◄ WORLD II · THE FOLDTHE OCHO · blue builds │ the machine │ red breaks

THE HODGKIN-HUXLEY MODEL

The equations that turned the nerve impulse into biophysics. Four coupled ODEs — one for voltage, three for the gates that open and close the ion channels — and out of them falls the action potential: an all-or-none spike that a sub-threshold nudge cannot make and a supra-threshold nudge cannot make bigger. Down the center, current goes in, the membrane integrates, the spike comes out. The blue team builds and defends it; the red team tries to break it.

source Hodgkin & Huxley, A quantitative description of membrane current and its application to conduction and excitation in nerve (1952), J. Physiol. 117, 500–544 — doi:10.1113/jphysiol.1952.sp004764. Rendered, not quoted.

◧ blue team · builds & defends
3

THE MODEL — one voltage, three gates

The membrane is a capacitor in parallel with three conductances. Charge balance gives one line:

C dV/dt = −g̅Na·m³h·(V−ENa) − g̅K·n⁴·(V−EK) − gL(V−EL) + I

Each gate obeys dx/dt = αx(V)(1−x) − βx(V)x — voltage-dependent opening and closing, staying in [0,1]. m is fast Na activation, h slow Na inactivation, n slow K activation.

channelg̅ (mS/cm²)E (mV)gate
Na⁺120+50m³h
K⁺36−77n⁴
leak0.3−54.4

AMBER Illustrative squid-giant-axon parameters, modern −65 mV resting convention. C = 1 µF/cm². Not medical advice.

5

THE LINEAGE — the impulse made equations AVAN

1952: Hodgkin and Huxley voltage-clamped the squid axon, measured Na and K currents separately, and fit the rate constants that predicted the spike shape and conduction velocity. Four ODEs, no fudge factor.

It is the biophysical root of the-action-potential, and the source it reduces to — collapse m,h,n into one recovery variable and you get the excitable phase plane of the-fitzhugh-nagumo. Each sphere is the next one's premise.

7

THE WITNESS live

The blue team's live check: re-integrate the model at a sub-threshold and a supra-threshold current and confirm the all-or-none signature. If red removes the sodium (window 6), this badge is where it shows.

▼ the machine ▼
4

DATA IN — the stimulus current in ↓

A brief depolarizing current pulse I (µA/cm², 0.5 ms) is injected into a resting membrane at −65 mV. That is the whole input — one number. Below a threshold the membrane just leaks the charge back; above it, the sodium gates catch and the spike ignites itself.

Slide the current below to feed the panel. The membrane does the rest — nothing about the spike shape is drawn by hand; it is integrated from the four equations above.

▼   inject the current into the membrane   ▼
0

▣ THE PANEL — the engine LIT

20 µA/cm²
V (mV)gNa = g̅·m³hgK = g̅·n⁴

Move the slider — the trace is integrated (forward Euler, dt = 0.01 ms) on the spot from C dV/dt and the three gate equations, never looked up.

▼   the membrane emits a spike (or does not)   ▼
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DATA OUT — the spike out ↓

What the machine produces, proven: below threshold, only a small passive bump; above it, a full ~100 mV action potential whose peak barely changes with how hard you push (all-or-none). Sodium conductance peaks first (m rises, then h falls); potassium follows and repolarizes past rest. Every gate stays in [0,1].

The blue team's witness (left) re-checks this signature live; the red team (right) tries to make it wrong.

red team · attacks & breaks ◨
1

THE ADVERSARY

WALL This is a space-clamped point membrane — no cable, no geometry, no propagation. It is a squid axon with two gated channels; a real neuron has dozens (Ca²⁺, many K⁺ subtypes, Ih), dendrites, and temperature (Q₁₀) dependence the fixed rates here ignore.

The parameters are illustrative, not a patient. Euler integration adds its own small error; a finer solver shifts the peak by a fraction of a millivolt. The model is a triumph of form — it does not diagnose, prescribe, or replace measurement.

2

THE GRAVEYARD

"The spike is the neuron amplifying its input." Cut. The energy is the membrane's own ionic gradients; the current only triggers a release. Peak height is nearly independent of stimulus — that is the whole point of all-or-none.

"Threshold is a fixed voltage." Cut, corrected. It is a moving boundary set by the race between m opening and h closing; it drifts with history (accommodation) and prior spikes (refractoriness).

"Potassium causes the spike." Cut. Na+ influx makes the upstroke; K+ efflux ends it. The engine proves the order: gNa peaks before gK.

6

THE TAMPER — break it

The red team's move: remove the sodium current (set g̅Na = 0). Without regenerative Na⁺ influx there is no upstroke — no current, however large, produces an all-or-none spike. The blue team's witness (window 7) is watching.

Delete the sodium channel and the membrane only charges passively — the witness re-integrates, finds no spike where one is required, and turns red. Nothing is faked; the attack is real and it is caught.