Biophysical Properties and Slow Voltage-Dependent Inactivation of a Sustained Sodium Current in Entorhinal Cortex Layer-II Principal Neurons: A Whole-Cell and Single-Channel Study

The functional and biophysical properties of a sustained, or “persistent,” Na(+) current (I (NaP)) responsible for the generation of subthreshold oscillatory activity in entorhinal cortex layer-II principal neurons (the “stellate cells”) were investigated with whole-cell, patch-clamp experiments. Both acutely dissociated cells and slices derived from adult rat entorhinal cortex were used. I (NaP) , activated by either slow voltage ramps or long-lasting depolarizing pulses, was prominent in both isolated and, especially, in situ neurons. The analysis of the gating properties of the transient Na(+) current (I (NaT)) in the same neurons revealed that the resulting time-independent “window” current (I (NaTW)) had both amplitude and voltage dependence not compatible with those of the observed I (NaP) , thus implying the existence of an alternative mechanism of persistent Na(+)-current generation. The tetrodotoxin-sensitive Na(+) currents evoked by slow voltage ramps decreased in amplitude with decreasing ramp slopes, thus suggesting that a time-dependent inactivation was taking place during ramp depolarizations. When ramps were preceded by increasingly positive, long-lasting voltage prepulses, I (NaP) was progressively, and eventually completely, inactivated. The V(1/2) of I (NaP) steady state inactivation was approximately −49 mV. The time dependence of the development of the inactivation was also studied by varying the duration of the inactivating prepulse: time constants ranging from ∼6.8 to ∼2.6 s, depending on the voltage level, were revealed. Moreover, the activation and inactivation properties of I (NaP) were such as to generate, within a relatively broad membrane-voltage range, a really persistent window current (I (NaPW)). Significantly, I (NaPW) was maximal at about the same voltage level at which subthreshold oscillations are expressed by the stellate cells. Indeed, at −50 mV, the I (NaPW) was shown to contribute to >80% of the persistent Na(+) current that sustains the subthreshold oscillations, whereas only the remaining part can be attributed to a classical Hodgkin-Huxley I (NaTW). Finally, the single-channel bases of I (NaP) slow inactivation and I (NaPW) generation were investigated in cell-attached experiments. Both phenomena were found to be underlain by repetitive, relatively prolonged late channel openings that appeared to undergo inactivation in a nearly irreversible manner at high depolarization levels (−10 mV), but not at more negative potentials (−40 mV).