Evidence map›Paper›PMID 36157120›Full record

ArticleWorld journal of gastroenterology2022

P2X7 receptor blockade decreases inflammation, apoptosis, and enteric neuron loss during

Ana A Q A Santos, Deiziane V S Costa, Danielle A Foschetti, Antoniella S G Duarte, Conceição S Martins, Pedro M G Soares, Patricia Castelucci, Gerly A C Brito

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Phenotypic switching of gastrointestinal smooth muscle cells and the regulatory role of macrophages: a literature review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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.

Ana A Q A SantosDepartment of Morphology, School of Medicine, Federal University of Ceara, Fortaleza 60430-170, Ceara, Brazil.
Deiziane V S CostaDepartment of Morphology, School of Medicine, Federal University of Ceara, Fortaleza 60430-170, Ceara, Brazil.
Danielle A FoschettiDepartment of Pathology and Legal Medicine, School of Medicine, Federal University of Ceara, Fortaleza 60430-170, Ceara, Brazil.
Antoniella S G DuarteDepartment of Morphology (UFC), Federal University of Ceara, Fortaleza 60430-170, Ceara, Brazil.
Conceição S MartinsDepartment of Morphology, School of Medicine, Federal University of Ceara, Fortaleza 60430-170, Ceara, Brazil.
Pedro M G SoaresDepartment of Morphology, School of Medicine, Federal University of Ceara, Fortaleza 60430-170, Ceara, Brazil.
Patricia CastelucciDepartment of Anatomy, Institute of Biomedical Sciences, University of São Paulo, Sao Paulo 05508-270, Brazil.
Gerly A C BritoDepartment of Morphology, Federal University of Ceara, Fortaleza 60140-170, Ceara, Brazil. gerlybrito@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

aimTo characterize a specific population of TcdA-affected myenteric neurons and investigate the role of the P2X7 receptor in TcdA-induced ileal inflammation, cell death, and the changes in the enteric nervous system in mice.

methodsSwiss mice were used to model TcdA-induced ileitis in ileal loops exposed to TcdA (50 μg/Loop) for 4 h. To investigate the role of the P2X7 receptor, Brilliant Blue G (50 mg/kg, i.p.), which is a nonspecific P2X7 receptor antagonist, or A438079 (0.7 μg/mouse, i.p.), which is a competitive P2X7 receptor antagonist, were injected one hour prior to TcdA challenge. Ileal samples were collected to analyze the expression of the P2X7 receptor (by quantitative real-time polymerase chain reaction and immunohistochemistry), the population of myenteric enteric neurons (immunofluorescence), histological damage, intestinal inflammation, cell death (terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling), neuronal loss, and S100B synthesis (immunohistochemistry).

resultsTcdA upregulated (

conclusionOur findings demonstrated that TcdA induced the upregulation of the P2X7 receptor, which promoted enteric neuron loss, S100B synthesis, tissue damage, inflammation, and cell death in the mouse ileum. These findings contribute to the future directions in understanding the mechanism involved in intestinal dysfunction reported in patients after

Indexed as

Bacterial ToxinsClostridioides difficileIleitisAnimalsApoptosisBiotinCalbindin 2Choline O-AcetyltransferaseDNA NucleotidylexotransferaseEnterotoxinsInflammationInterleukin-6Interleukin-8MiceNeuronsPurinergic P2X Receptor AntagonistsBacterial ToxinsBiotinCalbindin 2Choline O-AcetyltransferaseDNA NucleotidylexotransferaseEnterotoxinsInterleukin-6Interleukin-8Purinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7Tumor Necrosis Factor-alphaClostridioides difficileClostridioides difficile toxin AEnteric gliaEnteric nervous systemEnteric neuronP2X7 receptor

Identifiers

PMID36157120
PMCPMC9403433

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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.