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Acute inhibition of nitric oxide exacerbates airway hyperresponsiveness, eosinophilia and C-C chemokine generation in a murine model of fungal asthma.

AbstractOBJECTIVE AND DESIGN:
This study examined the role of nitric oxide in changes in airway physiology and inflammation in a murine model of fungal allergy induced by Aspergillus fumigatus (A. fumigatus) by treatment of A. fumigatus-sensitized mice with NG-nitro-L-arginine methyl ester (L-NAME) or D-NAME (8 mg/kg; i.p.).
MATERIALS AND METHODS:
Female CBA/J mice received A. fumigatus antigen dissolved in incomplete Freund's adjuvant (10 mg/100 ml i.p. and s.c.) followed 2 weeks later by A. fumigatus antigens (20 mg; i.n.) and a subsequent i.t. challenge 4 days later. Airway physiology and inflammation were examined (24 to 72 h) following i.t. challenge.
RESULTS:
L-NAME-treated mice had lower lung nitrite levels 24 h after A. fumigatus challenge, but higher airway hyperresponsiveness and inflammation compared to D-NAME controls. Airway inflammation in the L-NAME treatment group (72 h) was characterized by a greater bronchoalveolar lavage (BAL), peribronchial eosinophilia and augmented levels of CC chemokines compared to controls.
CONCLUSIONS:
These findings suggest that nitric oxide is an important modulator of airway hyperresponsiveness, inflammation and C-C chemokine generation during allergic airway responses to A. fumigatus.
AuthorsK Blease, S L Kunkel, C M Hogaboam
JournalInflammation research : official journal of the European Histamine Research Society ... [et al.] (Inflamm Res) Vol. 49 Issue 6 Pg. 297-304 (Jun 2000) ISSN: 1023-3830 [Print] Switzerland
PMID10939620 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Chemokines, CC
  • Nitric Oxide
  • Immunoglobulin E
  • NG-Nitroarginine Methyl Ester
Topics
  • Animals
  • Aspergillus fumigatus (immunology)
  • Asthma (physiopathology)
  • Bronchial Hyperreactivity (etiology)
  • Chemokines, CC (biosynthesis)
  • Eosinophilia (etiology)
  • Female
  • Immunoglobulin E (blood)
  • Mice
  • Mice, Inbred CBA
  • NG-Nitroarginine Methyl Ester (pharmacology)
  • Nitric Oxide (physiology)

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