The activation of
tachykinin NK receptors by
neuropeptides may induce the recruitment of eosinophils in vivo. The aim of the present study was to investigate the effects and underlying mechanism(s) of the action of
tachykinin receptor antagonists on eosinophil recruitment in a model of allergic
pleurisy in mice. Pretreatment of immunized mice with
capsaicin partially prevented the recruitment of eosinophils after
antigen challenge, suggesting the potential contribution of sensory nerves for the recruitment of eosinophils Local (10-50 nmol per pleural cavity) or systemic (100-300 nmol per animal) pretreatment with the
tachykinin NK1 receptor antagonist
SR140333 prevented the recruitment of eosinophils induced by
antigen challenge of immunized mice. Neither
tachykinin NK2 nor NK3 receptor antagonists suppressed eosinophil recruitment. Pretreatment with
SR140333 failed to prevent the
antigen-induced increase of
interleukin-5 concentrations in the pleural cavity. Similarly,
SR140333 failed to affect the bone marrow
eosinophilia observed at 48 h after
antigen challenge of immunized mice.
SR140333 induced a significant increase in the concentrations of
antigen-induced eotaxin at 6 h after challenge.
Antigen challenge of immunized mice induced a significant increase of Leucotriene B4 (
LTB4) concentrations at 6 h after challenge. Pretreatment with
SR140333 prevented the
antigen-induced increase of
LTB4 concentrations. Our data suggest an important role for NK1 receptor activation with consequent
LTB4 release and eosinophil recruitment in a model of allergic
pleurisy in the mouse.
Tachykinins appear to be released mainly from peripheral endings of
capsaicin-sensitive sensory neurons and may act on mast cells to facilitate
antigen-driven release of
LTB4.