Intra-luminal exposure of murine airways to peroxynitrite causes inflammation but not hyperresponsiveness

Inflamm Res. 2002 Jan;51(1):33-7. doi: 10.1007/pl00000279.

Abstract

Objective and design: There is increasing evidence for the involvement of reactive nitrogen species like peroxynitrite (ONOO-) in airway pathology, for example during allergic airway inflammation. Therefore, the effect of peroxynitrite exposure on airway responsiveness and inflammation was studied.

Materials: Male BALB/c mice were treated intra-tracheally with authentic peroxynitrite and the peroxynitrite donor 3-morpholinosydnonimine (SIN-1). Control animals received decomposed solutions of peroxynitrite and SIN- 1.

Methods: Airway inflammation was monitored by bronchoalveolar lavage, three and seven days after administration. Airway responsiveness to methacholine and acetylcholine was measured on day 1, 2, 3 and 7 post administration using whole body plethysmography.

Results: Intra-tracheal administration of peroxynitrite 200 microM in 50 microl phosphate buffered saline (PBS) induced a significant increase in macrophages (>35%, p < 0.05) in the airway lumen three days after administration. In contrast, neither intra-tracheal administration of authentic peroxynitrite (up to 5 mM) nor the peroxynitrite donor SIN-1 (1 mM, both intra-tracheal and nebulized) changed airway responsiveness to methacholine. Moreover, peroxynitrite (5 mM) did not alter responsiveness to acetylcholine.

Conclusion: Administration of peroxynitrite directly into the airways of BALB/c mice, induces airway inflammation, but not airway hyperresponsiveness. It is suggested that antioxidants in the epithelial lining fluid and/or the epithelium itself form an efficient barrier, which prevents peroxynitrite from reaching putative targets in the airway interstitium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Bronchi / drug effects*
  • Bronchial Hyperreactivity / chemically induced*
  • Inflammation / chemically induced*
  • Male
  • Methacholine Chloride / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Molsidomine / analogs & derivatives
  • Molsidomine / pharmacology
  • Peroxynitrous Acid / toxicity*
  • Trachea / drug effects*
  • Tyrosine / analogs & derivatives*
  • Tyrosine / analysis

Substances

  • Methacholine Chloride
  • Peroxynitrous Acid
  • 3-nitrotyrosine
  • Tyrosine
  • linsidomine
  • Molsidomine
  • Acetylcholine