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Tolerance, physical dependence, and Δ9-THC-like interoceptive effects of cannabinol in mice.

S. Vanegas, J. Marusich, J. Maturano, D. Sarlah, S. G. Kinsey

Drug and Alcohol Dependence September 1, 2026 DOI: 10.1016/j.drugalcdep.2026.113341 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical animal study Peer reviewed
Population Adult C57BL/6 mice
Interventions Cannabinol (CBN) rimonabant WIN 55 212-2 THC
Duration CBN administered twice daily for five days; withdrawal assessed on the sixth day
Measures Tetrad battery, tail suspension test, drug discrimination
Topics Addiction Cannabis
Key points Repeated CBN administration in mice produced tolerance to cannabimimetic effects and physical dependence, evidenced by rimonabant-precipitated withdrawal. CBN fully substituted for THC in discrimination tests, and CBN plus THC attenuated THC's psychoactive effects.

Abstract

Background: AND PURPOSE Cannabinoids, including Δ9-tetrahydrocannabinol (THC) and synthetic CB1 agonists elicit acute psychotropic effects that undergo tolerance with repeated exposure. In contrast, the effects of prolonged cannabinol (CBN) use are unknown. This study examined (1) the effects of repeated CBN administration on classic cannabimimetic outcomes, (2) whether these effects undergo tolerance or induce physical dependence, and (3) the THC-like discriminative stimulus effects of CBN, including whether CBN alters THC's discriminative stimulus. EXPERIMENTAL APPROACH Adult C57BL/6 mice were administered CBN twice daily for five days and tested in the tetrad battery to measure tolerance. On the sixth day, rimonabant was administered and somatic signs of withdrawal (i.e., head twitches and paw tremors) and struggling in the tail suspension test were assessed. Cross-tolerance to the CB1/CB2 agonist WIN 55,212-2 was also assessed in mice repeatedly administered CBN. A separate cohort of mice was trained to discriminate THC from vehicle. KEY RESULTS Mice displayed tolerance to CBN-induced catalepsy, antinociception, and hypothermia. Cannabimimetic effects of WIN 55,212-2 were attenuated in CBN-treated mice, indicating cross-tolerance. Similarly, rimonabant induced somatic withdrawal signs and increased struggling in CBN-treated mice. Finally, CBN fully substituted for THC. Although rimonabant substantially lowered the psychoactive effects of THC, the specific dose tested was less effective in lowering CBN's psychoactive effects. Administration of CBN plus THC also attenuated THC's psychoactive effects.

Conclusion: AND IMPLICATIONS These data indicate that repeated CBN administration induces tolerance and physical dependence and that CBN reduces THC's psychoactive effects.

In the evidence

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  • Repeated cannabinol administration produced tolerance to cannabimimetic effects and physical dependence evidenced by rimonabant-precipitated withdrawal, and cannabinol fully substituted for THC in discrimination tests.

    Synthesized

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