ATP reduces voltage-activated K+ current in cultured rat hippocampal neurons

Pflugers Arch. 1994 Nov;429(1):143-5. doi: 10.1007/BF02584042.

Abstract

Effects of extracellular ATP were investigated in cultured rat hippocampal neurons using whole-cell voltage-clamp techniques. When a depolarizing step to +10 mV was applied from a holding potential of -60 mV, an outward K+ current was activated. ATP (3 to 300 microM) reduced the K+ current. Among adenosine derivatives, ADP (100 microM) slightly inhibited the K+ current, and AMP or adenosine (100 microM) was ineffective. UTP was as potent as ATP and alpha,beta-methylene ATP was less effective than ATP. The inhibition by ATP of the K+ current was abolished by inclusion of 2 mM GDP beta S in the intracellular solution. The results indicate that ATP inhibits K+ channels in rat hippocampal neurons through UTP-responsive P2-purinoceptors coupled with GTP-binding proteins.

MeSH terms

  • Adenosine / analogs & derivatives
  • Adenosine / pharmacology
  • Adenosine Triphosphate / pharmacology*
  • Animals
  • Cells, Cultured
  • Electrophysiology
  • GTP-Binding Proteins / metabolism
  • Hippocampus / cytology
  • Hippocampus / drug effects
  • Hippocampus / metabolism*
  • Neurons / drug effects
  • Neurons / metabolism*
  • Patch-Clamp Techniques
  • Potassium Channels / drug effects
  • Potassium Channels / metabolism*
  • Purinergic P2 Receptor Antagonists
  • Rats

Substances

  • Potassium Channels
  • Purinergic P2 Receptor Antagonists
  • Adenosine Triphosphate
  • GTP-Binding Proteins
  • Adenosine