Gal T J
Department of Anesthesiology, University of Virginia, Charlottesville 22908.
Clin Pharmacol Ther. 1989 Jan;45(1):66-71. doi: 10.1038/clpt.1989.10.
In a placebo-controlled, single-blind study we evaluated the ability of three large doses of naloxone (1.0, 5.0, and 10 mg) to antagonize the established respiratory-depressant effects of a common analgesic dose of intravenous buprenorphine (0.3 mg/70 kg). This dose of buprenorphine consistently reduced indexes of CO2 responsiveness to about one half of their control values, much like comparable doses of other opioid analgesics. One milligram of naloxone had little effect on this respiratory depression. Both 5 and 10 mg produced consistent reversal, which was more complete with the larger dose. The reversal effect of naloxone did not occur immediately as is characteristic with morphine and other opioids but rather appeared to reach a maximum 3 hours after reversal. These findings indicate that high doses of naloxone are required to antagonize buprenorphine and naloxone's limited efficacy results not from its short duration of action but rather its relative inability to displace buprenorphine already bound to opioid receptors.
在一项安慰剂对照的单盲研究中,我们评估了三种大剂量纳洛酮(1.0、5.0和10毫克)拮抗常用镇痛剂量静脉注射丁丙诺啡(0.3毫克/70千克)已确立的呼吸抑制作用的能力。该剂量的丁丙诺啡持续将二氧化碳反应性指标降低至对照值的约一半,这与其他阿片类镇痛药的相当剂量情况非常相似。1毫克纳洛酮对这种呼吸抑制作用几乎没有影响。5毫克和10毫克均产生了持续的逆转作用,且较大剂量的逆转作用更完全。纳洛酮的逆转作用不像吗啡和其他阿片类药物那样立即出现,而是在逆转后3小时似乎达到最大值。这些发现表明,需要高剂量纳洛酮来拮抗丁丙诺啡,且纳洛酮疗效有限并非源于其作用持续时间短,而是其相对无法取代已与阿片受体结合的丁丙诺啡。