When many channels are activated, channel opening is a stochastic
process and the total current recorded is the sum of the
currents flowing through the individual channels. Once a
channel opens there is a very high probability that it will
go into the inactivateable state.
‘ v’ applied step voltage, ‘I’ individual channel currents
and below summated currents. The membrane currents recorded by Hodgkin & Huxley
can be seen to form when many channels are activated. The current recorded at
a single node of Ranvier represents the contribution of many thousands of ion
channels.
The probability that a channel is in the active, conducting
state is a function of the transmembrane potential. When
step changes in the membrane potential are applied and peak
sodium currents are measured and plotted as a function of
the magnitude of the step change in membrane potential, the
curve shown in blue is recorded when the ion channels in
the test patch of membrane were in the inactive/activateable
state .
When an intermediate potential is applied, only a fraction of the channels are
opened, yellow line, too few to achieve threshold for generating an action potential.
If these channels are given time to become inactivateable, and, a second stimulus
pulse applied at value that is capable of activating all activatable channels
(and before the inactivatable channels have recovered), only those activateable
channels are activated leaving the patch unable to develop sufficient depolarization
to initiate a propagated action potential.
This concept may find utility in the creation of virtual
excitation sites that are separated some distance from an
actual electrode site, i.e. axons close to the electrode
will be incapable of generating a propagating action potential
because too many sodium ion channels are temporarily placed
in the inactivatable state.