Effects of cannabinoid agonists and antagonists in male rats discriminating the synthetic cannabinoid AM2201

• Published in: European journal of pharmacology Vol. 960; p. 176168
• Main Authors: AlKhelb, Dalal, Burke, Emily L, Zvonok, Alexander, Iliopoulos-Tsoutsouvas, Christos, Georgiadis, Markos-Orestis, Jiang, Shan, Ho, Thanh C, Nikas, Spyros P, Makriyannis, Alexandros, Desai, Rajeev I
• Format: Journal Article
• Language: English
• Published: Netherlands 05.12.2023
• Subjects: Animals; Atropine Derivatives; Cannabinoid Receptor Agonists - pharmacology; Cannabinoids - pharmacology; Dose-Response Relationship, Drug; Dronabinol - pharmacology; Drug Inverse Agonism; Fentanyl; Male; Rats; Receptor, Cannabinoid, CB1; Drug discrimination; AM2201 discrimination; Cannabinoid antagonists; Cannabinoid agonists; Δ-THC; CB partial agonists; Cannabinoid receptors
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/j.ejphar.2023.176168

The synthetic forms of delta-9-tetrahydrocannabinol (Δ -THC), dronabinol or nabilone, have been approved to treat several indications. However, due to safety concerns their clinical utility remains limited. Consequently, there is a need for developing cannabinoid (CB) ligands that display better behavioral pharmacological profiles than Δ -THC. Here, we utilized drug discrimination methods to compare the interoceptive effects of CB ligands that vary in potency, efficacy, and selectivity at the CB receptors, including two ligands, AM411 and AM4089, that show CB partial agonist-like actions in vitro. Male rats were trained to discriminate 0.1 mg/kg AM2201 from saline under a fixed-ratio (FR) 10 response schedule of food reinforcement. After establishing AM2201's discriminative-stimulus effects, pretreatment tests with the CB antagonist/inverse agonist rimonabant blocked AM2201's effects, whereas the peripherally-restricted antagonist AM6545 had no effect. Next, the generalization profiles of AM411 and AM4089 with CB full agonists (JWH-018, CP-55,940, AM8936), partial agonist (Δ -THC), and non-cannabinoids (fentanyl, atropine) were compared. The CBs either fully (AM2201, CP-55,940, JWH-018, AM8936, Δ -THC) or partially (AM411, AM4089) substituted for AM2201, whereas fentanyl and atropine did not produce AM2201-like effects. All CB drugs were more potent than Δ -THC and correlation analysis confirmed that the relative behavioral potencies of CBs corresponded strongly with their relative affinities at the CB but not CB receptors. Together, our results further demonstrate that AM411 and AM4089 exhibit better pharmacological profiles compared to Δ -THC, in that they are more potent and display in vivo partial agonist-like actions that are centrally mediated via CB receptors.