Pulmonary inflammatory response and immunomodulation to multiple trauma and hemorrhagic shock in pigs

PLoS One. 2022 Dec 7;17(12):e0278766. doi: 10.1371/journal.pone.0278766. eCollection 2022.

Abstract

Background: Patients suffering from severe trauma experience substantial immunological stress. Lung injury is a known risk factor for the development of posttraumatic complications, but information on the long-term course of the pulmonary inflammatory response and treatment with mild hypothermia are scarce.

Aim: To investigate the pulmonary inflammatory response to multiple trauma and hemorrhagic shock in a porcine model of combined trauma and to assess the immunomodulatory properties of mild hypothermia.

Methods: Following induction of trauma (blunt chest trauma, liver laceration, tibia fracture), two degrees of hemorrhagic shock (45 and 50%) over 90 (n = 30) and 120 min. (n = 20) were induced. Animals were randomized to hypothermia (33°C) or normothermia (38°C). We evaluated bronchoalveolar lavage (BAL) fluid and tissue levels of cytokines and investigated changes in microRNA- and gene-expression as well as tissue apoptosis.

Results: We observed a significant induction of Interleukin (IL) 1β, IL-6, IL-8, and Cyclooxygenase-2 mRNA in lung tissue. Likewise, an increased IL-6 protein concentration could be detected in BAL-fluid, with a slight decrease of IL-6 protein in animals treated with hypothermia. Lower IL-10 protein levels in normothermia and higher IL-10 protein concentrations in hypothermia accompanied this trend. Tissue apoptosis increased after trauma. However, intervention with hypothermia did not result in a meaningful reduction of pro-inflammatory biomarkers or tissue apoptosis.

Conclusion: We observed signs of a time-dependent pulmonary inflammation and apoptosis at the site of severe trauma, and to a lower extent in the trauma-distant lung. Intervention with mild hypothermia had no considerable effect during 48 hours following trauma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Interleukin-10
  • Interleukin-6
  • Lung
  • Multiple Trauma* / complications
  • Multiple Trauma* / therapy
  • Shock, Hemorrhagic* / therapy
  • Swine
  • Thoracic Injuries* / complications
  • Thoracic Injuries* / therapy
  • Wounds, Nonpenetrating*

Substances

  • Interleukin-10
  • Interleukin-6

Associated data

  • figshare/10.6084/m9.figshare.21324561.v1

Grants and funding

The work was supported by the Stiftung P.E. Kempkes (https://www.uni-marburg.de/de/forschung/foerderung/stiftung-pekempkes) and a doctoral scholarship from the Faculty of Medicine of Philipps-Universität Marburg (https://www.unimarburg.de/de/fb20) to MAO, the German Research Foundation (DFG SFB-TR84; https://www.dfg.de/) to B.S. (C1), the Bundesministerium für Bildung und Forschung (PermedCOPD – FKZ 01EK2203A, JPI-AMR – FKZ 01Kl1702; ERACoSysMed2 – SysMed-COPD – FKZ 031L0140; https://www.bmbf.de/) to BS, the Von-Behring- Röntgen-Stiftung (66-LV07; https://www.br-stiftung.de/) to BS, and Hessisches Ministerium für Wissenschaft und Kunst (LOEWE research cluster Diffusible Signals, B1; https://proloewe.de/en/research-initiatives/by-topic/diffusible-signals) to BS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.