Evidence map›Paper›PMID 27219328›Full record

ArticlePloS one2016

Palmitoylethanolamide Modulates Inflammation-Associated Vascular Endothelial Growth Factor (VEGF) Signaling via the Akt/mTOR Pathway in a Selective Peroxisome Proliferator-Activated Receptor Alpha (PPAR-α)-Dependent Manner.

Giovanni Sarnelli, Alessandra D'Alessandro, Teresa Iuvone, Elena Capoccia, Stefano Gigli, Marcella Pesce, Luisa Seguella, Nicola Nobile, Giovanni Aprea, Francesco Maione and 4 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07609810 (The Effect of Palmitoylethanolamide on the Clinical Outcomes in Ulcerative Colitis Patients), which is not on this map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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.

NCT07609810 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

The Effect of Palmitoylethanolamide on the Clinical Outcomes in Ulcerative Colitis Patients

TypeinterventionalSponsorAin Shams UniversityRan2026 to 2029Enrolled60ConditionsUlcerative Colitis (UC)ArmsPalmitoylethanolamide (PEA), Placebo
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Endothelial CEPT1 Promotes Angiogenesis Through PPARα and VEGF-A Signaling.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. EngineeredInternational journal of molecular sciences · 2021
    Article
  15. A Palmitoylethanolamide ProducingFrontiers in pharmacology · 2021
    Article
  16. The Basal Pharmacology of Palmitoylethanolamide.International journal of molecular sciences · 2020
    Review
  17. Article
  18. Review
  19. Article
  20. 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

14 authors at 2 institutions in 1 country.

Giovanni SarnelliDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Alessandra D'AlessandroDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Teresa IuvoneDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Elena CapocciaDepartment of Physiology and Pharmacology 'Vittorio Erspamer', La Sapienza University of Rome, Rome, Italy.
Stefano GigliDepartment of Physiology and Pharmacology 'Vittorio Erspamer', La Sapienza University of Rome, Rome, Italy.
Marcella PesceDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Luisa SeguellaDepartment of Physiology and Pharmacology 'Vittorio Erspamer', La Sapienza University of Rome, Rome, Italy.
Nicola NobileDepartment of Physiology and Pharmacology 'Vittorio Erspamer', La Sapienza University of Rome, Rome, Italy.
Giovanni ApreaDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Francesco MaioneDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Giovanni Domenico de PalmaDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Rosario CuomoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Luca SteardoDepartment of Physiology and Pharmacology 'Vittorio Erspamer', La Sapienza University of Rome, Rome, Italy.
Giuseppe EspositoDepartment of Physiology and Pharmacology 'Vittorio Erspamer', La Sapienza University of Rome, Rome, Italy.
University of Naples Federico II · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimAngiogenesis is emerging as a pivotal process in chronic inflammatory pathologies, promoting immune infiltration and prompting carcinogenesis. Ulcerative Colitis (UC) and Crohn's Disease (CD) represent paradigmatic examples of intestinal chronic inflammatory conditions in which the process of neovascularization correlates with the severity and progression of the diseases. Molecules able to target the angiogenesis have thus the potential to synergistically affect the disease course. Beyond its anti-inflammatory effect, palmitoylethanolamide (PEA) is able to reduce angiogenesis in several chronic inflammatory conditions, but no data about its anti-angiogenic activity in colitis have been produced, yet.

methodsThe effects of PEA on inflammation-associated angiogenesis in mice with dextran sulphate sodium (DSS)-induced colitis and in patients with UC were assessed. The release of Vascular Endothelial Growth Factor (VEGF), the hemoglobin tissue content, the expression of CD31 and of phosphatidylinositol 3-kinase/Akt/mammalian-target-of-rapamycin (mTOR) signaling axis were all evaluated in the presence of different concentrations of PEA and concomitant administration of PPAR-α and -γ antagonists.

resultsOur results demonstrated that PEA, in a selective peroxisome proliferator activated receptor (PPAR)-α dependent mechanism, inhibits colitis-associated angiogenesis, decreasing VEGF release and new vessels formation. Furthermore, we demonstrated that the mTOR/Akt axis regulates, at least partly, the angiogenic process in IBD and that PEA directly affects this pathway.

conclusionsOur results suggest that PEA may improve inflammation-driven angiogenesis in colonic mucosa, thus reducing the mucosal damage and potentially affecting disease progression and the shift towards the carcinogenesis.

Indexed as

AdultAmidesAnimalsCells, CulturedColitisColitis, UlcerativeDextran SulfateDisease Models, AnimalEthanolaminesFemaleHumansMaleMiceMiddle AgedPalmitic AcidsPPAR alphaAmidesDextran SulfateEthanolaminesMTOR protein, humanpalmidrolPalmitic AcidsPPAR alphaProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID27219328
PMCPMC4878779
OpenAlexW2406668813

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.