Gatch Michael B, Forster Michael J
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas, USA.
Behav Pharmacol. 2015 Aug;26(5):460-8. doi: 10.1097/FBP.0000000000000150.
When synthetic cannabinoid compounds became controlled by state and federal governments, different, noncontrolled compounds began to appear as marijuana substitutes. Unlike the scheduled cannabinoids, the newer compounds have not been characterized for potency and efficacy in preclinical studies. The purpose of these experiments was to determine whether some of the more recent synthetic compounds sold as marijuana substitutes have behavioral effects similar to those of Δ-tetrahydrocannabinol (Δ-THC), the pharmacologically active compound in marijuana. The compounds UR-144, XLR-11, AKB-48 (APINACA), PB-22 (QUPIC), 5F-PB-22, and AB-FUBINACA were tested for locomotor depressant effects in male Swiss-Webster mice and subsequently for their ability to substitute for Δ-THC (3 mg/kg, intraperitoneally) in drug discrimination experiments with male Sprague-Dawley rats. UR-144, XLR-11, AKB-48, and AB-FUBINACA each decreased locomotor activity for up to 90 min, whereas PB-22 and 5F-PB-22 produced depressant effects lasting 120-150 min. Each of the compounds fully substituted for the discriminative stimulus effects of Δ-THC. These findings confirm the suggestion that these compounds have marijuana-like psychoactive effects and abuse liability.
当合成大麻素化合物受到州和联邦政府管控时,不同的、不受管控的化合物开始作为大麻替代品出现。与列入管制的大麻素不同,这些较新的化合物在临床前研究中尚未对其效力和功效进行表征。这些实验的目的是确定一些作为大麻替代品出售的最新合成化合物是否具有与Δ-四氢大麻酚(Δ-THC,大麻中的药理活性化合物)类似的行为效应。对化合物UR-144、XLR-11、AKB-48(APINACA)、PB-22(QUPIC)、5F-PB-22和AB-FUBINACA在雄性瑞士韦伯斯特小鼠中进行了运动抑制作用测试,随后在雄性斯普拉格-道利大鼠的药物辨别实验中测试了它们替代Δ-THC(3毫克/千克,腹腔注射)的能力。UR-144、XLR-11、AKB-48和AB-FUBINACA各自降低运动活性长达90分钟,而PB-22和5F-PB-22产生持续120 - 150分钟的抑制作用。每种化合物都能完全替代Δ-THC的辨别刺激效应。这些发现证实了这些化合物具有类似大麻的精神活性作用和滥用可能性的推测。