Response of the Pulmonary Surfactant System To Phosgene

Author:

Frosolono M.F.1,Currie William D.2

Affiliation:

1. Department of Clinical Research, Medical Division, The Burroughs Wellcome Company, 3030 Cornwallis Road, Research Triangle Park, North Carolina 27709, Division of Radiobiology, Department of Radiology, Duke University Medical Center, Durham, North Carolina 27710

2. Division of Radiobiology, Department of Radiology, Duke University Medical Center, Durham, North Carolina 27710

Abstract

Rats were exposed to 240 ppm·min phosgene (1.0 ppm for 4 hrs) in a Rochester-type chamber. At intervals thereafter over a 4 day period, lungs were removed for determination of wet weight; total, microsomal and surfactant protein concentrations; surfactant phospholipid concentrations; and 1-acyl-2-lyso-phosphatidylcholine: palmitoyl-CoA acyl transferase activity. Immediately upon termination of the phosgene exposure, microsomal protein and acyl transferase activity were reduced below, and lung wet weight was elevated above, control levels. From Day 1 through Day 3 after the exposure, all measured parameters, except for the phosphatidylinositol constituent of the surfactant fraction, were increased above the control values. In general, maximum levels were observed on Day 2; however, the acyl transferase activity and surfactant concentration continued to increase on Day 3. The results suggest (a) components of the pulmonary surfactant system may be involved in maintenance of pulmonary fluid balance and (b) the presence of excess water in the lungs as a result of phosgene exposure may represent a signal for increased synthesis of anti-edematogenic materials in order to promote removal of the inappropriate fluid.

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health,Toxicology

Reference19 articles.

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2. Scarpelli, E.M., Perinatal Respiration in Pulmonary Physiology of the Fetus, Newborn, and Child , edited by E.M. Scarpelli, pp. 116-139, Philadelphia, Lea and Febiger, 1968.

3. Isolation, characterization, and surface chemistry of a surface-active fraction from dog lung

4. Lung surface-active fraction as a model system for macromolecular ultrastructural studies with Crotalus atrox venom

5. Frosolono, M.F., Lung, in Lipid Metabolism in Mammals, Vol. 2, edited by F. Snyder, pp. 1-38, New York , Plenum Press, 1977.

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