WE investigated the role of glycine in felbamate hypoxic neuroprotecti
on using the rat hippocampal slice. Following hypoxic exposure, CA1 or
thodromic PS recovered a mean 26 +/- 3% of original amplitude; treatme
nt with 1.3 mM felbamate, a recently developed anticonvulsant, increas
ed this recovery to 95 +/- 3%. However, the addition of 10 muM glycine
with felbamate during hypoxia, reduced this recovery to 16 +/- 12%. T
he glycine EC50 for reversal of felbamate hypoxic protection was found
to be 4.4 muM. Glycine 10 muM given during hypoxia without felbamate,
slightly exacerbated subsequent injury, with 13 +/- 3% recovery seen.
Glycine 100 muM given alone under normoxic conditions showed no effec
t. Reversal of felbamate hypoxic protection was specific for glycine,
and was not seen with 50 muM glutamate. These results suggest that fel
bamate neuroprotection from hypoxia occurs through a glycine interacti
on.