Inactivation viewed through single sodium channels.

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Abstract
Recordings of the Na current in tissue-cultured [rat] GH3 cells show that the rate of inactivation in whole cell and averaged single channel records is voltage dependent: .tau.h varied e-fold/.apprx. 26 mV. The source of this voltage dependence was investigated by examining the voltage dependence of individual rate constants, estimated by maximum likelihood analysis of single channel records, in a 5-state kinetic model. The rate constant for inactivating from the open state, rather than closing, increased with depolarization, as did the probability that an open channel inactivates. The rate constant for closing from the open state had the opposite voltage dependence. Both rate constants contributed to the mean open time, which was not very voltage dependent. Both open time and burst duration were less than .tau.h for voltages up to -20 mV. The slowest time constant of activation, .tau.m, was measured from whole cell records, by fitting a single exponential either to tail currents or to activating currents in trypsin-treated cells, in which the inactivation was abolished. .tau.m was a bell-shaped function of voltage and had a voltage dependence similar to .tau.h at voltages more positive than -35 mV, but was smaller than .tau.h. At potentials more negative than about -10 mV, individual channels may open and close several times before inactivating. Averaged single channel records, which correspond with macroscopic current elicited by a depolarization, are best described by a convolution of the 1st latency density with the autocorrelation functin rather than with 1 - (channel open time distribution). The voltage dependence of inactivation from the open state, in addition to that of the activation process, is a significant factor in determining the voltage dependence of macroscopic inactivation. Although the rates of activation and inactivation overlapped greatly, independent and coupled inactivation could not be statistically distinguished for 2 models examined. Although rates of activation affect the observed rate of inactivation at intermediate voltages, extrapolation of estimates of rate constants suggests that at very depolarized voltages the activation process is so fast that it is an insignificant factor in the time course of inactivation. Prediction of gating currents shows that an inherently voltage-dependent inactivation process need not produce a conspicuous component in the gating current.