Lehmann Christian, Birnbaum Jürgen, Lührs Carsten, Rückbeil Oskar, Spies Claudia, Ziemer Sabine, Gründling Matthias, Pavlovic Dragan, Usichenko Taras, Wendt Michael, Kox Wolfgang J
Klinik für Anästhesiologie und Intensivmedizin, Ernst-Moritz-Arndt-Universität Greifswald, F.-Loeffler-Strasse 23, 17489, Greifswald, Germany.
Klinik für Anaesthesiologie und operative Intensivmedizin, Universitätsklinikum Charité, Humboldt-Universität zu Berlin, Schumannstrasse 20/21, 10117, Berlin, Germany.
Intensive Care Med. 2004 Feb;30(2):309-314. doi: 10.1007/s00134-003-2042-2. Epub 2003 Oct 29.
To determine the effects of C1 esterase inhibitor (C1-INH) administration on intestinal functional capillary density, leukocyte adherence, and mesenteric plasma extravasation during experimental endotoxemia.
Prospective, randomized, controlled animal study in the experimental laboratory of a university.
42 male Wistar rats.
The animals were divided into three groups. One half of the animals of each group underwent studies of intestinal functional capillary density and leukocyte adherence on venular endothelium by intravital fluorescence microscopy. In the other half of the animals mesenteric plasma extravasation (FITC albumin) was determined by intravital fluorescence microscopy. Treatment groups received endotoxin infusion of 2.5 mg/kg per hour (group 2 and 3) and 100 U/kg b.w. C1-INH (group 3) during the 2 h of endotoxemia.
Endotoxemia resulted in a significant decrease in mucosal functional capillary density (18.5% vs. controls), which was reduced by C1-INH administration (9.5%). Treatment with C1-INH also significantly attenuated intestinal leukocyte adherence in submucosal venules (35% vs. endotoxin group) and mesenteric plasma extravasation (44% vs. endotoxin group).
C1-INH administration diminishes endotoxin-induced changes in the intestinal microcirculation during experimental endotoxemia.
确定给予C1酯酶抑制剂(C1-INH)对实验性内毒素血症期间肠道功能性毛细血管密度、白细胞黏附和肠系膜血浆外渗的影响。
在一所大学的实验室内进行的前瞻性、随机、对照动物研究。
42只雄性Wistar大鼠。
将动物分为三组。每组动物的一半通过活体荧光显微镜检查研究肠道功能性毛细血管密度和白细胞在小静脉内皮上的黏附情况。另一半动物通过活体荧光显微镜检查测定肠系膜血浆外渗(异硫氰酸荧光素标记的白蛋白)。在内毒素血症的2小时期间,治疗组接受每小时2.5mg/kg的内毒素输注(第2组和第3组)以及100U/kg体重的C1-INH(第3组)。
内毒素血症导致黏膜功能性毛细血管密度显著降低(与对照组相比降低18.5%),而给予C1-INH可使其降低幅度减小(降低9.5%)。C1-INH治疗还显著减轻了黏膜下小静脉中的肠道白细胞黏附(与内毒素组相比降低35%)和肠系膜血浆外渗(与内毒素组相比降低44%)。
给予C1-INH可减轻实验性内毒素血症期间内毒素诱导的肠道微循环变化。