La Vincente S F, White J M, Somogyi A A, Bochner F, Chapleo C B
Discipline of Pharmacology, School of Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Clin Pharmacol Ther. 2008 Jan;83(1):144-52. doi: 10.1038/sj.clpt.6100262. Epub 2007 Jun 13.
Animal studies have demonstrated that co-administration of an ultra-low-dose opioid antagonist with an opioid agonist may result in enhanced analgesia. Investigation of this effect in humans has been limited and produced inconsistent findings, with previous reports suggesting that dose ratio may be critical to analgesic potentiation. The aim of the current investigation was to determine whether buprenorphine analgesia could be enhanced with the addition of ultra-low-dose naloxone among healthy volunteers, using a range of dose ratios. Tolerance to cold pressor pain was significantly greater with the combination of buprenorphine and naloxone compared to buprenorphine alone, and this effect was dose ratio dependent. Importantly, this enhanced analgesia occurred without an increase in adverse effects; indeed at some ratios, respiratory depression was attenuated. These findings demonstrate that the addition of ultra-low-dose naloxone can enhance the analgesic effect of buprenorphine in humans without a concurrent increase in side effects.
动物研究表明,将超低剂量阿片类拮抗剂与阿片类激动剂联合使用可能会增强镇痛效果。在人体中对这种效应的研究有限,且结果不一致,之前的报告表明剂量比可能是镇痛增强的关键。当前研究的目的是确定在健康志愿者中,添加超低剂量纳洛酮是否能使用一系列剂量比增强丁丙诺啡的镇痛效果。与单独使用丁丙诺啡相比,丁丙诺啡和纳洛酮联合使用时对冷压痛的耐受性显著更高,且这种效应取决于剂量比。重要的是,这种增强的镇痛效果并未伴随不良反应的增加;事实上,在某些比例下,呼吸抑制有所减轻。这些发现表明,添加超低剂量纳洛酮可增强丁丙诺啡在人体中的镇痛效果,同时不会增加副作用。