Evidence map›Paper›PMID 26092099›Full record

ArticleCardiovascular research2015

Cannabidiol causes endothelium-dependent vasorelaxation of human mesenteric arteries via CB1 activation.

Christopher P Stanley, William H Hind, Cristina Tufarelli, Saoirse E O'Sullivan

Open access · hybridAbstract read
In one paragraph

Article in Cardiovascular research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 94 citations in OpenAlex.

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  7. Cannabidiol Toxicity Driven by Hydroxyquinone Formation.Chemical research in toxicology · 2025
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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

4 authors at 2 institutions in 1 country.

Christopher P StanleySchool of Medicine, University of Nottingham, Royal Derby Hospital, Derby DE22 3DT, UK.
William H HindSchool of Medicine, University of Nottingham, Royal Derby Hospital, Derby DE22 3DT, UK.
Cristina TufarelliSchool of Medicine, University of Nottingham, Royal Derby Hospital, Derby DE22 3DT, UK.
Saoirse E O'SullivanSchool of Medicine, University of Nottingham, Royal Derby Hospital, Derby DE22 3DT, UK mbzso@nottingham.ac.uk.
Royal Derby Hospital · GBUniversity of Nottingham · GB

Funding

British Heart Foundation FS/09/007/26170British Heart Foundation FS/09/061
6 · The paper itself

Abstract

aimsThe protective effects of cannabidiol (CBD) have been widely shown in preclinical models and have translated into medicines for the treatment of multiple sclerosis and epilepsy. However, the direct vascular effects of CBD in humans are unknown. METHODS AND

resultsUsing wire myography, the vascular effects of CBD were assessed in human mesenteric arteries, and the mechanisms of action probed pharmacologically. CBD-induced intracellular signalling was characterized using human aortic endothelial cells (HAECs). CBD caused acute, non-recoverable vasorelaxation of human mesenteric arteries with an Rmax of ∼ 40%. This was inhibited by cannabinoid receptor 1 (CB1) receptor antagonists, desensitization of transient receptor potential channels using capsaicin, removal of the endothelium, and inhibition of potassium efflux. There was no role for cannabinoid receptor-2 (CB2) receptor, peroxisome proliferator activated receptor (PPAR)γ, the novel endothelial cannabinoid receptor (CBe), or cyclooxygenase. CBD-induced vasorelaxation was blunted in males, and in patients with type 2 diabetes or hypercholesterolemia. In HAECs, CBD significantly reduced phosphorylated JNK, NFκB, p70s6 K and STAT5, and significantly increased phosphorylated CREB, ERK1/2, and Akt levels. CBD also increased phosphorylated eNOS (ser1177), which was correlated with increased levels of ERK1/2 and Akt levels. CB1 receptor antagonism prevented the increase in eNOS phosphorylation.

conclusionThis study shows, for the first time, that CBD causes vasorelaxation of human mesenteric arteries via activation of CB1 and TRP channels, and is endothelium- and nitric oxide-dependent.

Indexed as

AdultAgedAged, 80 and overCannabidiolEndothelium, VascularFemaleHumansMaleMesenteric ArteriesMiddle AgedMultiple SclerosisNitric OxideReceptor, Cannabinoid, CB1VasodilationVasodilator AgentsCannabidiolNitric OxideReceptor, Cannabinoid, CB1Vasodilator AgentsCannabidiolCannabinoidEndotheliumHumanVasorelaxation

Identifiers

PMID26092099
PMCPMC4540144
OpenAlexW1844376968

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.