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. 2002 Aug 15;22(16):6891–6899. doi: 10.1523/JNEUROSCI.22-16-06891.2002

Fig. 3.

Fig. 3.

Effect of external Na+reduction on the decay phase of Ca2+ transients.A, Two Ca2+ transients from the same cell were superimposed. The traces indicated with NaCl and LiCl were obtained in normal Tyrode's solution (145 mm[Na+]o) and in low Na+ condition (20 mm[Na+]o and 125 mm[Li+]o), respectively. The K pipette solution (for its composition, see Materials and Methods) containing 50 μm fura-2 was used for the internal solution. Calibration: 2 sec, 200 nm. The decay phases of the traces indicated with NaCl and LiCl were fitted with the following bi-exponential equations: 0.20 μm · exp (−0.19t) + 1.18 μm · exp (−1.42t) and 0.19 μm · exp(−0.13t) + 1.02 μm · exp(−0.48t), respectively. Inset, The plot of the time derivatives (−d[Ca2+]/dt) of the decay phases of the two Ca2+ transients as a function of Δ[Ca2+]i (white dots, NaCl; black dots, LiCl). B, The instantaneous γ values at various Δ[Ca2+] were calculated by dividing the time derivatives (insetin A) by Δ[Ca2+](t) and were fitted with fourth-order polynomial functions (fNa, a fit to γ in the normal condition; fLi, a fit to γ in the low [Na+]o condition). The difference between the two polynomial fits was plotted as asolid line (marked byfNafLi). The fraction of γ inhibited by the reduction of [Na+]o, (fNafLi)/fNa, was plotted as gray open circles (the right ordinate).