Evidence map›Paper›PMID 32286500›Full record

ArticleScientific reports2020

Melatonin modulates red-ox state and decreases viability of rat pancreatic stellate cells.

Antonio Gonzalez, Matias Estaras, Salome Martinez-Morcillo, Remigio Martinez, Alfredo García, Mario Estévez, Patricia Santofimia-Castaño, Jose A Tapia, Noelia Moreno, Marcos Pérez-López and 8 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

18 authors.

Antonio GonzalezInstitute of Molecular Pathology Biomarkers, University of Extremadura, Caceres, Spain. agmateos@unex.es.ORCID http://orcid.org/0000-0001-8380-0270
Matias EstarasInstitute of Molecular Pathology Biomarkers, University of Extremadura, Caceres, Spain.
Salome Martinez-MorcilloUnit of Toxicology, Veterinary Faculty, University of Extremadura, Caceres, Spain.
Remigio MartinezDepartment of Animal Health, Veterinary Faculty, University of Extremadura, Caceres, Spain.ORCID http://orcid.org/0000-0002-5908-9447
Alfredo GarcíaDepartment of Animal Production, CICYTEX-La Orden, Guadajira, Badajoz, Spain.
Mario EstévezIPROCAR Research Institute, Food Technology, University of Extremadura, 10003, Cáceres, Spain.ORCID http://orcid.org/0000-0002-8509-2789
Patricia Santofimia-CastañoCentre de Recherche en Cancérologie de Marseille, INSERM U1068, CNRS UMR 7258, Aix-Marseille Université and Institut Paoli-Calmettes, Parc Scientifique et Technologique de Luminy, Marseille, France.
Jose A TapiaInstitute of Molecular Pathology Biomarkers, University of Extremadura, Caceres, Spain.
Noelia MorenoInstitute of Molecular Pathology Biomarkers, University of Extremadura, Caceres, Spain.
Marcos Pérez-LópezUnit of Toxicology, Veterinary Faculty, University of Extremadura, Caceres, Spain.
María P MíguezUnit of Toxicology, Veterinary Faculty, University of Extremadura, Caceres, Spain.
Gerardo Blanco-FernándezHepatobiliary-Pancreatic Surgery and Liver Transplant Unit, Infanta Cristina Hospital, Badajoz, Spain.ORCID http://orcid.org/0000-0003-4845-5306
Diego Lopez-GuerraHepatobiliary-Pancreatic Surgery and Liver Transplant Unit, Infanta Cristina Hospital, Badajoz, Spain.ORCID http://orcid.org/0000-0001-9763-4402
Miguel Fernandez-BermejoDepartment of Gastroenterology, San Pedro de Alcantara Hospital, Caceres, Spain.
Jose M MateosDepartment of Gastroenterology, San Pedro de Alcantara Hospital, Caceres, Spain.
Daniel VaraDepartment of Gastroenterology, San Pedro de Alcantara Hospital, Caceres, Spain.
Vicente RonceroUnit of Histology and Pathological Anatomy, Veterinary Faculty, University of Extremadura, Caceres, Spain.
Gines M SalidoInstitute of Molecular Pathology Biomarkers, University of Extremadura, Caceres, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work we have studied the effects of pharmacological concentrations of melatonin (1 µM-1 mM) on pancreatic stellate cells (PSC). Cell viability was analyzed by AlamarBlue test. Production of reactive oxygen species (ROS) was monitored following CM-H

Indexed as

AnimalsAntioxidantsCatalaseCell SurvivalGene Expression RegulationGlutathioneGlutathione DisulfideHeme Oxygenase-1HumansMelatoninMembrane Potential, MitochondrialNF-E2-Related Factor 2Oxidation-ReductionPancreatic Stellate CellsRatsReactive Oxygen SpeciesAntioxidantsCatalaseGlutathioneGlutathione DisulfideHeme Oxygenase-1MelatoninNfe2l2 protein, ratNF-E2-Related Factor 2Reactive Oxygen SpeciesSuperoxide Dismutase

Identifiers

PMID32286500
PMCPMC7156707

What Socratic 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 Socratic graph.