Evidence map›Paper›PMID 37365380›Full record

ArticleWorld journal of microbiology & biotechnology2023

Synergistic synbiotic containing fructooligosaccharides and Lactobacillus delbrueckii CIDCA 133 alleviates chemotherapy-induced intestinal mucositis in mice.

Laísa Macedo Tavares, Luís Cláudio Lima de Jesus, Viviane Lima Batista, Fernanda Alvarenga Lima Barroso, Andria Dos Santos Freitas, Gabriela Munis Campos, Monique Ferrary Américo, Tales Fernando da Silva, Nina Dias Coelho-Rocha, Giovanna Angeli Belo and 10 more

Abstract read
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In one paragraph

Article in World journal of microbiology & biotechnology, 2023. 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
1.6field-weighted citation impact, top 16% of its field
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, 6 citations in OpenAlex.

  1. Review
  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

20 authors at 2 institutions in 2 countries.

Laísa Macedo Tavares *Department of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Luís Cláudio Lima de Jesus *Department of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Viviane Lima BatistaDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Fernanda Alvarenga Lima BarrosoDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Andria Dos Santos FreitasDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Gabriela Munis CamposDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Monique Ferrary AméricoDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Tales Fernando da SilvaDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Nina Dias Coelho-RochaDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Giovanna Angeli BeloDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Mariana Martins DrumondFederal Center for Technological Education of Minas Gerais, Department of Biological Sciences, Belo Horizonte, Brazil.
Pamela Mancha-AgrestiFederal Center for Technological Education of Minas Gerais, Department of Biological Sciences, Belo Horizonte, Brazil.
Kátia Duarte VitalDepartment of Clinical and Toxicological Analysis, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Simone Odília Antunes FernandesDepartment of Clinical and Toxicological Analysis, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Valbert Nascimento CardosoDepartment of Clinical and Toxicological Analysis, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Alexander BirbrairDepartment of General Pathology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Enio FerreiraDepartment of General Pathology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Flaviano Santos MartinsDepartment of Microbiology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Juliana Guimarães LagunaDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Vasco AzevedoDepartment of Genetics, Ecology, and Evolution, Federal University of Minas Gerais, Belo Horizonte, Brazil. vascoariston@gmail.com.
Universidade Federal de Minas Gerais · BRFederal Center for Technological Education of Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal mucositis is a commonly reported side effect in oncology patients undergoing chemotherapy and radiotherapy. Probiotics, prebiotics, and synbiotics have been investigated as alternative therapeutic approaches against intestinal mucositis due to their well-known anti-inflammatory properties and health benefits to the host. Previous studies showed that the potential probiotic Lactobacillus delbrueckii CIDCA 133 and the prebiotic Fructooligosaccharides (FOS) alleviated the 5-Fluorouracil (5-FU) chemotherapy-induced intestinal mucosa damage. Based on these previous beneficial effects, this work evaluated the anti-inflammatory property of the synbiotic formulation containing L. delbrueckii CIDCA 133 and FOS in mice intestinal mucosa inflammation induced by 5-FU. This work showed that the synbiotic formulation was able to modulate inflammatory parameters, including reduction of cellular inflammatory infiltration, gene expression downregulation of Tlr2, Nfkb1, and Tnf, and upregulation of the immunoregulatory Il10 cytokine, thus protecting the intestinal mucosa from epithelial damage caused by the 5-FU. The synbiotic also improved the epithelial barrier function by upregulating mRNA transcript levels of the short chain fatty acid (SCFA)-associated GPR43 receptor and the occludin tight junction protein, with the subsequent reduction of paracellular intestinal permeability. The data obtained showed that this synbiotic formulation could be a promising adjuvant treatment to be explored against inflammatory damage caused by 5-FU chemotherapy.

Indexed as

Antineoplastic AgentsLactobacillus delbrueckiiMucositisProbioticsSynbioticsAnimalsFluorouracilIntestinal MucosaMiceOligosaccharidesPrebioticsAntineoplastic AgentsFluorouracilfructooligosaccharideOligosaccharidesPrebioticsChemotherapyImmunomodulationIntestinal barrierIntestinal damageSynbiotic

Identifiers

PMID37365380
OpenAlexW4382182169

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.