Enhancement of the endotoxin recognition pathway by ventilation with a large tidal volume in rabbits

Am J Physiol Lung Cell Mol Physiol. 2004 Jun;286(6):L1114-21. doi: 10.1152/ajplung.00296.2003. Epub 2003 Nov 21.

Abstract

Ventilation with a small tidal volume (V(t)) is associated with better clinical outcomes than with a large V(t), particularly in critical settings, including acute lung injury. To determine whether V(t) influences the lipopolysaccaharide (LPS) recognition pathway, we studied CD14 expression in rabbit lungs and the release of TNF-alpha by cultured alveolar macrophages after 240 min of ventilation with a large (20 ml/kg) vs. a small (5 ml/kg) V(t). We also applied small or large V(t) to lungs instilled with 50 microg/kg of LPS. The alveolar macrophages collected after large V(t) ventilation revealed a 20-fold increase in LPS-induced TNF-alpha release compared with those collected after small V(t) ventilation, whereas TNF-alpha was undetectable without LPS stimulation. In animals ventilated with a large V(t), the expression of CD14 mRNA in whole lung homogenates and the expression of CD14 protein on alveolar macrophages, assessed by immunohistochemistry, were both significantly increased in the absence of LPS stimulation. A large V(t) applied to LPS-instilled lungs increased the pulmonary albumin permeability and TNF-alpha release into the plasma. These results suggest that mechanical stress caused by a large V(t) sensitizes the lungs to endotoxin, a phenomenon that may occur partially via the upregulation of CD14.

Publication types

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

MeSH terms

  • Albumins / metabolism
  • Animals
  • Bronchoalveolar Lavage Fluid / cytology
  • Bronchoalveolar Lavage Fluid / immunology
  • Cells, Cultured
  • Gene Expression
  • Leukocyte Count
  • Lipopolysaccharide Receptors / genetics
  • Lipopolysaccharide Receptors / metabolism
  • Lipopolysaccharides / pharmacology*
  • Lung / drug effects
  • Lung / immunology
  • Lung / metabolism
  • Macrophages, Alveolar / cytology
  • Macrophages, Alveolar / metabolism
  • Male
  • Neutrophils / cytology
  • RNA, Messenger / analysis
  • Rabbits
  • Respiration, Artificial / adverse effects*
  • Respiratory Distress Syndrome / etiology*
  • Respiratory Distress Syndrome / immunology
  • Respiratory Distress Syndrome / metabolism*
  • Tidal Volume*
  • Tumor Necrosis Factor-alpha / metabolism
  • Up-Regulation

Substances

  • Albumins
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha