Relationship between L-glutamate-regulated intracellular Na+ dynamics and ATP hydrolysis in astrocytes.

Details

Serval ID
serval:BIB_38C159ACF0EC
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Relationship between L-glutamate-regulated intracellular Na+ dynamics and ATP hydrolysis in astrocytes.
Journal
Journal of Neural Transmission
Author(s)
Magistretti P.J., Chatton J.Y.
ISSN
0300-9564
Publication state
Published
Issued date
2005
Peer-reviewed
Oui
Volume
112
Number
1
Pages
77-85
Language
english
Notes
SAPHIRID:61578
Abstract
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.
Keywords
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
Create date
10/03/2008 10:58
Last modification date
20/08/2019 13:28
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