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新型大麻素激动剂AZD1940对下颌第三磨牙拔除术后疼痛的镇痛效果评估。

Evaluation of the analgesic efficacy of AZD1940, a novel cannabinoid agonist, on post-operative pain after lower third molar surgical removal.

作者信息

Kalliomäki Jarkko, Segerdahl Märta, Webster Lynn, Reimfelt Annika, Huizar Karin, Annas Peter, Karlsten Rolf, Quiding Hans

机构信息

AstraZeneca R&D Södertälje, Södertälje, Sweden.

Lifetree Clinical Research, 3838 South, 700 East, Suite 202, Salt Lake City, UT 84106, USA.

出版信息

Scand J Pain. 2013 Jan 1;4(1):17-22. doi: 10.1016/j.sjpain.2012.08.004.

DOI:10.1016/j.sjpain.2012.08.004
PMID:29913883
Abstract

Aim To evaluate the analgesic efficacy of AZD1940, a novel peripherally acting cannabinoid CB1/CB2 receptor agonist, in patients undergoing third molar surgical removal. Methods This was a randomized, double-blind, placebo-controlled study in patients scheduled for surgical removal of an impacted lower third molar. Patients received a single oral dose of 800 μg AZD1940, 500 mg naproxen or placebo 1.5 h before surgery. The dose of 800 μg AZD1940 was selected based on earlier data from a single dose study in man, in which it was identified as the highest well tolerated dose. Ongoing post-operative pain (primary variable) and pain on jaw movement were assessed on a visual analog scale (VAS, 0-100 mm) from 0 to 8h postoperatively, deriving the area under the curve of ongoing pain (VAS AUC0-8h), and of pain on jaw movement (VASJM AUC0-8h). The time to requesting rescue medication (acetaminophen) was recorded. Subjective cannabinoid effects were assessed by the visual analog mood scale (VAMS). Results In total, 151 patients were randomized to AZD1940 (n = 61), placebo (n = 59) or naproxen (n = 31). There was no statistically significant difference in pain VAS AUC0-8h or in VASJM AUC0-8h between AZD1940 and placebo. Naproxen significantly reduced both pain VAS AUC0-8h and VASJM AUC0-8h as compared with placebo (p < 0.0001 for both). Significantly fewer patients on naproxen requested rescue medication and the duration of time to rescue was greater, as compared with placebo, whereas there were no significant differences between AZD1940 and placebo in these outcome variables. Statistically significant increases in VAMS items "sedated" and "high" were observed after AZD1940 compared with placebo. The increases in VAMS were numerically small compared with previous findings with a centrally acting cannabinoid. The most commonly observed adverse events (AE) on treatment with AZD1940 were postural dizziness (80% of subjects), nausea (26%), hypotension (21%) and headache (13%), most AE being mild to moderate. Conclusion The CB1/CB2 receptor agonist AZD1940 did not reduce post-operative pain after lower third molar surgical removal at doses exerting subjective cannabinoid effects. Implications Activation of peripheral CB1/CB2 receptors per se is probably of less clinical relevance for the treatment of acute nociceptive pain in man.

摘要

目的 评估新型外周作用大麻素CB1/CB2受体激动剂AZD1940在接受第三磨牙拔除手术患者中的镇痛效果。方法 这是一项针对计划手术拔除下颌阻生第三磨牙患者的随机、双盲、安慰剂对照研究。患者在手术前1.5小时接受单次口服800μg AZD1940、500mg萘普生或安慰剂。800μg AZD1940的剂量是根据早期人体单剂量研究数据选定的,该剂量被确定为耐受性良好的最高剂量。术后持续疼痛(主要变量)和下颌运动时的疼痛通过视觉模拟量表(VAS,0 - 100mm)在术后0至8小时进行评估,得出持续疼痛的曲线下面积(VAS AUC0 - 8h)以及下颌运动时疼痛的曲线下面积(VASJM AUC0 - 8h)。记录请求使用急救药物(对乙酰氨基酚)的时间。通过视觉模拟情绪量表(VAMS)评估主观大麻素效应。结果 总共151例患者被随机分为AZD1940组(n = 61)、安慰剂组(n = 59)或萘普生组(n = 31)。AZD1940组与安慰剂组在疼痛VAS AUC0 - 8h或VASJM AUC0 - 8h方面无统计学显著差异。与安慰剂相比,萘普生显著降低了疼痛VAS AUC0 - 8h和VASJM AUC0 - 8h(两者p < 0.0001)。与安慰剂相比,服用萘普生的患者请求急救药物的人数显著减少,且急救时间更长,而在这些结果变量方面,AZD1940组与安慰剂组无显著差异。与安慰剂相比,AZD1940治疗后VAMS项目“镇静”和“兴奋”有统计学显著增加。与先前使用中枢作用大麻素的研究结果相比,VAMS的增加在数值上较小。使用AZD1940治疗时最常观察到的不良事件(AE)是体位性头晕(80%的受试者)、恶心(26%)、低血压(21%)和头痛(13%),大多数AE为轻至中度。结论 在产生主观大麻素效应的剂量下,CB1/CB2受体激动剂AZD1940并未减轻下颌第三磨牙拔除术后的疼痛。启示 外周CB1/CB2受体的激活本身可能对人类急性伤害性疼痛的治疗临床相关性较小。

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