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. 2003 Oct 24;554(Pt 3):659–672. doi: 10.1113/jphysiol.2003.055806

Figure 3. Pharmacological characterization of the two outward currents Ir and Is.

Figure 3

Ir was analysed at the potential +70 mV, whereas Is was tested at +20 mV to avoid contamination by Ir (see Methods). A, effects of the K+ channel blockers Ba2+ (1 mm), 4-aminopyridine (4-AP, 3 mm), E-4031 (5 μm), HMR1556 (1 μm), linopirdine (10 μm) and of the chloride channel blocker DIDS (200 μm). Outward current amplitudes in the presence of blockers were normalized to predrug amplitudes. Numbers in columns give the number of cells tested. B, effects of tetraethylammonium on outward current amplitudes. The effects of all compounds were reversible upon washout. *P < 0.05, **P < 0.01, ***P < 0.001; Student's paired t test.