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. 1998 Sep 15;511(Pt 3):827–836. doi: 10.1111/j.1469-7793.1998.827bg.x

Figure 3. Effect of Cd2+ on Ito in rat myocytes.

Figure 3

ICa,L was blocked by 0 mM Ca2+o-5 mM Mg2+o. A, decrease of Ito by Cd2+ (0.3 mM). Current activated by a step from a holding potential of -80 to 0 mV. Traces in the absence (□) and in the presence of Cd2+ (•) are superimposed. Inset, voltage-clamp protocol (20 ms prepulse to -40 mV to inactivate INa not shown). B, increase of Ito by Cd2+. Current activated by a step to +60 mV after a 1 s prepulse to -30 mV in the absence (□) and presence of Cd2+ (•). Only currents during the test pulse are shown. Inset, voltage-clamp protocol. C, effect of Cd2+ on steady-state activation and inactivation curves. □, control; •, Cd2+; ▵, second control. The effect of Cd2+ was reversible.