Amyotrophic lateral sclerosis is a progressive fatal disorder devastating t
he spinal cord and brain in humans; Excitotoxicity has been suggested to be
involved in the pathogenesis of amyotrophic lateral sclerosis. This hypoth
esis has driven a wealth of basic research and stimulated development of ne
uroprotective therapies for chronic neurdegenerative disorders. As a result
of these efforts, riluzole, an antiglutamatergic drug, has been establishe
d in the therapy of amyotrophic lateral sclerosis. A transgenic mouse showi
ng features of amyotrophic lateral sclerosis has been subsequently engineer
ed enabling studies of the disease irt vivo. However, despite-considerable
progress, the etiology of amyotrophic lateral sclerosis remains obscure and
the disturbances in excitatory neurotransmission should by no means be reg
arded as exclusive to the pathogenesis of the disease.