Basolateral regulation of pHi in proximal tubules of avian loopless and long-looped nephrons in bicarbonate
Abstract
In isolated, nonperfused chicken proximal tubules from both loopless reptilian-type and long-looped mammalian-type nephrons, resting intracellular pH (pHi), measured with pH-sensitive fluorescent dye 2′,7′-bis(2-carboxyethyl)-5,6-carboxyfluorescein (BCECF), was ∼7.1 under control HCO3– conditions [20 mM N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid (HEPES)/5 mM HCO3–-buffered medium with pH 7.4 at 37°C] and was reduced to ∼6.8 in response to NH4Cl pulse. The rate of recovery of pHi (dpHi/dt) from this level to the resting level in proximal tubules from both nephron types was (1) significantly reduced by the removal of Na+ or both Na+ and Cl– from the bath, and (2) unaffected by the removal of Cl– from the bath or the presence of a high K+ concentration or Ba2+ in the bath. In proximal tubules from long-looped mammalian-type, but not loopless reptilian-type, nephrons, dpHi/dt was significantly reduced by the addition of either 5-(N-ethyl-N-isopropyl) amiloride (EIPA) or 4,4′-diisothiocyanostilbene-2,2′disulfonate (DIDS) to the bath. These data suggest that a Na+/H+ exchanger and most likely a Na+-dependent Cl–/HCO3– exchanger are involved in basolateral regulation of pHi in mammalian-type nephrons whereas none of the commonly identified basolateral acid-base transporters appear to be involved in regulation of pHi in reptilian-type nephrons. J. Exp. Zool. 284:174–187, 1999. © 1999 Wiley-Liss, Inc.