Although the isolated chicken embryo retina has been a very useful in
vitro preparation for studying mechanisms of excitotoxicity, it is an
avian rather than mammalian tissue and its embryonic age makes it unsu
itable for a full range of developmental and aging studies. Therefore,
we have explored the feasibility of using the rat retina at various a
ges for in vitro excitotoxicity studies. In this model, retinal segmen
ts were isolated in artificial cerebrospinal fluid (CSF) at 5 degrees
C then incubated under various conditions at 30 degrees C and assessed
histologically for signs of neurodegenerative changes. Retinal segmen
ts from 7-, 30-, 120- and 660-day-old rats incubated in CSF for 3 h an
d from 30-day-old rats incubated for 24 h retained a normal histologic
al appearance. Thus, this preparation is suitable for in vitro studies
pertaining to either acute or delayed excitotoxic phenomena in the ma
mmalian CNS at any age from infancy to old age. Excitotoxin agonist ex
periments in the 30-day-old rat retina revealed the surprising result
that the non-NMDA agonists, kainate and AMPA, at a low concentration (
100 mu M) damaged a much larger number of retinal neurons than NMDA di
d at a very high concentration (10 mM).