Evidence map›Paper›PMID 30868511›Full record

ArticleJournal of physiology and biochemistry2019

Melatonin induces reactive oxygen species generation and changes in glutathione levels and reduces viability in human pancreatic stellate cells.

Matias Estaras, Noelia Moreno, Patricia Santofimia-Castaño, Salome Martinez-Morcillo, Vicente Roncero, Gerardo Blanco, Diego Lopez, Miguel Fernandez-Bermejo, Jose M Mateos, Juan L Iovanna and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of physiology and biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 30 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

12 authors at 4 institutions in 2 countries.

Matias EstarasDepartment of Physiology, Institute of Molecular Pathology Biomarkers, University of Extremadura, Avenida Universidad s/n, 10003, Cáceres, Spain.
Noelia MorenoDepartment of Physiology, Institute of Molecular Pathology Biomarkers, University of Extremadura, Avenida Universidad s/n, 10003, Cáceres, Spain.
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.
Salome Martinez-MorcilloUnit of Toxicology, Veterinary Faculty, University of Extremadura, Cáceres, Spain.
Vicente RonceroUnit of Histology and Pathological Anatomy, Veterinary Faculty, University of Extremadura, Cáceres, Spain.
Gerardo BlancoHepatobiliary-Pancreatic Surgery and Liver Transplant Unit, Infanta Cristina Hospital, Badajoz, Spain.
Diego LopezHepatobiliary-Pancreatic Surgery and Liver Transplant Unit, Infanta Cristina Hospital, Badajoz, Spain.
Miguel Fernandez-BermejoDepartment of Gastroenterology, San Pedro de Alcantara Hospital, Cáceres, Spain.
Jose M MateosDepartment of Gastroenterology, San Pedro de Alcantara Hospital, Cáceres, Spain.
Juan L IovannaCentre 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.
Gines M SalidoDepartment of Physiology, Institute of Molecular Pathology Biomarkers, University of Extremadura, Avenida Universidad s/n, 10003, Cáceres, Spain.
Antonio GonzalezDepartment of Physiology, Institute of Molecular Pathology Biomarkers, University of Extremadura, Avenida Universidad s/n, 10003, Cáceres, Spain. agmateos@unex.es.ORCID http://orcid.org/0000-0001-8380-0270
Universidad de Extremadura · ESCentre National de la Recherche Scientifique · FRHospital San Pedro de Alcántara · ESHospital Universitario Infanta Cristina · ES

Funding

Consejería de Educación y Empleo, Junta de Extremadura IB16006Ministerio de Economía, Industria y Competitividad, Gobierno de España BFU2016-79259-RMinisterio de Economía, Industria y Competitividad, Gobierno de España UNEX13-1E-1608
6 · The paper itself

Abstract

In this study, the effects of pharmacological concentrations of melatonin (1 μM-1 mM) on human pancreatic stellate cells (HPSCs) have been examined. Cell type-specific markers and expression of melatonin receptors were analyzed by western blot analysis. Changes in intracellular free Ca

Indexed as

AnimalsCalciumCells, CulturedCell SurvivalGlutathioneGlutathione DisulfideHumansMelatoninMicePancreasPancreatic Stellate CellsRatsReactive Oxygen SpeciesReceptor, Melatonin, MT1CalciumGlutathioneGlutathione DisulfideMelatoninMTNR1A protein, humanReactive Oxygen SpeciesReceptor, Melatonin, MT1CalciumCell viabilityGlutathioneHuman pancreatic stellate cellsMelatonin

Identifiers

PMID30868511
OpenAlexW2921110195

What Socratic holds

Textmetadata
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.