Gracely R H, Dubner R, Wolskee P J, Deeter W R
Nature. 1983;306(5940):264-5. doi: 10.1038/306264a0.
The discovery of an endogenous opioid-mediated analgesic system has led to the search for its physiological roles and how it might be activated in natural conditions. Environmental and surgical stress and certain forms of transcutaneous electrical stimulation or acupuncture appear to activate this system. Several studies also suggest that this opioid system mediates placebo analgesia. Placebo reduces post-surgical pain in comparison with no treatment, and this analgesia is apparently reversed by the opioid antagonist, naloxone. However, these studies did not indicate whether naloxone and placebo exert their effects by common or by separate mechanisms. By administering hidden infusions of naloxone (in subjects unaware that the medication was being given) separate from the administration of a placebo, we were able to assess the effects of these two treatments independently. We report here evidence that placebo analgesia can occur after blockade of opioid mechanisms by naloxone and that naloxone can produce hyperalgesia independent of the placebo effect. The combined action of these effects is sufficient to explain the reversal of placebo analgesia by naloxone.
内源性阿片介导的镇痛系统的发现促使人们探寻其生理作用以及在自然条件下可能被激活的方式。环境和手术应激以及某些形式的经皮电刺激或针灸似乎能激活该系统。多项研究还表明,这种阿片系统介导安慰剂镇痛。与不治疗相比,安慰剂可减轻术后疼痛,且这种镇痛作用显然会被阿片拮抗剂纳洛酮逆转。然而,这些研究并未表明纳洛酮和安慰剂是通过共同机制还是单独机制发挥作用。通过在受试者不知情的情况下单独给予纳洛酮(隐藏输注),与给予安慰剂分开进行,我们能够独立评估这两种治疗的效果。我们在此报告的证据表明,纳洛酮阻断阿片机制后仍可出现安慰剂镇痛,且纳洛酮可产生与安慰剂效应无关的痛觉过敏。这些效应的联合作用足以解释纳洛酮对安慰剂镇痛的逆转作用。