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Pulmonary Biophysics and Bioengineering Research Laboratory, Departments of Medicine and Chemical Engineering, University of Illinois at Chicago, Chicago 60680; and Veterans Affairs Chicago Health Care System, Chicago, Illinois 60612
Received 7 March 1996; accepted in final form 10 June 1997.
Winters, Scot L., and Donovan B. Yeates. Interaction
between ion transporters and the mucociliary transport system in dog
and baboon. J. Appl. Physiol. 83(4):
1348-1359, 1997.
To gain insight into the role of epithelial ion
channels, pumps, and cotransporters in regulating airway water and
mucociliary transport, we administered inhibitors of the
Na+ channel (amiloride),
3Na-2K-adenosinetriphosphatase (acetylstrophanthidin), and Na-K-2Cl
cotransporter (furosemide) to anesthetized dogs and/or baboons.
Tracheal ciliary beat frequency was measured by using heterodyne laser
light scattering. Tracheal mucus velocity (TMV) and bronchial
mucociliary clearance (BMC) or lung mucociliary clearance were measured
by using radioaerosols and nuclear imaging. Respiratory tract fluid
output was collected by using a secretion-collecting endotracheal tube.
In six dogs, amiloride aerosol [lung deposition, 96 ± 11 µg
(means ± SE)] had minimal effect, whereas
acetylstrophanthidin aerosol (lung deposition, 71 ± 9 µg)
increased BMC, and furosemide (40 mg iv) markedly increased TMV. In
five baboons, TMV increased after iv furosemide administration (2 mg/kg) as well as by aerosol (lung deposition, 20 ± 3 mg), coincident with increases in ciliary-mucus coupling from 11.5 ± 0.1 to 29.5 ± 0.4 and 46.5 ± 0.7 µm/beat, respectively.
Furosemide also increased lung mucociliary clearance in baboons. In
dogs, respiratory tract fluid output increased after intravenous
furosemide from 2.2 ± 0.5 to 6.8 ± 1.7 mg/min. When combined
with dry-air inhalation, furosemide failed to stimulate TMV and
reversed the inhibition of BMC by dry air. Thus pharmacological manipulation of the Na-K-2Cl cotransporter and the
3Na-2K-adenosinetriphosphatase pump may provide increases of clinical
relevance in airway hydration and mucociliary transport.
fluid transport; ciliary beat; ion transport; water balance; mucus transport
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