Department of Anesthesiology, Cheng-Hsin General Hospital, Taipei, Taiwan, ROC.
Department of Pharmacology, National Defense Medical Center, Taipei, Taiwan, ROC; Department of Anesthesiology, Mackay Memorial Hospital, Taipei, Taiwan, ROC.
J Chin Med Assoc. 2017 Jul;80(7):432-441. doi: 10.1016/j.jcma.2016.12.008. Epub 2017 May 3.
In patients with severe sepsis, pro-inflammatory cytokines and subsequent activation of tissue factors trigger a cascade of events that lead to coagulation dysfunction and multiple organ failure. It has been shown that levosimendan has protective effects against tissue injury caused by endotoxin. The purpose of this study was to evaluate the effects of levosimendan on consumptive coagulopathy and organ dysfunction in an endotoxemic animal model induced by lipopolysaccharide (LPS).
Forty-six male adult Wistar rats were randomly divided into four groups: 1) control group (n = 10), an intravenous infusion of 5% dextrose 1.2 mL/kg for 20 min and 0.03 mL/kg/min for 4 h; 2) the levosimendan-treated control group (n = 12), an intravenous levosimendan infusion (24 μg/kg for 20 min plus 0.6 μg/kg/min for 4 h); 3) the LPS group (n = 12), an intravenous LPS (4 mg/kg) infusion followed by dextrose administration; and 4) the levosimendan-treated LPS group (n = 12), an intravenous LPS infusion followed by levosimendan treatment. Various parameters of hemodynamics, biochemistry, hemostasis and inflammatory response were examined during the experimental period.
The administration of levosimendan significantly attenuated (i) consumptive coagulopathy displayed by thromboelastography, (ii) the decreases of platelet count and plasma fibrinogen level, (iii) injury in the lung, liver and kidney, and (iv) the rise in plasma interleukin-6 in rats treated with LPS.
The treatment of LPS rats with levosimendan was found to reduce organ injury and coagulopathy. These protective effects may be attributed to the anti-inflammatory effects of this drug.
在严重脓毒症患者中,促炎细胞因子和随后组织因子的激活引发了一系列事件,导致凝血功能障碍和多器官衰竭。已经表明,左西孟旦对内毒素引起的组织损伤具有保护作用。本研究旨在评估左西孟旦对脂多糖(LPS)诱导的内毒素血症动物模型消耗性凝血病和器官功能障碍的影响。
46 只成年雄性 Wistar 大鼠随机分为四组:1)对照组(n=10),静脉输注 5%葡萄糖 1.2 mL/kg,持续 20 分钟,然后以 0.03 mL/kg/min 的速度输注 4 小时;2)左西孟旦治疗对照组(n=12),静脉输注左西孟旦(24μg/kg 持续 20 分钟,然后以 0.6μg/kg/min 的速度输注 4 小时);3)LPS 组(n=12),静脉输注 LPS(4mg/kg),然后给予葡萄糖;4)左西孟旦治疗 LPS 组(n=12),静脉输注 LPS 后给予左西孟旦治疗。在实验期间检查了血流动力学、生化、止血和炎症反应的各种参数。
左西孟旦的给药显著减轻了(i)血栓弹性图显示的消耗性凝血病,(ii)血小板计数和血浆纤维蛋白原水平的降低,(iii)肺、肝和肾的损伤,以及(iv)LPS 处理大鼠血浆白细胞介素-6 的升高。
在 LPS 大鼠中使用左西孟旦治疗可减少器官损伤和凝血病。这些保护作用可能归因于该药物的抗炎作用。