Rapid responses to aldosterone in human distal colon

Aldosterone at normal physiological levels induces rapid increases in intracellular calcium and pH in human distal colon. The end target of these rapid signaling responses an basolateral K+ channels. Using spectrofluorescence microscopy and Ussing chamber techniques, we have shown that aldosterone activates basolateral Na/H exchange via a protein kinase C and calcium-dependent signaling pathway. The resultant intracellular alkalinization up-regulates an adenosine triphosphate (ATP)-dependent K+ channel (K-ATP) and inhibits a Ca2+-dependent K+ channel (K-Ca). In Ussing chamber experiments, we have shown that the K-ATP channel is required to drive sodium absorption, whereas the K-Ca channel is necessary for both cyclic adenosine monophosphate and calcium-dependent chloride secretion. The rapid effects of aldosterone on intracellular calcium, pH, protein kinase C and K-ATP, K-Ca channels are insensitive to cycloheximide, actinomycin D, and spironalactone, indicating a nongenomic mechanism of action. We propose that the physiological role for the rapid nongenomic effect of aldosterone is to prime pluripotential epithelia for absorption by simultaneously up-regulating K-ATP channels to drive absorption through surface cells and down-regulating the secretory capacity by inhibiting K-Ca channels involved in secretion through crypt cells. (C) 1999 Elsevier Science Inc. All rights reserved.