Evidence map›Paper›PMID 34958108›Full record

ArticleMolecular medicine reports2022

CD4

Ivonne Maciel Arciniega-Martínez, Aldo Arturo Reséndiz Albor, Luz María Cárdenas Jaramillo, Juan Manuel Gutiérrez-Meza, Ramcés Falfán-Valencia, Belen Mendoza Arroyo, Mariazell Yépez-Ortega, Judith Pacheco-Yépez, Edgar Abarca-Rojano

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors at 2 institutions in 1 country.

Ivonne Maciel Arciniega-MartínezPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Aldo Arturo Reséndiz AlborPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Luz María Cárdenas JaramilloMorphology Coordination, Department of Basic Disciplinary Training, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Juan Manuel Gutiérrez-MezaPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Ramcés Falfán-ValenciaHLA Laboratory, National Institute of Respiratory Diseases Ismael Cosío Villegas, 14080 Mexico City, México.
Belen Mendoza ArroyoPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Mariazell Yépez-OrtegaPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Judith Pacheco-YépezPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Edgar Abarca-RojanoPostgraduate Studies and Research Section, Superior School of Medicine, National Polytechnic Institute, 11340 Mexico City, México.
Tecnológico Nacional de México · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Life stress may influence symptom onset and severity in certain gastrointestinal disorders in association with a dysregulated intestinal barrier. It has been widely accepted that stress triggers the hypothalamus‑pituitary‑adrenal (HPA) axis, releasing corticosterone, which promotes intestinal permeability. In response, colonic inflammation alters mucosal immune homeostasis and destroys the colonic architecture, leading to severe intestinal diseases. Endogenous substance P (SP) does not inhibit the initial extent of the HPA axis response to restraint stress, but it reduces the duration of the stress, suggesting that SP plays an important role in the transition between acute and chronic stress. The present study aimed to investigate the effect of two groups of mice exposed to stress, including acute and chronic stress. The corticosterone was evaluated by ELISA, colon samples were obtained to detected polymorphonuclear cells by hematoxylin and eosin staining, goblet and mast cells were identified by immunocytochemistry and cytokine‑producing CD4

Indexed as

AnimalsCadherinsCD4-Positive T-LymphocytesClaudin-1ColonCorticosteroneDisease Models, AnimalGoblet CellsInflammationInterleukin-4MaleMast CellsMiceMice, Inbred BALB CMucous MembraneStress Disorders, Traumatic, AcuteCadherinsCdh1 protein, mouseClaudin-1Cldn1 protein, mouseCorticosteroneIl4 protein, mouseInterleukin-4Substance Pacute stressCD4+/IL‑4+ lymphocyteschronic stresscolonintestinemast and goblet cellssubstance P

Identifiers

PMID34958108
PMCPMC8767552
OpenAlexW4200183851

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.