The relationship between some beta-adrenergic mediated responses and plasma concentrations of adrenaline and cyclic AMP in man

Acta Endocrinol (Copenh). 1990 Jan;122(1):115-20. doi: 10.1530/acta.0.1220115.

Abstract

To test the hypothesis that increments in plasma cyclic AMP during beta-adrenergic stimulation reflect integrated second messenger function of the tissues activated by the agonist, graded adrenaline infusion resulting in plasma adrenaline concentrations within the physiological range was performed in 8 healthy subjects with and without concomitant beta-adrenoceptor blockade by iv propranolol. A significant correlation was found between increments in plasma adrenaline and plasma cyclic AMP in the experiments without beta-blockade; during concomitant beta-blockade the increase in plasma cyclic AMP concentrations at low adrenaline infusion rates was prevented, whereas a small increase in cyclic AMP was found at high adrenaline infusion rates, probably owing to incomplete beta-receptor blockade. Likewise, the adrenaline-induced increments in blood substrates (glucose, lactate, glycerol and beta hydroxybutyric acid) were significantly reduced but not completely prevented by beta-blockade. We conclude that an altered relationship between beta-agonist concentrations and plasma cyclic AMP may provide evidence for the existence of differences in beta-adrenergic sensitivity in man.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / administration & dosage
  • Adult
  • Blood Pressure / drug effects
  • Catecholamines / blood*
  • Cyclic AMP / blood*
  • Epinephrine / administration & dosage*
  • Epinephrine / blood
  • Glucagon / blood
  • Heart Rate / drug effects
  • Humans
  • Infusions, Intravenous
  • Insulin / blood
  • Intestinal Mucosa / metabolism
  • Male
  • Pancreas / metabolism
  • Propranolol / administration & dosage
  • Receptors, Adrenergic, beta / drug effects*
  • Receptors, Adrenergic, beta / physiology

Substances

  • Adrenergic beta-Antagonists
  • Catecholamines
  • Insulin
  • Receptors, Adrenergic, beta
  • Glucagon
  • Propranolol
  • Cyclic AMP
  • Epinephrine