Evidence map›Paper›PMID 39705234›Full record

ArticlePloS one2024

Cannabis sativa extracts inhibit LDL oxidation and the formation of foam cells in vitro, acting as potential multi-step inhibitors of atherosclerosis development.

Bruno Musetti, Alejandra Kun, David Menchaca, Alejandra Rodríguez-Haralambides, Javier Varela, Leonor Thomson, Edward M Bahnson

Abstract read
In one paragraph

Article in PloS one, 2024. 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. Review
  2. Review
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

7 authors.

Bruno MusettiFacultad de Ciencias, Instituto de Química Biológica, Laboratorio de Enzimología, Universidad de la República, Montevideo, Uruguay.
Alejandra KunFacultad de Ciencias, Biología Celular del Sistema Nervioso Periférico-DPAN-IIBCE, Instituto de Investigaciones Biológicas Clemente Estable, Sección Bioquímica, Montevideo, Uruguay.
David MenchacaLaboratorio Química Bioanalítica, Instituto Polo Tecnológico de Pando, Facultad de Química, Universidad de la República, Uruguay.
Alejandra Rodríguez-HaralambidesLaboratorio Química Bioanalítica, Instituto Polo Tecnológico de Pando, Facultad de Química, Universidad de la República, Uruguay.ORCID 0000-0001-8587-3297
Javier VarelaFacultad de Ciencias, Laboratorio de Química Orgánica y Medicinal, de la República, Uruguay.
Leonor ThomsonFacultad de Ciencias, Instituto de Química Biológica, Laboratorio de Enzimología, Universidad de la República, Montevideo, Uruguay.
Edward M BahnsonDepartment of Cell Biology & Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States of America.ORCID 0000-0001-8578-0517

Funding

Cell-Mediated Targeted Redox Intervention for the Treatment and Prevention of AtherosclerosisK01HL145354 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BAHNSON, EDWARD M · 2020 to 2023
$528k
NHLBI NIH HHS K01 HL145354
6 · The paper itself

Abstract

Atherosclerotic disease is the leading cause of death world-wide. Our goal was to explore the effect of phytocannabinoids on the molecular mechanisms triggering the development of the atheromatous lesion. Three cannabis sativa extracts of different chemotypes were chemically characterized by UPLC-DAD. The capacity of the extracts to prevent the oxidation of LDL, the formation of foam cells and the activation of an inflammatory response by J774 cells, were monitored by UV-Vis spectrometry, confocal-microscopy and western blot. Three varieties of cannabis sativa, with high (E1), intermediate (E2) and low (E3) THC/CBD ratios were selected. The three cannabis extracts inhibited the oxidation of LDL by copper ions and the formation of foam cells by J774.1 cells challenged with oxLDL (ED50 5-12 μg mL-1). The effect of the cannabinoid extracts on the endocytic process was independent of the canonical cannabinoid receptors, CB1 and CB2, but related to the action of non-canonical receptors (TRPV1, TRPV4 and GPR55), involved in calcium signaling. Decreased levels of CD36 and OLR1 scavenger receptors were, at least partially, responsible for the diminished uptake of oxLDL induced by phytocannabinoids. The downregulation of CD36 and OLR1 could be explained by the observed inhibitory effect of the cannabis extracts on the activation of the NFκB pathway by oxLDL. Phytocannabinoids interfere with the main events leading to the development of the atheromatous plaque, opening new venues on atherosclerosis therapy.

Indexed as

AtherosclerosisCannabisFoam CellsLipoproteins, LDLOxidation-ReductionPlant ExtractsAnimalsCD36 AntigensCell LineHumansMiceNF-kappa BCD36 AntigensLipoproteins, LDLNF-kappa Boxidized low density lipoproteinPlant Extracts

Identifiers

PMID39705234
PMCPMC11661628

What OpenQuestion holds

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Registered trials

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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.