Determination of the muscarinic receptor subtype mediating vasodilatation

Br J Pharmacol. 1985 Jan;84(1):3-5.

Abstract

The muscarinic receptor mediating vasodilatation of the rabbit aorta and dog femoral artery has been assessed using muscarinic antagonists. With the exception of pirenzepine, the antagonist affinities were similar to those reported for the ileal receptors and dissimilar to those reported for the atrial receptors. Pirenzepine exhibited an affinity (7.54) intermediate between that reported for the CNS receptors (8.4) and that reported for the ileal receptors (6.77). This value for pirenzepine was confirmed using acetylcholine as the agonist and using the dog femoral artery as the vascular tissue. It is concluded that the muscarinic receptor profile mediating vasodilatation is not easily accommodated into the current receptor classification.

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Aorta, Thoracic / drug effects
  • Atropine / pharmacology
  • Benzodiazepinones / pharmacology
  • Carbachol / pharmacology
  • Dogs
  • Female
  • Femoral Artery / drug effects
  • Gallamine Triethiodide / pharmacology
  • In Vitro Techniques
  • Male
  • Pancuronium / pharmacology
  • Parasympatholytics / pharmacology*
  • Phenethylamines / pharmacology
  • Piperidines / pharmacology
  • Pirenzepine
  • Rabbits
  • Receptors, Muscarinic / drug effects*
  • Vasodilation / drug effects*

Substances

  • Benzodiazepinones
  • Parasympatholytics
  • Phenethylamines
  • Piperidines
  • Receptors, Muscarinic
  • Pirenzepine
  • secoverine
  • Atropine
  • 4-diphenylacetoxy-1,1-dimethylpiperidinium
  • Carbachol
  • Pancuronium
  • Acetylcholine
  • Gallamine Triethiodide