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Separate and combined effects of the cannabinoid agonists nabilone and Δ⁹-THC in humans discriminating Δ⁹-THC.

Joshua A Lile, Thomas H Kelly, Lon R Hays

Drug and Alcohol Dependence July 1, 2011 DOI: 10.1016/j.drugalcdep.2010.11.019 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Drug-discrimination study Peer reviewed
Sample size 6
Population Cannabis users
Interventions Nabilone Δ⁹-tetrahydrocannabinol (Δ⁹-THC)
Dose Nabilone 0, 1 and 3 mg; Δ⁹-THC 0, 5, 15 and 30 mg; training dose 30 mg oral Δ⁹-THC
Measures multiple-choice procedure, self-report measures, task performance measures, physiological measures
Topics Cannabis
Key points Nabilone shared discriminative-stimulus and subjective effects with Δ⁹-THC in cannabis users and, when combined with Δ⁹-THC, shifted its discriminative effects leftward/upward and enhanced its effects on other measures. The authors indicate nabilone would likely be safe and well tolerated when combined with cannabis, supporting future research on cross-tolerance and reduced cannabis use.

Abstract

Agonist replacement treatment is a promising strategy to manage cannabis-use disorders. The aim of this study was to assess the combined effects of the synthetic cannabinoid agonist nabilone and Δ⁹-tetrahydrocannabinol (Δ⁹-THC) using drug-discrimination procedures, which are sensitive to drug interactions. Testing the concurrent administration of nabilone and Δ⁹-THC was also conducted to provide initial safety and tolerability data, which is important because cannabis users will likely lapse during treatment. Six cannabis users learned to discriminate 30 mg oral Δ⁹-THC from placebo and then received nabilone (0, 1 and 3mg) and Δ⁹-THC (0, 5, 15 and 30 mg), alone and in combination. Subjects completed the multiple-choice procedure to assess drug reinforcement, and self-report, task performance and physiological measures were collected. Δ⁹-THC and nabilone alone shared discriminative-stimulus effects with the training dose of Δ⁹-THC, increased crossover point on the multiple-choice procedure, produced overlapping subject ratings and decreased skin temperature. Nabilone alone also elevated heart rate. In combination, nabilone shifted the discriminative-stimulus effects of Δ⁹-THC leftward/upward and enhanced Δ⁹-THC effects on the other outcome measures. These results replicate a previous study demonstrating that nabilone shares agonist effects with the active constituent of cannabis in cannabis users, and contribute further by indicating that nabilone would likely be safe and well tolerated when combined with cannabis. These data support the conduct of future studies to determine if nabilone treatment would produce cross-tolerance to the abuse-related effects of cannabis and reduce cannabis use.

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