Xu Xuefeng, Jia Chune, Luo Sa, Li Yanming, Xiao Fei, Dai Huaping, Wang Chen
National Clinical Research Centre for Respiratory Diseases, Beijing Hospital, Beijing, 100730, China.
Department of Surgical Intensive Care Medicine, Beijing An Zhen Hospital, Capital Medical University, No. 2 Anzhen Rd., Chao-Yang District, Beijing, 100029, China.
Ann Intensive Care. 2017 Aug 14;7(1):84. doi: 10.1186/s13613-017-0287-0.
Blood purification is an emerging approach to dampening the cytokine storm. This study aims to assess the efficacy of HA330 resin-directed hemoadsorption (HA) on endotoxin-induced porcine acute respiratory distress syndrome (ARDS) model.
Twenty-four Chinese domestic pigs were allocated into saline group receiving intravenous infusion of saline (N = 6) and endotoxin group receiving intravenous infusion of LPS (N = 18). When ALI model was initially diagnosed, six pigs in the LPS and saline group were killed for BALF and histopathological analysis. The remaining 12 pigs in LPS group received 3-h HA (N = 6) or HA-sham (N = 6) treatment, respectively. Following another 5-h observation, animals were killed. Variables on hemodynamics, blood gases and lung mechanics were recorded at a series of time points. Differentially expressed cytokines and proteins were determined by ELISA and proteomics.
HA treatment significantly improved injured oxygenation induced by LPS. HA also partially improved the barrier permeability and reduced lung edema and inflammation/injury induced by LPS infusion. Proteomic analysis showed the differentially expressed proteins between HA- and HA-sham-treated groups mostly belonged to the categories of acute inflammation/immune response, and proteolysis.
Hemoadsorption improved ARDS possibly by blunting the cytokine storm and by restoring homeostasis of the disordered proteome milieu in the exudative phase.
血液净化是一种抑制细胞因子风暴的新兴方法。本研究旨在评估HA330树脂直接血液吸附(HA)对内毒素诱导的猪急性呼吸窘迫综合征(ARDS)模型的疗效。
将24头中国家猪分为接受静脉输注生理盐水的生理盐水组(N = 6)和接受静脉输注脂多糖的内毒素组(N = 18)。当最初诊断出ALI模型时,将内毒素组和生理盐水组中的6头猪处死以进行支气管肺泡灌洗(BALF)和组织病理学分析。内毒素组中剩余的12头猪分别接受3小时的HA(N = 6)或假HA(N = 6)治疗。在另外5小时的观察后,将动物处死。在一系列时间点记录血流动力学、血气和肺力学方面的变量。通过酶联免疫吸附测定(ELISA)和蛋白质组学确定差异表达的细胞因子和蛋白质。
HA治疗显著改善了由脂多糖诱导的受损氧合。HA还部分改善了屏障通透性,并减少了由脂多糖输注引起的肺水肿和炎症/损伤。蛋白质组学分析表明,HA治疗组和假HA治疗组之间差异表达的蛋白质大多属于急性炎症/免疫反应和蛋白水解类别。
血液吸附可能通过抑制细胞因子风暴和恢复渗出期紊乱蛋白质组环境的稳态来改善ARDS。