Evidence map›Paper›PMID 41409292›Full record

ArticleFrontiers in immunology2025

Immunomodulatory and anti-inflammatory effects of agave fructans in atopic dermatitis: gut microbiota and short-chain fatty acid implication.

Marcela Rios-Carlos, Mariela Jiménez, Daniel Cervantes-García, Laura Elena Córdova-Dávalos, Lidia E Verduzco, Francisco Javier Enríquez-Medrano, Omar Fabela-Sánchez, Luis G Bermúdez-Humarán, Eva Salinas

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Bioactive Potential ofPharmaceuticals (Basel, Switzerland) · 2026
    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

9 authors.

Marcela Rios-CarlosLaboratory of Immunology, Department of Microbiology, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Mariela JiménezLaboratory of Immunology, Department of Microbiology, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Daniel Cervantes-GarcíaLaboratory of Immunology, Department of Microbiology, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Laura Elena Córdova-DávalosLaboratory of Immunology, Department of Microbiology, Autonomous University of Aguascalientes, Aguascalientes, Mexico.
Lidia E VerduzcoDepartment of Sustainable and Protected Agriculture, Technological University of Northern Aguascalientes, La Estación Rincón, Rincón de Romos, Aguascalientes, Mexico.
Francisco Javier Enríquez-MedranoDepartment of Macromolecular Chemistry and Nanomaterials, Center for Research in Applied Chemistry (CIQA), Saltillo, Mexico.
Omar Fabela-SánchezSecretariat of Science, Humanities, Technologies and Innovation (SECIHTI), Mexico City, Mexico.
Luis G Bermúdez-HumaránMicalis Institute, Université Paris-Saclay, INRAE, AgroParisTech, Jouy-en-Josas, France.
Eva SalinasLaboratory of Immunology, Department of Microbiology, Autonomous University of Aguascalientes, Aguascalientes, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Atopic dermatitis (AD) is a chronic inflammatory skin disorder resulting from the interplay of genetic and environmental factors, with a dysregulated type-2 immune response. The association between AD onset and intestinal dysbiosis supports research into nutritional interventions such as fermentable fibers intake. Agave-derived fructans (AFs) display prebiotic activity, modulating gut microbial communities that may positively influence immune functions. In this study, we evaluated the anti-inflammatory and immunomodulatory effects of oral AFs in a rat AD model. Methods: AD-like lesions were induced in the ear of Wistar rats by frequent application of 2,4-dinitrochlorobenzene (DNCB). AFs (0.1, 1, 5 g/kg) from Results: Treatment with AFs at 0.1 g/kg significantly reduced ear thickness at 1- and 6-hours post-DNCB application. Similarly, ear edema at 1 hour was attenuated, and inhibition of the NF-κB inflammatory pathway was detected. After AFs treatment at 0.1 g/kg, serum IgE levels were normalized to those of control animals. All AFs significantly decreased dermal mast cell and eosinophil counts, as well as epidermal thickening, with greater efficacy observed at lower doses. The scratching behavior remained unchanged across groups. AFs reduced Conclusion: AFs exhibit anti-inflammatory, immunoregulatory, and microbiota-modulatory properties in both the gut and skin compartments, in a non-linear dose-response manner. These findings suggest that the intake of AFs may contribute to the therapeutic management of AD.

Indexed as

AgaveAnti-Inflammatory AgentsDermatitis, AtopicFatty Acids, VolatileFructansGastrointestinal MicrobiomeAnimalsCytokinesDinitrochlorobenzeneDisease Models, AnimalMalePrebioticsRatsRats, WistarSkinAnti-Inflammatory AgentsCytokinesDinitrochlorobenzeneFatty Acids, VolatileFructansPrebioticsagave fructansatopic dermatitismicrobiotaprebioticshort-chain fatty acids

Identifiers

PMID41409292
PMCPMC12705406

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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.