NeuroLogic: Fundamentals

EEG Fundamentals

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Read the signal, then report what it shows

This self-paced course is designed for neurology residents and clinicians beginning to read scalp EEG. Each topic combines an explanation, a model or clinical example, and a short check. Experienced readers can use individual lessons for review.

About 5 hours 40 minutes53 short lessons · learn in order or choose a topic from Contents

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Answer the short pre-test before you start, and the matching post-test after the last lesson. Together they show what the course teaches you and help us improve it. A random study code pairs the two; no names or email addresses are collected.

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By the end, you can:

  • Explain where the scalp signal comes from and why a channel compares two inputs.
  • Use the 10–20 map, montages, filters, and polarity to describe what appears on a page.
  • Recognize common background, sleep, artifact, and abnormal patterns, then organize a report.

Course topics

Many lessons open with a short narrated video that covers the same ground; watch it first, then read on. To watch them back to back, open Videos. Under each video are its chapters, a transcript and a short quiz.

From cortex to channel

Concept

Follow five steps from cortical current to recorded channel. This sequence explains polarity, montage subtraction, and the limits of scalp localization.

  1. Source population: Synaptic currents create graded postsynaptic potentials in cortical neurons. Single axonal action potentials are too brief and spatially scattered to dominate routine scalp EEG.
  2. Open field: Millions of similarly oriented pyramidal cells, over several square centimeters of cortex (often 10 cm² or more for a spike seen on the scalp), must be active with enough synchrony for their extracellular fields to add instead of cancel.
  3. Volume conduction: The summed field spreads through brain, cerebrospinal fluid, skull, and scalp. This passive journey attenuates and spatially blurs the signal; it does not create a new rhythm.
  4. Electrode potential: Each scalp electrode samples the local extracellular potential produced by the mixture of fields that reaches it. An electrode has no meaningful absolute voltage by itself.
  5. Channel difference: The amplifier displays Input 1 minus Input 2. The waveform therefore belongs to a channel (a comparison), not to either electrode alone.
Synchrony makes the signal
Synchrony, not a single conductor

A crowd is quiet at a distance when everyone speaks independently and loud when many people clap together. Cortical synchrony likewise emerges from interacting thalamocortical and intracortical networks; the thalamus is important for several rhythms, but it is not the sole conductor of EEG.

Scalp detection generally requires synchronous activation across several square centimeters of cortex; often-cited estimates begin around 6 cm², and most spikes seen on the scalp involve 10 cm² or more (Tao 2005), but detectability varies with depth, orientation, synchrony, amplitude, and competing background activity.

Hand-drawn cross section: nine aligned pyramidal neurons in the cortex whose extracellular fields add and spread upward through cerebrospinal fluid, skull and scalp to one scalp electrode, with numbered notes on alignment, summation and volume conduction
Aligned cortical populations generate a cumulative extracellular field; volume conduction carries a blurred, attenuated version to the scalp electrode.

The diagram above traced cortex → extracellular field → volume conduction → electrode. Routine scalp EEG reflects the summed postsynaptic fields of synchronized cortical populations, not individual axonal spikes.

Spot check Follow the diagram from cortex to scalp. Which signal contributes most directly to routine scalp EEG?

Ions, channels and membrane voltage

Concept

Every EEG signal begins as current crossing neuronal membranes. These three step-by-step drawings build the cellular vocabulary the rest of the course uses, one click at a time: why a neuron rests near −70 mV, how voltage-gated channels produce a 1‑ms action potential, and how excitatory and inhibitory postsynaptic potentials add.

Millivolts inside, microvolts at the scalp. Membrane voltages are tens of millivolts (mV): rest is about −70 mV and an action potential peaks near +30 mV. Scalp EEG is measured in microvolts (µV), roughly a thousand times smaller, because the electrode records only small extracellular currents summed across many cells and weakened by cerebrospinal fluid, skull and scalp.

