Tier 3 — preclinical

Quercetin Protects Intestinal Barrier Integrity in Inflammation and Oxidative Stress

Olugbenga Balogun, Hye Won Kang
Nutrients 2026 18(13):2169

Bibliography

PubMed
PMID 42451170
PubMed Central
PMC13363914
Funding
Funding was not confirmed from the indexed record; consult the original publication.
Competing interests
The authors declare no conflicts of interest.

Study snapshot

DesignDietary intervention and intestinal mechanism study in mice
ModelAnimal or laboratory evidence
SampleHigh-fat and low-fat diet mouse groups; exact group sizes not stated in the indexed abstract
InterventionDiet with or without 1% quercetin in experimental mice
DurationExperimental feeding schedule; exact duration requires full methods
EndpointsModel-specific outcomes; see methods and findings

What the study showed, in plain terms

Published in 2026, this source examined gut and intestinal health. Design: Dietary intervention and intestinal mechanism study in mice. Sample/model: High-fat and low-fat diet mouse groups; exact group sizes not stated in the indexed abstract. The exposure or intervention was Diet with or without 1% quercetin in experimental mice. Follow-up or treatment period: Experimental feeding schedule; exact duration requires full methods.

Quercetin improved selected intestinal-barrier, inflammatory and signalling measures in high-fat-fed mice.

Animal dietary exposure and mechanistic endpoints. Human gut-repair efficacy, an oral clinical dose and treatment of IBS or IBD were not established.

Continue with Quercetin Data Center

For topic-level interpretation, read Quercetin for Gut Health: Microbiome and Barrier Evidence. This is a related guide; the citation panel separately identifies articles that directly cite this paper.

Key findings

  • Quercetin improved selected intestinal-barrier, inflammatory and signalling measures in high-fat-fed mice.
  • The recorded outcome domains were Model-specific outcomes; see methods and findings.
  • The result applies to the tested exposure: Diet with or without 1% quercetin in experimental mice; Experimental feeding schedule; exact duration requires full methods.

What this study can and cannot tell us

  • Animal dietary exposure and mechanistic endpoints. Human gut-repair efficacy, an oral clinical dose and treatment of IBS or IBD were not established.
  • Cell concentrations, species, disease models and experimental routes cannot be converted directly into an effective or safe oral human regimen.
  • Source basis: Source check: PubMed abstract and indexed metadata; full methods were not independently confirmed for this record. Missing method details, funding information or participant denominators are not inferred.

Citation network

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