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Determinants of surfactant function in acute lung injury and early recovery.

Abstract
Relationships between lung function and surfactant function and composition were examined during the evolution of acute lung injury in guinea pigs. Lung mechanics and gas exchange were assessed 12, 24, or 48 h after exposure to nebulized lipopolysaccharide (LPS). Bronchoalveolar lavage (BAL) fluid was processed for phospholipid and protein contents and surfactant protein (SP) A and SP-B levels; surfactant function was measured by pulsating bubble surfactometry. Lung elastance, tissue resistance, and arterial-alveolar gradient were moderately elevated by 12 h after LPS exposure and continued to increase over the first 24 h but began to recover between 24 and 48 h. Similarly, the absolute amount of 30,000 g pelleted SP-A and SP-B, the phospholipid content of BAL fluid, and surfactant function declined over the first 24 h after exposure, with recovery between 24 and 48 h. BAL fluid total protein content increased steadily over the first 48 h after LPS nebulization. In this model of acute lung injury, the intra-alveolar repletion of surfactant components in early recovery led to improved surfactant function despite the presence of potentially inhibitory plasma proteins.
AuthorsR Mora, S Arold, Y Marzan, B Suki, E P Ingenito
JournalAmerican journal of physiology. Lung cellular and molecular physiology (Am J Physiol Lung Cell Mol Physiol) Vol. 279 Issue 2 Pg. L342-9 (Aug 2000) ISSN: 1040-0605 [Print] United States
PMID10926558 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Lipopolysaccharides
  • Phospholipids
  • Proteins
  • Proteolipids
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Surfactants
Topics
  • Administration, Inhalation
  • Animals
  • Blotting, Western
  • Bronchoalveolar Lavage Fluid (chemistry, cytology)
  • Cell Count
  • Disease Models, Animal
  • Guinea Pigs
  • Infusions, Intravenous
  • Lipopolysaccharides (administration & dosage)
  • Male
  • Phospholipids (analysis)
  • Proteins (analysis)
  • Proteolipids (metabolism)
  • Pulmonary Gas Exchange (physiology)
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Surfactants (metabolism)
  • Recovery of Function (physiology)
  • Respiratory Distress Syndrome (metabolism)

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