Goldman equation

The GHK voltage equation for ${\displaystyle M}$ monovalent positive ionic species and ${\displaystyle A}$ negative:

${\displaystyle E_{m}={\frac {RT}{F}}\ln {\left({\frac {\sum _{i}^{n}P_{M_{i}^{+}}[M_{i}^{+}]_{\mathrm {out} }+\sum _{j}^{m}P_{A_{j}^{-}}[A_{j}^{-}]_{\mathrm {in} }}{\sum _{i}^{n}P_{M_{i}^{+}}[M_{i}^{+}]_{\mathrm {in} }+\sum _{j}^{m}P_{A_{j}^{-}}[A_{j}^{-}]_{\mathrm {out} }}}\right)}}$

This results in the following if we consider a membrane separating two ${\displaystyle \mathrm {K} _{x}\mathrm {Na} _{1-x}\mathrm {Cl} }$-solutions:[1][2][3]

${\displaystyle E_{m,\mathrm {K} _{x}\mathrm {\text{Na}} _{1-x}\mathrm {Cl} }={\frac {RT}{F}}\ln {\left({\frac {P_{\text{Na}}[{\text{Na}}^{+}]_{\mathrm {out} }+P_{\text{K}}[{\text{K}}^{+}]_{\mathrm {out} }+P_{\text{Cl}}[{\text{Cl}}^{-}]_{\mathrm {in} }}{P_{\text{Na}}[{\text{Na}}^{+}]_{\mathrm {in} }+P_{\text{K}}[{\text{K}}^{+}]_{\mathrm {in} }+P_{\text{Cl}}[{\text{Cl}}^{-}]_{\mathrm {out} }}}\right)}}$

It is "Nernst-like" but has a term for each permeant ion:

${\displaystyle E_{m,{\text{Na}}}={\frac {RT}{F}}\ln {\left({\frac {P_{\text{Na}}[{\text{Na}}^{+}]_{\mathrm {out} }}{P_{\text{Na}}[{\text{Na}}^{+}]_{\mathrm {in} }}}\right)}={\frac {RT}{F}}\ln {\left({\frac {[{\text{Na}}^{+}]_{\mathrm {out} }}{[{\text{Na}}^{+}]_{\mathrm {in} }}}\right)}}$

• ${\displaystyle E_{m}}$ = the membrane potential (in volts, equivalent to joules per coulomb)
• ${\displaystyle P_{\mathrm {ion} }}$ = the selectivity for that ion (in meters per second)
• ${\displaystyle [\mathrm {ion} ]_{\mathrm {out} }}$ = the extracellular concentration of that ion (in moles per cubic meter, to match the other SI units)[4]
• ${\displaystyle [\mathrm {ion} ]_{\mathrm {in} }}$ = the intracellular concentration of that ion (in moles per cubic meter)[4]
• ${\displaystyle R}$ = the ideal gas constant (joules per kelvin per mole)[4]
• ${\displaystyle T}$ = the temperature in kelvins[4]
• ${\displaystyle F}$ = Faraday's constant (coulombs per mole)

${\displaystyle {\frac {RT}{F}}}$ is approximately 26.7 mV at human body temperature (37 °C); when factoring in the change-of-base formula between the natural logarithm, ln, and logarithm with base 10 ${\displaystyle ([\log _{10}\exp(1)]^{-1}=\ln(10)=2.30258...)}$, it becomes ${\displaystyle 26.7\,\mathrm {mV} \cdot 2.303=61.5\,\mathrm {mV} }$, a value often used in neuroscience.

${\displaystyle E_{X}=61.5\,\mathrm {mV} \cdot \log {\left({\frac {[X^{+}]_{\mathrm {out} }}{[X^{+}]_{\mathrm {in} }}}\right)}=-61.5\,\mathrm {mV} \cdot \log {\left({\frac {[X^{-}]_{\mathrm {out} }}{[X^{-}]_{\mathrm {in} }}}\right)}}$

The ionic charge determines the sign of the membrane potential contribution. During an action potential, although the membrane potential changes about 100mV, the concentrations of ions inside and outside the cell do not change significantly. They are always very close to their respective concentrations when the membrane is at their resting potential.

Goldman's equation seeks to determine the voltage E_m across a membrane.[5] A Cartesian coordinate system is used to describe the system, with the z direction being perpendicular to the membrane. Assuming that the system is symmetrical in the x and y directions (around and along the axon, respectively), only the z direction need be considered; thus, the voltage E_m is the integral of the z component of the electric field across the membrane.

