Resting Potential Calculators
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Ionic Basis of Resting Potential
At rest, K⁺ concentration is high inside (~140 mM) and low outside (~5 mM). Na⁺ is high outside (~145 mM) and low inside (~12 mM). Cl⁻ is predominantly extracellular. The membrane at rest is most permeable to K⁺ through inward-rectifying K⁺ leak channels. K⁺ diffuses outward down its concentration gradient, leaving behind negative charges and creating a negative interior — the resting potential.
The Na⁺/K⁺ Pump
The Na⁺/K⁺-ATPase pump actively transports 3 Na⁺ out and 2 K⁺ in per ATP hydrolyzed, maintaining the ion gradients that drive the resting potential. It also directly contributes −3 to −5 mV to the resting potential by being electrogenic (unequal ion transport). Without the pump, ion gradients would dissipate and cells would depolarize.
The Goldman-Hodgkin-Katz (GHK) Equation
The Goldman equation calculates Vm from the relative permeabilities and concentrations of K⁺, Na⁺, and Cl⁻:
Vm = (RT/F) × ln[(PK[K⁺]o + PNa[Na⁺]o + PCl[Cl⁻]i) / (PK[K⁺]i + PNa[Na⁺]i + PCl[Cl⁻]o)]
At rest, PK >> PNa, so the resting potential approaches the Nernst equilibrium potential for K⁺ (EK ≈ −90 mV), but is slightly depolarized from this value due to Na⁺ leak permeability.
Resting Potential and Excitability
The resting potential sets the 'electrical baseline' from which action potentials are generated. Hyperpolarization (more negative Vm) makes cells less excitable; depolarization (less negative Vm) moves Vm closer to the action potential threshold (~−55 mV for neurons). Many neurotransmitters and drugs act by modulating resting permeabilities to Na⁺, K⁺, or Cl⁻.
Glossary
Frequently Asked Questions
The resting membrane potential (~−70 mV in neurons) is the voltage difference across the cell membrane when the cell is not firing. It is caused by the unequal distribution of ions — particularly K⁺ (high inside), Na⁺ (high outside), and Cl⁻ (high outside) — and the selective permeability of the resting membrane, which is much more permeable to K⁺ than Na⁺. K⁺ diffuses outward down its concentration gradient, leaving the cell interior negatively charged.
The Na⁺/K⁺-ATPase pump uses ATP to transport 3 Na⁺ out of the cell and 2 K⁺ into the cell, actively maintaining the ion concentration gradients that drive the resting potential. Without this pump, Na⁺ would leak in and K⁺ would leak out until gradients dissipated. The pump also contributes directly ~3–5 mV to the resting potential because it is electrogenic (transports more positive charges out than in).
The Goldman-Hodgkin-Katz equation calculates the membrane potential from the concentrations and relative permeabilities of all permeant ions (typically K⁺, Na⁺, Cl⁻). It generalizes the Nernst equation for a single ion to multiple ions. At rest, K⁺ permeability dominates, pulling Vm toward EK (~−90 mV). Because some Na⁺ permeability also exists, the actual resting potential is around −70 mV, slightly depolarized from EK.
The resting potential determines how far the membrane voltage is from the action potential threshold (~−55 mV). A more negative resting potential (hyperpolarization) means a larger depolarization is needed to fire an action potential, making the cell less excitable. A less negative resting potential (depolarization) brings Vm closer to threshold, increasing excitability. Inhibitory neurotransmitters (GABA, glycine) hyperpolarize cells; excitatory neurotransmitters (glutamate) depolarize them.