Evidence map›Paper›PMID 41390618›Full record

ArticleBMC microbiology2025

The effects of postbiotics and glycyrrhetinic acid on immune response and inflammation-related genes during H. pylori eradication therapy.

Erhan Tek, Nizami Duran, Elif Yaprak Colak, Gulay Gulbol Duran, Tuncer Kutlu, Hamdullah Suphi Bayraktar, Sibel Dagli, Mehmet Demir

Abstract read
In one paragraph

Article in BMC microbiology, 2025. 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
–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

2 citing papers in PubMed.

  1. Combined Effect ofFoods (Basel, Switzerland) · 2026
    Article
  2. Review
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

8 authors.

Erhan TekDepartment of Medical Microbiology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.
Nizami DuranDepartment of Medical Microbiology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye. nduran@mku.edu.tr.ORCID 0000-0002-2766-3491
Elif Yaprak ColakDepartment of Medical Microbiology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.
Gulay Gulbol DuranDepartment of Medical Biology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.
Tuncer KutluDepartment of Pathology, Veterinary Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.
Hamdullah Suphi BayraktarDepartment of Medical Microbiology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.
Sibel DagliDepartment of Medical Microbiology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.
Mehmet DemirDepartment of Gastroenterology, Medical Faculty, Hatay Mustafa Kemal University, Antakya-Hatay, 31060, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThis study aims to test the effectiveness of postbiotics from Streptococcus thermophilus and Lactobacillus casei, along with Glycyrrhetinic acid, against H. pylori in both AGS cells (a human gastric adenocarcinoma cell line) and an experimental rat gastritis model.

methodThe effectiveness of the compounds (postbiotics and G. acid) against H. pylori was evaluated by measuring the expression levels of various genes, including NF-κB, IL-1β, IL-6, IL-8, IL-10, TNF-α, COX-2, FOX-M1, and IL-33 in AGS cells using the Real-Time PCR method. Additionally, bacterial loads in gastric tissue were quantified using culture-based colony-forming unit (CFU) analysis and expressed as log₁₀ CFU/g. The study also evaluated the effectiveness of combinations of these components in the rat gastritis model through microbiological and histopathological analyses.

resultsThe postbiotics of S. thermophilus and L. casei have shown a significant reduction in the expression level of NF-κB when compared to the control group. The S. thermophilus plus L. casei treatment group showed a 10-fold decrease in NF-κB expression, while the G. acid plus L. casei treatment group showed a 5-fold decrease. TNF-α expression levels were also lower in the S. thermophilus and L. casei treatment groups with 10-fold and 5-fold reductions, respectively. The expression of IL-1β was significantly reduced in all treatment groups compared to the control group, with a 10-fold decrease in expression. The S. thermophilus plus L. casei treatment group exhibited a 10-fold reduction in IL-6 release, a proinflammatory cytokine. Similarly, the expression of IL-8 was reduced by 10-fold and 2-fold in the S. thermophilus and L. casei treatment groups, respectively. Additionally, bacterial loads in gastric tissue were quantified using culture-based colony-forming unit (CFU) analysis and expressed as log₁₀ CFU/g. The mean bacterial load in the infected control group was 6.14 ± 0.18 log₁₀ CFU/g, while the quaternary treatment group (S. thermophilus + L. casei + G. acid + antibiotic) achieved complete eradication with no detectable colonies (0.00 ± 0.00 log₁₀ CFU/g). Ternary and binary treatment groups exhibited intermediate bacterial loads, ranging from approximately 1.63 ± 0.09 to 3.24 ± 0.17 log₁₀ CFU/g, indicating partial efficacy compared to the control group.

conclusionThese promising findings can pave the way for the development of novel therapeutic approaches for treating H. pylori-associated gastritis. The combination of molecular (gene expression) and microbiological (CFU) data demonstrates the multi-dimensional efficacy of postbiotics and glycyrrhetinic acid as potential adjunctive agents.

Indexed as

GastritisGlycyrrhetinic AcidHelicobacter InfectionsHelicobacter pyloriLacticaseibacillus caseiStreptococcus thermophilusAnimalsBacterial LoadCell Line, TumorCytokinesDisease Models, AnimalGene Expression ProfilingHumansMaleRatsCytokinesGlycyrrhetinic AcidAGS cell lineGlycyrrhetinic acidH.pyloriInflammation-related gene expressionL.caseiMicrobiological eradicationPostbioticsS.thermophilus

Identifiers

PMID41390618
PMCPMC12821235

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.