Mester Anita, Magyar Zsuzsanna, Sogor Viktoria, Tanczos Bence, Stark Yoav, Cherniavsky Konstantin, Bidiga Laszlo, Peto Katalin, Nemeth Norbert
Department of Operative Techniques and Surgical Research, Faculty of Medicine, University of Debrecen, Hungary.
Department of Pathology, University of Debrecen, Hungary.
Clin Hemorheol Microcirc. 2018;68(1):35-44. doi: 10.3233/CH-170278.
Intestinal ischemia-reperfusion (I/R) is a potentially life-threatening situation and its pathomechanism is not fully understood yet.
To investigate the early micro-rheological, microcirculatory and morphological consequences of intestinal I/R in a rat model.
CD rats were anesthetized and subjected to Control (n = 7) or I/R (n = 7) groups. Left femoral artery cannulation and median laparotomy were performed. In the I/R group the superior mesenteric artery was clamped for 30 minutes. Blood samples were taken before (Base) and after the ischemia, at the 30th, 60th and 120th minutes of the reperfusion (R-30, R-60, R-120). Hematological parameters, erythrocyte deformability and aggregation were determined. On the jejunum, the liver and the right kidney laser Doppler flowmetry tests were completed. At the end of experiment histological samples were taken.
Hematocrit, leukocyte and platelet counts increased during the reperfusion. Erythrocyte deformability worsened versus Control. All erythrocyte aggregation index values of I/R group increased gradually. Intestinal microcirculatory blood flux units (BFU) did not recover completely after ischemia, at R-30 liver BFU values were lower, and kidney values decreased by R-120. Histology showed signs of I/R injury.
Micro-rheological parameters may show early and significant deterioration during the reperfusion that might contribute further to microcirculatory alterations.
肠道缺血再灌注(I/R)是一种潜在的危及生命的情况,其发病机制尚未完全明确。
在大鼠模型中研究肠道I/R早期的微观流变学、微循环及形态学变化。
将CD大鼠麻醉后分为对照组(n = 7)和I/R组(n = 7)。进行左股动脉插管及正中剖腹术。I/R组中,肠系膜上动脉夹闭30分钟。在缺血前(基础值)、缺血后以及再灌注第30、60和120分钟(R-30、R-60、R-120)采集血样。测定血液学参数、红细胞变形性和聚集性。在空肠、肝脏和右肾完成激光多普勒血流仪检测。实验结束时采集组织学样本。
再灌注期间血细胞比容、白细胞和血小板计数增加。与对照组相比,红细胞变形性变差。I/R组所有红细胞聚集指数值逐渐升高。缺血后肠道微循环血流量单位(BFU)未完全恢复,R-30时肝脏BFU值较低,R-120时肾脏BFU值降低。组织学显示有I/R损伤迹象。
微观流变学参数在再灌注期间可能出现早期且显著的恶化,这可能进一步导致微循环改变。