NO chemical events in the human airway during the immediate and late antigen-induced asthmatic response
- Raed A. Dweik*,
- Suzy A. A. Comhair*,†,
- Benjamin Gaston‡,
- Frederik B. J. M. Thunnissen§,
- Carol Farver¶,
- Mary Jane Thomassen*,‖,
- Mani Kavuru*,
- Jeffrey Hammel**,
- Husam M. Abu-Soud‖, and
- Serpil C. Erzurum*,†,‡‡
- Departments of *Pulmonary and Critical Care Medicine, †Cancer Biology, ¶Pathology, ‖Cell Biology, and **Biostatistics and Epidemiology, Cleveland Clinic Foundation, Lerner Research Institute, Cleveland, OH 44195; ‡Department of Pediatric Medicine, University of Virginia Health Sciences Center, Charlottesville, VA 22908; and §Department of Pathology, Canisius Wilhelmina Ziekenhuis, Nijmegen, The Netherlands 6500
-
Communicated by Cynthia M. Beall, Case Western University, Cleveland, OH (received for review September 15, 2000)
Abstract
A wealth of evidence supports increased NO (NO⋅) in asthma,
but its roles are unknown. To investigate how NO participates in
inflammatory airway events in asthma, we measured NO⋅ and
NO⋅ chemical reaction products [nitrite, nitrate,
S-nitrosothiols (SNO), and nitrotyrosine] before,
immediately and 48 h after bronchoscopic antigen (Ag) challenge of
the peripheral airways in atopic asthmatic individuals and nonatopic
healthy controls. Strikingly, NO
was the only
NO⋅ derivative to increase during the immediate Ag-induced
asthmatic response and continued to increase over 2-fold at 48 h
after Ag challenge in contrast to controls [P <
0.05]. NO
was not affected by Ag challenge at 10
min or 48 h after Ag challenge. Although SNO was not detectable in
asthmatic airways at baseline or immediately after Ag, SNO increased
during the late response to levels found in healthy controls. A model
of NO⋅ dynamics derived from the current findings predicts that
NO⋅ may have harmful effects through formation of peroxynitrite,
but also subserves an antioxidant role by consuming reactive oxygen
species during the immediate asthmatic response, whereas nitrosylation
during the late asthmatic response generates SNO, safe reservoirs for
removal of toxic NO⋅ derivatives.
Footnotes
-
↵ ‡‡ To whom reprint requests should be addressed at: Cleveland Clinic Foundation, 9500 Euclid Avenue/A90, Cleveland, OH 44195. E-mail: erzurus{at}ccf.org.
- Abbreviations:
- Ag,
- antigen;
- BAL,
- bronchoalveolar lavage;
- NOS,
- NO synthase;
- SNO,
- S-nitrosothiols;
- ROS,
- reactive oxygen species
- Copyright © 2001, The National Academy of Sciences





