Sneyd J R, Langton J A, Allan L G, Peacock J E, Rowbotham D J
Anaesthesia Research Group, Peninsula Medical School, The John Bull Building, Tamar Science Park, Drake Circus, Plymouth PL6 8BU, and Department of Anaesthesia, Northwick Park Hospital, Harrow, UK.
Br J Anaesth. 2007 May;98(5):672-6. doi: 10.1093/bja/aem075. Epub 2007 Apr 7.
Adenosine is analgesic in humans, and the selective adenosine A1 receptor agonist GR79236X has significant anti-nociceptive activity in an animal pain model of inflammatory pain.
Seventy-nine patients with moderate pain after third molar extraction under general anaesthesia were randomized to receive a 15 min double-blind infusion containing either GR79236X 4 microg kg-1, GR79236X 10 microg kg-1, diclofenac 50 mg, or saline placebo. Rescue analgesia was promptly available to all patients.
Meaningful pain relief (mild or no pain) was attained by 9 (47%) patients in the placebo group, 12 (63%) patients in the GR79236 4 microg kg-1 group, 10 (48%) patients in the 10 microg kg-1 group, and 16 (80%) patients in the diclofenac 50 mg group. Neither dose of GR79236 produced a significant improvement over placebo, but diclofenac was superior to both placebo (P=0.036) and GR79236 10 microg kg-1 (P=0.034). Median times to rescue or additional analgesia were 62, 100, 60, and 363 min for patients receiving placebo, GR79236 4 microg kg-1, 10 microg kg-1, and diclofenac 50 mg, respectively (diclofenac significantly longer than placebo, P=0.002 log-rank test). Pain control was poor in the placebo group and in both GR79236 groups, with between 79 and 86% of patients having good pain control (i.e. mild or no pain) for <20% of the time compared with only 30% of patients who received diclofenac.
We found no evidence of efficacy of GR79236 compared with placebo, but the active control diclofenac was effective. It is possible that a higher dose of GR79236 might have been effective or that i.v. administration of this drug does not achieve appropriate concentrations in the brain or peripheral nerves.
腺苷对人类具有镇痛作用,选择性腺苷A1受体激动剂GR79236X在炎症性疼痛的动物疼痛模型中具有显著的抗伤害感受活性。
79例在全身麻醉下拔除第三磨牙后出现中度疼痛的患者被随机分配接受15分钟的双盲输注,输注液中分别含有4微克/千克GR79236X、10微克/千克GR79236X、50毫克双氯芬酸或生理盐水安慰剂。所有患者均可立即获得解救性镇痛。
安慰剂组9例(47%)患者、4微克/千克GR79236组12例(63%)患者、10微克/千克组10例(48%)患者以及50毫克双氯芬酸组16例(80%)患者实现了有意义的疼痛缓解(轻度或无疼痛)。两种剂量的GR79236均未比安慰剂产生显著改善,但双氯芬酸优于安慰剂(P = 0.036)和10微克/千克GR79236(P = 0.034)。接受安慰剂、4微克/千克GR79236、10微克/千克GR79236和50毫克双氯芬酸的患者解救或额外镇痛的中位时间分别为62、100、60和363分钟(双氯芬酸显著长于安慰剂,对数秩检验P = 0.002)。安慰剂组和两个GR79236组的疼痛控制较差,79%至86%的患者在不到20%的时间内实现了良好的疼痛控制(即轻度或无疼痛),而接受双氯芬酸的患者只有30%。
我们未发现GR79236与安慰剂相比有效的证据,但活性对照双氯芬酸是有效的。可能更高剂量的GR79236会有效,或者静脉注射该药物在大脑或周围神经中未达到合适的浓度。