Evidence map›Paper›PMID 25517879›Full record

ArticleGut microbes2015

Lactobacillus rhamnosus CNCM I-3690 and the commensal bacterium Faecalibacterium prausnitzii A2-165 exhibit similar protective effects to induced barrier hyper-permeability in mice.

L Laval, R Martin, J N Natividad, F Chain, S Miquel, C Desclée de Maredsous, S Capronnier, H Sokol, E F Verdu, J E T van Hylckama Vlieg and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Gut microbes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

111 citing papers in PubMed, 210 citations in OpenAlex.

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51 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 3 countries.

L Lavala INRA ; Commensal and Probiotics-Host Interactions Laboratory ; UMR 1319 Micalis ; F-78350; Jouy-en-Josas , France.
R Martin
J N Natividad
F Chain
S Miquel
C Desclée de Maredsous
S Capronnier
H Sokol
E F Verdu
J E T van Hylckama Vlieg
L G Bermúdez-Humarán
T Smokvina
P Langella
AgroParisTech · FRDanone (France) · FRDigestive Health Research Institute · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Impaired gut barrier function has been reported in a wide range of diseases and syndromes and in some functional gastrointestinal disorders. In addition, there is increasing evidence that suggests the gut microbiota tightly regulates gut barrier function and recent studies demonstrate that probiotic bacteria can enhance barrier integrity. Here, we aimed to investigate the effects of Lactobacillus rhamnosus CNCM I-3690 on intestinal barrier function. In vitro results using a Caco-2 monolayer cells stimulated with TNF-α confirmed the anti-inflammatory nature of the strain CNCM I-3690 and pointed out a putative role for the protection of the epithelial function. Next, we tested the protective effects of L. rhamnosus CNCM I-3690 in a mouse model of increased colonic permeability. Most importantly, we compared its performance to that of the well-known beneficial human commensal bacterium Faecalibacterium prauznitzii A2-165. Increased colonic permeability was normalized by both strains to a similar degree. Modulation of apical tight junction proteins expression was then analyzed to decipher the mechanism underlying this effect. We showed that CNCM I-3690 partially restored the function of the intestinal barrier and increased the levels of tight junction proteins Occludin and E-cadherin. The results indicate L. rhamnosus CNCM I-3690 is as effective as the commensal anti-inflammatory bacterium F. prausnitzii to treat functional barrier abnormalities.

Indexed as

Animal ExperimentationAnimalsAnti-Inflammatory AgentsCaco-2 CellsClostridiumEpithelial CellsGene Expression ProfilingHumansIntestinal MucosaLacticaseibacillus rhamnosusMaleMice, Inbred C57BLPermeabilityProbioticsTight Junction ProteinsTreatment OutcomeAnti-Inflammatory AgentsTight Junction ProteinsTumor Necrosis Factor-alphaAJs, adherence junctions; CNCM, Collection Nationale de Cultures de Microorganismes; DNBS, DiNitroBenzene Sulfonic; EOS, extremely oxygen sensitive; GVHD, graft-versus-host disease; IBD, inflammatory bowel diseases; IBS, irritable bowel syndrome; LAB, lacapical junction proteinslactobacilliprobiotics

Identifiers

PMID25517879
PMCPMC4615674
OpenAlexW1982040117

What OpenQuestion holds

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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.