Ferrario Manuela, Brunelli Laura, Su Fuhong, Herpain Antoine, Pastorelli Roberta
Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.
Department of Environmental Health Sciences, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Front Physiol. 2019 Jan 28;10:11. doi: 10.3389/fphys.2019.00011. eCollection 2019.
Septic shock is a medical emergency and is one of the main causes of mortality in critically ill patients. Given the pathophysiological complexity of sepsis spectrum and progression in clinical settings, animal models become essential tools to improve patient care, and to understand key mechanisms that may remain masked from the heterogeneity of clinical practice. Our aim was to verify whether the metabolic constellations we previously reported for septic shock patients appear also in our septic shock swine model as systemic markers of early disturbances in energy metabolism and hepatic homeostasis. Septic shock was induced in anesthetized, instrumented, and ventilated adult swines by polymicrobial peritonitis. Hemodynamic and serial measurements of arterial and mixed venous blood gasses were made. Laboratory measurements and mass spectrometry-based targeted quantitative plasma metabolomics were performed in blood samples collected at baseline, at shock and at fully resuscitation after fluids and vasopressors administration. Data elaboration was performed by multilevel and multivariate analysis. Changes in hemodynamic, blood chemistry, and inflammatory markers were in line with a septic shock phenotype. Time course alteration of systemic metabolites were characterized by marked decreased in phosphatidylcholines and lysophosphatidylcholines species, altered alanine-glucose cycle and inter-organ amino acid metabolism, pointing toward an early hepatic impairment similarly to what we previously reported for septic shock. This is the first study in which an experimental swine model of septic shock recapitulates the main metabolic derangements reported in a clinical setting of shock. These events occur within hours from infections and may act as early metabolic features to assist in evaluating subclinical hepatic alterations and pave the way to improve the management of septic shock.
脓毒性休克是一种医疗急症,是重症患者死亡的主要原因之一。鉴于脓毒症谱系在临床环境中的病理生理复杂性和进展情况,动物模型成为改善患者护理以及了解可能因临床实践异质性而被掩盖的关键机制的重要工具。我们的目的是验证我们之前报道的脓毒性休克患者的代谢模式是否也出现在我们的脓毒性休克猪模型中,作为能量代谢和肝脏内稳态早期紊乱的系统标志物。通过多微生物性腹膜炎在麻醉、插管和通气的成年猪中诱导脓毒性休克。进行血流动力学以及动脉血和混合静脉血气的系列测量。在基线、休克时以及在给予液体和血管加压药后完全复苏时采集的血样中进行实验室测量和基于质谱的靶向定量血浆代谢组学分析。通过多水平和多变量分析进行数据处理。血流动力学、血液化学和炎症标志物的变化与脓毒性休克表型一致。全身代谢物的时间进程变化表现为磷脂酰胆碱和溶血磷脂酰胆碱种类显著减少、丙氨酸 - 葡萄糖循环改变以及器官间氨基酸代谢改变,这表明早期肝脏受损,与我们之前对脓毒性休克的报道相似。这是第一项在脓毒性休克实验猪模型中重现休克临床环境中报道的主要代谢紊乱的研究。这些事件在感染后数小时内发生,可能作为早期代谢特征,有助于评估亚临床肝脏改变,并为改善脓毒性休克的管理铺平道路。