Mannitol triggers mast cell-dependent contractions of human small bronchi and prostacyclin bronchoprotection

Abstract

Background: Clinical research supports that exercise-induced bronchoconstriction (EIB) is caused by hyperosmolar triggering of mast cells. The reaction can be mimicked by inhalation of mannitol, but it has paradoxically previously not been possible to replicate this mode of action of mannitol in isolated airways.

Objective: We sought to establish an ex vivo model of EIB in human small bronchi.

Methods: Small bronchi (inner diameter, 0.5-2 mm) from macroscopically healthy human lung tissue were obtained from 48 patients and mounted in organ baths. Contractions and mediator release were analyzed after challenge with hyperosmolar mannitol (850 mOsm).

Results: Ten minutes of exposure to mannitol caused a small initial contraction (12% ± 1% of maximum) that was followed by a second and much larger contraction (maximum effect [E_max], 47% ± 5%) when mannitol was washed out. The mast cell stabilizer cromolyn reduced the second contraction (E_max, 27% ± 3%). Furthermore, this main contraction was abolished by the combination of antagonists of histamine and cysteinyl leukotrienes in the presence of indomethacin. Mannitol increased the release of the mast cell mediators histamine (9.0-fold), cysteinyl leukotrienes (4.5-fold), and prostaglandin (PG) D₂ (5.4-fold), as well as PGE₂ (6.3-fold) and the prostacyclin metabolite 6-keto PGF_1α (5.7-fold). In contrast, indomethacin alone enhanced the bronchoconstriction (E_max, 68% ± 6%). Likewise, receptor antagonists for PGE₂ (EP₂ and EP₄) and prostacyclin (IP) also enhanced the mannitol-induced bronchoconstriction (E_max, 67% ± 5%, 66% ± 4%, and 68% ± 3%, respectively). In bronchi precontracted by carbachol, the IP receptor agonist cicaprost induced profound relaxation.

Conclusion: This new protocol established an in vitro model for studies of EIB in isolated human bronchi. The IP receptor might be a new target for asthma treatment.

Keywords: EP(2) receptor; EP(4) receptor; Hyperosmolar challenge; exercise-induced bronchoconstriction; histamine; nonsteroidal anti-inflammatory drugs; prostacyclin receptor; prostaglandin D(2); prostaglandin E(2); prostaglandin I(2).