Voltage dependence of slow inactivation in Shaker potassium channels results from changes in relative K+ and Na+ permeabilities

Time constants of slow inactivation were investigated in NH2-terminal delet ed Shaker potassium channels using macro-patch recordings from Xenopus oocy tes. Slow inactivation is voltage insensitive in physiological solutions or in simple experimental solutions such as K-o(+)//K-i(+) or Na-o(+)//K-i(+) . However, when [Na+](i) is increased while [K+](i) is reduced, voltage sen sitivity appears ill the slow inactivation rates at positive potentials. In such solutions, the I-V curves show a region of negative slope conductance between similar to 0 and +60 mV, with strongly increased outward current a t more positive voltages, yielding an N-shaped curvature. These changes in peak outward currents are associated with marked changes in the dominant sl ow inactivation time constant from similar to 1.5 s at potentials less than approximately +60 mV to similar to 30 ms at more than +150 mV. Since slow inactivation in Shaker channels is extremely sensitive to die concentration s and species of permeant ions, more rapid entry into slow inactivated stat e(s) might indicate decreased K+ permeation and increased Na+ permeation at positive potentials. However, the N-shaped I-V curve becomes fully develop ed before the onset of significant slow inactivation, indicating that this N-shaped I-V does not arise from permeability changes associated with entry into slow inactivated states. Thus, changes in the relative contributions of K+ and Na+ ions to outward currents could arise either: (a) from depleti ons of [K+](i) sufficient to permit increased Na+ permeation, or (b) from v oltage-dependent changes in K+ and Na+ permeabilities. Our results rule out the first of these mechanisms. Furthermore, effects of changing [K+](i) an d [K+](o) on ramp I-V waveforms suggest that applied potential directly aff ects relative permeation by K+ and Na+ ions. Therefore, we conclude that th e voltage sensitivity of slow inactivation rates arises indirectly as a res ult of voltage-dependent changes in the ion occupancy of these channels, an d demonstrate that simple barrier models can predict such voltage-dependent changes in relative permeabilities.