Negus S S, Dykstra L A
Curriculum in Neurobiology, University of North Carolina, Chapel Hill 27599.
Eur J Pharmacol. 1988 Oct 26;156(1):77-86. doi: 10.1016/0014-2999(88)90149-5.
Buprenorphine produced a dose-dependent antagonism of the selective kappa opioid agonist U50,488 in squirrel monkeys responding under the shock titration procedure. In one group of four monkeys, 0.003-0.01 mg/kg buprenorphine produced dose-dependent rightward shifts in the individual U50,488 dose-effect curves and increased the A50 value for U50,488 more than 2-fold in each monkey. Furthermore, 0.01 mg/kg buprenorphine antagonized a maximally effective dose of U50,488 in these monkeys. Buprenorphine (0.01-0.1 mg/kg) also produced rightward shifts in the group U50,488 dose-effect curve for a second group of three monkeys. Buprenorphine's antagonism of U50,488 was probably not a consequence of any mu opioid antagonist properties of buprenorphine in this procedure since (1) buprenorphine produced an inconsistent antagonism of the selective mu agonist fentanyl, and (2) the selective mu antagonist beta-funaltrexamine did not antagonize U50,488. These results support the hypothesis that buprenorphine has kappa antagonist activity in the shock titration procedure.
在松鼠猴的电击滴定程序中,丁丙诺啡对选择性κ阿片受体激动剂U50,488产生了剂量依赖性拮抗作用。在一组四只猴子中,0.003 - 0.01mg/kg的丁丙诺啡使个体U50,488剂量效应曲线产生剂量依赖性右移,并且在每只猴子中使U50,488的A50值增加了2倍以上。此外,0.01mg/kg的丁丙诺啡拮抗了这些猴子中U50,488的最大有效剂量。丁丙诺啡(0.01 - 0.1mg/kg)也使第二组三只猴子的群体U50,488剂量效应曲线右移。在该程序中,丁丙诺啡对U50,488的拮抗作用可能不是其任何μ阿片受体拮抗特性的结果,因为(1)丁丙诺啡对选择性μ激动剂芬太尼的拮抗作用不一致,并且(2)选择性μ拮抗剂β-氟纳曲明不拮抗U50,488。这些结果支持了丁丙诺啡在电击滴定程序中具有κ拮抗剂活性这一假说。