EXTENDING THE MARGIN OF SAFETY OF PRESERVATION PERIOD FOR RESUSCITATION OF ISCHEMICALLY DAMAGED PANCREAS DURING PRESERVATION USING THE TWO-LAYER(UNIVERSITY OF WISCONSIN SOLUTION/PERFLUOROCHEMICAL) METHOD AT 20??C WITH THROMBOXANE A2 SYNTHESIS INHIBITOR OKY046

Abstract
We have shown that 5-hr preservation using the two-layer (University of Wisconsin solution/perfluorochemical) method at 20 °C allows ATP synthesis and makes it possible to resuscitate a canine pancreas subjected to 90 min of warm ischemia. However, 8 hr of preservation using this method caused a disturbance of vascular microcirculation and did not resuscitate the grafts. The aim of this study was to examine the effect of thromboxane A2 synthesis inhibitor OKY046 on vascular endothelial cells and ATP tissue levels of canine pancreas during preservation using the two-layer (University of Wisconsin solution/perfluorochemical) method at 20 °C, and vascular microcirculation and pancreas viability after transplantation. Graft viability was judged by graft survival following autotransplantation. ATP tissue levels were measured by high-performance liquid chromatography at the end of preservation. Viability of the vascular endothelial cells was judged using nuclear trypan blue uptake of the graft after preservation. Pancreatic tissue perfusion was measured using an H2clearance technique after reperfusion. Pancreas grafts subjected to 90 min of warm ischemia were not viable(0/5). However, 5-hr preservation made it possible to recover the pancreas(5/5); 8-hr preservation was not successful (0/3). ATP tissue levels after 5-hr and 8-hr preservation were 9.40±2.09 and 7.37±1.06μmol/g dry weight, respectively, and OKY046 did not affect ATP synthesis during 8-hr preservation (8.44±0.92 μmol/g dry weight). The percentage of nuclear trypan blue uptake of endothelial cells in 8-hr-preserved grafts was 37.6±11.6% and was significantly higher than the value in 5-hr-preserved grafts (5.0±3.0%;P<0.01). However, OKY046 significantly reduced trypan blue uptake in 8-hr-preserved grafts (8.2±3.6%;P<0.01). Pancreatic tissue perfusion in 8-hr-preserved grafts after 2 hr of reperfusion was 28.5±7.5 ml/min/100 g, and was significantly lower than the value in 5-hr-preserved grafts(57.1±4.4 ml/min/100 g; P<0.01), but OKY046 dramatically improved pancreatic tissue perfusion (97.1±14.6 ml/min/100 g; P<0.01). As a consequence, 8-hr-preserved grafts were resuscitated (4/5). We conclude that OKY046 protects the vascular endothelium during preservation by the two-layer method at 20 °C and consequently improves vascular microcirculation on reperfusion. Together with ATP synthesis, which is essential for repairing damaged cells, the canine pancreas graft subjected to 90 min of warm ischemia is resuscitated during 8-hr preservation by the two-layer method at 20 °C. This method holds promise for pancreas-kidney transplantation from cardiac arrest donors.

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