Abstract

The contribution of mast cells (MCs) to inflammatory response and lung remodeling in COPD is not well documented. Aim: to assess the effect of MC degranulation blockade on inflammatory response outcome and lung tissue structure in COPD model. Methods: Model of COPD was induced in rats by NO 2 (15-19 ppm) exposure: 1,5-2 h/day for 60 days. Sodium cromoglicate (SC, Aventis) was used as MC membrane stabilizer. From 30th to 60th day one group was inhaled with SC before NO 2 exposure, control group received 0.9% NaCl. Lung sections were stained with H&E and toluidine blue for MCs. Bronchoalveolar lavage fluid (BALF) cytogram was determined. The levels of mast cell tryptase (MCT) and chymase (MCC), TNFa, surfactant protein B (SP-B) were measured in BALF by ELISA. Results: A lot of MCs, inflammatory infiltration, foci of emphysema were revealed in control lung tissue. The BALF levels of TNFa, SP-B, MCT and MCC increased respectively 10-, 2-, 6- and 3-fold (p Conclusion: The results confirm the involvement of MCs in the development of airway inflammation. Prevention of MC degranulation reduces the activity of the airway inflammation and severity of lung tissue remodeling in rats with COPD model.

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