Figure 4
Comparison of observed and model-simulated changes in the mean Na+ and K+ content of RBCs during the dehydration-rehydration protocol. RBCs were treated as described for Figure 1A and sampled for their Na+ and K+ contents, measured by flame photometry (see “Materials and methods”). (B) The Lew-Bookchin red cell model41 was used to simulate the sequence followed in the experiment of Figure 3A to estimate the required changes in Na+ and K+ permeabilities (PNa, PK) that would reproduce the extents and time course of the measured mean Na+ and K+ content changes in panel A. The PNa and PK values used for the fit shown were 0.015 h−1 (PNa through Pcat, a 10-fold increase over the normal mean electrodiffusional component of the Na+ permeability of about 0.0015 h−1 41,43) and 10 h−1 (PK through Gardos channels), respectively. The electrodiffusional anion permeability was set at 50 h−1 to represent the effect of 10 mM SCN−.42

Comparison of observed and model-simulated changes in the mean Na+ and K+ content of RBCs during the dehydration-rehydration protocol. RBCs were treated as described for Figure 1A and sampled for their Na+ and K+ contents, measured by flame photometry (see “Materials and methods”). (B) The Lew-Bookchin red cell model41  was used to simulate the sequence followed in the experiment of Figure 3A to estimate the required changes in Na+ and K+ permeabilities (PNa, PK) that would reproduce the extents and time course of the measured mean Na+ and K+ content changes in panel A. The PNa and PK values used for the fit shown were 0.015 h−1 (PNa through Pcat, a 10-fold increase over the normal mean electrodiffusional component of the Na+ permeability of about 0.0015 h−1 41,43 ) and 10 h−1 (PK through Gardos channels), respectively. The electrodiffusional anion permeability was set at 50 h−1 to represent the effect of 10 mM SCN.42 

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