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Departments of 1 Medicine and 2 Chemical Engineering, University of Illinois at Chicago, and 3 Department of Veterans Affairs, Veterans Affairs Chicago Health Care System, Chicago, Illinois 60612
To investigate the regulation of respiratory tract fluid
output (RTFO), we collected the RTFO in an anesthetized canine model after a series of pharmacological interventions (inhibition of Na+-K+-ATPase or
Na+-K+-2Cl
cotransporter, 250 µl) and physiological challenges (ionic and/or osmotic perturbation
in airway lumen, 250 µl). Whereas 250 µl of aerosolized 0.9%
saline caused a transient increase in RTFO, a 250-µl
bumetanide-induced increase in RTFO was evident for 18 min and a
250-µl acetylstrophanthidin-induced increase in RTFO persisted for at
least 30 min. Dry air ventilation decreased the responses of RTFO to
the saline (sham) and acetylstrophanthidin intervention but not the
bumetanide intervention. Delivery of 250 mosmol/kgH2O
ion-free mannitol (250 µl) caused marked increases in RTFO that were
little affected by the administration of acetylstrophanthidin or
bumetanide 30 min before these challenges. A 250-µl 550 mosmol/kgH2O ion-free mannitol challenge caused a more
marked and prolonged increase in RTFO. Thus aerosol delivery of a low
dose of a cardiac glycoside or a near-isosmotic, ion-free, impermeant
osmolyte solution may be therapeutically useful by increasing the
clearance of secretions from the tracheobronchial airways.
mucus collection; acetylstrophanthidin; bumetanide; airway humidity; mucociliary transport
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