Figure 12.
Effect of several potassium channel blockers on the IK(Ca) of the AS-HEL cells. IK(Ca) was activated by dialyzing AS-HEL cells with an internal solution containing 1 μM Ca2+. (a) Once IK(Ca) was activated, the cells were superfused with an external solution containing either 10 μM quinine, 10 mM TEA, 100 nM apamin, 100 μM d-tubocurarine (d-TC) or 1 μM clotrimazole (CLT). Data are shown as mean ± SEM (four cells in each group) of the outward current elicited by a voltage step to +60 mV from a holding potential of −80 mV, before (solid column) or during (open column) exposure to the indicated potassium channel blocker. IK(Ca) is significantly inhibited by 1 μM clotrimazole and 10 mM TEA (*P < 0.05, paired t test). (b) AS-HEL cells were superfused with different concentrations of CTX after activation of the IK(Ca). Current–voltage relationship shows the shift of reversal potentials upon CTX treatment (four to six cells in each group). (c) The data from b for the voltage step to +60 mV are replotted as a function of the concentration of CTX. The data were fit using the Hill equation: I = I max/[1 + (C 1/2/C)n] with n = 0.9 and C 1/2 = 21 nM.