Published ahead of print on January 12, 2004, doi:10.1165/rcmb.2003-0178OC
© 2004 American Thoracic Society DOI: 10.1165/rcmb.2003-0178OC Short-Term Smoke Exposure Attenuates Ovalbumin-Induced Airway Inflammation in Allergic MiceDepartment of Pathology and Laboratory Medicine, and Department of Pulmonology, University Hospital Groningen, Groningen, The Netherlands Address correspondence to: B. N. Melgert, Ph.D., Department of Pathology and Laboratory Medicine, University Hospital Groningen, P.O. Box 30.001, 9700 RB, Groningen, The Netherlands. E-mail: B.N.Melgert{at}path.azg.nl Little is known about effects of smoking on airway inflammation in asthma. We tested the hypothesis that smoking enhances established airway inflammation in a mouse model of allergic asthma. C57Bl/6j mice were sensitized to ovalbumin (OVA) and challenged with OVA (OVA-mice) or sham-sensitized to phosphate-buffered saline (PBS) and challenged with PBS aerosols (PBS-mice) for 7 wk. At 4 wk, mice were additionally exposed to air (nonsmoking controls) or mainstream smoke for 3 wk. Using whole body plethysmography, we found OVA-induced bronchoconstriction to be significantly inhibited in smoking OVA-mice as compared with nonsmoking OVA-mice (1 ± 2% increase versus 22 ± 6% increase in enhanced pause, respectively). Smoking did not change airway hyperresponsiveness (AHR) to methacholine in PBS-mice, yet significantly attenuated AHR in OVA-mice 24 h after OVA challenge as compared with nonsmoking mice. This was accompanied by reduced eosinophil numbers in lung lavage fluid and tissue of smoking OVA-mice compared with nonsmoking OVA-mice. In contrast to our hypothesis, short-term smoking reduced responsiveness to OVA and methacholine in OVA-mice and decreased airway inflammation when compared with nonsmoking mice. This effect of smoking may be different for long-term smoking, in which remodeling effects of smoking can be expected to interrelate with remodeling changes caused by asthmatic disease.
Abbreviations: airway hyperresponsiveness, AHR bronchoalveolar lavage, BAL carbon monoxide, CO enzyme-linked immunosorbent assay, ELISA interleukin, IL methacholine, MCh ovalbumin, OVA phosphate-buffered saline, PBS enhanced pause, Penh
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