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Vol. 286, Issue 2, 806-811, August 1998
Department of Surgery, University of Kentucky College of Medicine,
Lexington, Kentucky
Exogenous adenosine produces numerous beneficial effects in ischemic
myocardium, but pharmacological doses of adenosine are required to
exert these effects. This is thought to be due to the rapid metabolism
of adenosine by coronary endothelium, although there is no direct
evidence supporting this hypothesis in the ischemic/reperfused heart.
The purpose of this study was to determine the relationship between
vascular and interstitial fluid (ISF) adenosine levels during
adenosine-induced cardioprotection. Isolated perfused rat hearts were
submitted to 30-min global normothermic ischemia and 30- min
reperfusion. Left ventricular developed pressure (LVDP) was measured
with a fluid-filled latex balloon, and ISF adenosine was estimated with
cardiac microdialysis. Control hearts were compared with hearts treated
with increasing doses of adenosine (1, 10 and 100 µM) for 10 min
immediately preceding ischemia. Adenosine produced dose-dependent
increases in coronary effluent adenosine levels, but only 10 and 100 µM adenosine increased dialysate adenosine concentrations. All
adenosine doses increased coronary flow to the same extent, but only
the two higher doses decreased spontaneous heart rate. Control and 1 µM adenosine-treated hearts recovered 60 ± 3% and 46 ± 7% of preischemic LVDP, respectively, whereas 10 and 100 µM
adenosine improved recovery to 80 ± 5% and 90 ± 4% of
preischemic LVDP, respectively, after 30-min reperfusion. Because ISF
bathes the cardiac myocytes, these results are consistent with the
hypothesis that adenosine protects the ischemic rat heart via the activation of cardiac myocyte adenosine
receptors.