Evidence map›Paper›PMID 42883229›Full record

ArticleMolecules (Basel, Switzerland)2026

Impact of Cannabidiol and Its Synthetic Derivative on Fentanyl Consumption and Fentanyl-Induced Neurometabolic Alterations in Mice.

Dalal A AlKhelb, Jomana M Alahmadi, Maisa S Alqarni, Syed Rizwan Ahamad, Alaa Alnoor Alameen, Ahmed Altuwaijri, Shakir D AlSharari, Fawaz Alasmari

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Dalal A AlKhelbDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-4888-0698
Jomana M AlahmadiDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Maisa S AlqarniDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Syed Rizwan AhamadDepartment of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Alaa Alnoor AlameenDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-4073-2375
Ahmed AltuwaijriDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0009-0006-8129-4507
Shakir D AlSharariDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-4263-3610
Fawaz AlasmariDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0003-2382-5892

Funding

King Saud University W25-14
6 · The paper itself

Abstract

backgroundOpioid use disorder (OUD) remains a critical global health challenge, with highly potent synthetic opioids like fentanyl contributing to overdose deaths. The available treatments have limitations. The endocannabinoid system has emerged steadily as a therapeutic target for the opioid crisis due to its modulatory effects on opioid reward and withdrawal and its involvement in regulating inflammation. These studies investigate the potential of cannabidiol (CBD) and its synthetic derivative (L-1β IN-1) in mitigating fentanyl effects.

methodsC57BL/6 male mice were used in several behavioral assays: two-bottle choice (TBC) to measure fentanyl reward/seeking behaviors, hot plate to assess antinociception, and marble burying to evaluate compulsive/adverse effects. Additionally, a neurometabolic study was conducted to evaluate the impact of chronic high doses of fentanyl alone and in combination with CBD or L-1β-IN-1 on brain metabolic signatures.

resultsThe mice consistently preferred to drink fentanyl, and i.p. injections of 10 mg/kg CBD or 5-25 mg/kg of L-1β-IN-1 decreased the fentanyl preference scores to values below 0.5. The antinociceptive effects of pretreatment groups showed a trend of enhanced analgesic effects in the hot plate assay. However, they showed no significant changes in the marble-burying assay, suggesting that pretreatment with these compounds lacks acute stereotypic effects. The Fentanyl metabolomics revealed robust metabolic activation with fentanyl alone, while CBD or L-1β-IN-1 showed different profiles in modulating these fentanyl-induced metabolic signatures.

conclusionsThese studies provide evidence about the in vivo behavioral and neurometabolic profiles of fentanyl after pretreatment with CBD and synthetic CBD, presenting them as possible pharmacological tools for OUD research.

Indexed as

Analgesics, OpioidCannabidiolFentanylOpioid-Related DisordersAnimalsBehavior, AnimalBrainMaleMiceMice, Inbred C57BLAnalgesics, OpioidCannabidiolFentanylcannabidiolfentanylmetabolomicneurotoxicityopioidstwo-bottle choice

Identifiers

PMID42883229
PMCPMC13666421

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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.