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Self-administration of delta9-tetrahydrocannabinol (THC) by drug naive squirrel monkeys.

Zuzana Justinova, Gianluigi Tanda, Godfrey H Redhi, Steven R Goldberg

Psychopharmacology September 2003 DOI: 10.1007/s00213-003-1484-0 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational animal study (intravenous self-administration experiment) Peer reviewed
Population Drug-naive squirrel monkeys with no history of exposure to other drugs
Intervention delta9-tetrahydrocannabinol (THC)
Dose 1 to 16 microg/kg per injection (tested doses); 0.2 ml injections
Duration Acquisition reached in 11-34 sessions; dose-response testing followed
Topics Cannabis
Key findings THC functioned as a reinforcer in drug-naive squirrel monkeys, sustaining intravenous self-administration above vehicle levels at 2, 4, and 8 micrograms per kilogram per injection, with maximal responding at 4 micrograms per kilogram. Response rates, injections per session, and total THC intake were two- to three-fold greater than in earlier monkeys with a history of cocaine self-administration, suggesting that prior drug exposure is not required for THC self-administration.

Abstract

Interest in therapeutic activities of cannabinoids has been restrained by the fact that they are most often mediated through activation of cannabinoid CB1 receptors, the same receptors that mediate the effects of delta9-tetrahydrocannabinol (THC) and are responsible for the abuse liability of marijuana. Persistent intravenous self-administration of THC by animals was first demonstrated in squirrel monkeys and shown to be mediated by CB1 receptors, but monkeys in the study had a history of cocaine self-administration, raising the possibility that persistent neurobiological adaptations might subsequently predispose animals to self-administer THC. To demonstrate persistent intravenous self-administration of THC in drug-naive squirrel monkeys. Monkeys with no history of exposure to other drugs learned to press a lever for intravenous injections (0.2 ml in 0.2 s) of THC under a 10-response, fixed-ratio schedule with a 60-s time-out after each injection. Acquisition of THC self-administration was rapid and the final schedule was reached in 11-34 sessions. Dose of THC was then varied from 1 to 16 microg/kg per injection with vehicle extinction following each dose of THC. THC maintained significantly higher numbers of self-administered injections per session and higher rates of responding than vehicle at doses of 2, 4 and 8 microg/kg per injection, with maximal rates of responding at 4 microg/kg per injection. Response rates, injections per session and total THC intake per session were two- to three-fold greater in monkeys with no history of exposure to other drugs compared to previous findings in monkeys with a history of cocaine self-administration. THC can act as an effective reinforcer of drug-taking behavior in monkeys with no history of exposure to other drugs, suggesting that self-administration of THC by monkeys provides a reliable animal model of human marijuana abuse.

Comparable studies

Other preclinical and animal studies on cannabis, most cited first.

Study Year Design Participants
Cognitive Impairment Induced by Delta9-tetrahydrocannabinol Occurs through Heteromers between Cannabinoid CB1 and Serotonin 5-HT2A Receptors Mice 2015 Preclinical study
Interaction of drugs of abuse and maintenance treatments with human P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2). hMDR1- and hBCRP-transfected HEK293 cells and hMDR1- and hBCRP-MDCKII cells 2010 In vitro study
Long-term hippocampal interneuronopathy drives sex-dimorphic spatial memory impairment induced by prenatal THC exposure Mice prenatally exposed to THC, including conditional CB1R knockout mice 2020 Animal experimental study
Chronic cannabis promotes pro-hallucinogenic signaling of 5-HT2A receptors through Akt/mTOR pathway Mice exposed to chronic THC early in life 2018 Animal experimental study
Effects of cannabinoid drugs on the deficit of prepulse inhibition of startle in an animal model of schizophrenia: the SHR strain Spontaneously hypertensive rats (SHRs) and Wistar rats 2014 Animal experimental study

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