Contrasting effects of tetraethylammonium and 4-aminopyridine on the gastrointestinal function of mice

Eur J Pharmacol. 2005 Feb 21;509(2-3):179-85. doi: 10.1016/j.ejphar.2005.01.013.

Abstract

Many different K+ channels have been identified in the gastrointestinal tract, and the two classical K+ channel blockers, tetraethylammonium and 4-aminopyridine, show different sensitivity for these channels. The aim of the present study was to compare the effects of tetraethylammonium and 4-aminopyridine on the gastrointestinal function of mice. 4-Aminopyridine (5 mg/kg, p.o.) inhibited, but tetraethylammonium (40 mg/kg, p.o.) enhanced, the intestinal propulsion of a charcoal suspension in conscious mice. Studies in vitro showed that perfusion of 5 mM 4-aminopyridine increased the maximal contractile force and minimal relaxation force, and decreased the amplitude and frequency of the peristaltic contraction of the isolated duodenum. However, perfusion of 5 mM tetraethylammonium increased the maximal contractile force, the minimal relaxation force and the amplitude of the contraction. The effects of tetraethylammonium and 4-aminopyridine on the duodenal contraction could be abolished completely by application of 5 microM verapamil. Our results in vivo and in vitro showed that tetraethylammonium and 4-aminopyridine had contrasting effects on the gastrointestinal function of mice.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Aminopyridine / pharmacology*
  • Animals
  • Duodenum / drug effects
  • Duodenum / physiology
  • Gastric Acid / metabolism
  • Gastric Fundus / drug effects
  • Gastric Fundus / physiology
  • Gastric Mucosa / metabolism
  • Gastrointestinal Motility / drug effects
  • Gastrointestinal Tract / drug effects*
  • Gastrointestinal Tract / physiology
  • Gastrointestinal Transit / drug effects
  • In Vitro Techniques
  • Mice
  • Muscle Contraction / drug effects
  • Potassium Channel Blockers / pharmacology
  • Rats
  • Rats, Wistar
  • Stomach / drug effects
  • Tetraethylammonium / pharmacology*

Substances

  • Potassium Channel Blockers
  • Tetraethylammonium
  • 4-Aminopyridine