Evidence map›Paper›PMID 39880402›Full record

ArticleChemical research in toxicology2025

Cannabidiol Toxicity Driven by Hydroxyquinone Formation.

Metzli I Montero, Pravien S Rajaram, Jose E Zamora Alvarado, Kara E McCloskey, Ryan D Baxter, Roberto C Andresen Eguiluz

Abstract read
In one paragraph

Article in Chemical research in toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Pravien S Rajaram
Jose E Zamora Alvarado
Kara E McCloskey
Roberto C Andresen EguiluzORCID 0000-0002-5209-4112

Funding

G-RISE at UC MercedT32GM141862 · NIGMS · UNIVERSITY OF CALIFORNIA, MERCED · PI GOPINATHAN, AJAY, LIWANG, ANDY · 2021 to 2025
$2.7M
NIGMS NIH HHS T32 GM141862
6 · The paper itself

Abstract

Oxidative byproducts of cannabidiol (CBD) are known to be cytotoxic. However, CBD susceptibility to oxidation and resulting toxicity dissolved in two common solvents, ethanol (EtOH) and dimethyl sulfoxide (DMSO), is seldom discussed. Furthermore, CBD products contain a wide range of concentrations, making it challenging to link general health risks associated with CBD cytotoxicity. Here, we report on the effect of CBD and CBD analogues dissolved in EtOH or DMSO at various concentrations. The cells used in these studies were human umbilical vascular endothelial cells (HUVECs). Our findings show significant CBD oxidation to cannabidiol-quinone (CBD-Q) and subsequent cytotoxicity, occurring at 10 μM concentration, regardless of the solution delivery vehicle. Moreover, a new analogue of CBD, cannabidiol-diacetate (CBD-DA), exhibits significantly more stability and reduced toxicity compared with CBD or CBD-Q, respectively. This knowledge is important for determining concentration-dependent health risks of complex cannabinoid mixtures and establishing legal limits.

Indexed as

CannabidiolQuinonesCells, CulturedCell SurvivalDimethyl SulfoxideDose-Response Relationship, DrugHumansHuman Umbilical Vein Endothelial CellsMolecular StructureOxidation-ReductionCannabidiolDimethyl SulfoxideQuinones

Identifiers

PMID39880402
PMCPMC11837211

What OpenQuestion holds

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LicenceCC BY
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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.