Sodium channel modulators prevent oxygen and glucose deprivation injury and glutamate release in rat neocortical cultures

Summary Neocortical cultures were deprived of oxygen and glucose to model ischemic neuronal injury. We used a graded series of periods of oxygen and glucose deprivation, providing graded insults. Cell death was measured by release of lactate dehydrogenase (LDH). One hundred and twenty to 240 min of deprivation caused graded increases in glutamate overflow, LDH release and 45 Ca influx. Curves of LDH release with respect to deprivation time were shifted to longer intervals by treatment with tetrodotoxin (TTX; 3, 30 or 300 nM), phenytoin (10, 30 or 100 μM), lidocaine (10, 30 or 100 μM) or the N -methyl- d -aspartate antagonist CPP [3(2-carboxypiperazine-4-yl)propyl-1-phosphonic acid, 3, 10, 30 or 100 μM]. Combined treatment with TTX and CPP caused pronounced rightward shifts of LDH deprivation curves. Our results indicate that Na + channel blockade is neuroprotective in neocortex cultures. Our results also suggest that neuroprotection with Na + channel blockers may be due to inhibition of glutamate release.