Watch ions flow through open channels! Green channels allow ion passage, creating concentration gradients that drive membrane voltage. Five Na⁺/K⁺ pumps (numbered 1-5) work continuously to maintain ion gradients. The oscilloscope shows real-time voltage changes from -120mV to +100mV with threshold at -60mV. The trace turns red during action potentials above threshold. Use the offset control to shift the entire voltage display by ±100mV.
Green trace : Normal membrane potential (below -60mV)
Red trace : Action potential (above -60mV threshold)
Red dashed line : Fixed threshold at -60mV
Yellow sweep line: Current recording position
Red dashed line : Action potential threshold (-60mV, fixed)
Red dotted line : Sodium equilibrium potential (ENa, ~+60mV, moves with concentrations)
Blue dotted line : Potassium equilibrium potential (EK, ~-90mV, moves with concentrations)
1. Set stimulus strength to 50-70 mV
2. Click "Stimulate" button
3. Watch voltage rise above -60mV threshold
4. Observe the complete spike cycle: depolarization → repolarization → hyperpolarization
• If no spike occurs: increase stimulus strength or Na⁺ channel permeability
• For bigger spikes: increase Na⁺ permeability
• For longer spikes: decrease K⁺ permeability
Na⁺ channels (red ions): Open rapidly above -60mV, cause depolarization
K⁺ channels (blue ions): Open slowly above -60mV, cause repolarization
Leak channels: Always open, allow mixed ion flow
Green channels: Open and allow ion passage
Gray channels: Closed, block ion flow
Function: Transport 3 Na⁺ out for every 2 K⁺ in
Energy: Uses ATP (yellow pulsing circles)
Purpose: Maintains concentration gradients
Animation: Red arrows (Na⁺ out), blue arrows (K⁺ in)
Na⁺ Channels: Controls action potential amplitude (default: 0.04)
K⁺ Channels: Controls repolarization speed (default: 1.0)
Cl⁻ Channels: Minor effect on resting potential (default: 0.05)
Pump Rate: Speed of Na⁺/K⁺ gradient maintenance (0-3x normal)
Temperature: Affects ion movement speed (20-40°C)
Stimulus Strength: Depolarization amount (0-100 mV)
Offset: Shifts display by ±100mV (simulates measurement artifacts)
Voltage: Current membrane potential (includes offset)
Phase: Current state (Resting, Depolarizing, Action Potential, etc.)
Na⁺ Conductance: Whether sodium channels are open
Ion Flux: Rate of ion movement across membrane
Shows real-time Na⁺, K⁺, and Cl⁻ levels inside and outside the cell
Equilibrium potentials (ENa, EK) update based on these concentrations
• Block Na⁺ channels: Set Na⁺ permeability to 0, try to stimulate
• Block K⁺ channels: Set K⁺ permeability to 0, observe prolonged spikes
• Disable pumps: Set pump rate to 0, watch gradients decay
• Temperature effects: Change temperature, observe ion movement changes
• Offset experiments: Use offset to simulate different recording conditions
• Multiple stimuli: Create trains of action potentials
This simulation uses real neurophysiological parameters:
• Hodgkin-Huxley channel kinetics
• Goldman-Hodgkin-Katz voltage calculations
• Realistic ion concentrations and equilibrium potentials
• Accurate Na⁺/K⁺ pump stoichiometry (3:2 ratio)
• Physiological temperature dependence
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