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组织型纤溶酶原激活物减轻异氰酸甲酯所致气道阻塞和死亡率。

Alleviation of methyl isocyanate-induced airway obstruction and mortality by tissue plasminogen activator.

机构信息

Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.

Division of Cell Biology, Department of Pediatrics, National Jewish Health, Denver, Colorado.

出版信息

Ann N Y Acad Sci. 2020 Nov;1479(1):134-147. doi: 10.1111/nyas.14344. Epub 2020 Mar 31.

Abstract

Methyl isocyanate (MIC, "Bhopal agent") is a highly reactive, toxic industrial chemical. Inhalation of high levels (500-1000 ppm) of MIC vapor is almost uniformly fatal. No therapeutic interventions other than supportive care have been described that can delay the onset of illness or death due to MIC. Recently, we found that inhalation of MIC caused the appearance of activated tissue factor in circulation with subsequent activation of the coagulation cascade. Herein, we report that MIC exposure (500 ppm for 30 min, nose-only) caused deposition of fibrin-rich casts in the conducting airways resulting in respiratory failure and death within 24 h in a rat model (LC ). We thus investigated the effect of airway delivery of the fibrinolytic agent tissue plasminogen activator (tPA) on mortality and morbidity in this model. Intratracheal administration of tPA was initiated 11 h post MIC exposure and repeated every 4 h for the duration of the study. Treatment with tPA afforded nearly 60% survival at 24 h post MIC exposure and was associated with decreased airway fibrin casts, stabilization of hypoxemia and respiratory distress, and improved acidosis. This work supports the potential of airway-delivered tPA therapy as a useful countermeasure in stabilizing victims of high-level MIC exposure.

摘要

甲基异氰酸酯(MIC,“博帕尔试剂”)是一种高反应性、有毒的工业化学品。吸入高浓度(500-1000ppm)的 MIC 蒸气几乎是致命的。除了支持性护理外,尚未描述任何可以延迟 MIC 引起的疾病发作或死亡的治疗干预措施。最近,我们发现 MIC 吸入会导致循环中出现激活的组织因子,随后激活凝血级联反应。在此,我们报告 MIC 暴露(500ppm 暴露 30 分钟,仅通过鼻腔)会导致富含纤维蛋白的铸型在传导气道中沉积,从而导致呼吸衰竭,并在 LC 大鼠模型中在 24 小时内死亡。因此,我们研究了气道给予纤维蛋白溶解剂组织纤溶酶原激活剂(tPA)对该模型死亡率和发病率的影响。在 MIC 暴露后 11 小时开始进行气管内 tPA 给药,并在研究期间每 4 小时重复一次。在 MIC 暴露后 24 小时,tPA 治疗的存活率接近 60%,与气道纤维蛋白铸型减少、低氧血症和呼吸窘迫稳定以及酸中毒改善相关。这项工作支持气道给予 tPA 治疗作为稳定高浓度 MIC 暴露受害者的一种有用对策的潜力。

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