Evidence map›Paper›PMID 27998021›Full record

ArticleJournal of cellular and molecular medicine2017

Melanocortin receptor agonists MCR

Rosa Maisto, Carlo Gesualdo, Maria Consiglia Trotta, Paolo Grieco, Francesco Testa, Francesca Simonelli, Jorge Miquel Barcia, Michele D'Amico, Clara Di Filippo, Settimio Rossi

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
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  5. Therapeutic Potential of Fingolimod in Diabetes Mellitus and Its Chronic Complications.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
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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

10 authors at 5 institutions in 2 countries.

Rosa MaistoDepartment of Experimental Medicine, Division of Pharmacology, Second University of Naples, Naples, Italy.
Carlo GesualdoMultidisciplinary Department of Medical-Surgical and Dental Specialities, Second University of Naples, Naples, Italy.
Maria Consiglia TrottaDepartment of Experimental Medicine, Division of Pharmacology, Second University of Naples, Naples, Italy.
Paolo GriecoPharmacy Department, University of Naples Federico II, Naples, Italy.
Francesco TestaMultidisciplinary Department of Medical-Surgical and Dental Specialities, Second University of Naples, Naples, Italy.
Francesca SimonelliMultidisciplinary Department of Medical-Surgical and Dental Specialities, Second University of Naples, Naples, Italy.
Jorge Miquel BarciaSchool of Medicine, University of Valencia, Valencia, Spain.
Michele D'AmicoDepartment of Experimental Medicine, Division of Pharmacology, Second University of Naples, Naples, Italy.
Clara Di FilippoDepartment of Experimental Medicine, Division of Pharmacology, Second University of Naples, Naples, Italy.
Settimio RossiMultidisciplinary Department of Medical-Surgical and Dental Specialities, Second University of Naples, Naples, Italy.
University of Campania "Luigi Vanvitelli" · ITFederico II University Hospital · ITPegaso University · ITUniversitat de València · ESUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal photoreceptors are particularly vulnerable to local high-glucose concentrations. Oxidative stress is a risk factor for diabetic retinopathy development. Melanocortin receptors represent a family of G-protein-coupled receptors classified in five subtypes and are expressed in retina. Our previous data indicate that subtypes 1 and 5 receptor agonists exert a protective role on experimental diabetic retinopathy. This study focuses on their role in primary retinal cell cultures in high-glucose concentrations. After eye enucleation from wild-type male C57BL/6 mice, retinal cells were isolated, plated in high-glucose concentration and treated with melanocortin receptors 1 and 5 agonists and antagonists. Immunocytochemical and biochemical analysis showed that treatment with melanocortin receptors 1 and 5 agonists reduced anti-inflammatory cytokines and chemokines and enhanced manganese superoxide dismutase and glutathione peroxidase levels, preserving photoreceptor integrity. According with these evidences, we propose a major role of melanocortin receptors 1 and 5 on primary retinal cell response against high glucose or oxidative insults.

Indexed as

AnimalsAntioxidantsBlotting, WesternEnzyme-Linked Immunosorbent AssayGene Expression RegulationGlucoseGlutathione PeroxidaseImmunohistochemistryMaleMice, Inbred C57BLNeuroprotectionOpsinsPhotoreceptor Cells, VertebratePrimary Cell CultureReceptors, MelanocortinStaining and LabelingAntioxidantsGlucoseGlutathione PeroxidaseOpsinsReceptors, MelanocortinSuperoxide Dismutasehyperglycaemiamelanocortin receptor agonistsoxidative stressphotoreceptorsprimary retinal cell cultures

Identifiers

PMID27998021
PMCPMC5387132
OpenAlexW2562584932

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.