Different acid secretagogues activate different Na+/H+exchanger isoforms in rabbit parietal cells

Abstract

Rabbit parietal cells express three Na+/H+exchanger isoforms (NHE1, NHE2, and NHE4). We investigated the effects of carbachol, histamine, and forskolin on Na+/H+exchange activity and acid formation in cultured rabbit parietal cells and tested the effect of NHE isoform-specific inhibition on agonist-induced Na+/H+exchange. Carbachol (10−4 M) was the weakest acid secretagogue but caused the strongest Na+/H+exchange activation, which was completely blocked by 1 μM HOE-642 (selective for NHE1); histamine (10−4 M) and forskolin (10−5 M) were stronger stimulants of [14C]aminopyrine accumulation but weaker stimulants of Na+/H+exchange activity. HOE-642 (1 μM) reduced forskolin-stimulated Na+/H+exchange activity by 35%, and 25 μM HOE-642 (inhibits NHE1 and -2) inhibited an additional 13%, but 500 μM dimethyl amiloride (inhibits NHE1, -2, and -4) caused complete inhibition. The presence of 5% CO2-[Formula: see text]markedly reduced agonist-stimulated H+ efflux rates, suggesting that the anion exchanger is also activated. Hyperosmolarity also activated Na+/H+exchange. Our data suggest that, in rabbit parietal cells, Ca2+-dependent stimulation causes a selective activation of NHE1, whereas cAMP-dependent stimulation activates NHE1, NHE2, and more strongly NHE4. Because intracellular pH (pHi) did not change in the presence of CO2-[Formula: see text]and concomitant activation of Na+/H+and anion exchange is one of the volume regulatory mechanisms, we speculate that the physiological significance of secretagogue-induced Na+/H+exchange activation may not be related to pHi but to volume regulation during acid secretion.