Effect of cholinergic and adrenergic receptor blockade on arrhythmogenic activity of endothelin-1 during inhibition of nitric oxide synthesis in awake mice

Bull Exp Biol Med. 2004 Feb;137(2):111-3. doi: 10.1023/b:bebm.0000028115.53995.e0.
[Article in English, Russian]

Abstract

We studied the effects of blockade of nicotinic receptors in sympathetic and parasympathetic ganglia (hexamethonium), muscarinic receptors (atropine), and beta1-adrenoceptors (atenolol) on arrhythmogenic activity of endothelin-1 during inhibition of nitric oxide synthesis with Nomega-nitro-L-arginine in NMRI mice. Atropine reduced, while hexamethonium completely abolished the arrhythmogenic effect of endothelin-1 during nitric oxide synthase inhibition. Atenolol potentiated arrhythmogenic activity of Nomega-nitro-L-arginine, but endothelin-1 had no effect on the incidence of arrhythmias under these conditions.

MeSH terms

  • Adrenergic Antagonists / pharmacology*
  • Animals
  • Arrhythmias, Cardiac / chemically induced
  • Arrhythmias, Cardiac / metabolism
  • Arrhythmias, Cardiac / prevention & control*
  • Atenolol / pharmacology
  • Atropine / pharmacology
  • Cholinergic Antagonists / pharmacology*
  • Endothelin-1 / pharmacology
  • Hexamethonium / pharmacology
  • Male
  • Mice
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitric Oxide / biosynthesis

Substances

  • Adrenergic Antagonists
  • Cholinergic Antagonists
  • Endothelin-1
  • Nitric Oxide
  • Hexamethonium
  • Atenolol
  • Atropine
  • NG-Nitroarginine Methyl Ester