Blockade of human atrial 5-HT4 receptors by SB 207710, a selective and high affinity 5-HT4 receptor antagonist

Naunyn Schmiedebergs Arch Pharmacol. 1994 May;349(5):546-8. doi: 10.1007/BF00169146.

Abstract

The mode of antagonism of 5-hydroxytryptamine-induced positive inotropic effects by the highly selective 5-HT4 receptor antagonist SB 207710 (1-butyl-4-piperidinyl) methyl 8-amino-7-iodo-1,4-benzodioxan-5-carboxylate) was investigated on isolated preparations of human right atrial appendage. SB 207710 caused concentration-dependent (0.1-10 nmol/l) surmountable antagonism of the effects of 5-hydroxytryptamine with a pKB (mol/l) of 10.1. Due to its high selectivity and affinity, SB 207710 could be a powerful tool for the comparison of human atrial 5-HT4 receptors with 5-HT4 receptors of other organs of man and other species.

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Aged
  • Aged, 80 and over
  • Dioxanes / pharmacology*
  • Female
  • Heart Atria / drug effects
  • Humans
  • Imidazoles / pharmacology
  • Male
  • Middle Aged
  • Myocardial Contraction / drug effects*
  • Piperidines / pharmacology*
  • Serotonin / pharmacology
  • Serotonin Antagonists*

Substances

  • Adrenergic beta-Antagonists
  • Dioxanes
  • Imidazoles
  • Piperidines
  • SB 207710
  • Serotonin Antagonists
  • Serotonin
  • CGP 20712A