Suppression by cholinesterase inhibition of a Ca(2+)-independent efflux of [3H]acetylcholine from the neuromuscular junction of the isolated rat diaphragm

Eur J Pharmacol. 1992 Oct 20;221(2-3):371-6. doi: 10.1016/0014-2999(92)90725-j.

Abstract

Endplate preparations of the left rat hemidiaphragm were incubated with [3H]choline to label neuronal acetylcholine stores. Elevation of the concentration (13.5-135 mmol/l) of extracellular potassium chloride (KCl) stimulated the release of [3H]acetylcholine in a concentration-dependent manner. KCl (27 mmol/l) still caused a significant efflux of [3H]acetylcholine in a Ca(2+)-free medium. Inhibitors of cholinesterase (physostigmine, diisopropylfluorophosphate) suppressed by 80% this Ca(2+)-independent efflux of [3H]acetylcholine. Vesamicol (10 mumol/l), the blocker of the vesicular acetylcholine carrier, also suppressed the stimulated, Ca(2+)-independent efflux of [3H]acetylcholine. The inhibitory effect of physostigmine was not prevented by muscarine or nicotine receptor antagonists, but the inhibitory effect was lost when the stimulus strength was increased (81 mmol/l KCl). The present experiments showed cholinesterase inhibition to suppress a Ca(2+)-independent efflux of [3H]acetylcholine, probably by interference with a membrane-bound acetylcholine carrier.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / analysis
  • Acetylcholine / metabolism*
  • Animals
  • Calcium / physiology*
  • Choline / analysis
  • Cholinesterase Inhibitors / pharmacology*
  • Diaphragm
  • Female
  • In Vitro Techniques
  • Male
  • Neuromuscular Junction / metabolism*
  • Physostigmine / pharmacology
  • Piperidines / pharmacology
  • Potassium Chloride / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Tritium

Substances

  • Cholinesterase Inhibitors
  • Piperidines
  • Tritium
  • vesamicol
  • Potassium Chloride
  • Physostigmine
  • Choline
  • Acetylcholine
  • Calcium