Evidence map›Paper›PMID 29863387›Full record

ArticleExperimental and clinical psychopharmacology2018

Influence of tiagabine maintenance on cannabis effects and related behaviors in daily cannabis users.

Michael J Wesley, Philip M Westgate, William W Stoops, Thomas H Kelly, Lon R Hays, Joshua A Lile

Abstract readControlled Clinical Trial
In one paragraph

Article in Experimental and clinical psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Pharmacotherapy for Cannabis Use Disorder: Preclinical and Clinical Models.Current topics in behavioral neurosciences · 2026
    Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Michael J WesleyDepartment of Behavioral Science.
Philip M WestgateDepartment of Biostatistics, University of Kentucky College of Public Health.
William W StoopsDepartment of Behavioral Science.
Thomas H KellyDepartment of Behavioral Science.
Lon R HaysDepartment of Psychiatry.
Joshua A LileDepartment of Behavioral Science.

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
The impact of electronic cigarettes (e-cigs) on perinatal immune responsiveness and birth outcomes in AppalachiaR01DA040694 · NIDA · UNIVERSITY OF KENTUCKY · PI ASHFORD, KRISTIN H. · 2015 to 2018
$2.5M
Human Laboratory Screening of Pregabalin and Tiagabine for Cannabis DependenceR01DA036550 · NIDA · UNIVERSITY OF KENTUCKY · PI LILE, JOSHUA ANTHONY · 2014 to 2019
$2.1M
GABA Drugs for Cannabis-Use Disorders: Initial Mechanistic Studies in HumansR01DA025605 · NIDA · UNIVERSITY OF KENTUCKY · PI LILE, JOSHUA ANTHONY · 2008 to 2011
$1.4M
Neural Mechanisms of Cannabinoid-Impaired Decision-Making in Emerging AdultsK01DA043652 · NIDA · UNIVERSITY OF KENTUCKY · PI WESLEY, MICHAEL J · 2018 to 2022
$792k
NCATS NIH HHS UL1 TR001998NIDA NIH HHS K01 DA043652NIDA NIH HHS R01 DA025605NIDA NIH HHS R01 DA036550University of Kentucky Center for Clinical and Translational Science
6 · The paper itself

Abstract

No medications are approved for cannabis use disorder (CUD). Gamma-aminobutyric acid (GABA) reuptake is modulated by cannabinoid (CB) receptor agonists, and there are shared effects between CB agonists and the GABA reuptake inhibitor tiagabine. This overlapping neuropharmacology suggested that tiagabine might be useful for CUD. The study determined the ability of tiagabine maintenance to reduce cannabis self-administration using a placebo-controlled, double-blind, counterbalanced, within-subjects design. Nontreatment-seeking daily cannabis users (N = 12; 3 female, 9 male) completed two 12-day outpatient maintenance phases (0 or 12 mg of tiagabine/day). Each phase consisted of a safety session, 7 maintenance days, and 4 experimental sessions. During experimental sessions, maintenance continued and participants completed two 2-day blocks of sampling and self-administration sessions to determine the reinforcing effects of smoked cannabis (0% and 5.9% Δ9-tetrahydrocannabinol). Naturalistic cannabis use, the subjective, performance and physiological response to cannabis, as well as side effects, sleep quality, craving, other self-reported substance use, and observer ratings were also measured. Cannabis functioned as a reinforcer and produced prototypical effects (e.g., increased heart rate and ratings of "high"), but tiagabine generally did not impact the effects of cannabis, or alter naturalistic use. Furthermore, tiagabine produced small, but significant, increases on 2 subscales of a Marijuana Craving Questionnaire, and reductions in both the amount of time slept in the past 24 hr and ratings of positive mood upon awakening. These human laboratory results from a sample of nontreatment-seeking cannabis users do not support the potential efficacy of 12 mg of tiagabine as a stand-alone pharmacotherapy for CUD. (PsycINFO Database Record

Indexed as

AdultAffectCannabinoid Receptor AgonistsCannabisCravingDouble-Blind MethodDronabinolFemaleGABA Uptake InhibitorsHallucinogensHumansMaleMarijuana AbuseMarijuana SmokingMarijuana UseReinforcement, PsychologyCannabinoid Receptor AgonistsDronabinolGABA Uptake InhibitorsHallucinogensTiagabine

Identifiers

PMID29863387
PMCPMC5990026

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.