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Vol. 285, Issue 2, 602-607, May 1998
Johns Hopkins Asthma and Allergy Center, Baltimore, Maryland
The role of endogenous 5-lipoxygenase products in modulating
tachykinergic neurotransmission in guinea pig isolated trachea was
investigated. Tachykinin-containing afferent nerve fibers were
stimulated with either electrical field stimulation or antidromic stimulation of the right vagus nerve. This resulted in contractions of
the isolated caudal trachea and bronchus that could be blocked with
either tetrodotoxin or a combination of neurokinin-1 and neurokinin-2
receptor antagonists. The 5-lipoxygenase inhibitor ZD 2138 (1 µM)
significantly inhibited these neurally mediated tachykinergic
contractions, by approximately 50%, yet had no effect on the
contractions evoked by stimulating tachykinergic fibers in an action
potential-independent fashion with capsaicin or by exogenously applied
neurokinin A. The effect of ZD 2138 on action potential-driven
tachykinergic contractions was mimicked by pobilukast, pranlukast,
montelukast and zafirlukast, four structurally unrelated antagonists of
the cysteinyl leukotriene 1 receptor subtype. Pobilukast had no effect
on the tachykinergic contraction in tissues pretreated with ZD 2138. Likewise, ZD 2138 had no effect on the tachykinergic contractions in
tissues pretreated with pobilukast. Intracellular electrophysiological
recording of the membrane properties of jugular ganglion neurons, the
source of tachykinins in the guinea pig trachea/bronchus, demonstrated
that leukotriene D4 caused a membrane depolarization of
vagal afferent C-fiber neurons and an increase in input impedance, both
of which were abolished by zafirlukast. Taken together, these data
indicate that in the resting guinea pig isolated trachea/bronchus,
endogenous 5-lipoxygenase activity leads to the production of cysteinyl
leukotrienes that amplify action potential-dependent release of
tachykinins from airway afferent nerve fibers.
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