According to Goldman's model, only two factors influence the motion of ions across a permeable membrane: the average electric field and the difference in ionic concentration from one side of the membrane to the other. The electric field is assumed to be constant across the membrane, so that it can be set equal to E_m/L, where L is the thickness of the membrane. For a given ion denoted A with valence n_A, its flux j_A—in other words, the number of ions crossing per time and per area of the membrane—is given by the formula

${\displaystyle j_{\mathrm {A} }=-D_{\mathrm {A} }\left({\frac {d\left[\mathrm {A} \right]}{dz}}-{\frac {n_{\mathrm {A} }F}{RT}}{\frac {E_{m}}{L}}\left[\mathrm {A} \right]\right)}$

The first term corresponds to Fick's law of diffusion, which gives the flux due to diffusion down the concentration gradient, i.e., from high to low concentration. The constant D_A is the diffusion constant of the ion A. The second term reflects the flux due to the electric field, which increases linearly with the electric field; Formally, it is [A] multiplied by the drift velocity of the ions, with the drift velocity expressed using the Stokes–Einstein relation applied to electrophoretic mobility. The constants here are the charge valence n_A of the ion A (e.g., +1 for K⁺, +2 for Ca²⁺ and −1 for Cl⁻), the temperature T (in kelvins), the molar gas constant R, and the faraday F, which is the total charge of a mole of electrons.

This is a first-order ODE of the form y' = ay + b, with y = [A] and y' = d[A]/dz; integrating both sides from z=0 to z=L with the boundary conditions [A](0) = [A]_in and [A](L) = [A]_out, one gets the solution

${\displaystyle j_{\mathrm {A} }=\mu n_{\mathrm {A} }P_{\mathrm {A} }{\frac {\left[\mathrm {A} \right]_{\mathrm {out} }-\left[\mathrm {A} \right]_{\mathrm {in} }e^{n_{\mathrm {A} }\mu }}{1-e^{n_{\mathrm {A} }\mu }}}}$

where μ is a dimensionless number

${\displaystyle \mu ={\frac {FE_{m}}{RT}}}$

and P_A is the ionic permeability, defined here as

${\displaystyle P_{\mathrm {A} }={\frac {D_{\mathrm {A} }}{L}}}$

The electric current density J_A equals the charge q_A of the ion multiplied by the flux j_A

${\displaystyle J_{A}=q_{\mathrm {A} }j_{\mathrm {A} }}$

Current density has units of (Amperes/m²). Molar flux has units of (mol/(s m²)). Thus, to get current density from molar flux one needs to multiply by Faraday's constant F (Coulombs/mol). F will then cancel from the equation below. Since the valence has already been accounted for above, the charge q_A of each ion in the equation above, therefore, should be interpreted as +1 or -1 depending on the polarity of the ion.

There is such a current associated with every type of ion that can cross the membrane; this is because each type of ion would require a distinct membrane potential to balance diffusion, but there can only be one membrane potential. By assumption, at the Goldman voltage E_m, the total current density is zero

${\displaystyle J_{tot}=\sum _{A}J_{A}=0}$

(Although the current for each ion type considered here is nonzero, there are other pumps in the membrane, e.g. Na⁺/K⁺-ATPase, not considered here which serve to balance each individual ion's current, so that the ion concentrations on either side of the membrane do not change over time in equilibrium.) If all the ions are monovalent—that is, if all the n_A equal either +1 or -1—this equation can be written

${\displaystyle w-ve^{\mu }=0}$

whose solution is the Goldman equation

${\displaystyle {\frac {FE_{m}}{RT}}=\mu =\ln {\frac {w}{v}}}$

where

${\displaystyle w=\sum _{\mathrm {cations\ C} }P_{\mathrm {C} }\left[\mathrm {C} ^{+}\right]_{\mathrm {out} }+\sum _{\mathrm {anions\ A} }P_{\mathrm {A} }\left[\mathrm {A} ^{-}\right]_{\mathrm {in} }}$

${\displaystyle v=\sum _{\mathrm {cations\ C} }P_{\mathrm {C} }\left[\mathrm {C} ^{+}\right]_{\mathrm {in} }+\sum _{\mathrm {anions\ A} }P_{\mathrm {A} }\left[\mathrm {A} ^{-}\right]_{\mathrm {out} }}$

If divalent ions such as calcium are considered, terms such as e^2μ appear, which is the square of e^μ; in this case, the formula for the Goldman equation can be solved using the quadratic formula.

• Bioelectronics
• Cable theory
• GHK current equation
• Hindmarsh–Rose model
• Hodgkin–Huxley model
• Morris–Lecar model
• Nernst equation
• Saltatory conduction

• Subthreshold membrane phenomena Includes a well-explained derivation of the Goldman-Hodgkin-Katz equation
• Nernst/Goldman Equation Simulator Archived 2010-08-08 at the Wayback Machine
• Goldman-Hodgkin-Katz Equation Calculator
• Nernst/Goldman interactive Java applet The membrane voltage is calculated interactively as the number of ions are changed between the inside and outside of the cell.
• Potential, Impedance, and Rectification in Membranes by Goldman (1943)