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Alleviation of methyl isocyanate-induced airway obstruction and mortality by tissue plasminogen activator.
Nick, Heidi J; Rioux, Jacqueline S; Veress, Livia A; Bratcher, Preston E; Bloomquist, Leslie A; Anantharam, Poojya; Croutch, Claire R; Tuttle, Richard S; Peters, Eric; Sosna, William; White, Carl W.
Afiliación
  • Nick HJ; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Rioux JS; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Veress LA; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Bratcher PE; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Bloomquist LA; Division of Cell Biology, Department of Pediatrics, National Jewish Health, Denver, Colorado.
  • Anantharam P; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Croutch CR; MRIGlobal, Kansas City, Missouri.
  • Tuttle RS; MRIGlobal, Kansas City, Missouri.
  • Peters E; MRIGlobal, Kansas City, Missouri.
  • Sosna W; MRIGlobal, Kansas City, Missouri.
  • White CW; MRIGlobal, Kansas City, Missouri.
Ann N Y Acad Sci ; 1479(1): 134-147, 2020 11.
Article en En | MEDLINE | ID: mdl-32233099
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 (LC90-100 ). 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Activador de Tejido Plasminógeno / Isocianatos / Obstrucción de las Vías Aéreas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Ann N Y Acad Sci Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Activador de Tejido Plasminógeno / Isocianatos / Obstrucción de las Vías Aéreas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Ann N Y Acad Sci Año: 2020 Tipo del documento: Article
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