Before examining the ionic mechanisms of action potentials, it is first necessary
to understand the ionic mechanisms of the resting potential. The two phenomena
are intimately related. The story of the resting potential goes back to the early
1900's when Julius Bernstein suggested that the resting potential (Vm) was equal
to the potassium equilibrium potential (EK). Where
The key to understanding the resting potential is the fact that ions are distributed
unequally on the inside and outside of cells, and that cell membranes are selectively
permeable to different ions. K+ is particularly important for the
resting potential. The membrane is highly permeable to K+. In addition,
the inside of the cell has a high concentration of K+ ([K+]i)
and the outside of the cell has a low concentration of K+ ([K+]o).
Thus, K+ will naturally move by diffusion from its region of high
concentration to its region of low concentration. Consequently, the positive
K+ ions leaving the inner surface of the membrane leave behind some
negatively charged ions. That negative charge attracts the positive charge of
the K+ ion that is leaving and tends to "pull it back". Thus, there
will be an electrical force directed inward that will tend to counterbalance
the diffusional force directed outward. Eventually, an equilibrium will be established;
the concentration force moving K+ out will balance the electrical
force holding it in. The potential at which that balance is achieved is called
the Nernst Equilibrium Potential.
Figure 1.4
An experiment to test Bernstein's hypothesis that the membrane
potential is equal to the Nernst Equilibrium Potential (i.e.,
Vm = EK) is illustrated to the left.
The K+ concentration outside the cell was systematically
varied while the membrane potential was measured. Also shown is the line
that is predicted by the Nernst Equation. The experimentally measured points
are very close to this line. Moreover, because of the logarithmic relationship
in the Nernst equation, a change in concentration of K+ by a
factor of 10 results in a 60 mV change in potential.
Note, however, that there are some deviations in the figure at left
from what is predicted by the Nernst equation. Thus, one cannot conclude
that Vm = EK. Such deviations indicate that another
ion is also involved in generating the resting potential. That ion is Na+.
The high concentration of Na+ outside the cell and relatively
low concentration inside the cell results in a chemical (diffusional) driving
force for Na+ influx. There is also an electrical driving force
because the inside of the cell is negative and this negativity attracts
the positive sodium ions. Consequently, if the cell has a small permeability
to sodium, Na+ will move across the membrane and the membrane
potential would be more depolarized than would be expected from the K+
equilibrium potential.
Goldman-Hodgkin and Katz (GHK) Equation
When a membrane is permeable to two different ions, the Nernst equation
can no longer be used to precisely determine the membrane potential. It
is possible, however, to apply the GHK equation. This equation describes
the potential across a membrane that is permeable to both Na+
and K+.
Note that is the ratio of Na+
permeability (PNa) to K+ permeability (PK).
Note also that if the permeability of the membrane to Na+ is 0, then
alpha in the GHK is 0, and the Goldman-Hodgkin-Katz equation reduces to the
Nernst equilibrium potential for K+. If the permeability of the membrane
to Na+ is very high and the potassium permeability is very low, the
[Na+] terms become very large, dominating the equation compared to
the [K+] terms, and the GHK equation reduces to the Nernst equilibrium
potential for Na+.
If the GHK equation is applied to the same data
in Figure 1.4, there is a much better fit. The value of alpha needed to
obtain this good fit was 0.01. This means that the potassium K+
permeability is 100 times the Na+ permeability. In summary, the
resting potential is due not only to the fact that there is a high permeability
to K+. There is also a slight permeability to Na+,
which tends to make the membrane potential slightly more positive than it
would have been if the membrane were permeable to K+ alone.
Figure 1.5
Membrane Potential Laboratory
Click here to go to the interactive Membrane
Potential Laboratory to experiment with the effects of altering external
or internal potassium ion concentration and membrane permeability to sodium
and potassium ions. Predictions are made using the Nernst and the Goldman, Hodgkin,
Katz equations.
Membrane Potential Laboratory
Test Your Knowledge
1. If a nerve membrane suddenly
became equally permeable to both Na+ and K+, the
membrane potential would:
A. Not change B. Approach the new K+ equilibrium
potential C. Approach the new Na+ equilibrium
potential D. Approach a value of about 0 mV E. Approach a constant value of about +55
mV
2. If the concentration of K+
in the cytoplasm of an invertebrate axon is changed to a new value of
200 mM (Note: for this axon normal [K]o = 20 mM and normal
[K]i = 400 mM):
A. The membrane potential would become more
negative B. The K+ equilibrium potential
would change by 60 mV C. The K+ equilibrium potential
would be about -60 mV D. The K+ equilibrium potential
would be about -18 mV E. An action potential would be initiated