Rodriguez Jesse S, McMahon Lance R
Department of Pharmacology, The University of Texas Health Science Center at San Antonio, USA.
Department of Pharmacology, The University of Texas Health Science Center at San Antonio, USA.
Eur J Pharmacol. 2014 Oct 5;740:151-9. doi: 10.1016/j.ejphar.2014.06.023. Epub 2014 Jun 24.
Several effects of the abused synthetic cannabinoid JWH-018 were compared to those of Δ9-tetrahydrocannabinol (Δ9-THC) in rhesus monkeys. JWH-018 (0.1 mg/kg i.v.) was established as a discriminative stimulus and rimonabant was used to examine mechanisms responsible for discrimination as well as operant response rate-decreasing and hypothermic effects. JWH-018 dose-dependently increased drug-lever responding (ED50=0.01 mg/kg) and decreased response rate (ED50=0.064 mg/kg). Among various cannabinoids, the relative potency for producing discriminative stimulus and rate-decreasing effects was the same: CP-55940=JWH-018>Δ9-THC=WIN-55212-2=JWH-073. The benzodiazepine agonist midazolam and the NMDA antagonist ketamine did not exert JWH-018 like discriminative stimulus effects up to doses that disrupted responding. JWH-018 and Δ9-THC decreased rectal temperature by 2.2 and 2.8°C, respectively; the doses decreasing temperature by 2°C were 0.21 and 1.14 mg/kg, respectively. Antagonism did not differ between JWH-018 and Δ9-THC, but did differ among effects. The apparent affinities of rimonabant calculated in the presence of JWH-018 and Δ9-THC were not different from each other for antagonism of discriminative stimulus effects (6.58 and 6.59, respectively) or hypothermic effects (7.08 and 7.19, respectively). Apparent affinity estimates are consistent with the same receptors mediating the discriminative stimulus and hypothermic effects of both JWH-018 and Δ9-THC. However, there was more limited and less orderly antagonism of rate-decreasing effects, suggesting that an additional receptor mechanism is involved in mediating the effects of cannabinoids on response rate. Overall, these results strongly suggest that JWH-018 and Δ9-THC act at the same receptors to produce several of their shared psychopharmacological effects.
在恒河猴中,比较了滥用的合成大麻素JWH - 018与Δ9 - 四氢大麻酚(Δ9 - THC)的几种效应。将JWH - 018(0.1毫克/千克静脉注射)确立为一种辨别刺激物,并使用利莫那班来研究负责辨别以及操作反应率降低和体温过低效应的机制。JWH - 018剂量依赖性地增加药物杠杆反应(半数有效剂量[ED50]=0.01毫克/千克)并降低反应率(ED50=0.064毫克/千克)。在各种大麻素中,产生辨别刺激和反应率降低效应的相对效力相同:CP - 55940 = JWH - 018>Δ9 - THC = WIN - 55212 - 2 = JWH - 073。苯二氮䓬激动剂咪达唑仑和N - 甲基 - D - 天冬氨酸(NMDA)拮抗剂氯胺酮在达到破坏反应的剂量之前,不会产生类似JWH - 018的辨别刺激效应。JWH - 018和Δ9 - THC分别使直肠温度降低2.2℃和2.8℃;使温度降低2℃的剂量分别为0.21毫克/千克和1.14毫克/千克。JWH - 018和Δ9 - THC之间的拮抗作用没有差异,但在不同效应之间存在差异。在JWH - 018和Δ9 - THC存在的情况下计算得出的利莫那班对辨别刺激效应拮抗作用的表观亲和力(分别为6.58和6.59)以及对体温过低效应拮抗作用的表观亲和力(分别为7.08和7.19)彼此没有差异。表观亲和力估计值与介导JWH - 018和Δ9 - THC的辨别刺激和体温过低效应的相同受体一致。然而,对反应率降低效应的拮抗作用更有限且不太规律,这表明大麻素对反应率的影响涉及额外的受体机制。总体而言,这些结果强烈表明JWH - 018和Δ9 - THC作用于相同的受体以产生它们的几种共同的精神药理学效应。