Bauer C, Siaplaouras S, Soule H R, Moyle M, Marzi I
Department of Anesthesiology and Critical Care Medicine, University of Saarland Medical School, Homburg-Saar, Germany.
Shock. 1995 Sep;4(3):187-92. doi: 10.1097/00024382-199509000-00006.
This study was designed to assess the effect of neutrophil inhibitory factor (NIF), a novel specific inhibitor of CD11b/CD18 on hepatic leukocyte trafficking by intravital microscopy 5 h after hemorrhagic shock. Anesthetized rats were instrumented for invasive hemodynamical monitoring. Hemorrhagic shock was induced for 60 min by withdrawal of arterial blood (mean arterial blood pressure = 40 mmHg). Rats were adequately resuscitated for 5 h to achieve a mean arterial blood pressure > 100 mmHg and were randomly assigned to blinded treatment with NIF or placebo control protein administered as a single intravenous bolus (10 mg/kg) at the time of resuscitation. Intrahepatic leukocyte adhesion was evaluated by in vivo fluorescence microscopy. There were no significant differences observed in hemodynamic parameters between the shock groups throughout the study, however, NIF significantly reduced firm leukocyte adhesion in liver sinusoids. The results suggest that NIF may be beneficial in the attenuation of the pathological shock-induced leukocyte adhesion.
本研究旨在通过活体显微镜观察评估中性粒细胞抑制因子(NIF),一种新型的CD11b/CD18特异性抑制剂,在失血性休克5小时后对肝脏白细胞运输的影响。将麻醉的大鼠进行有创血流动力学监测。通过抽取动脉血诱导失血性休克60分钟(平均动脉血压=40 mmHg)。大鼠充分复苏5小时,以使平均动脉血压>100 mmHg,并在复苏时随机分配接受NIF或安慰剂对照蛋白的盲法治疗,以单次静脉推注(10 mg/kg)给药。通过体内荧光显微镜评估肝内白细胞黏附。在整个研究过程中,休克组之间的血流动力学参数未观察到显著差异,然而,NIF显著降低了肝血窦中牢固的白细胞黏附。结果表明,NIF可能有助于减轻病理性休克诱导的白细胞黏附。