Studies on concurrent alpha- and beta-adrenoceptor blocking action of S-596 (arotinolol)

Jpn Heart J. 1983 Nov;24(6):925-33. doi: 10.1536/ihj.24.925.

Abstract

The effects of a therapeutic dose of oral S-596 upon the cardiovascular response to intravenous isoproterenol and noradrenaline were studied in 2 hypertensive and 4 normotensive subjects in order to evaluate the drug's mode of action. After oral administration of S-596, mean blood pressure rose slightly and the heart rate decreased. In addition, cardiac output decreased considerably and total peripheral resistance increased. However pulmonary arterial end-diastolic pressure and right atrial pressure were not affected by S-596 administration. Before S-596, intravenous isoproterenol increased both heart rate and pulse pressure in a dose-dependent manner. Similarly, intravenous noradrenaline increased both systolic and diastolic pressures. Following 15 mg of S-596, the effects of isoproterenol were antagonized such that the cumulative log-dose-response curves of the mean isoproterenol-induced increases in heart rate and reductions in diastolic pressure were shifted in parallel to the right. At the same time, the mean noradrenaline-induced increases in blood pressure were also antagonized in a competitive manner. The mean ratio of alpha- and beta-components was calculated as: (formula: see text) From this result it can be suggested that the alpha-adrenoceptor blockade potency of this drug is approximately one-eight of its beta-adrenoceptor blockade potency.

MeSH terms

  • Adrenergic alpha-Antagonists / pharmacology*
  • Adrenergic beta-Antagonists / pharmacology*
  • Adult
  • Aged
  • Blood Pressure / drug effects
  • Cardiac Output / drug effects
  • Female
  • Heart Rate / drug effects
  • Hemodynamics / drug effects*
  • Humans
  • Hypertension / physiopathology
  • Isoproterenol / antagonists & inhibitors
  • Isoproterenol / pharmacology
  • Male
  • Middle Aged
  • Norepinephrine / pharmacology
  • Propanolamines / administration & dosage
  • Propanolamines / pharmacology*
  • Stroke Volume / drug effects

Substances

  • Adrenergic alpha-Antagonists
  • Adrenergic beta-Antagonists
  • Propanolamines
  • arotinolol
  • Isoproterenol
  • Norepinephrine