Typical values in a mature mammalian neuron. They vary with cell type and age.
IonInsideOutsideEquilibrium potential
K⁺about 140 mM3–5 mMabout −90 to −100 mV
Na⁺10–15 mMabout 145 mMabout +60 to +70 mV
Cl⁻4–10 mMabout 110 mMabout −65 to −90 mV
Ca²⁺about 0.0001 mMabout 2 mMabove +120 mV

Where these ideas return

  • Potassium sets rest. Because resting permeability is dominated by K⁺, a rise in extracellular K⁺ during intense firing depolarizes neighboring neurons and favors seizure spread.
  • Sodium-channel inactivation sets refractoriness. Carbamazepine, phenytoin and lamotrigine stabilize the fast-inactivated state; lacosamide enhances slow inactivation.
  • GABA-A receptors are Cl⁻ channels. Benzodiazepines and barbiturates act here. In immature neurons, high intracellular Cl⁻ can make gamma-aminobutyric acid (GABA) depolarizing, one proposed but debated reason these drugs work less reliably in neonatal seizures.
  • Postsynaptic potentials outlast action potentials. Their long, overlapping currents are what summate into the scalp EEG, the subject of the next two lessons.

Step back through the first drawing: the voltage falls toward EK when K⁺ leak channels open, and only a small Na⁺ leak pulls it back toward −70 mV.

Spot check A cortical neuron rests near −70 mV. Which process sets most of that voltage?

Why EEG sees synapses, not single-neuron spikes

Concept

Routine scalp EEG is dominated by the extracellular fields of synchronized cortical postsynaptic currents. Duration helps explain temporal summation, but spatial alignment, cancellation, source extent, depth, and the competing background also determine detectability.

Predict: keep the cells aligned and increase their timing spread. Which event loses more of its summed peak: a brief biphasic action-potential-like event or a longer postsynaptic event?

The model below runs both events side by side. Each panel shows twelve model cells, standing for a much larger population, and the sum a distant electrode would receive.

Hand-drawn stadium crowd in two halves with the same eighteen people in each. Left, labeled random noise: everyone does something different, and the summed trace beneath is small and jagged. Right, labeled synchronized signal: everyone raises both arms together, and the summed trace beneath is a large, smooth wave.
Same number of people on both sides. Only the timing differs.

Drag the timing spread down to 0 ms and up to 25 ms (it starts at 6 ms) and watch the right panel, then flip half the cells. Timing dispersion and geometric cancellation are different mechanisms. Watch what each does to the two sums.

Snapshot: at the combined peak

Postsynaptic potentialseach lasts about 60 ms

Sum keeps of its aligned height

Action potentialseach lasts about 1 ms

Sum keeps of its aligned height

Each row is one model cell; a filled dot means it is active at the cursor. The bottom trace is the sum of the rows above it, in relative field units, not membrane voltage. Replay sweeps 120 ms in six seconds.

Why routine scalp EEG is dominated by postsynaptic fields

Brief axonal events have unfavorable temporal and spatial summation at the scalp. A quiet trace does not imply silent neurons. Likewise, synchrony is not itself epileptiform: alpha rhythms and sleep graphoelements also reflect organized population activity.

Two meanings of “spike.” A single axonal action potential lasts about 1 ms. An EEG spike is a 20–70 ms scalp waveform generated by a population of neurons. The terms describe different levels of physiology.

Compare the timing spread with the length of each event. Two events add only while they overlap in time.

Spot check Twelve aligned cortical cells each produce the same event, but their timing now spreads over about 10 ms. Which summed signal loses more of its peak at a distant electrode?

Timing dispersion and geometric cancellation are different mechanisms. Here the timing is perfect; only the direction changes.

Spot check In a population with perfectly matched timing and strength, half of the cells are turned to point the opposite way. What happens to the summed field?

From ion flow to EEG polarity

Concept

Start with the extracellular space, because that is where the EEG electrode listens. A sink is a membrane region where conventional positive current enters the neuron. Removing positive charge makes the nearby extracellular space relatively negative. A source is the return-current region, where positive current leaves the cell and the extracellular space becomes relatively positive.

Pyramidal cells are aligned perpendicular to the cortical surface. When many of them activate together, the sink and source fields add as an open field. Move the synaptic current from the apical dendrites to the soma and the dipole flips, even though the cellular event can still be excitatory.

Try: switch between an excitatory postsynaptic potential (EPSP) and an inhibitory postsynaptic potential (IPSP), then move the synapse from apical dendrite to soma. Watch the extracellular sign and the scalp deflection change together.

