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首页> 外文期刊>British journal of anaesthesia >Gut microcirculatory and mitochondrial effects of hyperdynamic endotoxaemic shock and norepinephrine treatment
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Gut microcirculatory and mitochondrial effects of hyperdynamic endotoxaemic shock and norepinephrine treatment

机译:内毒素血症性休克和去甲肾上腺素治疗的肠道微循环和线粒体作用

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摘要

BackgroundMicrocirculatory and mitochondrial dysfunction are important factors in the development of septic shock. In this study, we investigated the effects of fluid resuscitated endotoxaemic shock and norepinephrine treatment on intestinal microcirculation and mitochondrial function in sheep. MethodsEight anaesthetized sheep received an i.v. infusion of endotoxin. After 24 h, mean arterial pressure (MAP) was restored to baseline levels with a norepinephrine infusion. Five sheep served as sham experiments. Central and regional haemodynamics were monitored, and ileal microcirculation was evaluated with laser Doppler and sidestream dark-field videomicroscopy techniques. Gut mucosal acidosis was assessed by air tonometry, and ileal wall biopsies were analysed for mitochondrial activity. ResultsAfter 24 h of endotoxaemia, the animals had developed hyperdynamic shock with systemic and mucosal acidosis. Although superior mesenteric artery (SMA) flow was higher than the baseline values, ileal microcirculatory perfusion and mitochondrial complex I activity decreased. After norepinephrine was started, SMA flow, ileal microcirculation, and mucosal acidosis remained unchanged. Although no statistically significant difference could be demonstrated, norepinephrine increased mitochondrial complex I activity in five of the six animals from which ileal biopsies were taken. ConclusionsAlthough fluid resuscitated endotoxaemic shock increased regional blood flow, microcirculatory and mitochondrial alterations were still present. Restoring MAP with norepinephrine did not affect ileal microcirculation or mucosal acidosis, indicating that perfusion pressure manipulation is of limited importance to the intestinal microcirculation in established endotoxaemic shock.
机译:背景微循环和线粒体功能障碍是感染性休克发展的重要因素。在这项研究中,我们调查了液体复苏的内毒素休克和去甲肾上腺素对绵羊肠道微循环和线粒体功能的影响。方法八只麻醉的绵羊接受静脉注射。输注内毒素。 24小时后,通过去甲肾上腺素输注将平均动脉压(MAP)恢复至基线水平。五只羊作为假实验。监测中央和区域血流动力学,并用激光多普勒和侧流暗场视频显微镜技术评估回肠微循环。通过空气眼压计评估肠粘膜酸中毒,并分析回肠壁活检组织的线粒体活性。结果内毒素血症24小时后,动物出现全身性和粘膜酸中毒的高动力性休克。尽管肠系膜上动脉(SMA)流量高于基线值,但回肠微循环灌注和线粒体复合体I活性降低。去甲肾上腺素开始后,SMA流量,回肠微循环和粘膜酸中毒保持不变。尽管没有统计学上的显着差异,但去甲肾上腺素在进行回肠活检的六只动物中有五只增加了线粒体复合体I的活性。结论尽管液体复苏的内毒素休克增加了局部血流量,但仍存在微循环和线粒体改变。用去甲肾上腺素恢复MAP不会影响回肠微循环或粘膜酸中毒,这表明在已建立的内毒素休克中,灌注压力操纵对肠道微循环的重要性有限。

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