Cultures of septal and hippocampal neurons from fetal rat and dorsal r
oot ganglion neurons from embryonic chick were pretreated with GM1 gan
glioside or cycloheximide and then supplemented with toxic concentrati
ons of ethanol. GM1 provided significant protection against ethanol ne
urotoxicity in each population. The inhibition of protein synthesis by
cycloheximide, however, which protects against cell death resulting f
rom withdrawal of neurotrophic factor support, did not ameliorate etha
nol-induced neuronal loss.