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Melanocortin receptor agonists MCR (1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture
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 previ...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387132/ https://www.ncbi.nlm.nih.gov/pubmed/27998021 http://dx.doi.org/10.1111/jcmm.13036 |
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author | Maisto, Rosa Gesualdo, Carlo Trotta, Maria Consiglia Grieco, Paolo Testa, Francesco Simonelli, Francesca Barcia, Jorge Miquel D'Amico, Michele Di Filippo, Clara Rossi, Settimio |
author_facet | Maisto, Rosa Gesualdo, Carlo Trotta, Maria Consiglia Grieco, Paolo Testa, Francesco Simonelli, Francesca Barcia, Jorge Miquel D'Amico, Michele Di Filippo, Clara Rossi, Settimio |
author_sort | Maisto, Rosa |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5387132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53871322017-05-01 Melanocortin receptor agonists MCR (1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture Maisto, Rosa Gesualdo, Carlo Trotta, Maria Consiglia Grieco, Paolo Testa, Francesco Simonelli, Francesca Barcia, Jorge Miquel D'Amico, Michele Di Filippo, Clara Rossi, Settimio J Cell Mol Med Original Articles 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. John Wiley and Sons Inc. 2016-12-20 2017-05 /pmc/articles/PMC5387132/ /pubmed/27998021 http://dx.doi.org/10.1111/jcmm.13036 Text en © 2016 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Maisto, Rosa Gesualdo, Carlo Trotta, Maria Consiglia Grieco, Paolo Testa, Francesco Simonelli, Francesca Barcia, Jorge Miquel D'Amico, Michele Di Filippo, Clara Rossi, Settimio Melanocortin receptor agonists MCR (1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
title | Melanocortin receptor agonists MCR
(1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
title_full | Melanocortin receptor agonists MCR
(1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
title_fullStr | Melanocortin receptor agonists MCR
(1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
title_full_unstemmed | Melanocortin receptor agonists MCR
(1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
title_short | Melanocortin receptor agonists MCR
(1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
title_sort | melanocortin receptor agonists mcr
(1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387132/ https://www.ncbi.nlm.nih.gov/pubmed/27998021 http://dx.doi.org/10.1111/jcmm.13036 |
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