Nitric oxide activates Ca2+-activated K+ channels in cultured bovine adrenal chromaffin cells

Neurosci Lett. 1998 May 29;248(2):127-9. doi: 10.1016/s0304-3940(98)00316-4.

Abstract

The effects of sodium nitroprusside (SNP) on Ca2+-dependent K+ (KCa) channels in cultured bovine adrenal chromaffin cells were investigated using single channel recording patch-clamp techniques. KCa channels were activated by application of 100 microM SNP to the extracellular side of cell-attached patches. Methylene blue (300 microM), an inhibitor of soluble guanylate cyclase, or H-8 (1 microM), a protein kinase inhibitor with relative specificity for cGMP-dependent protein kinase, diminished but did not completely abolish the SNP-induced KCa channel activation. Diethylamine/NO complex (DEA/NO), an NO donor, also activated KCa channels in cell-attached patches. Furthermore, application of 100 microM SNP or 100 nM DEA/NO to the intracellular surface of excised inside-out patches also activated KCa channels in the bath solution which contained 1 microM Ca2+. These results indicate that SNP is capable of activating the KCa channel via cGMP-dependent and -independent mechanisms. These studies demonstrate that NO may serve as an important regulatory mechanism for catecholamine secretion in chromaffin cells via the activation of KCa channels.

MeSH terms

  • Adrenal Medulla / cytology
  • Adrenal Medulla / drug effects
  • Adrenal Medulla / metabolism*
  • Animals
  • Calcium / metabolism*
  • Catecholamines / metabolism
  • Cattle
  • Cells, Cultured
  • Chromaffin Cells / drug effects
  • Chromaffin Cells / metabolism*
  • Cyclic GMP-Dependent Protein Kinases / antagonists & inhibitors
  • Enzyme Inhibitors / pharmacology
  • Guanylate Cyclase / antagonists & inhibitors
  • Hydrazines / pharmacology
  • Isoquinolines / pharmacology
  • Methylene Blue / pharmacology
  • Nitric Oxide / physiology*
  • Nitrogen Oxides
  • Nitroprusside / pharmacology
  • Patch-Clamp Techniques
  • Potassium Channels / drug effects
  • Potassium Channels / metabolism*
  • Potassium Channels / physiology

Substances

  • Catecholamines
  • Enzyme Inhibitors
  • Hydrazines
  • Isoquinolines
  • Nitrogen Oxides
  • Potassium Channels
  • Nitroprusside
  • Nitric Oxide
  • N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide
  • 1,1-diethyl-2-hydroxy-2-nitrosohydrazine
  • Cyclic GMP-Dependent Protein Kinases
  • Guanylate Cyclase
  • Calcium
  • Methylene Blue