Competitive blockade of alpha-adrenergic receptors in rat heart by prazosin

Acta Pharmacol Toxicol (Copenh). 1980 Sep;47(3):217-22. doi: 10.1111/j.1600-0773.1980.tb01563.x.

Abstract

Phenylephrine (PE) in presence of propranolol evokes an alpha-adrenergic inotropic response in rat heart. The time course of this response is characterized by a transient decrease in maximal developed tension (Tmax) to subcontrol levels (negative phase of the inotropic response) followed by an increase which reaches maximum after 4-5 min. (positive phase of the inotropic response). Prazosin (PRZ), a selective alpha 1-receptor blocker, inhibited preferentially the positive phase of the inotropic response and displaced the dose-response curve of PE to the right in nanomolar concentrations, indicating a competitive mechanism of inhibition. Phentolamine, a non-selective alpha-blocker, blocked both the negative and the positive phase of the inotropic response to about the same degree. PRZ appears to be a competitive alpha-adrenergic antagonist with high affinity in rat heart. Two populations of alpha-adrenergic receptors may be present: one stimulatory (alpha 1) and one inhibitory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Antagonists*
  • Animals
  • Heart / drug effects*
  • In Vitro Techniques
  • Male
  • Myocardial Contraction / drug effects
  • Papillary Muscles / drug effects
  • Phentolamine / pharmacology
  • Phenylephrine / pharmacology
  • Prazosin / pharmacology*
  • Propranolol / pharmacology
  • Quinazolines / pharmacology*
  • Rats

Substances

  • Adrenergic alpha-Antagonists
  • Quinazolines
  • Phenylephrine
  • Propranolol
  • Prazosin
  • Phentolamine