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Acute Effects of a Single, Oral dose of d9-tetrahydrocannabinol (THC) and Cannabidiol (CBD) Administration in Healthy Volunteers

Rocío Martín‐Santos, José Alexandre S. Crippa, Albert Batalla, Sagnik Bhattacharyya, Zerrin Atakan, Stefan Borgwardt, Paul Allen, Marc L. Seal, Klaus Langohr, Magı́ Farré, AW. Zuardi, Philip Mcguire

Current Pharmaceutical Design September 12, 2012 DOI: 10.2174/138161212802884780 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized controlled trial Placebo-controlled Double-blind Peer reviewed
Sample size 16
Population Healthy male subjects
Interventions THC CBD
Dose THC 10 mg, CBD 600 mg
Duration 3 hours post drug administration
Topics Cannabis CBD
Keywords Placebo Sedation Delta-9-tetrahydrocannabinol Oral administration Anesthesia Analysis of variance Pharmacology Cannabinoid
Citations 288
Key findings THC produced anxiety, dysphoria, positive psychotic symptoms, sedation, subjective intoxication, and increased heart rate, while CBD showed no differences from placebo on any measure.

Abstract

Rationale: Animal and humans studies suggest that the two main constituents of cannabis sativa, delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) have quite different acute effects. However, to date the two compounds have largely been studied separately.

Objective: To evaluate and compare the acute pharmacological effects of both THC and CBD in the same human volunteers.

Methods: A randomised, double-blind, cross-over, placebo controlled trial was conducted in 16 healthy male subjects. Oral THC 10 mg or CBD 600 mg or placebo was administered in three consecutive sessions, at one-month interval. Physiological measures and symptom ratings were assessed before, and at 1, 2 and 3 hours post drug administration. The area under the curve (AUC) between baseline and 3 hours, and the maximum absolute change from baseline at 2 hours were analysed by one-way repeated measures analysis of variance, with drug condition (THC or CBD or placebo) as the factor.

Results: Relative to both placebo and CBD, administration of THC was associated with anxiety, dysphoria, positive psychotic symptoms, physical and mental sedation, subjective intoxication (AUC and effect at 2 hours: p < 0.01), an increase in heart rate (p < 0.05). There were no differences between CBD and placebo on any symptomatic, physiological variable.

Conclusions: In healthy volunteers, THC has marked acute behavioural and physiological effects, whereas CBD has proven to be safe and well tolerated.

In the evidence

This study is part of the evidence base for a synthesis in the library. Here is how each one recorded it.

  • CBD 600 mg produced no differences from placebo on any symptomatic or physiological measure, while THC produced anxiety, dysphoria, psychotic symptoms, sedation, and increased heart rate.

    Synthesized

Comparable studies

Other randomized controlled trials on CBD, most cited first.

Study Year Design Participants
Cannabidiol inhibits THC-elicited paranoid symptoms and hippocampal-dependent memory impairment Healthy participants 2012 Randomized controlled trial n = 48
Distinct Effects of Δ9-Tetrahydrocannabinol and Cannabidiol on Neural Activation During Emotional Processing Healthy, English-native, right-handed men who had used cannabis 15 times or less in... 2009 Double-blind, randomized, placebo-controlled crossover trial n = 15
Inverted U-Shaped Dose-Response Curve of the Anxiolytic Effect of Cannabidiol during Public Speaking in Real Life Healthy subjects aged 18 to 35 years 2017 Randomized controlled trial n = 60
Modulation of Mediotemporal and Ventrostriatal Function in Humans by Δ9-Tetrahydrocannabinol Healthy, native English-speaking, right-handed men of white race/ethnicity who had used... 2009 Randomized controlled trial n = 15
Cannabidiol (CBD) content in vaporized cannabis does not prevent tetrahydrocannabinol (THC)-induced impairment of driving and cognition Healthy volunteers with a history of light cannabis use 2019 Randomized, double-blind, within-subjects crossover n = 14

Citations in the library

Cited by 45

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