Intracellular ATP depletion inhibits swelling-induced D-[3H]aspartate release from primary astrocyte cultures

被引:28
|
作者
Rutledge, EM
Mongin, AA
Kimelberg, HK [1 ]
机构
[1] Albany Med Coll, Dept Pharmacol & Neurosci, Albany, NY 12208 USA
[2] Albany Med Coll, Div Neurosurg, Albany, NY 12208 USA
[3] Albany Med Coll, Neuropharmacol & Neurosci Res Grp, Albany, NY 12208 USA
[4] Natl Acad Sci Belarus, Inst Photobiol, Minsk 220072, BELARUS
关键词
astrocyte; excitotoxicity; cell swelling; energy depletion; volume-sensitive organic osmolyte-anion channel;
D O I
10.1016/S0006-8993(99)01805-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Volume expansion-sensing outward rectifier (VSOR) anion channel, also referred to as volume-sensitive organic osmolyte-anion channel (VSOAC), appears to be responsible for cell swelling-induced amino acid release in a variety of cells. One prominent feature of the VSOR/VSOAC is that non-hydrolyzed intracellular ATP binding to the channel or an accessory protein is required for its activation. In this study, the effect of intracellular ATP depletion on the swelling-induced release of D-[H-3]aspartate from rat primary astrocyte cultures due to exposure to either high K+ or hypotonic media was studied. When the cells were pretreated for 10 min with a combination of the metabolic inhibitors 2-deoxyglucose and rotenone, 100 mM K+ media- or hypotonic media-induced D-[H-3]aspartate release was completely suppressed. Added separately, each inhibitor showed only partial or no inhibition of D-[H-3]aspartate release, which correlated with its relative effectiveness in decreasing intracellular ATP levels. These data are consistent with the view that during high [K+](o) or hypotonic media-induced swelling of primary astrocyte cultures an ATP-dependent swelling-activated VSOAC channel is responsible for D-[H-3]aspartate release and close to normal ATP is required for full channel activation. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
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