Interactive current field

Move the synapse, then follow the charge

Synaptic current and the surrounding field The highlighted synapse creates a local sink or source. The scalp field and EEG deflection update with the selected synaptic event and location. − Scalpelectrode Active synapse Negative sink Return current Positive source Conventional current
Result at the scalp

EEG deflection

Relative negativity is displayed upward Negative → up

Compared with a fixed, quiet reference.

Schematic shape, not a measured voltage.

At the synapseNegative extracellular sink
Directly aboveRelative negativity
DisplayUpward deflection
About this model

This figure represents an aligned population of pyramidal cells, with a fixed quiet reference. The return current is distributed across the membrane; its arrows show a simplified circuit.

The EPSP example uses inward Na+ current. The IPSP example uses inward Cl− current at a mature, hyperpolarizing synapse. Inhibition depends on ionic driving force and conductance, so polarity alone does not identify excitation, inhibition, or a neurotransmitter.

Apical EPSPsuperficial sinknegative, displayed up
Deep EPSPdeep sinksurface positive, displayed down
Apical IPSPsuperficial sourcepositive, displayed down
Deep IPSPdeep sourcesurface negative, displayed up

Keep the order straight: identify where current crosses the membrane, decide whether the nearby extracellular space is a sink or source, determine the dipole orientation, and only then predict the scalp polarity. Clinical EEG displays relative negativity upward.

Use the polarity rules and ion lab above: inward positive current at a superficial synapse removes positive charge from the nearby extracellular space, leaving relative negativity at the electrode.

Spot check Positive current enters a superficial apical dendrite during an EPSP. What does the nearby extracellular electrode sample?

Dipole orientation and scalp maxima

Concept

Pyramidal cells stand perpendicular to the cortical surface, and the cortex is folded, so the fold decides which way the dipole points. A cell on a gyral crown points its dipole up at the scalp. A cell on a sulcal wall points sideways. Orientation changes the scalp field. The field maximum alone cannot uniquely determine the generator.

Try these three comparisons:

  1. Change orientation: select Radial, Oblique, then Tangential. Watch where the largest field moves and compare the Electrode overhead reading.
  2. Change depth: return to Radial and increase Source depth from 1.0 to 2.0. Watch the curve and the Peak strength reading.
  3. Compare two sources: reset depth to 1.0, then toggle Add an opposing source. Compare the field’s strength and shape with one source versus two.

How the cortex sets orientation

Radial · toward the scalp

The highlighted cell turns with the cortical fold. Its long axis stays perpendicular to the local surface.

Where the scalp field is largest

Blue −, upward · Red +, downward

Scalp potential produced by a dipole at the selected orientation
The ring marks the electrode directly above the first source. The curve shows position, not time, on a fixed field scale.
Electrode overhead
Largest field
Peak strength
About this model

The fold illustrates orientation; the depth slider separately controls source depth in relative units. The added source has equal strength, opposite orientation, and a fixed separation of 0.4 units. It is shown in the field panel.

Point dipoles in a homogeneous conductor, with zero reference at infinity. Field units are relative, not microvolts; the radial peak at depth 1 is 100 units. Electrode colors show polarity. Source symbols are schematic. A scalp maximum cannot uniquely locate a cortical source.

At 90° in this model: the field is zero directly above the source, with opposite-polarity peaks on either side. Neither peak alone locates the underlying cortical generator.

Why deep sources hide

Greater depth reduces and broadens the field in this model. Opposing cortical populations can partially or completely cancel, depending on their relative timing, strength, and geometry. Orientation and depth are separate variables; neither alone determines scalp detectability.

EEG and magnetoencephalography (MEG) provide complementary views. In a spherical approximation, MEG is preferentially sensitive to tangential sources, while EEG detects radial and tangential components. Real anatomy and noise also affect both recordings.

A pyramidal cell stands perpendicular to its own patch of cortex. On a sulcal wall, which way does that point relative to the scalp?

Spot check A focal discharge arises from cortex on the wall of a sulcus, so its dipole lies tangential to the scalp. What does the scalp field show?

Once the field reaches the scalp, the next task is naming the electrode sites that sample it.