Relationship between L-glutamate-regulated intracellular Na+ dynamics and ATP hydrolysis in astrocytes.
Détails
ID Serval
serval:BIB_38C159ACF0EC
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Relationship between L-glutamate-regulated intracellular Na+ dynamics and ATP hydrolysis in astrocytes.
Périodique
Journal of Neural Transmission
ISSN
0300-9564
Statut éditorial
Publié
Date de publication
2005
Peer-reviewed
Oui
Volume
112
Numéro
1
Pages
77-85
Langue
anglais
Notes
SAPHIRID:61578
Résumé
Glutamate uptake into astrocytes and the resulting increase in intracellular Na+ (Na+(i)) have been identified as a key signal coupling excitatory neuronal activity to increased glucose utilization. Arguments based mostly on mathematical modeling led to the conclusion that physiological concentrations of glutamate more than double astrocytic Na+/K+-ATPase activity, which should proportionally increase its ATP hydrolysis rate. This hypothesis was tested in the present study by fluorescence monitoring of free Mg2+ (Mg2+(i)), a parameter that inversely correlates with ATP levels. Glutamate application measurably increased Mg2+(i) (i.e. decreased ATP), which was reversible after glutamate washout. Na+(i) and ATP changes were then directly compared by simultaneous Na+(i) and Mg2+ imaging. Glutamate increased both parameters with different rates and blocking the Na+/K+-ATPase during the glutamate-evoked Na+(i) response, resulted in a drop of Mg2+(i) levels (i.e. increased ATP). Taken together, this study demonstrates the tight correlation between glutamate transport, Na+ homeostasis and ATP levels in astrocytes.
Mots-clé
Adenosine Triphosphate/metabolism, Animals, Astrocytes/metabolism, Astrocytes/physiology, Cells, Cultured, Dose-Response Relationship, Drug, Glutamic Acid/pharmacology, Glutamic Acid/physiology, Hydrolysis/drug effects, Intracellular Fluid/drug effects, Intracellular Fluid/metabolism, Male, Mice, Sodium/physiology
Pubmed
Web of science
Création de la notice
10/03/2008 10:58
Dernière modification de la notice
20/08/2019 13:28