Evidence map›Paper›PMID 29686308›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

Unique treatment potential of cannabidiol for the prevention of relapse to drug use: preclinical proof of principle.

Gustavo Gonzalez-Cuevas, Remi Martin-Fardon, Tony M Kerr, David G Stouffer, Loren H Parsons, Dana C Hammell, Stan L Banks, Audra L Stinchcomb, Friedbert Weiss

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 2 pooled it
12.2field-weighted citation impact, top 1% of its field
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

77 citing papers in PubMed, 2 syntheses or guidelines pooled it, 154 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. The neural and psychophysiological effects of cannabidiol in youth with alcohol use disorder: A randomized controlled clinical trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Trial
  6. Trial
  7. Trial
  8. Review
  9. Article
  10. Article
  11. Article
  12. Cannabidiol as a treatment for cocaine use disorder: a scoping review.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Article
  13. Article
  14. Article
  15. Cannabidiol mitigates alcohol dependence and withdrawal with neuroprotective effects in the basolateral amygdala and striatum.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  16. Review
  17. Cannabidiol: Pharmaceutical formulations and biomedical applications.Iranian journal of basic medical sciences · 2026
    Review
  18. Article
  19. High hopes, hard realities: cannabidiol shows no acute effects in youth with alcohol use disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  20. Article

17 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Gustavo Gonzalez-CuevasDepartment of Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road (SP30-2120), La Jolla, CA, 92037, USA.
Remi Martin-FardonDepartment of Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road (SP30-2120), La Jolla, CA, 92037, USA.ORCID http://orcid.org/0000-0002-7470-5885
Tony M KerrDepartment of Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road (SP30-2120), La Jolla, CA, 92037, USA.
David G StoufferDepartment of Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road (SP30-2120), La Jolla, CA, 92037, USA.
Loren H ParsonsDepartment of Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road (SP30-2120), La Jolla, CA, 92037, USA.
Dana C HammellUniversity of Maryland, School of Pharmacy, Baltimore, MD, 21201, USA.
Stan L BanksZynerba Pharmaceuticals, Devon, PA, 19333, USA.
Audra L StinchcombUniversity of Maryland, School of Pharmacy, Baltimore, MD, 21201, USA.
Friedbert WeissDepartment of Neuroscience, The Scripps Research Institute, 10550 North Torrey Pines Road (SP30-2120), La Jolla, CA, 92037, USA. bweiss@scripps.edu.ORCID http://orcid.org/0000-0001-6211-6058
Scripps Research Institute · USUniversity of Maryland, Baltimore · USZynerba Pharmaceuticals (United States) · US

Funding

EtOH Seeking and Relapse: Therapeutic Potential of Transdermal CannabidiolR01AA022082 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI WEISS, FRIEDBERT · 2014 to 2018
$2.0M
Implementation of novel methodology to study the anti-relapse potential of cannabidiolR21DA039821 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI WEISS, FRIEDBERT · 2015 to 2016
$695k
Significance of withdrawal-related learning in EtOH craving and relapseR21AA021549 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI WEISS, FRIEDBERT · 2012 to 2013
$485k
NIAAA NIH HHS R01 AA022082NIAAA NIH HHS R21 AA021549NIDA NIH HHS R21 DA039821
6 · The paper itself

Abstract

Cannabidiol (CBD), the major non-psychoactive constituent of Cannabis sativa, has received attention for therapeutic potential in treating neurologic and psychiatric disorders. Recently, CBD has also been explored for potential in treating drug addiction. Substance use disorders are chronically relapsing conditions and relapse risk persists for multiple reasons including craving induced by drug contexts, susceptibility to stress, elevated anxiety, and impaired impulse control. Here, we evaluated the "anti-relapse" potential of a transdermal CBD preparation in animal models of drug seeking, anxiety and impulsivity. Rats with alcohol or cocaine self-administration histories received transdermal CBD at 24 h intervals for 7 days and were tested for context and stress-induced reinstatement, as well as experimental anxiety on the elevated plus maze. Effects on impulsive behavior were established using a delay-discounting task following recovery from a 7-day dependence-inducing alcohol intoxication regimen. CBD attenuated context-induced and stress-induced drug seeking without tolerance, sedative effects, or interference with normal motivated behavior. Following treatment termination, reinstatement remained attenuated up to ≈5 months although plasma and brain CBD levels remained detectable only for 3 days. CBD also reduced experimental anxiety and prevented the development of high impulsivity in rats with an alcohol dependence history. The results provide proof of principle supporting potential of CBD in relapse prevention along two dimensions: beneficial actions across several vulnerability states and long-lasting effects with only brief treatment. The findings also inform the ongoing medical marijuana debate concerning medical benefits of non-psychoactive cannabinoids and their promise for development and use as therapeutics.

Indexed as

Administration, CutaneousAlcoholismAnimalsAnxietyBrainCannabidiolCocaine-Related DisordersDrug-Seeking BehaviorImpulsive BehaviorMaleMotor ActivityRatsRats, WistarRecurrenceStress, PsychologicalSubstance-Related DisordersCannabidiol

Identifiers

PMID29686308
PMCPMC6098033
OpenAlexW2789955855

What OpenQuestion holds

Textmetadata
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.