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羟考酮与吗啡在多模式、组织分化实验性疼痛模型中的比较研究。

A comparative study of oxycodone and morphine in a multi-modal, tissue-differentiated experimental pain model.

作者信息

Staahl Camilla, Christrup Lona Louring, Andersen Søren Due, Arendt-Nielsen Lars, Drewes Asbjørn Mohr

机构信息

Center for Visceral Biomechanics and Pain, Department of Gastroenterology, University Hospital Aalborg, Denmark.

出版信息

Pain. 2006 Jul;123(1-2):28-36. doi: 10.1016/j.pain.2006.02.006. Epub 2006 Apr 4.

DOI:10.1016/j.pain.2006.02.006
PMID:16600508
Abstract

Visceral pain can be difficult to treat with classical mu-opioid agonists and it has been suggested to use opioids with distinct pharmacological profiles. In animal experiments, oxycodone has shown different effects compared to morphine, and clinical observations have shown that oxycodone may occasionally be superior to, e.g., morphine in the treatment of visceral pain. In the current study, we randomised 24 healthy subjects to treatment with either morphine (30 mg), oxycodone (15 mg) or placebo in a crossover study. The experimental pain model involved multi-modal (mechanical, thermal and electrical) pain tests in the skin, muscles and viscera. The pain tests were carried out at baseline and 30, 60 and 90 min after oral administration of the drugs. The model showed effect of the two opioids compared to placebo on all stimulus modalities in all three types of tissues (all P values <0.001). Both opioids attenuated the sensory response mainly to painful stimulations. Morphine and oxycodone were equipotent in pain modulation of the skin and muscles, but oxycodone had superior analgesic effect to both morphine and placebo on the mechanical (P<0.001) and thermal (P<0.001) stimulations of the oesophagus. In conclusion, the multi-modal and tissue-differentiated pain model could link findings from animal experiments to clinical findings. A different pharmacological profile of oxycodone compared to that of morphine was shown, and thus oxycodone may be a useful alternative to morphine in the treatment of visceral pain syndromes.

摘要

内脏痛很难用传统的μ-阿片受体激动剂进行治疗,因此有人建议使用具有不同药理学特性的阿片类药物。在动物实验中,羟考酮与吗啡相比显示出不同的效果,临床观察表明,在治疗内脏痛方面,羟考酮有时可能优于吗啡等药物。在本研究中,我们将24名健康受试者随机分为三组,在一项交叉研究中分别接受吗啡(30毫克)、羟考酮(15毫克)或安慰剂治疗。实验性疼痛模型涉及对皮肤、肌肉和内脏进行多模式(机械、热和电)疼痛测试。疼痛测试在基线时以及口服药物后30、60和90分钟进行。该模型显示,与安慰剂相比,两种阿片类药物对所有三种组织类型的所有刺激模式均有效果(所有P值<0.001)。两种阿片类药物都主要减弱了对疼痛刺激的感觉反应。吗啡和羟考酮在调节皮肤和肌肉疼痛方面效果相当,但在食管的机械性(P<0.001)和热性(P<0.001)刺激方面,羟考酮的镇痛效果优于吗啡和安慰剂。总之,这种多模式和组织差异化的疼痛模型可以将动物实验结果与临床结果联系起来。结果显示羟考酮与吗啡具有不同的药理学特性,因此在治疗内脏痛综合征方面,羟考酮可能是吗啡的一种有用替代品。

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