McLaughlin Peter J, Lu Dai, Winston Keisha M, Thakur Ganesh, Swezey Lynn A, Makriyannis Alexandros, Salamone John D
Department of Psychology, University of Connecticut, 406 Babbidge Rd. Storrs, CT, 06269-1020, USA.
Pharmacol Biochem Behav. 2005 May;81(1):78-88. doi: 10.1016/j.pbb.2005.02.005. Epub 2005 Apr 21.
AM 411 ((-)-1-adamantyl-Delta8-tetrahydrocannabinol) is a novel full agonist at cannabinoid CB1 receptors. The present studies were conducted to provide behavioral characterization of this compound in rats. It was hypothesized that AM 411 should produce behavioral effects similar to known cannabinoid agonists, and that these effects should be inhibited by co-treatment with a CB1 antagonist. In Experiments 1 and 2, AM 411 dose-dependently produced behaviors consistent with CB1 agonism, including analgesia, hypothermia, catalepsy and reductions in locomotion, which were blocked by a CB1-selective antagonist. In Experiment 3, AM 411 produced a dose-dependent suppression of lever-pressing on a fixed-ratio 5 (FR5) schedule, a task known to be sensitive to administration of CB1 agonists. Detailed analysis of the temporal patterns of operant responding showed that AM 411 altered the distribution of interresponse times. Experiment 4 showed that AM 411 decreased relative interior activity in the open field, which is suggestive of an anxiogenic effect. It is concluded that AM 411 produces CB1 agonist-like behavior with potency between that of WIN 55,212-2 and AM 356. AM 411 could be a useful tool for understanding the behavioral and neural effects of CB1 receptor stimulation.
AM 411((-)-1-金刚烷基-Δ8-四氢大麻酚)是一种新型的大麻素CB1受体完全激动剂。本研究旨在对该化合物在大鼠中的行为特征进行描述。研究假设AM 411应产生与已知大麻素激动剂相似的行为效应,并且这些效应应通过与CB1拮抗剂联合给药来抑制。在实验1和2中,AM 411剂量依赖性地产生了与CB1激动作用一致的行为,包括镇痛、体温过低、僵住症和运动减少,这些均被CB1选择性拮抗剂阻断。在实验3中,AM 411在固定比率5(FR5)的实验安排下对杠杆按压产生了剂量依赖性抑制,这是一项已知对CB1激动剂给药敏感的任务。对操作性反应的时间模式进行的详细分析表明,AM 411改变了反应间隔时间的分布。实验4表明,AM 411降低了旷场试验中的相对内部活动,这提示其具有致焦虑作用。结论是,AM 411产生CB1激动剂样行为,其效力介于WIN 55,212-2和AM 356之间。AM 411可能是理解CB1受体刺激的行为和神经效应的有用工具。