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. 2009 Dec 30;298(3):R642–R660. doi: 10.1152/ajpregu.00729.2009

Fig. 12.

Fig. 12.

Cl dependence, DIDS sensitivity, and Na+ independence of intracellular alkalinization in AeAE oocytes. A: representative recordings of pHi and membrane potential (Vm) in an AeAE oocyte exposed to a 5% CO2/33 mM HCO3 solution (solution III, Table 2) for 2 h prior. Extracellular concentrations (in mM) of Cl and DIDS are indicated. When extracellular [Cl] was lowered, it was replaced by gluconate. Solution changes are indicated by dashed vertical lines. Intervals a–d in the pHi trace indicate the intervals where rates of pHi change (ΔpHit) were measured. B: representative recordings of pHi and Vm in a H2O-injected oocyte, using a protocol similar to that described in A. C: summary of ΔpHit measurements. Shaded bars represent ΔpHit values of AeAE oocytes (number of oocytes shown in parentheses) during the intervals identified in A. The open bars represent H2O-injected oocytes at similar intervals. Values are means ± SE. Brackets connecting shaded and open bars represent comparisons in unpaired t-tests resulting in significant differences (***P < 0.001). a,bP < 0.001, categorization of the means of the AeAE oocytes as determined by a repeated-measures ANOVA and Newman-Keuls posttest. D: representative recording of pHi in an AeAE oocyte that examines the Na+ dependence of AeAE transport. Extracellular concentrations (in mM) of Cl and Na+ are indicated. A total of 6 AeAE oocytes were evaluated using this protocol.