Lung inflammatory responses and hyperinflation induced by an intratracheal exposure to lipopolysaccharide in rats

Lung. 2004;182(3):163-71. doi: 10.1007/s00408-004-1803-1.


Exposure of the respiratory tract to lipopolysaccharide (LPS) induces acute local inflammation and tissue injury associated with the various deliveries of LPS. To determine potential association of local inflammatory responses with respiratory tract dysfunction, infiltration of inflammatory cells, production of inflammatory mediators, lung hyperinflation and edema were measured in Wister rats 2, 4, and 24 h after an intratracheal administration of LPS at different doses (5, 50, 500 and 5000 microg/ml/kg). Lung hyperinflation determined by an increased excised lung gas volume was significantly increased 2 and 4 h after LPS instillation and lung edema occurred from 2 h onward. Peak BAL levels of TNFalpha appeared at 2 h, MCP-1 at 4 h, and IL-6 at 2 and 4 h, while BAL levels of IL-1beta were increased during 24 h after the intratracheal instillation of LPS. Neutrophilia in BAL fluid was noted from 2 h post-challenge. Our results demonstrate a clear dose-related change in the lung weight at 4 and 24 h, in the BAL levels of MCP-1 at 4 h, and IL-6 and IL-1beta at 2 and 4 h. It seems important to understand polymorphisms of LPS-induced lung hyperinflation and inflammation. Lung hyperinflation and inflammation may be independent during the development of acute lung injury.

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid / chemistry
  • Chemokine CCL2 / metabolism
  • Dose-Response Relationship, Drug
  • Female
  • Interleukin-1 / metabolism
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / toxicity*
  • Lung / drug effects
  • Lung / pathology
  • Lung Volume Measurements
  • Organ Size
  • Pneumonia / chemically induced*
  • Pneumonia / metabolism
  • Pneumonia / pathology*
  • Pulmonary Edema / chemically induced
  • Pulmonary Edema / metabolism
  • Pulmonary Edema / pathology
  • Rats
  • Rats, Wistar
  • Trachea*
  • Tumor Necrosis Factor-alpha / metabolism


  • Chemokine CCL2
  • Interleukin-1
  • Interleukin-6
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha