Neurocognition and subjective experience following acute doses of the synthetic cannabinoid JWH‐018: a phase 1, placebo‐controlled, pilot study
Eef L. Theunissen, Nadia R. P. W. Hutten, Natasha L. Mason, Stefan W. Toennes, Kim P. C. Kuypers, E. B. de Sousa Fernandes Perna, Johannes G. Ramaekers
British Journal of Pharmacology November 22, 2017 DOI: 10.1111/bph.14066 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Placebo-controlled crossover study Pilot study Peer reviewed |
|---|---|
| Sample size | 6 |
| Population | Healthy cannabis-experienced volunteers |
| Intervention | JWH-018 |
| Dose | 2 and 3 mg |
| Duration | 12 h after drug administration |
| Topics | Cannabis |
| Keywords | Synthetic cannabinoids Placebo Dosing Neurocognitive Pharmacology Anesthesia Cognition |
| Citations | 38 |
| Key points | Low doses of JWH-018 produced subjective feelings of high and impaired neurocognitive function despite low serum concentrations. |
Abstract
Background: AND
Purpose: Synthetic cannabinoids (often sold as Spice or K2) have become a very popular alternative to cannabis due to their easy access and portrayed safety. Controlled studies on the behavioural effects of synthetic cannabinoids are currently lacking, which hampers risk assessments of these compounds. EXPERIMENTAL APPROACH: This is a first attempt to assess the influence of a synthetic cannabinoid, JWH-018, on neurocognition and subjective experience in humans after controlled administration. JWH-018, 2 and 3 mg, was administered to six healthy cannabis-experienced volunteers in a placebo-controlled, cross-over study following an escalating dosing schedule. Participants were monitored for 12 h after drug administration, and several neurocognitive measures and subjective questionnaires were taken. KEY
Results: Serum concentrations of JWH-018 were highest after the 2 mg dose but generally low after administration of both doses. Both doses of JWH-018 were well tolerated, and no serious side effects were reported. Participants reported feeling more 'high' at 1 and 2 h after administration, particularly after the 2 mg dose. Behavioural impairments also emerged despite the low serum concentrations of JWH-018. The low dose of JWH-018 impaired performance on the tracking, divided attention and stop signal task.
Conclusion: AND
Implications: JWH-018 dosing in the present study resulted in drug concentrations that were generally low and not fully representative of common use. Yet initial impairments of neurocognitive function and subjective feelings of high did emerge despite low levels of JWH-018 in serum. Higher doses are needed to obtain a more representative risk profile of JWH-018.
Comparable studies
Other randomized controlled trials on cannabis, 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 |
| Acute Effects of a Single, Oral dose of d9-tetrahydrocannabinol (THC) and Cannabidiol (CBD) Administration in Healthy Volunteers Healthy male subjects | 2012 | Randomized controlled trial | n = 16 |
| 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 11
- What are the psychological effects of using synthetic cannabinoids? A systematic review Journal of Psychopharmacology February 21, 2019
- Neurocognition and Subjective Experience Following Acute Doses of the Synthetic Cannabinoid JWH-018: Responders Versus Nonresponders Cannabis and Cannabinoid Research February 27, 2019
- Psychotomimetic symptoms after a moderate dose of a synthetic cannabinoid (JWH-018): implications for psychosis Psychopharmacology January 26, 2021
- A Comparison of Acute Neurocognitive and Psychotomimetic Effects of a Synthetic Cannabinoid and Natural Cannabis at Psychotropic Dose Equivalence Frontiers in Psychiatry May 19, 2022
- How can we facilitate research on the risks and potential benefits of novel psychoactive substances? EClinicalMedicine June 19, 2026
and 6 more in the library
Cites 13
- Measurement of dissociative states with the Clinician‐Administered Dissociative States Scale (CADSS) Journal of Traumatic Stress 1998
- Psychedelic Effects of Ketamine in Healthy Volunteers Anesthesiology 1998
- Here today, gone tomorrow…and back again? A review of herbal marijuana alternatives (K2, Spice), synthetic cathinones (bath salts), kratom, Salvia divinorum, methoxetamine, and piperazines. Journal of Medical Toxicology March 1, 2012
- Cannabis and tolerance: acute drug impairment as a function of cannabis use history Scientific Reports May 26, 2016
- Neurocognitive performance following acute mephedrone administration, with and without alcohol Journal of Psychopharmacology August 25, 2016
and 8 more in the library