Evidence map›Paper›PMID 42123701›Full record

ArticleInternational journal of molecular sciences2026

Phenolic Compounds of Grape Pomace Skin Released During SHIME Colonic Fermentation Shape the Transcriptomic Profile of Tight Junctions, Improving the Barrier Properties in Caco-2 Cells.

Miltha Hidalgo, Francisca Vera, Alina Concepción-Alvarez, Vanessa Rubio, Bárbara Railef, Jorge Meneses-Pacheco, Macarena Moreno, Martina Oyarzún, Adriano Costa de Camargo, Raquel Bridi and 6 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Miltha HidalgoLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0003-2946-9470
Francisca VeraLaboratorio de Genómica y Genética de Interacciones Biológicas (LG2IB), Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0002-8515-7810
Alina Concepción-AlvarezLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0001-6161-5998
Vanessa RubioLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.
Bárbara RailefLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0009-0001-5067-0948
Jorge Meneses-PachecoLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0009-0007-7027-4778
Macarena MorenoLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.
Martina OyarzúnLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.
Adriano Costa de CamargoInstituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0001-9404-1193
Raquel BridiDepartment of Pharmacological and Toxicological Chemistry, Faculty of Chemical and Pharmaceutical Sciences, Universidad de Chile, Santiago 8380000, Chile.ORCID 0000-0002-3891-5770
Karen FuenzalidaLaboratorio de Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0001-8829-7336
Elva GonzalesLaboratorio Nutribreeding, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0003-4613-3020
Igor PachecoLaboratorio Nutribreeding, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0001-5057-0464
Carolina AñazcoLaboratorio de Bioquímica Nutricional, Escuela de Nutrición y Dietética, Carrera de Nutrición y Dietética, Facultad de Ciencias de la Rehabilitación y Calidad de Vida, Universidad San Sebastián, General Lagos #1190, Valdivia 5110773, Chile.ORCID 0000-0003-1311-9492
Rodrigo PulgarLaboratorio de Genómica y Genética de Interacciones Biológicas (LG2IB), Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.
Omar PorrasLaboratorio de Investigación en Nutrición Funcional, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, El Líbano 5524, Santiago 7830490, Chile.ORCID 0000-0001-6314-9345

Funding

Agencia Nacional de Investigación y Desarrollo 1212026Agencia Nacional de Investigación y Desarrollo 1221848Agencia Nacional de Investigación y Desarrollo 3240669Agencia Nacional de Investigación y Desarrollo EQM170092Institute of Nutrition and Food Technology Puente Research INTA/DID 2023Institute of Nutrition and Food Technology Research Doctoral Thesis Completion Project INTA/DID 2024
6 · The paper itself

Abstract

The association between dietary fiber and phenolic compounds allows the latter to reach the colon, where most polysaccharides undergo fermentation. This bioprocessing weakens the matrix and promotes the release of the phenolic compounds, which then exert beneficial effects on intestinal function. Although this notion is widely accepted, supporting evidence remains scarce. In this study, we subjected grape pomace skin to in vitro digestion to obtain an indigestible fraction suitable for SHIME bioreactors. Throughout these stages, we observed a sequential increase in the release of phenolic compounds, with colonic fermentation playing an important role. Although we did not observe an increase in short-chain fatty acid (SCFA) production by the gut microbiota, we performed a repeated-challenge design on differentiated Caco-2 monolayers. With this approach, we found that the phenolic-rich ferment prevented the transepithelial electrical resistance (TEER) drop on the second challenge and modulated the transcriptomic profile assessed by RNA-seq. Our findings indicate that the Caco-2 cellular responses mentioned above were SCFA-independent and likely due to the differential impact of phenolic compound load after colonic fermentation of grape pomace skin.

Indexed as

ColonFermentationPhenolsTight JunctionsTranscriptomeVitisCaco-2 CellsFatty Acids, VolatileHumansIntestinal Barrier FunctionFatty Acids, VolatilePhenolsCaco-2human colonic fermentationphenolic compoundsRNA-seqSCFATEER

Identifiers

PMID42123701
PMCPMC13163868

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Registered trials

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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.