Evidence map›Paper›PMID 41984887›Full record

ArticlePloS one2026

Xanthan gum intake modifies the colon microbiota profile and causes mild colon inflammation in rats.

Alessandra B Silva Rischiteli, Artur Francisco Silva-Neto, Paloma Korehisa Maza, Valter Tadeu Boldarine, Daniel Araki Ribeiro, Carolina Foot Gomes Moura, Marina Gomes Galvani, Raquel Galvão Figuerêdo, Giovana Jamar, Mariana de Moura Dias and 5 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

15 authors.

Alessandra B Silva RischiteliDepartment of Physiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.
Artur Francisco Silva-NetoDepartment of Physiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-3182-7425
Paloma Korehisa MazaDepartment of Physiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.
Valter Tadeu BoldarineDepartment of Physiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.
Daniel Araki RibeiroDepartment of Bioscience, Universidade Federal de São Paulo, Instituto de Saúde e Sociedade, Santos, São Paulo, Brazil.
Carolina Foot Gomes MouraDepartment of Bioscience, Universidade Federal de São Paulo, Instituto de Saúde e Sociedade, Santos, São Paulo, Brazil.
Marina Gomes GalvaniDepartment of Bioscience, Universidade Federal de São Paulo, Instituto de Saúde e Sociedade, Santos, São Paulo, Brazil.
Raquel Galvão FiguerêdoCancer Metabolism Research Group, Department of Surgery Laboratório de Investigação Médica (LIM26), Faculdade de Medicina, Universidade de São Paulo, São Paulo, São Paulo, Brazil.
Giovana JamarDepartment of Bioscience, Universidade Federal de São Paulo, Instituto de Saúde e Sociedade, Santos, São Paulo, Brazil.
Mariana de Moura DiasLaboratory of Clinical Analysis and Genomics, Department of Nutrition and Health, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
Larissa Casemiro Pacheco MonteiroLaboratory of Molecular Biotechnology, Department of Biochemistry and Molecular Biology, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
Tiago Antonio de Oliveira MendesLaboratory of Molecular Biotechnology, Department of Biochemistry and Molecular Biology, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
Lila Missae OyamaDepartment of Physiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-7078-6526
Daniela Caetano GonçalvesDepartment of Bioscience, Universidade Federal de São Paulo, Instituto de Saúde e Sociedade, Santos, São Paulo, Brazil.
Claudia Maria Oller do NascimentoDepartment of Physiology, Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xanthan gum is commonly used in the food industry to adjust food consistency and to improve the safety of swallowing liquids and food in people with dysphagia. The pro-inflammatory effect of xanthan gum is acknowledged in the literature. This study aimed to examine the effect of chronic xanthan gum supplementation in the diet on intestinal inflammatory processes in adult Wistar rats at three different doses. After the tenth week of treatment, white adipose tissue (epididymal, retroperitoneal, and mesenteric) was collected, and the distal colon was dissected and processed for cytokine and immunohistochemical analysis. Fecal matter from the colon was used for microbiota analysis. In general, the addition of xanthan gum at all doses promoted an inflammatory state as demonstrated by the high presence of lymphocytes. Also, it modified the content of the pro-inflammatory cytokines IL-1β and TNF-α compared to the control group. Regarding the colon barrier markers, xanthan gum increased the Claudin 2 and ZO-1 levels. The α diversity and relative abundance of Bacterioidetes (B), Firmicutes (F), F/B ratio were similar among the groups. Elusimicrobiota was increased. Our research, using an experimental model, confirmed the clinical assumption that xanthan gum is associated with the development of necrotizing enterocolitis in neonates. We validated the biological mechanism and metabolic pathway in the intestine of the deleterious effect of continuous use of xanthan gum. In conclusion, dietary xanthan gum induced moderate-grade inflammation and modified the colon gut barrier. Recent advances in the study of xanthan gum underscore the need for translational research bridging experimental findings and clinical practice.

Indexed as

ColitisColonMicrobiotaPolysaccharides, BacterialAnimalsCytokinesDietary SupplementsInflammationInterleukin-1betaMaleRatsRats, WistarTumor Necrosis Factor-alphaCytokinesInterleukin-1betaPolysaccharides, BacterialTumor Necrosis Factor-alphaxanthan gum

Identifiers

PMID41984887
PMCPMC13082600

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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.