Enhanced myocardial protection during global ischemia with 5’-nucleotidase inhibitors

• Published in: The Journal of thoracic and cardiovascular surgery Vol. 103; no. 1; pp. 73 - 77
• Main Authors: Bolling, Steven F., Olszanski, Douglas A., Bove, Edward L., Childs, Keith F.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.1992; AATS/WTSA
• Subjects: 5'-Nucleotidase - antagonists & inhibitors; Animals; Bicarbonates - pharmacology; Calcium Chloride - pharmacology; Cardioplegic Solutions - pharmacology; Dimethyl Sulfoxide - pharmacology; Magnesium - pharmacology; Myocardial Contraction - physiology; Myocardial Reperfusion Injury - physiopathology; Myocardial Reperfusion Injury - prevention & control; Pentoxifylline - pharmacology; Potassium Chloride - pharmacology; Rabbits; Sodium Chloride - pharmacology; Thioinosine - pharmacology
• ISSN: 0022-5223; 1097-685X
• DOI: 10.1016/S0022-5223(19)35068-8

Depletion of adenosine triphosphate precursors, such as myocardial adenosine, during global ischemia results in poor postischemic adenosine triphosphate repletion and functional recovery. Neonatal hearts may be more resistant to this deleterious effect of ischemia, because they are characterized by low 5’-nucleotidase activity, which may result in higher sustained endogenous myocardial adenosine triphosphate precursor levels during ischemia. Adult hearts, however, have high levels of 5’-nucleotidase activity leading to depleted precursors during ischemia and poor postischemic functional recovery. Augmenting myocardial adenosine exogenously during ischemia in adult hearts has a beneficial effect on recovery. The present study tested if preservation of nucleotide precursors, better adenosine triphosphate repletion, and enhanced postischemic myocardial recovery in adult hearts could be achieved with a “neonatal” strategy. Therefore 5’-nucleotidase inhibitors were administered to isolated, perfused adult rabbit hearts subjected to 120 minutes of ischemia (at 34° C) to determine if this improved functional recovery. Hearts received St. Thomas’ Hospital cardioplegic solution (control hearts) or cardioplegic solution containing 5’-nucleotidase inhibitors: pentoxifylline, thioinosine, [s-(p-nitrophenyl)-4-thioinosine], or thioinosine's dimethyl sulfoxide vehicle alone. After ischemia and reperfusion, recovery of systolic function, diastolic function, and myocardial oxygen consumption was significantly better with 5’-nucleotidase inhibition. No changes in coronary flow were noted. We speculate and are pursuing the theory that the mechanism of 5’-nucleotidase inhibition's favorable action is due to preventing the catabolism, transport, and loss of nucleotide precursors during ischemia, maintaining adenosine triphosphate precursor availability. (J Thorac Cardiovasc Surg 1992;103:73—7)