Dual inhibition of beta-adrenergic and angiotensin II receptors by a single antagonist: a functional role for receptor-receptor interaction in vivo

Circulation. 2003 Sep 30;108(13):1611-8. doi: 10.1161/01.CIR.0000092166.30360.78. Epub 2003 Sep 8.

Abstract

Background: Although the renin-angiotensin and the beta-adrenergic systems are interrelated, a direct interaction between beta-adrenergic receptors (betaARs) and angiotensin II type 1 receptors (AT1Rs) has not been identified.

Methods and results: Here, we provide evidence for a functional and physiological interaction between 2 G protein-coupled receptors: the betaAR and the AT1R. Selective blockade of betaARs in mouse cardiomyocytes inhibits angiotensin-induced contractility with an IC50 that is similar to its inhibition of isoproterenol-mediated contractility. Furthermore, administration of the angiotensin receptor blocker valsartan to intact mice results in a significant reduction in the maximal response to catecholamine-induced elevation of heart rate. The mechanism for this transinhibitory effect of beta-blockers and angiotensin receptor blockers is through receptor-G protein uncoupling; ie, beta-blockers interfere with AT1R-Gq coupling, and valsartan interferes with betaAR-Gs coupling. Finally, we demonstrate that AT1Rs and betaARs form constitutive complexes that are not affected by ligand stimulation. As a result of these interactions, a single receptor antagonist effectively blocks downstream signaling and trafficking of both receptors simultaneously.

Conclusions: We show that direct interactions between betaARs and AT1Rs may have profound consequences on the overall response to drugs that antagonize these receptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology*
  • Angiotensin II / antagonists & inhibitors
  • Angiotensin II / metabolism
  • Angiotensin Receptor Antagonists*
  • Animals
  • Binding, Competitive
  • COS Cells
  • Cell Line
  • Cells, Cultured
  • Female
  • Heart Rate / drug effects
  • Heterotrimeric GTP-Binding Proteins / metabolism
  • Humans
  • Isoproterenol / pharmacology
  • Macromolecular Substances
  • Mice
  • Mice, Inbred C57BL
  • Myocardial Contraction / drug effects
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / physiology
  • Propranolol / pharmacology
  • Receptor, Angiotensin, Type 1
  • Receptors, Adrenergic, beta / metabolism
  • Receptors, Angiotensin / metabolism
  • Signal Transduction / drug effects
  • Tetrazoles / pharmacology
  • Valine / analogs & derivatives*
  • Valine / pharmacology
  • Valsartan

Substances

  • Adrenergic beta-Antagonists
  • Angiotensin Receptor Antagonists
  • Macromolecular Substances
  • Receptor, Angiotensin, Type 1
  • Receptors, Adrenergic, beta
  • Receptors, Angiotensin
  • Tetrazoles
  • Angiotensin II
  • Valsartan
  • Propranolol
  • Heterotrimeric GTP-Binding Proteins
  • Valine
  • Isoproterenol