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A reversible model of acute lung injury based on ozone exposure

In this study inflammatory responses were determined in rat lungs 0, 1, 3, and 8 days following single 2- and 4-hr exposures to 1.8 ppm ozone. Analysis of lavage fluid immediately following exposure demonstrated enhanced lactate dehydrogenase activity and decreased numbers of lavageable macrophages...

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Autores principales: Bassett, D. J. P., Bowen-Kelly, E., Brewster, E. L., Elbon, C. L., Reichenbaugh, S. S., Bunton, T., Kerr, J. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087886/
https://www.ncbi.nlm.nih.gov/pubmed/3148794
http://dx.doi.org/10.1007/BF02714068
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author Bassett, D. J. P.
Bowen-Kelly, E.
Brewster, E. L.
Elbon, C. L.
Reichenbaugh, S. S.
Bunton, T.
Kerr, J. S.
author_facet Bassett, D. J. P.
Bowen-Kelly, E.
Brewster, E. L.
Elbon, C. L.
Reichenbaugh, S. S.
Bunton, T.
Kerr, J. S.
author_sort Bassett, D. J. P.
collection PubMed
description In this study inflammatory responses were determined in rat lungs 0, 1, 3, and 8 days following single 2- and 4-hr exposures to 1.8 ppm ozone. Analysis of lavage fluid immediately following exposure demonstrated enhanced lactate dehydrogenase activity and decreased numbers of lavageable macrophages but no alterations in albumin content. Similar analyses at one day postexposure demonstrated 282% and 456% increases in albumin content and enhanced numbers of lavageable neutrophils from a control value of 0.01 ± 0.01 to 0.27 ± 0.10 and 0.78 ± 0.11 million cells per lung for 2-hr and 4-hr exposures, respectively. The observed increased levels of albumin were also present at 3 days, at which time the number of lavageable neutrophils was not significantly different than control. At both one and 3 days postexposure, lavageable lymphocytes were significantly increased 10-fold from a control value of 0.03 ± 0.01 million cells per lung. However, the number of lavageable macrophages was unaltered on day 1, but enhanced on day 3, giving values of 0.67 ± 0.05 (control), 2.25 ± 0.46 (2 hr), and 2.70 ± 1.05 (4 hr) million cells per lung. By 8 days both inflammatory cell numbers and albumin levels had returned to control values. Since these data demonstrated different time courses for each inflammatory cell type, this reversible model of acute lung injury should be useful for establishing possible involvement of these cells in processes of lung injury.
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spelling pubmed-70878862020-03-23 A reversible model of acute lung injury based on ozone exposure Bassett, D. J. P. Bowen-Kelly, E. Brewster, E. L. Elbon, C. L. Reichenbaugh, S. S. Bunton, T. Kerr, J. S. Lung Article In this study inflammatory responses were determined in rat lungs 0, 1, 3, and 8 days following single 2- and 4-hr exposures to 1.8 ppm ozone. Analysis of lavage fluid immediately following exposure demonstrated enhanced lactate dehydrogenase activity and decreased numbers of lavageable macrophages but no alterations in albumin content. Similar analyses at one day postexposure demonstrated 282% and 456% increases in albumin content and enhanced numbers of lavageable neutrophils from a control value of 0.01 ± 0.01 to 0.27 ± 0.10 and 0.78 ± 0.11 million cells per lung for 2-hr and 4-hr exposures, respectively. The observed increased levels of albumin were also present at 3 days, at which time the number of lavageable neutrophils was not significantly different than control. At both one and 3 days postexposure, lavageable lymphocytes were significantly increased 10-fold from a control value of 0.03 ± 0.01 million cells per lung. However, the number of lavageable macrophages was unaltered on day 1, but enhanced on day 3, giving values of 0.67 ± 0.05 (control), 2.25 ± 0.46 (2 hr), and 2.70 ± 1.05 (4 hr) million cells per lung. By 8 days both inflammatory cell numbers and albumin levels had returned to control values. Since these data demonstrated different time courses for each inflammatory cell type, this reversible model of acute lung injury should be useful for establishing possible involvement of these cells in processes of lung injury. Springer-Verlag 1988 /pmc/articles/PMC7087886/ /pubmed/3148794 http://dx.doi.org/10.1007/BF02714068 Text en © Springer-Verlag New York, Inc 1988 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Bassett, D. J. P.
Bowen-Kelly, E.
Brewster, E. L.
Elbon, C. L.
Reichenbaugh, S. S.
Bunton, T.
Kerr, J. S.
A reversible model of acute lung injury based on ozone exposure
title A reversible model of acute lung injury based on ozone exposure
title_full A reversible model of acute lung injury based on ozone exposure
title_fullStr A reversible model of acute lung injury based on ozone exposure
title_full_unstemmed A reversible model of acute lung injury based on ozone exposure
title_short A reversible model of acute lung injury based on ozone exposure
title_sort reversible model of acute lung injury based on ozone exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087886/
https://www.ncbi.nlm.nih.gov/pubmed/3148794
http://dx.doi.org/10.1007/BF02714068
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