Matsumoto S, Kuroda Y, Fujita H, Tanioka Y, Sakai T, Hamano M, Kim Y, Suzuki Y, Ku Y, Saitoh Y
First Department of Surgery, Kobe University School of Medicine, Japan.
Transplantation. 1996 Oct 15;62(7):879-83. doi: 10.1097/00007890-199610150-00001.
We have shown that 5-hr preservation using the two-layer (University of Wisconsin solution/perfluorochemical) method at 20 degrees 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 degrees 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 H2 clearance 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+/-1.06 micromol/g dry weight, respectively, and OKY046 did not affect ATP synthesis during 8-hr preservation (8.44+/-0.92 micromol/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 degrees 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 degrees C. This method holds promise for pancreas-kidney transplantation from cardiac arrest donors.
我们已经表明,在20℃下使用两层法(威斯康星大学溶液/全氟化合物)保存5小时可使三磷酸腺苷(ATP)合成,并有可能使经历90分钟热缺血的犬胰腺复苏。然而,使用该方法保存8小时会导致血管微循环紊乱,且移植器官无法复苏。本研究的目的是检测血栓素A2合成抑制剂OKY046在20℃下使用两层法(威斯康星大学溶液/全氟化合物)保存犬胰腺期间对血管内皮细胞和ATP组织水平的影响,以及移植后血管微循环和胰腺活力。通过自体移植后的移植器官存活情况判断移植器官的活力。在保存结束时,通过高效液相色谱法测量ATP组织水平。使用保存后移植器官的台盼蓝核摄取来判断血管内皮细胞的活力。再灌注后,使用氢气清除技术测量胰腺组织灌注。经历90分钟热缺血的胰腺移植器官不可存活(0/5)。然而,5小时的保存使胰腺得以恢复(5/5);8小时的保存未成功(0/3)。5小时和8小时保存后的ATP组织水平分别为9.40±2.09和7.37±1.06微摩尔/克干重,且OKY046在8小时保存期间不影响ATP合成(8.44±0.92微摩尔/克干重)。8小时保存的移植器官中内皮细胞核摄取台盼蓝的百分比为37.6±11.6%,显著高于5小时保存的移植器官中的值(5.0±3.0%;P<0.01)。然而,OKY046显著降低了8小时保存的移植器官中台盼蓝的摄取(8.2±3.6%;P<0.01)。再灌注2小时后,8小时保存的移植器官中的胰腺组织灌注为28.5±7.5毫升/分钟/100克,显著低于5小时保存的移植器官中的值(57.1±4.4毫升/分钟/100克;P<0.01),但OKY046显著改善了胰腺组织灌注(97.1±14.6毫升/分钟/100克;P<0.01)。结果,8小时保存的移植器官得以复苏(4/5)。我们得出结论,OKY046在20℃下通过两层法保存期间保护血管内皮,从而改善再灌注时的血管微循环。与修复受损细胞所必需的ATP合成一起,经历90分钟热缺血的犬胰腺移植器官在20℃下通过两层法保存8小时期间得以复苏。该方法有望用于心脏骤停供体的胰肾联合移植。