Evidence map›Paper›PMID 37735539›Full record

ArticleCommunications biology2023

Olive oil-derived endocannabinoid-like mediators inhibit palatable food-induced reward and obesity.

Nicola Forte, Charlène Roussel, Brenda Marfella, Anna Lauritano, Rosaria Villano, Elvira De Leonibus, Emanuela Salviati, Tina Khalilzadehsabet, Giada Giorgini, Cristoforo Silvestri and 4 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
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  8. Nutrients · 2025
    Article
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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 7 institutions in 3 countries.

Nicola ForteInstitute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy.ORCID http://orcid.org/0000-0001-7488-7992
Charlène Roussel *Heart and Lung Research Institute of Université Laval, Québec City, QC, Canada.ORCID http://orcid.org/0000-0002-7127-8152
Brenda Marfella *Institute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy.ORCID http://orcid.org/0009-0000-3571-3906
Anna LauritanoInstitute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy.
Rosaria VillanoInstitute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy.
Elvira De LeonibusTelethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy.
Emanuela SalviatiDepartment of Pharmacy, University of Salerno, Fisciano (SA), Italy.
Tina KhalilzadehsabetHeart and Lung Research Institute of Université Laval, Québec City, QC, Canada.ORCID http://orcid.org/0000-0003-4631-3806
Giada GiorginiHeart and Lung Research Institute of Université Laval, Québec City, QC, Canada.
Cristoforo SilvestriHeart and Lung Research Institute of Université Laval, Québec City, QC, Canada.ORCID http://orcid.org/0000-0001-5635-1545
Fabiana PiscitelliInstitute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy.
Maria Pina MollicaDepartment of Biology, University of Naples Federico II, 80126, Naples, Italy.
Vincenzo Di MarzoInstitute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy. vdimarzo@icb.cnr.it.ORCID http://orcid.org/0000-0002-1490-3070
Luigia CristinoInstitute of Biomolecular Chemistry, National Research Council of Italy, Via Campi Flegrei 34, 80078, Pozzuoli (NA), Italy. luigia.cristino@icb.cnr.it.ORCID http://orcid.org/0000-0002-0182-4699
Institute of Applied Science and Intelligent Systems · ITUniversité Laval · CALung Institute · USNational Research Council · ITTecnologie Avanzate (Italy) · ITTelethon Institute Of Genetics And Medicine · ITUniversity of Salerno · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N-oleoylglycine (OlGly), a lipid derived from the basic component of olive oil, oleic acid, and N-oleoylalanine (OlAla) are endocannabinoid-like mediators. We report that OlGly and OlAla, by activating the peroxisome proliferator-activated receptor alpha (PPARα), reduce the rewarding properties of a highly palatable food, dopamine neuron firing in the ventral tegmental area, and the obesogenic effect of a high-fat diet rich in lard (HFD-L). An isocaloric olive oil HFD (HFD-O) reduced body weight gain compared to the HFD-L, in a manner reversed by PPARα antagonism, and enhanced brain and intestinal OlGly levels and gut microbial diversity. OlGly or OlAla treatment of HFD-L mice resulted in gut microbiota taxonomic changes partly similar to those induced by HFD-O. We suggest that OlGly and OlAla control body weight by counteracting highly palatable food overconsumption, and possibly rebalancing the gut microbiota, and provide a potential new mechanism of action for the obeso-preventive effects of olive oil-rich diets.

Indexed as

EndocannabinoidsPPAR alphaAnimalsBody WeightMiceObesityOlive OilEndocannabinoidsOlive OilPPAR alpha

Identifiers

PMID37735539
PMCPMC10514336
OpenAlexW4386935332

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.