Evidence map›Paper›PMID 36708234›Full record

ArticleThe FEBS journal2023

Synthetic cannabinoid receptor agonists are monoamine oxidase-A selective inhibitors.

Sarah A Hindson, Rachael C Andrews, Michael J Danson, Marc W van der Kamp, Amy E Manley, Oliver B Sutcliffe, Tom S F Haines, Tom P Freeman, Jennifer Scott, Stephen M Husbands and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The FEBS journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

14 authors at 3 institutions in 1 country.

Sarah A HindsonDepartment of Biology and Biochemistry, University of Bath, BA2 7AY, Bath, UK.
Rachael C AndrewsDepartment of Chemistry, University of Bath, BA2 7AY, Bath, UK.ORCID 0000-0002-7836-036X
Michael J DansonDepartment of Biology and Biochemistry, University of Bath, BA2 7AY, Bath, UK.
Marc W van der KampSchool of Biochemistry, University of Bristol, BS8 1TD, Bristol, UK.
Amy E ManleyFaculty of Health Sciences, University of Bristol, BS8 1TH, Bristol, UK.
Oliver B SutcliffeMANchester DRug Analysis & Knowledge Exchange (MANDRAKE), Department of Natural Sciences, Manchester Metropolitan University, M15 5GD, Manchester, UK.
Tom S F HainesDepartment of Computer Science, University of Bath, BA2 7AY, Bath, UK.
Tom P FreemanDepartment of Psychology, University of Bath, BA2 7AY, Bath, UK.
Jennifer ScottFaculty of Health Sciences, University of Bristol, BS8 1TH, Bristol, UK.
Stephen M HusbandsDepartment of Pharmacy and Pharmacology, University of Bath, BA2 7AY, Bath, UK.
Ian S BlagbroughDepartment of Pharmacy and Pharmacology, University of Bath, BA2 7AY, Bath, UK.
J L Ross AndersonSchool of Biochemistry, University of Bristol, BS8 1TD, Bristol, UK.
David R CarberyDepartment of Chemistry, University of Bath, BA2 7AY, Bath, UK.
Christopher R PudneyDepartment of Biology and Biochemistry, University of Bath, BA2 7AY, Bath, UK.ORCID 0000-0001-6211-0086
University of Bath · GBUniversity of Bristol · GBManchester Metropolitan University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L01386X/1Biotechnology and Biological Sciences Research Council BB/M026280/1
6 · The paper itself

Abstract

Synthetic cannabinoid receptor agonists (SCRAs) are one of the fastest growing classes of recreational drugs. Despite their growth in use, their vast chemical diversity and rapidly changing landscape of structures make understanding their effects challenging. In particular, the side effects for SCRA use are extremely diverse, but notably include severe outcomes such as cardiac arrest. These side effects appear at odds with the main putative mode of action, as full agonists of cannabinoid receptors. We have hypothesized that SCRAs may act as MAO inhibitors, owing to their structural similarity to known monoamine oxidase inhibitors (MAOI's) as well as matching clinical outcomes (hypertensive crisis) of 'monoaminergic toxicity' for users of MAOIs and some SCRA use. We have studied the potential for SCRA-mediated inhibition of MAO-A and MAO-B via a range of SCRAs used commonly in the UK, as well as structural analogues to prove the atomistic determinants of inhibition. By combining in silico and experimental kinetic studies we demonstrate that SCRAs are MAO-A-specific inhibitors and their affinity can vary significantly between SCRAs, most notably affected by the nature of the SCRA 'head' group. Our data allow us to posit a putative mechanism of inhibition. Crucially our data demonstrate that SCRA activity is not limited to just cannabinoid receptor agonism and that alternative interactions might account for some of the diversity of the observed side effects and that these effects can be SCRA-specific.

Indexed as

Cannabinoid Receptor AgonistsIllicit DrugsKineticsMonoamine OxidaseMonoamine Oxidase InhibitorsCannabinoid Receptor AgonistsIllicit DrugsMonoamine OxidaseMonoamine Oxidase Inhibitorsenzyme inhibitionflexible docking analysisMAO-AMAO-Bmonoamine oxidaseSCRAssynthetic cannabinoid receptor agonists

Identifiers

PMID36708234
PMCPMC10952593
OpenAlexW4318392924

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.