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Ionic Permeability of Insect Epithelia
Authors:HANRAHAN  JOHN W
Institution:Department of Zoology, University of British Columbia Vancouver, British Columbia V6T 2A9, Canada
Abstract:In general, ionic regulation will depend on active transportby epithelia and also on the permeability properties of thesetissues. Passive permeability has recently been studied in thehindgut of the desert locust Schistocerca gregaria using electrophysiologicaland radiotracer techniques. Although locust rectum has low electricalresistance, cell membranes provide the major route for transepithelialionic diffusion; i.e., the locust rectum is a tight epithelium.Potassium permeability (PK) is apparently regulated by luminalK and osmotic concentrations (local control), and also by thepeptide hormone CTSH (chloride transport-stimulating hormone).Transepithelial resistance declines when isolated recta areexposed to CTSH or its "second-messenger" cAMP (adenosine 3':5'-cyclicmonophosphate). Cyclic-AMP also stimulates K diffusion acrossrecta by 400%. Intracellular cable analysis indicatesthat cAMPlowers apical and basal membrane resistances (Ra and Rb, respectively)by {small tilde}80%; however different ionic permeabilitiesare affected at thelumen- and hemolymph-facing membranes: ThecAMP-induced decline in Ra, requires potassium whereas {delta}Rb isCl-dependent. The actions of cAMP on active transport and passivepermeability are complementary and would allow remarkably efficientcontrol over KC1 absorption in vivo. One hypothesis is as follows:CTSH elevates intracellular cAMP concentration by stimulatingadenyl cyclase. Cyclic-AMP enhances transepithelial Cl absorptionby stimulating a Cl pump in the apical membrane and also byincreasing the Cl permeability of the basal membrane. PassiveK absorption would also increase during cAMP stimulation sinceCl transport results in a more positive luminal potential, andbecause cAMP elevates transrectal PK. The mechanisms by whichmembrane permeability is regulated in insects have not yet beenstudied, but these might involve the modulation of ion channelsby cAMP- or calmodulin-dependent phosphorylation, Ca or calmodulinbinding, methylation, or insertion of new channels into themembrane.
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