Modulation of remifentanil-induced postinfusion hyperalgesia by the β-blocker propranolol in humans

被引:60
作者
Chu, Larry F. [1 ]
Cun, Tony [1 ]
Ngai, Lynn K. [1 ]
Kim, Julie E. [1 ]
Zamora, Abigail K. [1 ]
Young, Chelsea A. [1 ]
Angst, Martin S. [1 ]
Clark, David J. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
基金
美国国家卫生研究院;
关键词
Antagonist; beta(2)-Adrenergic receptor; Hyperalgesia; Mechanical stimulation; Propranolol; Remifentanil-induced postinfusion hyperalgesia; Thermal stimulation; OPIOID-INDUCED HYPERALGESIA; ADRENERGIC-RECEPTOR DENSITY; SHORT-TERM INFUSION; MORPHINE-TOLERANCE; PAIN SENSITIVITY; POSTOPERATIVE FENTANYL; INDUCED ANALGESIA; ABNORMAL PAIN; THERMAL PAIN; EVOKED PAIN;
D O I
10.1016/j.pain.2012.01.014
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Acute and chronic exposure to opioids has been associated with hyperalgesia in both animals and humans. A genetic analysis of opioid-induced hyperalgesia in mice linked the beta(2)-adrenergic receptor to mechanical sensitization after opioid exposure. In humans, expansion of the area of mechanical hyperalgesia surrounding an experimentally induced lesion after the cessation of remifentanil infusion is a commonly used model of opioid hyperalgesia (remifentanil-induced postinfusion hyperalgesia, RPH). The purpose of our translational study was to test the hypothesis that the beta-adrenergic receptor antagonist propranolol modulates the expression of RPH in humans. This double-blinded, randomized, placebo-controlled, crossover study was performed in 10 healthy human volunteers. During test sessions, intracutaneous electrical stimulation was used to generate areas of secondary mechanical hyperalgesia. The area of this sensitization was measured before, during, and after remifentanil infusion. Heat pain sensitivity was also followed. During one test session, subjects received propranolol infusion. We observed an average increase in the areas of secondary mechanical hyperalgesia to 141% of the baseline in subjects infused with remifentanil and placebo (P = 0.00040). However, when remifentanil infusion was combined with propranolol, the area of secondary hyperalgesia after terminating remifentanil was not significantly different than the area before beginning the opioid infusion (P = 0.13). Thermal hyperalgesia was not observed after remifentanil infusion. Propranolol infusion at the selected dose had minor hemodynamic effects. Concomitant infusion of propranolol with remifentanil prevented the expression of RPH. beta-adrenergic receptor blockade may be a useful pharmacological strategy for preventing hyperalgesia in patients exposed to opioids. (C) 2012 International Association for the Study of Pain. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:974 / 981
页数:8
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