FEEDBACK-REGULATION OF NA CHANNELS IN RAT CCT .4. MEDIATION BY ACTIVATION OF PROTEIN-KINASE-C

The hypothesis that feedback inhibition of the apical Na+ channels in the cortical collecting tubule (CCT) is mediated by activation of a Ca 2+-dependent protein kinase was tested using the patch-clamp technique . Na+ channel activity was monitored in cell-attached patches in princ ipal cells of split-open rat tubules. Mean number of open channels (NP o) and single-channel current (i) were measured at 37 degrees C during continuous tubule superfusion. Phorbol 12-myristate 13-acetate (PMA; 50 nM), an activator of protein kinase C (PKC), decreased NPo to 33% o f the control value. Staurosporine (200 nM), an inhibitor of PKC and o f Ca2+-calmodulin kinase II, practically abolished the effect of PMA. Ouabain (1 mM), reduced NPo to 29% of control values and decreased i. Ouabain did not downregulate the channels in tubules exposed to stauro sporine, although it still reduced i. Incubation of the tubules with 1 0 mu M KN-62, a specific cell membrane-permeable inhibitor of Ca2+-cal modulin kinase II, did not interfere with the ouabain-dependent downre gulation of the channels. The results support the view that the downre gulation caused by ouabain involves the Ca2+-dependent phosphorylation of the channel itself or of proteins regulating the channel.