CEFYBO   02669
CENTRO DE ESTUDIOS FARMACOLOGICOS Y BOTANICOS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Enriched environment protects the retina from diabetic damage in adult rats
Autor/es:
DORFMAN D; ARANDA ML; GONZÁLEZ FLEITAS MF; CHIANELLI MS; FERNANDEZ DC; ROSENSTEIN RE
Lugar:
Orlando
Reunión:
Congreso; ARVO Annual Meeting 2014; 2014
Institución organizadora:
ARVO
Resumen:
Enriched environment protects the retina from diabetic damage in adult rats Damian Dorfman1, Marcos L Aranda1, Maria F Gonzalez Fleitas1, Monica Chianelli1, Diego Carlos Fernandez1 and Ruth Estela Rosenstein1 1 Human Biochem/Sch of Med, University of Buenos Aires, Buenos Aires, Argentina Commercial Relationships: Damian Dorfman, None; Marcos Aranda, None; Maria Gonzalez Fleitas, None; Monica Chianelli, None; Diego Fernandez, None; Ruth Rosenstein, None Support: None Abstract Purpose:Diabetic retinopathy (DR) is a leading cause of acquired blindness. Available treatments are not very effective. Enriched environment (EE) allows freedom to move and exercise voluntarily in larger cage, with accessibility to complex stimuli as well as social interaction. We investigated the effect of EE housing on retinal damage induced by experimental diabetes. Methods:Diabetes was induced by an intraperitoneal injection of streptozotocin (STZ). EE consisted of big cages housing 6 animals, and containing several food hoppers, wheels and different objects repositioned once/day and fully substituted once/week. DR was evaluated in terms of: i) retinal function (electroretinogram (ERG) and oscillatory potentials (OPs)), ii) integrity of blood- retinal barrier (by albumin-Evan?s Blue complex leakage and astrocyte glial fibrillary acidic protein (GFAP) immunohistochemistry), iii) vascular endothelial growth factor (VEGF) levels (by Western blot and immunohistochemistry), and iv) retinal lipid peroxidation (thiobarbituric acid reactive substances, TBARS). Results:EE significantly preserved ERG a- and b-wave and OPs, avoided albumin-Evan?s blue leakage, and prevented the decrease in astrocyte GFAP levels in diabetic rats. EE prevented the increase in VEGF and TBARS levels induced by experimental diabetes. When EE housing started 7 weeks after diabetes onset, retinal function was significantly preserved. Conclusions:These results indicate that EE housing could become a novel and harmless therapeutic strategy in DR treatment.