Synaptosomal Glutamate Uptake Declines Progressively in the Spinal Cord of a Mutant Mouse with Motor Neuron Disease
- 1 April 1993
- journal article
- Published by Wiley in Journal of Neurochemistry
- Vol. 60 (4) , 1567-1569
- https://doi.org/10.1111/j.1471-4159.1993.tb03323.x
Abstract
It has been suggested that the degeneration of motor neurons in amyotrophic lateral sclerosis is a consequence of excitotoxicity resulting from a loss of synaptosomal glutamate uptake. The role of synaptosomal glutamate uptake in the pathogenesis of motor neuron disease was studied in the Mnd mouse. Glutamate uptake in spinal-cord synaptosomes declined in parallel with the onset of behavioral deficits in Mnd mice but lagged considerably behind the appearance of pathology in motor neurons. Glutamate uptake did not decline significantly in corpus striatum, and GABA uptake did not change significantly in either spinal cord or striatum. The presence of pronounced histopathological changes before the loss of glutamate uptake suggests that the decline of glutamate uptake is a consequence rather than the primary cause of motor neuron disease in the Mnd mouse.Keywords
This publication has 19 references indexed in Scilit:
- Accumulating autofluorescent material as a marker for early changes in the spinal cord of the Mnd mouseNeuromuscular Disorders, 1993
- Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS)Genomics, 1992
- Excitatory amino acids in amyotrophic lateral sclerosisAnnals of Neurology, 1991
- Amyotrophic lateral sclerosis: Amino acid levels in plasma and cerebrospinal fluidAnnals of Neurology, 1990
- Glutamate and aspartate immunoreactivity in corticospinal neurons of ratsJournal of Comparative Neurology, 1989
- Histopathology of the late-onset motor neuron degeneration (Mnd) mutant in the mouseJournal of Neurogenetics, 1987
- Histopathology of the late-onset motor neuron degeneration (Mnd) mutant in the mouseJournal of Neurogenetics, 1987
- Exogenous Glutamate Is Metabolized to Glutamine and Exported by Rat Primary Astrocyte CulturesJournal of Neurochemistry, 1986
- Improved Method for Isolating Synaptosomes from 11 Regions of One Rat Brain: Electron Microscopic and Biochemical Characterization and Use in the Study of Drug Effects on Nerve Terminal γ‐Aminobutyric Acid in VivoJournal of Neurochemistry, 1985
- Changes in whole tissue biosynthesis of γ-amino butyric acid (GABA) in basal ganglia of the dystonia (dtAlb) mouseLife Sciences, 1979