Evidence map›Paper›PMID 40877567›Full record

ReviewCurrent topics in behavioral neurosciences2026

Delta-9-tetrahydrocannabinol and Cannabidiol for Pain: Preclinical and Clinical Models.

H M Harris, C F Moore, B W Jenkins, M F Bedillion, E M Weerts, C A Arout

Abstract readReview
In one paragraph

Review in Current topics in behavioral neurosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Glucocorticoid-endocannabinoid crosstalk in the ventrolateral periaqueductal gray (vlPAG) promotes pain resolution.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  2. 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.

H M HarrisDepartment of Psychiatry, Division on Substance Use Disorders, Columbia University Irving Medical Center and New York State Psychiatric Institute, New York, NY, USA.
C F MooreDivision of Behavioral Biology, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
B W JenkinsDivision of Behavioral Biology, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
M F BedillionDepartment of Psychiatry, Division on Substance Use Disorders, Columbia University Irving Medical Center and New York State Psychiatric Institute, New York, NY, USA.
E M WeertsDivision of Behavioral Biology, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
C A AroutDepartment of Psychiatry, Division on Substance Use Disorders, Columbia University Irving Medical Center and New York State Psychiatric Institute, New York, NY, USA. caroline.arout@nyspi.columbia.edu.

Funding

Translational Clinical Research Fellowship on Substance Use DisordersT32DA007294 · NIDA · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Frances Rudnick Levin, Diana M Martinez · 1993 to 2026
$9.3M
Effects of Repeated CBD Administration on Cannabis Abuse-Liability and Analgesia: A Human Laboratory StudyK01DA056692 · NIDA · UNIVERSITY OF KENTUCKY · PI Hannah Marie Harris · 2024 to 2026
$540k
NIDA NIH HHS K01 DA056692NIDA NIH HHS T32 DA007294
6 · The paper itself

Abstract

Cannabinoids are increasingly being used to manage pain resulting from a variety of conditions. Both preclinical animal models and human studies have played a crucial role in advancing our knowledge of cannabinoids, their involvement in pain mechanisms, and their potential utility as novel analgesics. This chapter first reviews basic pain neurobiology and the most common experimental pain paradigms, which provide a basis for our discussion of preclinical, human laboratory, and clinical research characterizing the effectiveness of cannabinoids for managing pain. While a substantial body of literature exists describing these effects, findings are complex and largely mixed, dependent on the cannabinoid administered, route of administration, and pain modality/syndrome tested. Herein, we highlight the need for more rigorous, placebo-controlled research defining the therapeutic efficacy of cannabinoids. The chapter concludes by emphasizing the need for further investigation of other cannabis constituents (e.g., minor cannabinoids and terpenes), potential interactions between cannabinoids and other analgesic medications, as well as other emerging issues in the intersection between cannabinoids and pain management.

Indexed as

AnalgesicsCannabidiolDronabinolPainAnimalsDisease Models, AnimalHumansAnalgesicsCannabidiolDronabinolCannabidiolCannabisDelta-9-tetrahydrocannabinolPain

Identifiers

PMID40877567
PMCPMC12832180

What Socratic 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 Socratic graph.