR.S36827. Epub 2013 Jan 9.

Abstract

PURPOSE

Opioid therapy is associated with the development of tolerance and paradoxically increased sensitivity to pain. It has been suggested that buprenorphine is associated with a higher antihyperalgesia/analgesia ratio than μ-opioid receptor agonists. The primary outcome of this study was therefore to investigate relative differences in antihyperalgesia and analgesia effects between morphine and buprenorphine in an inflammatory pain model in volunteers. The secondary outcome was to examine the relationship between pain sensitivity and opioid-induced effects on analgesia, antihyperalgesia, and descending pain modulation.

SUBJECTS AND METHODS

Twenty-eight healthy subjects were included. The study was a double-blind, randomized, placebo-controlled, five-arm crossover study with a multimodal (electrical, mechanical, and thermal stimuli) testing technique. After baseline assessments, intravenous infusions of morphine (10/20 mg), buprenorphine (0.3/0.6 mg), or placebo (normal saline) were administered over a 210-minute period, during which a cold pressor test, heat injury (47°C, 7 minutes, 12.5 cm(2)), and the first postburn assessment were done. After completion of the drug infusions, two additional postburn assessments were done. The subjects were monitored during each 8-hour session by an anesthesiologist.

RESULTS

For nearly all tested variables, significant dose-dependent analgesic effects were demonstrated. The median antihyperalgesia/analgesia ratio (secondary hyperalgesia/heat injury relative to placebo) for low-dose morphine was 0.01 (interquartile range: -6.2; 9.9), 0.00 (-2.4; 2.1) for high-dose morphine, 0.03 (-1.8; 2.1) for low-dose buprenorphine, and 0.00 (-3.2; 1.1) for high-dose buprenorphine (P > 0.466). There were no significant differences in opioid responses between high and low pain-sensitive subjects (P > 0.286). High-dose buprenorphine, compared to placebo, was associated with a significantly enhanced action of the descending inhibitory pain control system (P = 0.004).

CONCLUSION

The present study, using multimodal testing technique, could not demonstrate any significant differences between morphine and buprenorphine in the profiles of antihyperalgesia and analgesia. Only high-dose buprenorphine was associated with a significant effect on the descending inhibitory pain control system.

摘要

目的

阿片类药物治疗与耐受性的发展有关,并且与疼痛敏感性增加有关。据认为,丁丙诺啡与μ-阿片受体激动剂相比,具有更高的抗痛觉过敏/镇痛比。因此,本研究的主要目的是在志愿者的炎症性疼痛模型中研究吗啡和丁丙诺啡在抗痛觉过敏和镇痛作用方面的相对差异。次要结果是检查疼痛敏感性与阿片类药物对镇痛、抗痛觉过敏和下行疼痛调节的影响之间的关系。

方法

纳入 28 名健康受试者。该研究是一项双盲、随机、安慰剂对照、五臂交叉研究,采用多模态(电、机械和热刺激)测试技术。在基线评估后,在 210 分钟内静脉输注吗啡(10/20mg)、丁丙诺啡(0.3/0.6mg)或安慰剂(生理盐水),在此期间进行冷加压试验、热损伤(47°C,7 分钟,12.5cm²)和第一次烧伤后评估。在药物输注完成后,再进行两次烧伤后评估。在每个 8 小时的治疗过程中,由麻醉师对受试者进行监测。

结果

对于几乎所有测试变量,都显示出明显的剂量依赖性镇痛作用。低剂量吗啡的中位数抗痛觉过敏/镇痛比(与安慰剂相比,二次痛觉过敏/热损伤)为 0.01(四分位距:-6.2;9.9),高剂量吗啡为 0.00(-2.4;2.1),低剂量丁丙诺啡为 0.03(-1.8;2.1),高剂量丁丙诺啡为 0.00(-3.2;1.1)(P>0.466)。高和低痛敏受试者之间的阿片类药物反应没有显著差异(P>0.286)。与安慰剂相比,高剂量丁丙诺啡与下行抑制性疼痛控制系统的作用显著增强相关(P=0.004)。

结论

本研究使用多模态测试技术,未能证明吗啡和丁丙诺啡在抗痛觉过敏和镇痛作用方面的特征存在任何显著差异。只有高剂量丁丙诺啡与下行抑制性疼痛控制系统的显著作用有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caed/3555550/1067f0f9c451/jpr-6-023f1.jpg

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