Adenosine inhibition of beta-adrenergic induced responses in aged hearts

Am J Physiol. 1993 Aug;265(2 Pt 2):H494-503. doi: 10.1152/ajpheart.1993.265.2.H494.

Abstract

Because adenosine has an antiadrenergic action in the heart, young (3-4 mo) and aged (18-20 mo) adult Sprague-Dawley and Fischer 344 rat hearts were perfused to determine whether interstitial adenosine plays a role in the reduced metabolic and mechanical responsiveness of the aged heart to beta-adrenergic stimulation. Interstitial adenosine was approximately twofold greater in aged hearts compared with young adult hearts, and 10(-8) M isoproterenol (ISO) further increased these levels. ISO increased myocardial adenosine 3',5'-cyclic monophosphate content, glycogen phosphorylase activity, and cardiac contractility by 83, 150, and 130%, respectively, in young hearts but only increased these variables by 45, 74, and 61%, respectively, in aged hearts. Sulfophenyl-theophylline prevented the reduced ISO-induced responsiveness of the above variables in aged hearts. Exogenously administered adenosine deaminase eliminated the reduced ISO-induced contractile responsiveness in aged hearts. The apparent activities of 5'-nucleotidase and adenosine deaminase were not significantly different in ventricular samples from young and aged hearts. These results suggest that the elevated interstitial level of adenosine exerts a greater antiadrenergic effect in the aged heart, rendering it less responsive to beta-adrenergic stimulation. The increased interstitial level of adenosine in the aged heart does not appear to be due to a difference in the activities of either 5'-nucleotidase or adenosine deaminase.

Publication types

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

MeSH terms

  • 5'-Nucleotidase / metabolism
  • Adenosine / pharmacology*
  • Adenosine Deaminase / pharmacology
  • Adrenergic beta-Antagonists / pharmacology*
  • Aging / metabolism*
  • Animals
  • Coronary Vessels
  • Cyclic AMP / metabolism
  • Extracellular Space / metabolism
  • Heart / drug effects
  • In Vitro Techniques
  • Inosine / metabolism
  • Male
  • Myocardial Contraction
  • Myocardium / metabolism*
  • Oxygen Consumption
  • Phosphorylases / metabolism
  • Rats
  • Rats, Inbred F344
  • Rats, Sprague-Dawley

Substances

  • Adrenergic beta-Antagonists
  • Inosine
  • Cyclic AMP
  • Phosphorylases
  • 5'-Nucleotidase
  • Adenosine Deaminase
  • Adenosine