Damage-associated molecular patterns in resuscitated hemorrhagic shock are mitigated by peritoneal fluid administration

Am J Physiol Lung Cell Mol Physiol. 2018 Sep 1;315(3):L339-L347. doi: 10.1152/ajplung.00183.2017. Epub 2018 May 3.

Abstract

Conventional resuscitation (CR) of hemorrhagic shock (HS), a significant cause of trauma mortality, is intravenous blood and fluids. CR restores central hemodynamics, but vital organ flow can drop, causing hypoperfusion, hypoxia, damage-associated molecular patterns (DAMPs), and remote organ dysfunction (i.e., lung). CR plus direct peritoneal resuscitation (DPR) prevents intestinal and hepatic hypoperfusion. We hypothesized that DPR prevents lung injury in HS/CR by altering DAMPs. Anesthetized male Sprague-Dawley rats were randomized to groups ( n = 8/group) in one of two sets: 1) sham (no HS, CR, or DPR), 2) HS/CR (HS = 40% mean arterial pressure (MAP) for 60 min, CR = shed blood + 2 volumes normal saline), or 3) HS/CR + DPR. The first set underwent whole lung blood flow by colorimetric microspheres. The second set underwent tissue collection for Luminex, ELISAs, and histopathology. Lipopolysaccharide (LPS) and DAMPs were measured in serum and/or lung, including cytokines, hyaluronic acid (HA), high-mobility group box 1 (HMGB1), Toll-like receptor 4 (TLR4), myeloid differentiation primary response 88 protein (MYD88), and TIR-domain-containing adapter-inducing interferon-β (TRIF). Statistics were by ANOVA and Tukey-Kramer test with a priori P < 0.05. HS/CR increased serum LPS, HA, HMGB1, and some cytokines [interleukin (IL)-1α, IL-1β, IL-6, and interferon-γ]. Lung TLR4 and MYD88 were increased but not TRIF compared with Shams. HS/CR + DPR decreased LPS, HA, cytokines, HMGB1, TLR4, and MYD88 levels but did not alter TRIF compared with HS/CR. The data suggest that gut-derived DAMPs can be modulated by adjunctive DPR to prevent activation of lung TLR-4-mediated processes. Also, DPR improved lung blood flow and reduced lung tissue injury. Adjunctive DPR in HS/CR potentially improves morbidity and mortality by downregulating the systemic DAMP response.

Keywords: DAMP; VEGF-A; damage-associated molecular pattern; dialysis fluid; direct peritoneal resuscitation; hemorrhage; peritoneal dialysis; pulmonary blood flow; rat; resuscitation.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blood Pressure
  • Cytokines / metabolism
  • Disease Models, Animal
  • Fluid Therapy*
  • HMGB1 Protein / metabolism
  • Lung Injury / metabolism
  • Lung Injury / pathology
  • Lung Injury / physiopathology
  • Lung Injury / prevention & control*
  • Male
  • Myeloid Differentiation Factor 88 / metabolism
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Resuscitation*
  • Shock, Hemorrhagic / metabolism
  • Shock, Hemorrhagic / pathology
  • Shock, Hemorrhagic / physiopathology
  • Shock, Hemorrhagic / therapy*
  • Toll-Like Receptor 4 / metabolism

Substances

  • Cytokines
  • HMGB1 Protein
  • Hbp1 protein, rat
  • Myd88 protein, rat
  • Myeloid Differentiation Factor 88
  • Tlr4 protein, rat
  • Toll-Like Receptor 4