Stimulation of airway sensory nerves by cyclosporin A and FK506 in guinea-pig isolated bronchus

1 We have investigated the contractile property of cyclosporin A. and FK506 in guinea-pig isolated bronchus. 2 Cyclosporin A (10 mu M) failed to significantly attenuate the excitatory non-adrenergic non-cholinergic (eNANC) and cholinergic contractile response (per cent methacholine E-max) induced by electrical held stimulation (EFS) . In contrast, eNANC responses were significantly attenuated by both the ne urokinin (NK)-1 and (NK)-2 receptor antagonists, N-acetyl-L-tryptophan 3,5- bis (trifluoromethyl)-benzyl and SR48968, respectively. 3 Cyclosporin A and FK506 caused a concentration-dependent contraction in g uinea-pig isolated bronchus, which was significantly attenuated by NK-1 and NK-2 receptor antagonists. The capsaicin receptor antagonist, capsazepine (10 mu M) significantly reduced the contractile response to cyclosporin A a nd capsaicin, but not to FK506. 4 The N-type calcium channel blocker, omega-Conotoxin (omega CTX: 10 nM), s ignificantly reduced the contractile response to FK506 and the eNANC respon se following EFS. In contrast, omega-CTX failed to significantly reduce the contractile potency to capsaicin or cyclosporin A. 5 In bronchial preparations desensitized by repeated application of capsaic in (1 mu M), the contractile responses to both cyclosporin A (100 mu M) and FK506 (100 mu M), were significantly reduced. In contrast, the contractile responses to substance P and neurokinin A (10 mu M) were not altered. Furt hermore, repeated application of cyclosporin A (100 mu M) significantly inh ibited the contractile response to capsaicin (1 mu M). 6 The findings from this study would indicate that cyclosporin A and FK506 mediate contraction of guinea-pig isolated bronchus secondary to the releas e of neuropeptides from airway sensory nerves. However, the release of sens ory neuropeptides appears to be mediated via different mechanisms for cyclo sporin A and FK506, the former by stimulation of the vanilloid receptor and the latter via opening of N-type calcium channels.