Evidence map›Paper›PMID 42204364›Full record

ArticlePediatric research2026

Urolithin A attenuates inflammation and enhances barrier integrity in an experimental NEC-in-a-Dish model.

Ahmad Salah Sami, Gergely Mozes, Corey M Jania, Erika Maldonado-Rosado, Austin J Hepperla, Nadia Ghetie, Vikram Puri, Lauren Bolzan, Yukihiro Yamaguchi, Lauren C Frazer and 4 more

Abstract read
In one paragraph

Article in Pediatric research, 2026. 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. Article
  2. Article
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.

Ahmad Salah SamiDivision of Pediatric Gastroenterology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Gergely MozesDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Corey M JaniaDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Erika Maldonado-RosadoBioinformatics and Analytics Research Collaborative (BARC), University of North Carolina, Chapel Hill, NC, USA.
Austin J HepperlaBioinformatics and Analytics Research Collaborative (BARC), University of North Carolina, Chapel Hill, NC, USA.
Nadia GhetieCarnegie Mellon University, Pittsburgh, PA, USA.
Vikram PuriDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Lauren BolzanDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Yukihiro YamaguchiDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Lauren C FrazerDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Stephen MackayDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Venkatakrishna JalaDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Natalia S AkopyantsDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Misty GoodDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. mistygood@unc.edu.ORCID http://orcid.org/0000-0002-0264-5721

Funding

Point of Care maternal milk concentration device to optimize neonatal growth with targeted nutrition supportR44HD110306 · NICHD · MOTHER'S MILK IS BEST, INC. · PI Elizabeth Randall Nelson · 2023 to 2026
$4.2M
Non-invasive analysis of methylated cell free DNA in necrotizing enterocolitisR01DK124614 · NIDDK · WASHINGTON UNIVERSITY · PI GOOD, MISTY L, PETERS, DAVID GERARD · 2021 to 2024
$2.5M
Neonatal gut-on-a-chip platform for high content drug testing and precision medicineR01HD105301 · NICHD · WASHINGTON UNIVERSITY · PI GOOD, MISTY L, MAGNESS, SCOTT T · 2021 to 2024
$2.4M
Reprogramming intestinal immunity in preterm neonates to prevent and cure necrotizing enterocolitisDP1DK140012 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MISTY L GOOD · 2024 to 2026
$2.2M
Regulation of signaling pathways mediating epithelial cell injury in the neonatal intestineK08DK140604 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRAZER, LAUREN CAROLE · 2024 to 2025
$348k
NIAID NIH HHS L40 AI178971NICHD NIH HHS R01 HD105301NICHD NIH HHS R44 HD110306NIDDK NIH HHS DP1 DK140012NIDDK NIH HHS K08 DK140604NIDDK NIH HHS R01 DK124614
6 · The paper itself

Abstract

background and hypothesisNecrotizing enterocolitis (NEC) is a devastating gastrointestinal disease in preterm infants, characterized by exaggerated inflammation and poorly understood pathogenesis. Aryl hydrocarbon receptor (AhR) signaling has been shown to reduce intestinal inflammation in colitis models. In these models, a microbial-derived AhR ligand, Urolithin A (UroA), has demonstrated anti-inflammatory properties and improved gut barrier function. We hypothesize that UroA attenuates inflammation and enhances epithelial barrier integrity in an in vitro NEC-in-a-Dish model.

methodsEnteroids derived from human neonatal intestinal tissue were pretreated with 100 µM UroA or 0.1% DMSO (vehicle) before a 6-h incubation with dysbiotic enteric bacteria cultured from an infant with NEC totalis (NEC-in-a-Dish). RNA sequencing was performed and analyzed for pro-inflammatory cytokine expression and pathway enrichment. Epithelial barrier integrity was evaluated using a fluorescein-isothiocyanate-dextran permeability assay on two-dimensional monolayers.

resultsUroA pretreatment decreased pro-inflammatory cytokine expression and enhanced barrier integrity. Transcriptomic analysis showed downregulation of NOD-like receptor, IL-17/Th17, NF-κB, and TLR signaling, and upregulation of AhR-dependent genes involved in antioxidant responses.

conclusionUroA reduces inflammation and strengthens epithelial barrier integrity in a NEC-in-a-Dish model through a variety of mechanisms. These findings support further investigation of dietary-derived metabolites as potential preventative strategies for NEC in preterm infants. IMPACT: Urolithin A (UroA), a microbiota-derived metabolite, reduces inflammation and enhances epithelial barrier integrity in a human neonatal in vitro model of necrotizing enterocolitis (NEC). This study is the first to demonstrate the protective effects of UroA in the neonatal small intestinal epithelium using a NEC-in-a-Dish model system. It also expands on the current understanding of the mechanism of action of UroA by revealing modulation of key inflammatory and oxidative stress pathways in neonatal tissue. These findings identify UroA as a promising candidate for dietary-based prevention strategies targeting epithelial injury in NEC.

Identifiers

PMID42204364
PMCPMC13641196

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