Exhaled Nitric Oxide Measurement in Workers in a Microwave Popcorn Production Plant
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1999/10/01
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Description:BACKGROUND: Recent evidence has shown that nitric oxide (NO) levels are increased in asthmatic airways. Although the role of NO in asthma is unknown, reactive metabolites of NO may lead to nitrotyrosine formation and promote airway dysfunction. OBJECTIVE: The aim of this study was to determine whether nitrotyrosine, as a marker of nitrating species, could be found in the airways and lung parenchyma of subjects with asthma who died of status asthmaticus or other nonrespiratory causes. METHODS: Lung tissue specimens were obtained from 5 patients who died of status asthmaticus, 2 asthmatic patients who died of nonrespiratory causes, and 6 nonasthmatic control subjects who died of nonrespiratory causes. Lung sections were stained for immunofluorescence with use of an antinitrotyrosine antibody, followed by a indiocarbocyanine (Cy5, Jackson Immunochemicals, Westgrove, Pa)-conjugated secondary antibody. RESULTS: Nonasthmatic lungs showed little or no nitrotyrosine staining, whereas asthmatic lungs demonstrated significantly more staining of nitrotyrosine residues distributed in both the airways and lung parenchyma. CONCLUSION: This study demonstrates the presence of nitrotyrosine, and hence evidence of formation of nitrating species, in the airways and lung parenchyma of patients with asthma who died of status asthmaticus or other nonrespiratory causes. This finding supports the concept that widespread airway and parenchymal inflammation occurs in asthma, and, more specifically, that NO and its reactive metabolites may play a pathophysiologic role in asthma. [Description provided by NIOSH]
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ISSN:0091-6749
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Volume:104
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Issue:4
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NIOSHTIC Number:nn:20030132
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Citation:J Allergy Clin Immunol 1999 Oct; 104(4 Pt 1):747-754
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Contact Point Address:Division of Pulmonary Disease and Critical Care Medicine, University of Vermont College of Medicine, Burlington, VT 05405
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Federal Fiscal Year:2000
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Performing Organization:Yale University, New Haven, Connecticut
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Peer Reviewed:True
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Part Number:1
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Start Date:19970901
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Source Full Name:Journal of Allergy and Clinical Immunology
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End Date:20020831
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Main Document Checksum:urn:sha-512:4435b260cbbdcf438cbdae27ef851c153dd186fcb985f7076b3945602bd5169c1ce0ce992ebedcfa2ba92ed7fd01ceb545d79ab346c0b8f80eaaa147b8fe4fbe
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