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

Brain Res. 1999 Sep 18;842(1):39-45. doi: 10.1016/s0006-8993(99)01805-3.

Abstract

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-[3H]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-[3H]aspartate release was completely suppressed. Added separately, each inhibitor showed only partial or no inhibition of D-[3H]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-[3H]aspartate release and close to normal ATP is required for full channel activation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / physiology*
  • Animals
  • Antimetabolites / pharmacology
  • Aspartic Acid / metabolism*
  • Astrocytes / metabolism*
  • Astrocytes / ultrastructure
  • Cell Size
  • Cells, Cultured
  • Hypotonic Solutions
  • Potassium / pharmacology
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Antimetabolites
  • Hypotonic Solutions
  • Aspartic Acid
  • Adenosine Triphosphate
  • Potassium