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. 2002 Feb 15;539(Pt 1):133–143. doi: 10.1113/jphysiol.2001.012940

Figure 4. Na+ efflux measurement.

Figure 4

A, a rabbit myocyte was first exposed to K+-free NT without divalent cations to cause Na+ loading of the cell. Then the cell was superfused with Na+-free solution (containing 4 mm K+) in the presence (outward leak) and absence (pump + leak) of 100 μm strophanthidin (10 mm ouabain was used for rat). The time course of [Na+]i decline was used to calculate d[Na+]i/dt. B, dependence of the rate of [Na+]i decrease on [Na+]i in the presence (leak) and absence (pump + leak) of strophanthidin. The difference between these two curves is the Na+ pump-mediated Na+ efflux. The outward leak depended linearly on [Na+]i with a slope of 0.036 ± 0.002 min−1 (n = 6) in rabbit and 0.069 ± 0.004 min−1 (n = 6) in rat myocytes. C, [Na+]i dependence of the Na+ efflux attributable to the Na+−K+ pump in rabbit (n = 6) and rat (n = 8) myocytes.