| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8351021 | Pharmacology Biochemistry and Behavior | 2014 | 6 Pages | 
Abstract
												Synthetic indole-derived cannabinoids, originally developed to probe cannabinoid CB1 and CB2 receptors, have become widely abused for their marijuana-like intoxicating properties. The present study examined the effects of indole-derived cannabinoids in rats trained to discriminate Î9-tetrahydrocannabinol (Î9-THC) from vehicle. In addition, the effects of Î9-THC in rats trained to discriminate JWH-018 from vehicle were assessed. Adult male Sprague-Dawley rats were trained to discriminate 3 mg/kg Î9-THC or 0.3 mg/kg JWH-018 from vehicle. JWH-018, JWH-073, and JWH-210 fully substituted in Î9-THC-trained rats and Î9-THC substituted in JWH-018-trained rats. In contrast, JWH-320, an indole-derived cannabinoid without affinity for CB1 receptors, failed to substitute for Î9-THC. Pre-treatment with 1 mg/kg rimonabant significantly reduced responding on the JWH-018-associated lever in JWH-018-trained rats. These results support the conclusion that the interoceptive effects of Î9-THC and synthetic indole-derived cannabinoids show a large degree of overlap, which is predictive of their use for their marijuana-like intoxicating properties. Characterization of the extent of pharmacological differences among structural classes of cannabinoids, and determination of their mechanisms remain important goals.
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											Authors
												Jenny L. Wiley, Timothy W. Lefever, Ricardo A. Cortes, Julie A. Marusich, 
											