Pulmonary surfactant in birds: coping with surface tension in a tubular lung

1  Departments of Pediatric Pulmonology and Neonatology, 2  Applied and Functional Anatomy, and 3  Respiratory Medicine, Hannover Medical School, 30625 Hannover, Germany; and 4  Child Health, Allergy and Inflammation Sciences Division, School of Medicine, University of Southampton, SO16 6YD Southamp...

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Veröffentlicht in:American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2001-07, Vol.281 (1), p.327-R337
Hauptverfasser: Bernhard, Wolfgang, Gebert, Andreas, Vieten, Gertrud, Rau, Gunnar A, Hohlfeld, Jens M, Postle, Anthony D, Freihorst, Joachim
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Sprache:eng
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Zusammenfassung:1  Departments of Pediatric Pulmonology and Neonatology, 2  Applied and Functional Anatomy, and 3  Respiratory Medicine, Hannover Medical School, 30625 Hannover, Germany; and 4  Child Health, Allergy and Inflammation Sciences Division, School of Medicine, University of Southampton, SO16 6YD Southampton, United Kingdom As birds have tubular lungs that do not contain alveoli, avian surfactant predominantly functions to maintain airflow in tubes rather than to prevent alveolar collapse. Consequently, we have evaluated structural, biochemical, and functional parameters of avian surfactant as a model for airway surfactant in the mammalian lung. Surfactant was isolated from duck, chicken, and pig lung lavage fluid by differential centrifugation. Electron microscopy revealed a uniform surfactant layer within the air capillaries of the bird lungs, and there was no tubular myelin in purified avian surfactants. Phosphatidylcholine molecular species of the various surfactants were measured by HPLC. Compared with pig surfactant, both bird surfactants were enriched in dipalmitoylphosphatidylcholine, the principle surface tension-lowering agent in surfactant, and depleted in palmitoylmyristoylphosphatidylcholine, the other disaturated phosphatidylcholine of mammalian surfactant. Surfactant protein (SP)-A was determined by immunoblot analysis, and SP-B and SP-C were determined by gel-filtration HPLC. Neither SP-A nor SP-C was detectable in either bird surfactant, but both preparations of surfactant contained SP-B. Surface tension function was determined using both the pulsating bubble surfactometer (PBS) and capillary surfactometer (CS). Under dynamic cycling conditions, where pig surfactant readily reached minimal surface tension values below 5 mN/m, neither avian surfactant reached values below 15 mN/m within 10 pulsations. However, maximal surface tension of avian surfactant was lower than that of porcine surfactant, and all surfactants were equally efficient in the CS. We conclude that a surfactant composed primarily of dipalmitoylphosphatidylcholine and SP-B is adequate to maintain patency of the air capillaries of the bird lung. avian lung surfactant; capillary surfactometer; dipalmitoylphosphatidylcholine; pulsating bubble surfactometer; surfactant function
ISSN:0363-6119
1522-1490
DOI:10.1152/ajpregu.2001.281.1.r327