Characterization of a murine model of endotoxin-induced acute lung injury

Shock. 2002 Apr;17(4):300-3. doi: 10.1097/00024382-200204000-00010.

Abstract

Endotoxin-induced microvascular lung injury in mice is a commonly used experimental model of the acute respiratory distress syndrome (ARDS). The present paper aimed to characterize this popular model in a comprehensive and systematic fashion. Male C57bl/6 mice (n = 5) were administered an LD55 dose of E. coli endotoxin (15 mg/kg, i.p.), and lungs were harvested at several time points and evaluated for injury as well as for expression of a variety of inflammatory mediators. Endotoxin induced many features characteristic of acute microvascular lung injury. These included early (1-2 h) expression of inflammatory mediators (IL-1alpha, IL-1beta, IL-4, IL-6, IL-10, TNF-alpha, interferon-alpha, interferon gamma, and MCP-1) and leukocyte accumulation in lung tissue (lung myeloperoxidase activity 18.5 +/- 7.8 U/g tissue, P < 0.05), followed by pulmonary edema (lung water content index 17.4% +/- 2.5%, P < 0.05) and mortality. Histopathological evaluation of lung tissue was compatible with these findings. The characterization of this murine model of endotoxin-induced microvascular injury will facilitate its utilization in ARDS research.

MeSH terms

  • Animals
  • Chemokines / biosynthesis
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Disease Models, Animal
  • Endotoxins / toxicity*
  • Gene Expression / drug effects
  • Humans
  • Inflammation Mediators / metabolism
  • Lung / drug effects*
  • Lung / metabolism
  • Lung / pathology
  • Lung Injury*
  • Mice
  • Mice, Inbred C57BL
  • Peroxidase / metabolism
  • Pulmonary Edema / chemically induced
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Respiratory Distress Syndrome / etiology

Substances

  • Chemokines
  • Cytokines
  • Endotoxins
  • Inflammation Mediators
  • RNA, Messenger
  • Peroxidase