Regulation of cAMP-sensitive colonic epithelial Na+ channel in oocyte expression system

In amphibian epithelia and in cortical collecting duct the antidiuretic pep tide arginine-vasopressin (AVP) stimulates activity of epithelial Na+ chann els (ENaCs). Generally, the AVP action upon Na+ (re)absorption is believed to be a cAMP/protein-kinase-A mediated mechanism. In the Xenopus oocyte exp ression system, however, a clear stimulation of ENaC activity by cAMP could not be reproduced with channel subunits cloned from A6 cells or rat colon. We have recently shown that membrane-permeant 8-(4-chloro-phenylthio)-cAMP (cpt-cAMP) stimulates activity of a hybrid ENaC in Xenopus oocytes, that c onsists of an alpha-subunit cloned from guinea-pig colon and the beta- and gamma -subunit originating from rat colon (gp alphar beta gamma ENaC). In t he present study, we have further investigated the mechanisms by which cpt- cAMP upregulates gp alphar beta gamma ENaC activity. Interestingly, we foun d AVP to stimulate the gp alphar beta gamma ENaC in oocytes. Also, treatmen t with GTP-gamma -S largely activated this channel. In contrast, as a confl icting result, forskolin had no stimulatory effect on the cAMP-sensitive gp alphar beta gamma ENaC. Experiments with Brefeldin A (BFA) or nocodazole s uggested that only a minor part of cpt-cAMP-induced activation is probably due to an additional translocation of channel proteins into the oocyte memb rane. In conclusion, the stimulatory effect of synthetic cpt-cAMP does not seem to be exclusively provided by classical cAMP/PKA-associated transducti on mechanisms, i.e., as in A6 cells.