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1 Department of Physiology,
Previous studies demonstrated that ACh-induced
liquid secretion by porcine bronchi is driven by active
Cl
and
HCO
3 secretion. The present study
was undertaken to determine whether this process was localized to
submucosal glands and mediated by the cystic fibrosis transmembrane
conductance regulator (CFTR). When excised, cannulated, and treated
with ACh, porcine bronchi secreted 15.6 ± 0.6 µl · cm
2 · h
1.
Removal of the surface epithelium did not significantly affect the rate
of secretion, indicating that the source of the liquid was the
submucosal glands. Pretreatment with diphenylamine-2-carboxylate, a
relatively nonselective
Cl
-channel blocker,
significantly reduced liquid secretion by 86%, whereas pretreatment
with DIDS, which inhibits a variety of
Cl
channels but not CFTR,
had no effect. When bronchi were pretreated with glibenclamide or
5-nitro-2-(3-phenylpropylamino)benzoic acid (both inhibitors of CFTR),
the rate of ACh-induced liquid secretion was significantly reduced by
39 and 91%, respectively, compared with controls. Agents that blocked
liquid secretion also caused disproportionate reductions in
HCO
3 secretion. Polyclonal
antibodies to the CFTR bound preferentially to submucosal gland ducts
and the surface epithelium, suggesting that this channel was localized
to these sites. These data suggest that ACh-induced gland liquid
secretion by porcine bronchi is driven by active secretion of both
Cl
and
HCO
3 and is mediated by the CFTR.
cystic fibrosis; cystic fibrosis transmembrane conductance regulator; bronchi; epithelium; exocrine glands
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