麻醉猪内毒素剂量呈对数增长时的炎症、凝血和循环反应

M. Lipcsey, A. Larsson, M. Eriksson, J. Sjölin
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引用次数: 28

摘要

虽然猪静脉内毒素休克模型被广泛用于实验性败血症,但内毒素剂量效应的研究很少。我们的主要目的是建立增加内毒素剂量对炎症、凝固和血流动力学效应变量的剂量反应,并确定在猪模型中进行评估的最佳时间点。第二个目的是研究不同反应之间的病理生理协变。20头麻醉仔猪静脉注射剂量分别为0.063 (n = 3)、0.25 (n = 3)、1.0 (n = 3)、4.0 (n = 3)、8 (n = 3)和16µg/kg/h (n = 2)的内毒素,另设无内毒素仔猪作为对照组(n = 3)。每小时的血小板和血红蛋白浓度,持续6小时。内毒素剂量的增加诱导了显著的对数对数细胞因子反应以及对数线性白细胞和血小板反应。在循环参数、血浆漏、低灌注和肺顺应性方面观察到显著的对数线性反应。在应答中注意到显著的协变。总之,对内毒素的对数对数或对数线性反应表明,在较低的预先存在的内毒素浓度下,给定剂量的效果更大,并且≤1 μ g/kg/h的较低剂量可能有利于研究实验药物或措施的潜在抗内毒素作用。
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Inflammatory, coagulatory and circulatory responses to logarithmic increases in the endotoxin dose in the anaesthetised pig
Although porcine intravenous endotoxin shock models are widely employed in experimental sepsis, endotoxin dose-effect studies are scarce. Our primary aim was to establish the dose response to increasing endotoxin doses in inflammatory, coagulatory and haemodynamic effect variables, as well as to determine the optimal time point for assessment in a pig model. A secondary aim was to study pathophysiological covariations between the different responses. Twenty anaesthetised piglets received endotoxin intravenously in doses of 0.063 (n = 3), 0.25 (n = 3), 1.0 ( n = 3), 4.0 (n = 3), 8 (n = 3) and 16 µg/kg/h (n = 2). In addition, non-endotoxin piglets constituted a control group (n = 3). Physiological variables were registered and blood samples analysed for TNF-α, IL-6, leukocyte, platelet and haemoglobin concentrations hourly for 6 h. Increases in the endotoxin dose induced significant log—log cytokine responses as well as log—linear leukocyte and platelet responses. Significant log—linear responses were observed for circulatory parameters, plasma leakage, hypoperfusion and pulmonary compliance. Significant covariations in the responses were noted. In conclusion, there were log—log or log—linear responses to endotoxin suggesting a greater effect of a given dose at lower pre-existing endotoxin concentrations and lower doses of ≤ 1 µg/kg/h may be of advantage in experiments designed to study potential anti-endotoxin effects of experimental drugs or measures.
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