Inhibition of high K+-evoked gamma-aminobutyric acid release by sodium nitroprusside in rat hippocampus

Eur J Pharmacol. 2003 Apr 25;467(1-3):119-23. doi: 10.1016/s0014-2999(03)01605-4.

Abstract

To clarify whether nitric oxide (NO) modifies high K(+)-evoked gamma-aminobutyric acid (GABA) release, we examined the effects of sodium nitroprusside, an NO donor; diethyldithiocarbamate, an NO trapper; dithiothreitol, a superoxide radical scavenger; and 1H-(1,2,4)oxadiazole(4,3-a)quinoxalin-1-one, a specific guanylyl cyclase inhibitor, on high (100 mM) K(+)-evoked GABA release from rat hippocampus in vivo using microdialysis. Perfusion with 0.5 or 5 mM sodium nitroprusside significantly reduced high K(+)-evoked GABA release. Co-perfusion with 0.5 mM sodium nitroprusside and 5 mM diethyldithiocarbamate or 0.5 mM 1H-(1,2,4)oxadiazole(4,3-a)quinoxalin-1-one significantly enhanced high K(+)-evoked GABA release. Co-perfusion with 0.5 mM sodium nitroprusside and 1 mM dithiothreitol tended to increase it. These results demonstrate that sodium nitroprusside reduces high K(+)-evoked GABA release both via an NO/cyclic GMP-dependent pathway and via an NO-dependent, but cyclic GMP-independent, pathway in rat hippocampus in vivo.

MeSH terms

  • Animals
  • Dithiothreitol / pharmacology
  • Ditiocarb / pharmacology
  • Free Radical Scavengers / pharmacology
  • Guanylate Cyclase / antagonists & inhibitors
  • Hippocampus / drug effects
  • Hippocampus / metabolism*
  • Male
  • Microdialysis
  • Nitric Oxide / physiology*
  • Nitric Oxide Donors / pharmacology*
  • Nitroprusside / pharmacology*
  • Oxadiazoles / pharmacology
  • Potassium / pharmacology*
  • Quinoxalines / pharmacology
  • Rats
  • Rats, Wistar
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • 1H-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one
  • Free Radical Scavengers
  • Nitric Oxide Donors
  • Oxadiazoles
  • Quinoxalines
  • Nitroprusside
  • Nitric Oxide
  • gamma-Aminobutyric Acid
  • Ditiocarb
  • Guanylate Cyclase
  • Potassium
  • Dithiothreitol