Electrophysiology Flashcards

1
Q

What are the advantages of electrophysiology?

A
  • Excellent temporal resolution (potential for excellent spatial resolution also)
  • Diverse, flexible techniques (wide and narrow field recording, invasive and non-invasive)
  • Biophysics are relatively well understood (direct measure of neural activity)
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2
Q

What are electrophysiological signals?

A

Summation of current contributions from cellular processes across a given area of neural tissue

Neurons are embedded in an extracellular medium (primarily interstitial fluid and extracellular matrix, highly conductive - acts as a volume conductor for any excitable membranes and transmembrane current)

Current superimposes in extracellular medium to generate an extracellular potential - signals can get messy

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3
Q

What do local field potentials represent?

A

Represents slow waveforms - dominated by synaptic activity

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4
Q

What does multiple-unit activity represent?

A

Extracellular action potentials - signals attenuate rapidly so difficult to detect over distances

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5
Q

What are the following abbrievations: EEG, ECoG, MEG?

A

EEG = electroencephalogram when recorded from the scalp
ECoG = electrocorticography when at the surface of the brain
MEG = magnetoencephalogram - magnetic moments produced by these electric currents

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6
Q

How has the local field potential definition changed?

A

Both definitions by Buzsaki
2004 - The local field potential is the extracellular current flow that reflects the linearly summed postsynaptic potentials from local cell groups

2012 - Any excitable membrane - whether it is a spine, dendrite, soma, axon or axon terminal - and any type of transmembrane current contributes to the extracellular field. The field is the superposition of all ionic processes, from fast action potentials to the slowest fluctuations in glia

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7
Q

What factors determines contribution to the LFP?

A

It depends - multiple sources whose proportional contribution vary based on recording site and technique
LFPs mostly represent slow events reflecting cooperative activity in neural populations

Two important factors determine the extent to which current contributes to an extracellular field
1. Synchrony of the current sources - sources occurring at roughly the same timescale
2. Architectural organisation of the network - allows the slow signals to overlap such that you can actually detect them

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8
Q

What contributes to the LFP?

A

Primary contribution typically from summation of synaptic activity
Potential minor contributions from
- Spiking related activity (fast action potentials, spike afterhyperpolarisation, calcium spikes)
- Intrinsic currents and resonances
- Gap junctions
- Glial cells

== Contributions depend on recording site

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9
Q

Briefly explain synaptic activity

A

Neurotransmitter action leads to ions flowing into the cell
Depending on the type of neurotransmitter, this leads to IPSPs - extracellular source or EPSPs - extracellular sink
Neurons always strive for electroneutrality so opposing ion flux along the neuron occurs
This leads to an extracellular sink in IPSPs and a extracellular source in EPSPs
This leads to generation of a dipole

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10
Q

Explain sources and sinks

A

Sinks and sources refer to the sign of the local field potential measured with extracellular electrodes

Excitation involves positive charges entering cells, depolarising them
When positive charges move into a cell, there is less positive charge outside the cell where the electrode is, so it becomes more negative - this is called a sink because the electrode records a negative deflection

Inhibition causes an active source in the case of negative ionic current - the extracellular potential at the source is positive

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11
Q

What is a dipole?

A

A molecule with an area of negative charge and an area of positive charge that are separated

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12
Q

Why is synaptic activity important for extracellular current flow?

A

They are slow which allows for overlap and summation which boosts detection

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13
Q

What is dipole theory?

A

When an excitatory neurotransmitter is released, positive ions flow into the dendrites, leaving a net negative voltage in the extracellular space – this creates a dipole.

Dipoles from different neurons and different regions summate and conduct to the skull and give rise to the characteristic peaks and troughs of the ERP waveform

A single extracellular event is ordinarily too small to be measured
Surface electrodes in human electrophysiology e.g., EEG mostly detect summated LFPs
Dipoles from multiple local neurons sum together - measurable as a single dipole whose magnitude reflects the number of summated dipoles

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14
Q

Why is cellular geometry important for dipoles?

A

Open field = layer V pyramidal cells
Maximum ion flow = strong LFP contribution
Spatial separation between sink and source allowing for ionic flow

Closed field = thalamocortical cells
Limited ion flow = weak LFP contribution
Source and sinks overlap resulting in limited ion flow

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15
Q

Why is the structure of layer V pyramidal cells ideal for dipoles?

A

Show ideal architecture for superposition of active dipoles
- Parallel apical dendrites
- Open field
- Perpendicular afferent inputs

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16
Q

How do cortical folds affect LFP?

A

When the cortical sheet bends to form a gyrus, the apical dendrites are pushed closer to each other on the concave side, and current density becomes higher compared to when the apical dendrites occupy the convex side of the curve. The influence of tissue curving on the LFP is particularly striking in the dentate gyrus–hippocampus–subiculum axis, where concave and convex bends alternate

17
Q

How do fast action potentials contribute to LFP?

A

Strongest potential single source of currents across the neuronal membrane - spikes generate large-amplitude voltage deflections, typically near the soma
Traditionally thought to have minimal contribution substantially to LFP and EEG due to short duration (<2ms) therefore a lack of synchronicity
However, spiking can contribute to high-frequency components of the ephys signal

18
Q

How are action potential spike afterhyperpolarisations important for LFPs?

A

Bursts of spikes are often followed by hyperpolarisation of the membrane
Afterhyperpolartisations can be as large and last as long as synaptic events meaning big, slow, potentially overlapping - crucial for dipole
Region dependent - when bursting of nearby neurons occurs in a temporally coordinated fashion e.g., hippocampal sharp-wave events associated with long-lasting afterhyperpolarisation

19
Q

How do calcium spikes contribute to LFPs?

A

Contributions to LFP not fully understood in vivo
Large amplitude, long duration Ca2+ spikes can have significant contribution to LFP
Diverse potential voltage-dependent triggers
- NMDA receptors EPSPs
- Action potential backpropagation
Observed experimentally from hippocampal pyramidal cells - NMDA mediated EPSPs produce slow calcium spikes

20
Q

How do gap junctions and glia contribute to LFPs?

A

Minor contributions from both, but worth considering
Gap junctions = do not involve any extracellular current flow, but can affect neuronal excitability and contribute indirectly to the LFP
Glia = may contribute to slow and infraslow field patterns

21
Q

How can we measure LFPs in vivo?

A

Invasive recordings from living animals
- Simultaneous LFP and MUA
- Deep brain or surface level
- Chronic or terminal implantation

Recent advancements in electrode arrays allow up to 2000 channels - most common = 16 channel electrode

Can’t easily analyse 2000 channels in a comprehensive way – although there are new advanced methods, post-analysis isn’t as advanced

22
Q

How can we measure LFPs in vitro?

A

Slice work (ex-vivo)
Neural tissue in artificial CSF - preserved neural functionality
Slice work = near perfect spatial resolution - great for studying circuits and systems

23
Q

What is surface level LFP detection?

A

Arises primarily from synchronised synaptic activity in populations of cortical pyramidal cells
Volume-conducted signal - as it reaches the edge of the volume it is travelling through, capacitance becomes responsible for the signal’s propagation
Detectable by EEG

24
Q

What are the frequency bands that rhythmic EEG is subdivided into?

A

Delta (0-4Hz)
Theta (4-8Hz)
Alpha (8-12Hz)
Beta (12-24Hz)
Gamma (24-40/80Hz)