Journal Article Epublish 4 citations
PubMed: 37108656 DOI: 10.3390/ijms24087494
Immunopathological Alterations after Blast Injury and Hemorrhage in a Swine Model of Prolonged Damage Control Resuscitation.
Int J Mol Sci 24(8)
Authors: Milomir O Simovic, Zhangsheng Yang, Bryan S Jordan, Tamara L Fraker, Tomas S Cancio, Michael L Lucas, Leopoldo C Cancio, Yansong Li
Affiliations
- US Army Institute of Surgical Research, Fort Sam Houston, San Antonio, TX 78234, USA.
- The Geneva Foundation, Tacoma, WA 98402, USA.
- US Army Institute of Surgical Research, Fort Sam Houston, San Antonio, TX 78234, USA. The Geneva Foundation, Tacoma, WA 98402, USA.
Abstract
Trauma-related hemorrhagic shock (HS) remains a leading cause of death among military and civilian trauma patients. We have previously shown that administration of complement and HMGB1 inhibitors attenuate morbidity and mortality 24 h after injury in a rat model of blast injury (BI) and HS. To further validate these results, this study aimed to develop a swine model and evaluate BI+HS-induced pathophysiology. Anesthetized Yucatan minipigs underwent combined BI and volume-controlled hemorrhage. After 30 min of shock, animals received an intravenous bolus of PlasmaLyte A and a continuous PlasmaLyte A infusion. The survival rate was 80% (4/5), and the non-survivor expired 72 min post-BI. Circulating organ-functional biomarkers, inflammatory biomarkers, histopathological evaluation, and CT scans indicated evidence of multiple-organ damage, systemic innate immunological activation, and local tissue inflammation in the injured animals. Interestingly, a rapid and dramatic increase in plasma levels of HMGB1 and C3a and markedly early myocarditis and encephalitis were associated with early death post-BI+HS. This study suggests that this model reflects the immunopathological alterations of polytrauma in humans during shock and prolonged damage control resuscitation. This experimental protocol could be helpful in the assessment of immunological damage control resuscitation approaches during the prolonged care of warfighters.
MeSH
Blast Injuries, Shock, Hemorrhagic, Resuscitation, Hemorrhage, Biomarkers, Multiple Trauma, Wounds And Injuries
Cited by
- An early HMGB1 rise 12 hours before creatinine predicts acute kidney injury and multiple organ failure in a smoke inhalation and burn swine model. Front Immunol, 2024
- Impact of Immunopathy and Coagulopathy on Multi-Organ Failure and Mortality in a Lethal Porcine Model of Controlled and Uncontrolled Hemorrhage. Int J Mol Sci, 2024
- A model to simulate human cardio-respiratory responses to different fluid resuscitation treatments after hemorrhagic injury. Front Physiol, 2025