ERJ
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Order Full text via Infotrieve
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Permissions
Right arrowRequest Permissions
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schmekel, B
Right arrow Articles by Venge, P
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schmekel, B
Right arrow Articles by Venge, P
Eur Respir J 1991; 4: 517-523
Copyright © ERS Journals Ltd 1991


Original Articles

The distribution of myeloperoxidase, eosinophil cationic protein, albumin and urea in sequential bronchoalveolar lavage

B Schmekel and P Venge

The distribution of myeloperoxidase (MPO) and eosinophil cationic protein (ECP), secreted from activated neutrophils and eosinophils, was estimated in bronchoalveolar lavage fluid in a sequential lavage study performed on 12 healthy subjects. Four 50 ml aliquots were sequentially injected into the right middle lobe and immediately aspirated. Recent studies, using radiological methods, have revealed proximal airway distribution of the first infused lavage aliquot, and more peripheral distribution of the following ones. We found significantly higher concentrations of MPO (p less than 0.001) and ECP (p less than 0.001) in the first aspirated aliquots as compared to the following three. These findings are compatible with the concept that these substances are, to a substantial part, distributed to the surface of the proximal airways. In contrast, the sequential recovery of albumin and urea showed a homogeneous recovery pattern. The findings were compatible with those of a small series of sixteen 10 ml lavage aliquots, sequentially infused and aspirated, also indicating a continuous diffusion of these small molecules through the lung membranes into the lavage fluid during the lavage process. We conclude that the difference in recovery pattern and distribution on the bronchial surface makes albumin and urea unsuitable as denominators in ratios to MPO and ECP, for the estimation of quantitative local concentration in epithelial lining fluid.


This article has been cited by other articles:


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
V. Brovkovych, X.-P. Gao, E. Ong, S. Brovkovych, M.-L. Brennan, X. Su, S. L. Hazen, A. B. Malik, and R. A. Skidgel
Augmented inducible nitric oxide synthase expression and increased NO production reduce sepsis-induced lung injury and mortality in myeloperoxidase-null mice
Am J Physiol Lung Cell Mol Physiol, July 1, 2008; 295(1): L96 - L103.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
M. B. Schabath, G. L. Delclos, M. M. Martynowicz, A. J. Greisinger, C. Lu, X. Wu, and M. R. Spitz
Opposing Effects of Emphysema, Hay Fever, and Select Genetic Variants on Lung Cancer Risk
Am. J. Epidemiol., March 1, 2005; 161(5): 412 - 422.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
M. B. Schabath, M. R. Spitz, X. Zhang, G. L. Delclos, and X. Wu
Genetic variants of myeloperoxidase and lung cancer risk
Carcinogenesis, June 1, 2000; 21(6): 1163 - 1166.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1991 by the European Respiratory Society.