THIS study examined high affinity Na+-dependent uptake of glutamate in
synaptosomal preparations from spinal cord in mice that express a dom
inant mutation of human copper/zinc superoxide dismutase (SOD1) and re
present an animal model of amyotrophic lateral sclerosis (ALS). Their
muscle strength was also monitored by a grip traction test throughout
their lifespan. The high affinity Na+-dependent uptake of [H-3]glutama
te was decreased between 120 and 150 days of age. A marked and signifi
cant decrease in V-max (-40.2%; p < 0.001) on whole spinal cord synapt
osomes was observed at 150 days, with no change in K-m. This significa
nt decrease was reached a week before the animals died (157.2 +/- 2.2
days) and corresponded to a considerable fall in muscle strength (25%
loss between 120 and 140 days, p < 0.001). The FALS mouse model theref
ore reproduces the decrease in glutamate uptake reported in humans suf
fering from sporadic or familial ALS. These results are discussed in t
erms of a possible tardive involvement of glutamate uptake deficiency
in human ALS. (C) 1998 Rapid Science Ltd.