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Cannabinoids, reward processing, and psychosis.

Brandon Gunasekera1, Kelly Diederen1, Sagnik Bhattacharyya2

  • 1Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, 16 De Crespigny Park, Box P067, London, SE5 8AF, UK.

Psychopharmacology
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PubMed
Summary

Cannabinoids like THC and CBD affect the brain's reward system and dopamine. While THC may induce psychosis-like symptoms, CBD might offer antipsychotic potential, but more research is needed.

Keywords:
Aberrant salienceCBDCannabidiolCannabisDopaminePETPsychosisReward processingSchizophreniaTHCfMRI

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Area of Science:

  • Neuroscience
  • Psychopharmacology
  • Neuroimaging

Background:

  • Psychotic disorders share neurobiological links with cannabinoid effects on reward processing.
  • Cannabinoids influence neurocognitive and neurochemical pathways crucial for reward functions.

Purpose of the Study:

  • To examine if delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) impact the reward system and dopamine.
  • To investigate the mechanisms behind THC's psychotomimetic and CBD's potential antipsychotic effects.

Main Methods:

  • A narrative review of preclinical and human studies on cannabinoid-induced dopamine signaling and reward processing.
  • Systematic search of neuroimaging studies involving acute cannabinoid challenges in healthy and psychotic individuals.

Main Results:

  • Psychosis is linked to increased striatal dopamine synthesis/release and altered reward processing.
  • Acute THC challenges show modest striatal dopamine effects, while chronic use may impair dopaminergic function.
  • THC modulates reward/salience regions (striatum, midbrain), with effects correlating to symptom severity; CBD may have opposing effects.

Conclusions:

  • THC and CBD modulate reward processing and its neural substrates.
  • The link between these modulations and the psychotomimetic/antipsychotic effects of cannabinoids requires further investigation.
  • Future research should explore endocannabinoid dysfunction, reward abnormalities, and psychosis.