Halothane Reduces Release of Adenosine, Inosine, and Lactate with Ischemia and Reperfusion in Isolated Hearts

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Abstract
. Isolated perfused guinea pig hearts were divided into three groups of perfusion at 25% (14 mm Hg), 10% (5.5 mm Hg), and 0% (no perfusion) from control perfusion pressure (PP, 55 mm Hg). Each of these PP groups was subdivided into three subgroups and perfused without halothane (control), with 0.23 ± 0.01 mM (0.74%) halothane, or with 0.51 ± 0.01 mM (1.65%) halothane. Halothane was present 10 min before reducing PP, during reduced PP (30 min), and for 10 min after reducing PP. Hypoperfusion was followed by 40 min of reperfusion at the control (100%, 55 mm Hg) PP. An additional group of control hearts was followed for the same period without reducing PP or perfusing with halothane. Exposure to 0.74% and 1.65% halothane, before reducing PP, decreased MVO2 and percent oxygen extraction (% O2E), but produced no significant change in coronary flow or release of ADE, ISO, or LAC. During early hypoperfusion (10 min) at 25% PP, 1.65% halothane significantly reduced release of ADE, INO, and LAC. During late hypoperfusion (40 min) the differences in LAC release diminished, but release of ADE and INO remained lower in the 1.65% halothane group. With early reperfusion there was a large increase in release of these metabolites, that was dependent on the decrease in perfusion pressure. The release of INO during reperfusion was reduced by halothane; however, ADE release increased with halothane suggesting less conversion of ADE to INO. The release of LAC was not affected by halothane. The reduction of cardiac work effected by halothane either before, during, or after graded reductions in PP may decrease the loss of purine substrate so that synthesis of high energy phosphates is less impaired. This study suggests that our earlier finding that halothane improved contractile function and reduced the severity of dysrhythmias in isolated hearts following graded reductions in PP is due, at least in part, to a decrease in oxygen demand relative to oxygen supply, resulting in a decrease in purine release. Address correspondence to Dr. Zeljko J. Bosnjak, Medical College of Wisconsin, Department of Anesthesiology, MFRC/A1000, 8701 West Watertown Plank Road, Milwaukee, WI 53226. Supported in part by Grants HL 01901 and HL 34708 from the National Institutes of Health. A preliminary report appears in abstract form in FASEB J 1991;5:A1049. Accepted for publication August 18, 1992. © 1993 International Anesthesia Research Society...

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