Evidence map›Paper›PMID 36430244›Full record

ArticleInternational journal of molecular sciences2022

Proton Pump Inhibitor Pantoprazole Modulates Intestinal Microbiota and Induces TLR4 Signaling and Fibrosis in Mouse Liver.

Heloisa B Assalin, Kelly Cristiane Gabriel De Almeida, Dioze Guadagnini, Andrey Santos, Caio J Teixeira, Silvana Bordin, Guilherme Z Rocha, Mario J A Saad

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Heloisa B AssalinDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13080-655, SP, Brazil.ORCID 0000-0003-1269-9624
Kelly Cristiane Gabriel De AlmeidaDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13080-655, SP, Brazil.
Dioze GuadagniniDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13080-655, SP, Brazil.
Andrey SantosDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13080-655, SP, Brazil.
Caio J TeixeiraDepartment of Physiology and Biophysics, Institute of Biomedical Science, University of Sao Paulo, Sao Paulo 05508-000, SP, Brazil.ORCID 0000-0002-4951-1130
Silvana BordinDepartment of Physiology and Biophysics, Institute of Biomedical Science, University of Sao Paulo, Sao Paulo 05508-000, SP, Brazil.ORCID 0000-0002-0192-8869
Guilherme Z RochaDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13080-655, SP, Brazil.ORCID 0000-0002-7403-3230
Mario J A SaadDepartment of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13080-655, SP, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade de São Paulo · BR

Funding

National Council for Scientific and Technological Development INCT Obesidade e Diabetes CNPq (465693/2014-8)São Paulo Research Foundation 2014/50907-5; 2019/03196-0; 2020/06397-3
6 · The paper itself

Abstract

Proton pump inhibitors (PPIs) are one of the most prescribed drugs around the world. PPIs induce microbiota modulation such as obesity both in humans and in animal models. However, since PPIs can induce microbiota modulation despite the absence of a high-fat diet or weight gain, it is an interesting model to correlate microbiota modulation with the establishment of non-alcoholic fatty liver disease (NAFLD). We investigated the effect of pantoprazole treatment on TLR4 signaling and liver histology in C57BL/6J mice for 60 days, trying to correlate microbiota modulation with some aspects of liver injury. We performed glucose (GTT) and insulin (ITT) tolerance tests, serum lipopolysaccharide (LPS) dosage, liver histology, liver and intestine extraction for Western blot and qPCR. Fecal microbiota were investigated via metagenomics. Chronic treatment with pantoprazole induced microbiota modulation and impaired ileum barrier integrity, without an association with insulin resistance. Furthermore, increased circulating LPS and increased Toll-like receptor 4 (TLR4) and TGFβ downstream signaling may have an important role in the development of the observed liver microvesicular steatosis and fibrosis. Finally, this model of PPI-induced changes in microbiota might be useful to investigate liver microvesicular steatosis and fibrosis.

Indexed as

Gastrointestinal MicrobiomeNon-alcoholic Fatty Liver DiseaseAnimalsFibrosisHumansLipopolysaccharidesMiceMice, Inbred C57BLPantoprazoleProton Pump InhibitorsToll-Like Receptor 4LipopolysaccharidesPantoprazoleProton Pump InhibitorsTLR4 protein, humanTlr4 protein, mouseToll-Like Receptor 4liver steatosismicrobiotaproton pump inhibitors

Identifiers

PMID36430244
PMCPMC9693486
OpenAlexW4308873524

What OpenQuestion holds

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LicenceCC BY
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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.