Evidence that cytosolic and ecto 5'-nucleotidases contribute equally to increased interstitial adenosine concentration during porcine myocardial ischemia

Abstract

The purpose of this study was to determine the roles of cytosolic and ecto 5'-nucleotidase in myocardial ischemia-induced increases in interstitial fluid (ISF) adenosine. Pentobarbital anesthetized, open chest pigs were instrumented with two microdialysis fibers in the distally perfused bed of the left anterior descending (LAD) coronary artery to estimate ISF metabolites. Fibers in control hearts were perfused with standard Krebs buffer. In two additional groups, after collecting one dialysate sample with normal Krebs, fibers were perfused with buffer supplemented with either L-homocysteine thiolactone (5 mM) or the ecto 5'-nucleotidase inhibitor α, β-methylene adenosine 5'-diphosphate (AOPCP, 5 mM). Hearts were then submitted to 60 minutes LAD occlusion and two hours reperfusion. Dialysate nucleosides and AMP were measured by high performance liquid chromatography. The local delivery of homocysteine did not alter preischemic dialysate adenosine concentration (0.30 ± 0.04 μM) compared to pre-homocysteine infusion (0.39 ± 0.04 μM) or control hearts (0.36 ± 0.04 μM), but AOPCP significantly decreased preischemic dialysate adenosine levels (from 0.36 ± 0.02 to 0.14 ± 0.03 μM). During LAD occlusion both homocysteine and AOPCP reduced dialysate levels by approximately 50 %. At 30 minutes ischemia dialysate adenosine concentrations were 19.47 ± 2.72, 11.41 ± 2.44, and 7.93 ± 1.01 μ:M in control, homocysteine, and AOPCP hearts, respectively. AOPCP significantly increased dialysate AMP levels; at 60 minutes ischemia AMP levels were 6.22 ± 2.97 μM in control hearts and 38.60 ± 5.69 μM in AOPCP treated hearts. These results suggest that both cytosolic and ecto 5'-nucleotidase contribute to ischemia-induced increases in ISF adenosine in porcine myocardium.