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Vol. 284, Issue 1, 370-377, 1998
The Johns Hopkins Asthma and Allergy Center (B.J.C., B.J.U.),
Baltimore, Maryland and
Justus-Liebig University, Institute for Anatomy
and Cell Biology (A.F.), Giessen, Germany
Previous studies indicated that antidromic stimulation of
capsaicin-sensitive vagal afferent fibers activated, via
peripheral release of tachykinins, nonadrenergic, noncholinergic
parasympathetic ganglion neurons that mediate relaxations of guinea pig
trachealis. On the basis of the effects of selective agonists and
inhibition with a nonselective receptor antagonist (SR 48968), we
speculated that tachykinin-mediated activation of
neurokinin3 (NK3) receptors might be involved.
Using the recently developed NK3-selective receptor
antagonist SR 142801, we further assessed the role of NK3
receptors in these relaxant responses. Relaxations of the guinea pig
trachea elicited by antidromic stimulation of capsaicin-sensitive vagal
afferent nerves were markedly inhibited by 0.3 µM SR 142801 and were
abolished by a combination of SR 142801 and either of the
NK1-selective receptor antagonists SR 140333 and CP 99994 (0.3 µM each). The NK3 receptor antagonist had similar
effects on the relaxant responses elicited by capsaicin and substance P, but it had no effect on relaxations of the trachealis elicited by
electrical field stimulation of the postganglionic nerves that innervate the trachealis or by stimulation of the preganglionic parasympathetic vagal nerves that innervate the trachea. These results
and the observation that the ganglion neurons that mediate these
responses are densely innervated by substance P-containing nerve fibers
lead us conclude that stimulation of capsaicin-sensitive visceral
afferent fibers activates, upon peripheral release of tachykinins,
nonadrenergic, noncholinergic inhibitory neurons innervating guinea pig
trachealis via activation of both NK3 and NK1 receptors.
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