Kaszaki J, Wolfárd A, Szalay L, Boros M
Institute of Surgical Research, University of Szeged, Szent-Györgyi Albert Medical and Pharmaceutical Center, Szeged, Hungary.
Transplant Proc. 2006 Apr;38(3):826-8. doi: 10.1016/j.transproceed.2006.02.152.
Our studies characterized the intestinal microcirculatory changes in canine models of intestinal hypoperfusion (hemorrhagic shock) or ischemia-reperfusion (small bowel autotransplantation). The villus microcirculatory parameters (functional capillary density, mean red blood cell velocity) were observed by intravital microscopy using orthogonal polarization spectral imaging. The leukocyte reaction (rolling and firm adherence) in the mesentery was quantified by using conventional fluorescence videomicroscopy. The investigations were aimed at determining whether the compromised intestinal villus perfusion could be influenced by endothelin-A receptor inhibition, volume resuscitation, or ischemic preconditioning. The results demonstrated the pathophysiological significance of endothelin-A receptor activation in ischemia-reperfusion-induced microcirculatory changes. Second, it was shown that colloid fluid therapy with hydroxyethyl-starch effectively ameliorated the microcirculatory consequences of hypovolemia, which correlated with a lower endothelin release. Third, ischemic preconditioning when applied 60 minutes before ischemia, inhibited the reperfusion-induced superoxide production, improved capillary perfusion, and attenuated leukocyte activation within the intestinal graft. Among the examined therapeutic strategies aimed at improving the outcome of intestinal microcirculatory dysfunction, endothelin-A receptor antagonist pretreatment and ischemic preconditioning are promising tools to decrease the harmful consequences of ischemia/reperfusion.
我们的研究对犬类肠灌注不足(失血性休克)或缺血再灌注(小肠自体移植)模型中的肠道微循环变化进行了特征描述。使用正交偏振光谱成像的活体显微镜观察绒毛微循环参数(功能性毛细血管密度、平均红细胞速度)。通过传统的荧光视频显微镜对肠系膜中的白细胞反应(滚动和牢固黏附)进行定量。这些研究旨在确定内皮素A受体抑制、容量复苏或缺血预处理是否会影响受损的肠绒毛灌注。结果证明了内皮素A受体激活在缺血再灌注诱导的微循环变化中的病理生理意义。其次,研究表明,用羟乙基淀粉进行胶体液治疗可有效改善低血容量引起的微循环后果,这与较低的内皮素释放相关。第三,在缺血前60分钟进行缺血预处理,可抑制再灌注诱导的超氧化物产生,改善毛细血管灌注,并减轻肠移植物内的白细胞激活。在旨在改善肠道微循环功能障碍结局的研究治疗策略中,内皮素A受体拮抗剂预处理和缺血预处理是减少缺血/再灌注有害后果的有前景的工具。