Pseudo-noncompetitive antagonism by BQ123 of intracellular calcium transients mediated by human ETA endothelin receptor

Biochem Biophys Res Commun. 1994 Apr 29;200(2):679-86. doi: 10.1006/bbrc.1994.1504.

Abstract

The family of endothelins, endothelin-1 (ET-1), ET-2 and ET-3, act on two subtypes of receptors called ETA and ETB receptors. BQ123 is an ETA-selective competitive antagonist. In this study, however, BQ123 inhibited ET-1-induced transients of cytosolic Ca2+ concentrations ([Ca2+]i) in an apparently noncompetitive manner in mouse L cell stably expressing cloned human ETA receptor. BQ123 (3-30 nM) did not change the EC50 of ET-1 (6.6 nM), but reduced the maximum responses down to 15.0%. In an non-equilibrium binding assay which mimicks the conditions of [Ca2+]i transient assay (cells were incubated with [125I]ET-1 only for 30 s), BQ123 (30 nM) constantly decreased the specific [125I]ET-1 binding to approximately 13% of that without the antagonist. Thus, the apparent noncompetitive antagonism by BQ123 of ETA receptor-mediated [Ca2+]i transient is due to the assay condition where the interactions of the agonist, antagonist and receptor remained non-equilibrium state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding, Competitive
  • Calcium / metabolism*
  • Cytosol / metabolism
  • Endothelin Receptor Antagonists*
  • Endothelins / metabolism
  • Humans
  • Kinetics
  • L Cells
  • Mice
  • Peptides, Cyclic / pharmacology*
  • Receptors, Endothelin / genetics
  • Receptors, Endothelin / metabolism*
  • Transfection

Substances

  • Endothelin Receptor Antagonists
  • Endothelins
  • Peptides, Cyclic
  • Receptors, Endothelin
  • cyclo(Trp-Asp-Pro-Val-Leu)
  • Calcium