Buprenorphine reduces central sensitization after repetitive C-fiber stimulation in rats

被引:6
作者
Kouya, PF [1 ]
Xu, XJ [1 ]
机构
[1] Huddinge Univ Hosp, Div Clin Neurophysiol, Karolinska Inst, Dept Lab Med, S-14186 Stockholm, Sweden
关键词
flexor reflex; morphine; NMDA receptor; opioids;
D O I
10.1016/j.neulet.2004.02.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The partial mu-opioid receptor. agonist buprenorphine produces antinociception through mechanisms different from those of classical opioids. In this study, we compared the effect of buprenorphine, and morphine on C-fiber conditioning stimulation (CS)-induced facilitation of the flexor reflex, a model of central sensitization in decerebrate, spinalized unanesthetized rats. Intraperitoneal morphine and buprenorphine moderately depressed the baseline flexor reflex to a similar extent at doses of 1-2 and 0.03-0.1 mg/kg, respectively. Buprenorphine significantly reduced C-fiber CS-induced reflex facilitation whereas morphine at 1 or 2 mg/kg had no effect. Thus, some of the atypical antinociceptive effects of buprenorphine may be derived from its effect on central sensitization. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:127 / 129
页数:3
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