Title

Inhibition by adenosine of catecholamine-induced increase in rat atrial contractility

UMMS Affiliation

Department of Physiology

Date

9-11-1980

Document Type

Article

Subjects

Acetylcholine; Adenosine; Animals; Atrial Function; Bucladesine; Calcium; Drug Synergism; Isoproterenol; Male; Myocardial Contraction; Rats; Time Factors

Disciplines

Cardiovascular Diseases | Physiology

Abstract

Because adenosine has been shown to attenuate the catecholamine-induced increase in myocardial cAMP formation and glycogen phosphorylase activity (Circ. Res. 43: 785-792, 1978), the present study was undertaken to determine whether the nucleoside inhibits the catecholamine-elicited increase in cardiac contractile state. Isolated rat atria were bathed in oxygenated physiologic saline and stimulated to contract isometrically at 2/s. Isoproterenol (0.1 microM) increased peak contractile force (PCF) by 96% and the rate of force development (+dF/dt) by 107%. Adenosine (10 microM) alone had no effect on these contractile parameters. Isoproterenol in the presence of adenosine increased PCF and +dF/dt only 15 and 14%, respectively. Elevation of bathing medium Ca2+ or administration of dibutyryl cAMP (DBcAMP) increased PCF and +dF/dt, but these responses were not decreased by adenosine. Inosine, adenine, adenosine 5'-monophosphate, and guanosine inhibited the isoproterenol-induced responses 5-22%. The results indicate that adenosine markedly inhibits, whereas some related purines only mildly attenuate, the catecholamine-elicited, but not the Ca2+- or DBcAMP-elicited, increases in contractility. Thus, adenosine may antagonize catecholamine-elicited glycogenolysis and enhanced contractile state in the heart by exerting an effect at the level of, or proximal to, cAMP formation.

Rights and Permissions

Citation: Am J Physiol. 1980 Sep;239(3):H365-70.

Related Resources

Link to article in PubMed

PubMed ID

6254373