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Cannabidiol in humans-the quest for therapeutic targets.

Simon Zhornitsky, Stéphane Potvin

Pharmaceuticals May 21, 2012 DOI: 10.3390/ph5050529 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Systematic review Randomized Peer reviewed
Population Healthy controls and clinical patients across 34 studies
Interventions Cannabidiol (CBD) CBD + ∆9-THC
Dose 150-600 mg/d
Topics CBD
Key findings Experimental studies indicate high-dose inhaled or intravenous CBD is required to inhibit the effects of a lower dose of THC, while evidence on whether oral/oromucosal CBD prolongs, intensifies, or inhibits THC effects is mixed. Preliminary clinical trials suggest high-dose oral CBD (150-600 mg/day) may exert therapeutic effects in social anxiety disorder, insomnia, and epilepsy, but may also cause mental sedation.

Abstract

Cannabidiol (CBD), a major phytocannabinoid constituent of cannabis, is attracting growing attention in medicine for its anxiolytic, antipsychotic, antiemetic and anti-inflammatory properties. However, up to this point, a comprehensive literature review of the effects of CBD in humans is lacking. The aim of the present systematic review is to examine the randomized and crossover studies that administered CBD to healthy controls and to clinical patients. A systematic search was performed in the electronic databases PubMed and EMBASE using the key word "cannabidiol". Both monotherapy and combination studies (e.g., CBD + ∆9-THC) were included. A total of 34 studies were identified: 16 of these were experimental studies, conducted in healthy subjects, and 18 were conducted in clinical populations, including multiple sclerosis (six studies), schizophrenia and bipolar mania (four studies), social anxiety disorder (two studies), neuropathic and cancer pain (two studies), cancer anorexia (one study), Huntington's disease (one study), insomnia (one study), and epilepsy (one study). Experimental studies indicate that a high-dose of inhaled/intravenous CBD is required to inhibit the effects of a lower dose of ∆9-THC. Moreover, some experimental and clinical studies suggest that oral/oromucosal CBD may prolong and/or intensify ∆9-THC-induced effects, whereas others suggest that it may inhibit ∆9-THC-induced effects. Finally, preliminary clinical trials suggest that high-dose oral CBD (150-600 mg/d) may exert a therapeutic effect for social anxiety disorder, insomnia and epilepsy, but also that it may cause mental sedation. Potential pharmacokinetic and pharmacodynamic explanations for these results are discussed.

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