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. 2012 Feb 1;302(10):C1436–C1451. doi: 10.1152/ajpcell.00063.2011

Fig. 11.

Fig. 11.

Luminal and basolateral Na+-dependent pHi regulation of principal cells (PCs) and intercalated cells (IC) in microperfused isolated collecting ducts (CDs) from control and orpk mutant mice. A: control CD. Simultaneously removing luminal (L) and basolateral (B) Na+ caused a small decrease in pHi (ab). Following an NH4+ prepulse-induced acid load (bcde), there was little pHi recovery in the continued absence of external Na+ (ef), or after returning luminal Na+ alone (fg). Subsequently returning basolateral Na+ elicited a pronounced increase in pHi (gh). NaR, Na-Ringer solution. B: orpk CD. The experimental protocol was identical to that shown in A. Removing luminal and basolateral Na+ elicited a more pronounced decrease in pHi (ab). Following the subsequent acid load (bcde) with little pHi recovery in the absence of luminal and basolateral Na+ (ef), returning luminal Na+ in the continued absence of basolateral Na+ elicited a large increase in pHi (fg), which was unaffected by then returning basolateral Na+ (gh). C: luminal and basolateral Na+-stimulated pHi recovery rates (ΔpHit). Using data from panel A- and B-type experiments, the luminal Na+ (NaL)-stimulated ΔpHit was calculated from the pHi recovery at point f in PCs and ICs from control (gray bars) and orpk (black bars) CDs. The basolateral Na+ (NaB)-stimulated ΔpHit was calculated from the pHi recovery at point g in PCs and ICs from control (gray bars) and orpk (black bars) CDs. *P < 0.05 vs control.