Negus S S, Picker M J, Dykstra L A
Curriculum in Neurobiology, University of North Carolina, Chapel Hill 27599.
Psychopharmacology (Berl). 1989;98(1):141-3. doi: 10.1007/BF00442021.
Buprenorphine was evaluated for its ability to act as a kappa opioid antagonist in rats responding under a fixed-ratio 30 schedule of food presentation both before and after the induction of morphine tolerance. Before the induction of morphine tolerance, both buprenorphine and the selective kappa agonist bremazocine decreased rates of responding in a dose-dependent manner, and buprenorphine (0.03 and 0.3 mg/kg) failed to antagonize bremazocine's rate-decreasing effects. Following the induction of morphine tolerance, the bremazocine dose-effect curve was unaffected, but a profound cross-tolerance developed to buprenorphine. Furthermore, buprenorphine (0.03, 0.3 and 1.0 mg/kg) produced a dose-dependent antagonism of the rate-decreasing effects of bremazocine in the morphine-tolerant rats. These results support the hypothesis that buprenorphine has antagonist activity at kappa opioid receptors.
在吗啡耐受诱导前后,对大鼠在固定比例30食物呈现时间表下反应时丁丙诺啡作为κ阿片受体拮抗剂的能力进行了评估。在吗啡耐受诱导前,丁丙诺啡和选择性κ激动剂布马佐辛均以剂量依赖性方式降低反应率,且丁丙诺啡(0.03和0.3毫克/千克)未能拮抗布马佐辛的反应率降低作用。吗啡耐受诱导后,布马佐辛的剂量效应曲线未受影响,但对丁丙诺啡产生了显著的交叉耐受。此外,丁丙诺啡(0.03、0.3和1.0毫克/千克)在吗啡耐受大鼠中对布马佐辛的反应率降低作用产生了剂量依赖性拮抗。这些结果支持丁丙诺啡在κ阿片受体具有拮抗活性的假说。