McMahon Lance R, France Charles P
Department of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229-3900, USA.
Exp Clin Psychopharmacol. 2003 Nov;11(4):286-93. doi: 10.1037/1064-1297.11.4.286.
This study examined whether the cannabinoid antagonist, SR 141716A, could be established as a discriminative stimulus in rhesus monkeys treated with delta -sup-9-tetrahydrocannabinol (delta -sup-9-THC). Stimulus control was established with SR 141716A (1.0 mg/kg) in 3 delta -sup-9-THC-treated monkeys (1.12 mg/kg/day) in 113-124 sessions. The SR 141716A discriminative stimulus was dose related, attenuated by an acute injection of delta -sup-9-THC, and not mimicked by cocaine or ketamine. SR 141716A-appropriate responding occasioned by temporary discontinuation of delta -sup-9-THC treatment was attenuated by delta -sup-9-THC and not ketamine. The SR 141716A discriminative stimulus in delta -sup-9-THC-treated monkeys appears to be mediated by cannabinoid receptors and could be related to delta -sup-9-THC withdrawal.
本研究检测了大麻素拮抗剂SR 141716A是否可在接受δ-9-四氢大麻酚(δ-9-THC)治疗的恒河猴中被确立为一种辨别刺激。在113 - 124次实验中,对3只接受δ-9-THC治疗(1.12 mg/kg/天)的恒河猴使用SR 141716A(1.0 mg/kg)确立刺激控制。SR 141716A辨别刺激与剂量相关,可被急性注射δ-9-THC减弱,且不会被可卡因或氯胺酮模拟。因暂时停止δ-9-THC治疗而引发的对SR 141716A的适当反应,可被δ-9-THC而非氯胺酮减弱。在接受δ-9-THC治疗的猴子中,SR 141716A辨别刺激似乎由大麻素受体介导,且可能与δ-9-THC戒断有关。