CEFYBO   02669
CENTRO DE ESTUDIOS FARMACOLOGICOS Y BOTANICOS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Tell me how you live, and I will tell you if your retina will be damaged: impact of the environment on the retina´s health
Autor/es:
DORFMAN D
Reunión:
Congreso; 16th International Congress on Photobiology; 2014
Resumen:
Ischemia
is a key component of several retinal diseases that are leading causes of
irreversible blindness. At present, there are no effective strategies for the
treatment of retinal ischemic damage. Recent evidences indicate that
environment conditions influence the visual system function. Enriched
environment (EE) constitutes a strategy that boosts exploratory, visual, and
cognitive activities, social interaction and voluntary physical exercise. In
this context, the aim of the present work was to analyze the effect of EE
housing against retinal damage induced by ischemia.
Adult male
Wistar rats were exposed to a standard environment (SE) or EE after retinal
ischemia for 3 weeks. 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. Retinal ischemia was induced by
increasing intraocular pressure to 120 mm Hg for 40 min. Retinal function was
weekly analysed and retinal morphology was analysed 3 weeks post-ischemia.
Macroglial reactivity (glial fibrillary acidic protein, GFAP) and synaptophysin
expression were assessed by immunohistochemistry. Anterograde transport from
the retina to the superior colliculus (SC) was examined after an intravitreal
injection of cholera toxin b-subunit.
In control animals, ischemia induced a
significant decrease in retinal function, whereas EE housing completely avoided
these alterations. In SE-housed animals, ischemia induced a significant retinal
ganglion cell loss, an increase in GFAP levels in Müller cells, and reduced
immunoreactivity for synaptophysin, which were prevented by EE housing. In
control animals, ischemia induced a deficit in the anterograde transport from
the retina to the superior colliculus, which was recovered by EE exposure.
These results suggest that the
exposure to an EE could become a new strategy for retinal ischemia treatment.