Melanocortin receptor agonists MCR1-5 protect photoreceptors from high-glucose damage and restore antioxidant enzymes in primary retinal cell culture

  • J Cell Mol Med. 2017 May;21(5):968-974. doi: 10.1111/jcmm.13036.
Rosa Maisto  1 Carlo Gesualdo  2 Maria Consiglia Trotta  1 Paolo Grieco  3 Francesco Testa  2 Francesca Simonelli  2 Jorge Miquel Barcia  4 Michele D'Amico  1 Clara Di Filippo  1 Settimio Rossi  2
Affiliations
  • 1. Department of Experimental Medicine, Division of Pharmacology, Second University of Naples, Naples, Italy.
  • 2. Multidisciplinary Department of Medical-Surgical and Dental Specialities, Second University of Naples, Naples, Italy.
  • 3. Pharmacy Department, University of Naples Federico II, Naples, Italy.
  • 4. School of Medicine, University of Valencia, Valencia, Spain.
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.

Keywords
hyperglycaemia; melanocortin receptor agonists; oxidative stress; photoreceptors; primary retinal cell cultures.