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- W2058175082 abstract "Amyotrophic lateral sclerosis is a fatal neurodegenerative disease and glutamate excitotoxicity has been implicated in its pathogenesis. Platelets contain a glutamate uptake system and express components of the glutamate–glutamine cycle, such as the predominant glial excitatory amino acid transporter 2 (EAAT2). In several neurological diseases platelets have proven to be systemic markers for the disease. We compared properties of key components of the glutamate–glutamine cycle in blood platelets of ALS patients and healthy controls. Platelets were analyzed for 3H-glutamate uptake in the presence or absence of thrombin and for EAAT2 and glutamine synthetase protein expression by Western blotting. Platelets of ALS patients showed a 37% increase in expression of glutamine synthetase, but normal expression of glutamate transporter EAAT2. Glutamate uptake in resting or thrombin-stimulated platelets did not differ significantly between platelets from ALS patients and controls. Thrombin-stimulation resulted in about a seven-fold increase in glutamate uptake. Our data suggest that glutamine synthetase may be a peripheral marker of ALS and encourage further investigation into the role of this enzyme in ALS." @default.
- W2058175082 created "2016-06-24" @default.
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- W2058175082 date "2006-03-01" @default.
- W2058175082 modified "2023-09-27" @default.
- W2058175082 title "Increased glutamine synthetase but normal EAAT2 expression in platelets of ALS patients" @default.
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- W2058175082 doi "https://doi.org/10.1016/j.neuint.2005.09.009" @default.
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