Modulation of neuroeffector transmission by endogenous nitric oxide: a role for acetylcholine receptor-activated nitric oxide formation, as indicated by measurements of nitric oxide/nitrite release

Eur J Pharmacol. 1993 Aug 24;240(2-3):235-42. doi: 10.1016/0014-2999(93)90904-v.

Abstract

Nitric oxide (NO) synthase inhibitors enhanced nerve-mediated contractile responses in guinea pig ileum longitudinal muscle, likely via a prejunctional effect on substance P-like neuroeffector transmission. Supporting a modulatory role for NO, application of NO through administration of acid sodium nitrite evoked marked inhibitory effects on responses to transmural nerve stimulation. Substance P-like responses to nerve stimulation were abolished by substance P receptor antagonists and were enhanced by atropine, indicating a cholinergic influence on substance P-like neuroeffector transmission. Since acetylcholine can evoke release of NO from endothelium, the possible role of acetylcholine in NO release in ileum was examined. The release of NO/nitrite, determined by chemiluminescence, was inhibited by NG-monomethyl-L-arginine (L-NMMA), by calcium removal, by tetrodotoxin or by atropine, indicating a nerve-mediated control of NO production. A basis for the NO release is likely to be spontaneous neuronal activity, where release of acetylcholine, with subsequent muscarinic receptor activation, contributes to stimulation of NO formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology*
  • Amino Acid Oxidoreductases / antagonists & inhibitors*
  • Animals
  • Arginine / analogs & derivatives
  • Arginine / pharmacology
  • Atropine / pharmacology
  • Electric Stimulation
  • Female
  • Guinea Pigs
  • Ileum / drug effects
  • Ileum / innervation
  • Ileum / metabolism
  • Ileum / physiology
  • Iris / drug effects
  • Iris / innervation
  • Iris / metabolism
  • Luminescent Measurements
  • Male
  • Muscle Contraction / drug effects
  • Muscle, Smooth / drug effects*
  • Muscle, Smooth / physiology
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase
  • Nitrites / metabolism
  • Rabbits
  • Receptors, Cholinergic / physiology*
  • Substance P / physiology
  • Synaptic Transmission / drug effects*
  • omega-N-Methylarginine

Substances

  • Nitrites
  • Receptors, Cholinergic
  • omega-N-Methylarginine
  • Nitric Oxide
  • Substance P
  • Atropine
  • Arginine
  • Nitric Oxide Synthase
  • Amino Acid Oxidoreductases
  • Acetylcholine