Abstract
Models of epithelial salt secretion, involving secondary active transport of Cl- [9], locate the K+ conductance of the plasma membrane exclusively in the basolateral membrane, although there is considerable experimental evidence to show that many secretory epithelia do have a significant apical K+ conductance. We have used an equivalent circuit model to examine the effect of an apical K+ conductance on the composition and flow rate of the fluid secreted by an epithelium in which secretion is driven by the secondary active transport of Cl-. The parameters of the model were chosen to be similar to those measured in the dog tracheal mucosa when stimulated with adrenaline to secrete. We find that placing a K+ conductance in the apical membrane can actually enhance secretion provided the proportion of the total cell K+ conductance in the apical membrane is not greater than about 60%, the enabling effect on secretion being maximal when the proportion is around 10-20%. We also find that even when the entire cell K+ conductance is located in the apical membrane, the secreted fluid remains relatively Na+ rich. Analysis of the sensitivity of model behavior to the choice of values for the parameters shows that the effects of an apical K+ conductance are enhanced by increasing the ratio of the paracellular resistance to the transcellular resistance.
MeSH Terms
Biological Transport, Active
Cell Membrane/metabolism
Chlorides/metabolism
Electric Conductivity
Epithelium/metabolism
Intercellular Junctions/metabolism
Models, Biological
Potassium Channels/metabolism
Sodium-Potassium-Exchanging ATPase/metabolism
Chemicals
Chlorides
Potassium Channels
Sodium-Potassium-Exchanging ATPase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cook D I
Department of Physiology, University of Sydney, New South Wales, Australia.
Young J A
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