Dependence of cell pH and buffer capacity on the extracellular acid-base change in the skeletal muscle of bullfrog.

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Abstract
Intracellular pH was measured with single- or double-barreled liquid ion-exchanger microelectrodes in the bullfrog sartorius muscle perfused in vitro. A neutral carrier ligand was used for pH sensor of microelectrodes. Average slopes of the single-barreled microelectrodes were -56.4 .+-. 1.34 mV/pH (n = 30) and the double-barreled -52.6 .+-. 1.34 mV/pH (n = 65). While changing acid-base parameters of bathing media (pHe from 6.7 to 8.4, PCO2 from 3.7 to 37 mmHg, and HCO3- concentrations from 5 to 75 .mu.M), paired muscle cell pH (pHi) and membrane potential (EM) values were determined at 23.degree. C. In control conditions (pHe = 7.6, HCO3- = 15 mM, PCO2 = 11 mmHg), pHi and EM (n = 20) averaged 6.99 .+-. 0.04 (S.E.) and -69.2 .+-. 2.2 mV, respectively. A negative correlation was observed between pHi and EM (correlation coefficient r = -0.564, p < 0.002). The change in EM per unit pH change was approximately -30 mV, indicating that the H+ distribution across the cell membrane only incompletely obeys the Donnan rule. The pHi varied more or less with pHe. Namely, changes in pHe and PCO2 at constant HCO3- produced relatively large changes in pHi, but elevation of pHe and HCO3- at constant PCO2 produced relatively minor rise in pHi. The stability of pHi or the size of buffer capacity were proportional to external HCO3- concentrations. These data suggested that a transmembrane distribution of buffer pairs depends largely on non-ionic diffusion of CO2-HCO3- buffer system and partly on ion fluxes of HCO3- or H+.

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