W. Bernauer, EFFECT OF ANTIARRHYTHMICS ON THE RELEASE OF ADENOSINE IN RAT HEARTS WITH CORONARY-OCCLUSION AND REPERFUSION, European journal of pharmacology, 283(1-3), 1995, pp. 91-98
In isolated perfused rat hearts the left coronary artery was occluded
for 5 min, with subsequent reperfusion for 20 min. During the reperfus
ion severe tachyarrhythmias were observed, with ventricular fibrillati
on occurring in all hearts. Simultaneously, large amounts of adenosine
and its degradation products inosine, hypoxanthine, xanthine and uric
acid were released into the coronary perfusate. The antiarrhythmics q
uinidine, lidocaine and gallopamil significantly decreased the release
. The effect of quinidine and lidocaine was linked with the antifibril
latory action of these drugs. Also the interruption of fibrillation im
mediately after its appearance by potassium chloride decreased the rel
ease of adenosine and its metabolites in a highly significant way. The
effect of gallopamil on the release was independent of an antifibrill
atory action. The findings indicate that different kinds of antiarrhyt
hmic drugs can affect the release of nucleosides and oxypurines in hea
rts with ischaemia and reperfusion.