Hyperventilation with dry air damages the bronchial mucosa, increases bronchovascular permeability, degranulates mast cells, and initiates inflammation in canine peripheral airways. All of these dry air-induced phenomena are believed to contribute to the development of airways hyperreactivity in humans, and may account for the increased incidence of asthma reported in elite winter athletes. The proposed research focuses on mechanisms that may contribute to the development and persistence of chronic asthma-like symptoms in a canine model of exercise-induced asthma. The general hypothesis is that repetitive hyperventilation with dry air stimulates a nonspecific immune response that results in airways hyperreactivity. Airway mucosal cells secrete a variety of proinflammatory eicosanoids and cytokines that may play an important role in the development of nonspecific airways hyperreactivity and non-allergic asthma. The specific hypothesis is that repetitive dry air challenge (DAC) causes airway injury and stimulates a Th-2 type response that results in a persistent asthma-like state.
The specific aims are to: 1) identify the stimulus responsible for repetitive hyperventilation-induced airways hyperreactivity; 2) use immunohistochemistry and image analysis to determine if repetitive hyperventilation with dry air stimulates CD4+ T lymphocyte migration; 3) identify mediators that potentially link repetitive hyperventilation-induced mucosal injury with eosinophilic inflammation in vivo using ELISA and RT-PCR; and 4) use drugs and monoclonal antibodies to investigate the role of a) eicosanoids, b) M2 receptor function, c) granulocyte infiltration, d) CD4+ lymphocyte infiltration, and e) Type-1/ Type-2 cytokine activity in the development of a repetitive DAC-induced asthma-like state. Finally, the use of a canine model will allow examination of the etiology of non-allergic small airways disease in normal dogs, and may provide valuable insights into the mechanisms involved in the development of hyperventilation-induced airway hyperreactivity and the pathogenesis of non-allergic asthma in humans.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL063186-01A1
Application #
6130102
Study Section
Special Emphasis Panel (ZRG1-ALTX-1 (01))
Project Start
2000-04-01
Project End
2002-03-31
Budget Start
2000-04-01
Budget End
2002-03-31
Support Year
1
Fiscal Year
2000
Total Cost
$396,566
Indirect Cost
Name
Johns Hopkins University
Department
Public Health & Prev Medicine
Type
Schools of Public Health
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Freed, Arthur N; McCulloch, Sharron; Meyers, Teresa et al. (2003) Neurokinins modulate hyperventilation-induced bronchoconstriction in canine peripheral airways. Am J Respir Crit Care Med 167:1102-8
Davis, Michael S; Schofield, Brian; Freed, Arthur N (2003) Repeated peripheral airway hyperpnea causes inflammation and remodeling in dogs. Med Sci Sports Exerc 35:608-16
Suzuki, Ryoichi; Freed, Arthur N (2002) Heparin inhibits hyperventilation-induced late-phase hyperreactivity in dogs. Am J Respir Crit Care Med 165:27-33
Davis, M S; Freed, A N (2001) Repeated hyperventilation causes peripheral airways inflammation, hyperreactivity, and impaired bronchodilation in dogs. Am J Respir Crit Care Med 164:785-9