Evidence map›Paper›PMID 37599675›Full record

ArticleFrontiers in nutrition2023

Palmitoylethanolamide counteracts high-fat diet-induced gut dysfunction by reprogramming microbiota composition and affecting tryptophan metabolism.

Claudio Pirozzi, Lorena Coretti, Nicola Opallo, Maria Bove, Chiara Annunziata, Federica Comella, Luigia Turco, Adriano Lama, Luigia Trabace, Rosaria Meli and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in nutrition, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 34 citations in OpenAlex.

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  4. Palmitoylethanolamide in Human and Animal Obesity.Molecules (Basel, Switzerland) · 2026
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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

12 authors at 2 institutions in 1 country.

Claudio PirozziDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Lorena CorettiDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Nicola OpalloDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Maria BoveDepartment of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.
Chiara AnnunziataDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Federica ComellaDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Luigia TurcoDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Adriano LamaDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Luigia TrabaceDepartment of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.
Rosaria MeliDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Francesca LemboDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
Giuseppina Mattace RasoDepartment of Pharmacy, School of Medicine, University of Naples Federico II, Naples, Italy.
University of Naples Federico II · ITUniversity of Foggia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is associated with gastrointestinal (GI) tract and central nervous system (CNS) disorders. High-fat diet (HFD) feeding-induced obesity in mice induces dysbiosis, causing a shift toward bacteria-derived metabolites with detrimental effects on metabolism and inflammation: events often contributing to the onset and progression of both GI and CNS disorders. Palmitoylethanolamide (PEA) is an endogenous lipid mediator with beneficial effects in mouse models of GI and CNS disorders. However, the mechanisms underlining its enteroprotective and neuroprotective effects still need to be fully understood. Here, we aimed to study the effects of PEA on intestinal inflammation and microbiota alterations resulting from lipid overnutrition. Ultramicronized PEA (30 mg/kg/die

Indexed as

gut-brain axisgut microbiotaN-acylethanolaminesobesityserotonin

Identifiers

PMID37599675
PMCPMC10434518
OpenAlexW4385446562

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.