Membrane Potential Calculators
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Resting Membrane Potential
Typical values: neurons ~−70 mV; cardiac muscle ~−90 mV; skeletal muscle ~−80 mV; red blood cells ~−10 mV. Set by: (1) Ion concentration gradients maintained by Na⁺/K⁺-ATPase (3 Na⁺ out / 2 K⁺ in per cycle — electrogenic). (2) Differential membrane permeability: K⁺ leak channels are open at rest → K⁺ diffuses out → negative charge inside. (3) Impermeant anions (proteins, organic phosphates) inside the cell contribute to intracellular negativity.
Nernst Equation (Single Ion)
E_ion = (RT/zF) × ln([ion]_out / [ion]_in)
At 37°C: E_ion = (61.5 mV / z) × log₁₀([ion]_out / [ion]_in).
E_K = (61.5/1) × log(5/140) = 61.5 × (−1.447) = −89 mV. E_Na = 61.5 × log(145/15) = +61 mV.
Goldman Equation (Multiple Ions)
V_m = (RT/F) × ln [(P_K[K]_o + P_Na[Na]_o + P_Cl[Cl]_i) / (P_K[K]_i + P_Na[Na]_i + P_Cl[Cl]_o)].
At rest: P_K : P_Na : P_Cl ≈ 1 : 0.04 : 0.45 → V_m ≈ −70 mV. During action potential: P_Na increases 500–1000× → V_m → +40 mV.
Action Potential Phases
Resting (−70 mV) → Threshold (−55 mV) → Rapid depolarization (Nav opens) → Overshoot (+40 mV) → Repolarization (Nav inactivates, Kv opens) → Hyperpolarization → Return to resting.
Glossary
Frequently Asked Questions
Membrane potential (V_m) is the electrical voltage across the cell membrane (inside relative to outside). Three factors determine resting V_m: (1) Ion concentration gradients: K⁺ is high inside (~140 mM) and low outside (~5 mM); Na⁺ is high outside (~145 mM) and low inside (~15 mM); maintained by Na⁺/K⁺-ATPase. (2) Differential membrane permeability: at rest, K⁺ channels (leak channels) are open; K⁺ flows outward down its concentration gradient, carrying positive charge out → inside becomes negative. (3) Fixed negative charges inside (large anions like proteins that cannot cross the membrane) contribute to intracellular negativity. Result: V_m ≈ −70 mV at rest.
The Nernst equation gives the membrane voltage at which there is no net flow of a specific ion (electrochemical equilibrium): E_ion = (RT/zF) × ln([ion]_outside/[ion]_inside). R = 8.314 J/mol/K; T = 310 K (37°C); F = 96,485 C/mol; z = charge. At 37°C: E_ion = (25.7 mV/z) × ln([out]/[in]) = (61.5 mV/z) × log₁₀([out]/[in]). E_K = (61.5/1) × log(5/140) = −89 mV. E_Na = 61.5 × log(145/15) = +61 mV. The resting V_m (−70 mV) lies between E_K and E_Na, weighted toward E_K by the higher K⁺ permeability.
The negative resting V_m arises from two main mechanisms: (1) Selective K⁺ permeability: at rest, K⁺ leak channels are the dominant open channels. K⁺ moves outward down its concentration gradient (high inside, low outside). As positive K⁺ ions leave, negative charge builds up inside — creating an electrical gradient opposing further K⁺ exit. Equilibrium: when electrical force = concentration force; V_m = E_K ≈ −89 mV (but partial Na⁺ and Cl⁻ permeability pulls V_m to ~−70 mV). (2) Na⁺/K⁺-ATPase: electrogenic pump exports 3 Na⁺ and imports 2 K⁺ per cycle → net outward positive charge → contributes ~−5 mV to V_m.
Depolarization: V_m becomes less negative (moves toward 0 mV or even positive). Caused by: Na⁺ or Ca²⁺ influx; K⁺ efflux reduction; Cl⁻ efflux. Example: action potential upstroke (Nav opens → Na⁺ rushes in → V_m goes from −70 to +40 mV). Hyperpolarization: V_m becomes more negative (moves away from 0 mV). Caused by: K⁺ efflux increase; Cl⁻ influx; GABA_A receptor activation (Cl⁻ influx). Example: afterhyperpolarization following an action potential (Kv channels slow to close → K⁺ efflux continues after Nav inactivation → V_m dips below −70 mV). Resting potential: the stable V_m maintained between stimuli (−70 mV in neurons). Threshold: ~−55 mV — the V_m at which enough Nav channels open to create positive feedback → action potential.