Week 5 - topic 2 Flashcards

1
Q

Methods of recording action potentials and post-synaptic potentials

A

These electrical events can be recorded:

  • Recording with Microelectrodes
  • Recording with Macroelectrodes (EEG)
  • Magnetoencephalography (MEG)
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2
Q

Recording with microelectrodes

A
  • Single Unit Recording: Recording of the electrical activity of a single neuron
  • Microelectrodes are made of very thin wires and have a very fine tip that can be used for single unit recording.
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3
Q

Recording with macroelectrodes

A
  • record the summed electrical activity of many neurons.

- EEG: an electrical brain potential recorded by placing electrodes on the scalp

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4
Q

Why use EEG’s?

A
  • Non-invasive, “on-line” recording of neural activity in real time
  • Clinically valuable - can be used to diagnose epilepsy and seizure disorder, detect abnormal brain states and classify sleep stages
Advantage = Excellent temporal resolution
Disadvantage = Poor spatial resolution
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5
Q

Magnetoencephalography (MEG)

A

A procedure that detects groups of synchronously activated neurons by means of the magnetic field induced by their electrical activity

  • > action potentials travelling down axons etc. produce magnetic fields
  • > MEG is performed with devices that contain an array of several SQUIDS that are placed in a particular way, such that a computer can determine the source of specific brain signals.
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6
Q

Clinical applications of magnetoencephalography (MEG)

A

Clinical applications = finding the source of seizures so that they can be removed surgically
Record neural activity from various cognitive tasks

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7
Q

Funcional imaging

A
  • When the neural activity in one part of the brain increases, so does metabolic activity in that region
  • The metabolic activity of specific brain regions can be measured non-invasively in living animals (and humans) via functional imaging.
  • Functional imaging = computerised method of detecting metabolic or chemical changes within the brain,
  • > Positron Emission Tomography (PET)
  • > functional MRI (fMRI)
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8
Q

Positron emission tomography

A

Positron emission tomography (PET) uses a radioactive tracer to localise activity in the brain. Thus, PET studies the function of the human brain

  • poor spatial and temporal resolution
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9
Q

Steps of a positron emission tomography

A
  • The person is injected with radioactive tracer that is specifically created in a lab fit for purpose (e.g. 2-DG - a sugar). The tracer dose is harmless.
  • The person is then placed into a machine that is similar to a CT scanner.
  • When the radioactive molecules of 2-DG decay, they emit subatomic particles called positrons.
  • The positrons meet nearby electrons and they destroy each other. This leads to the emission of gamma rays, which travel in opposite directions.
  • Sensors around the head pick up the gamma rays.
  • This information is used to produce images of slices of the brain that show variations in activity
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10
Q

functional Magnetic Resonance Imaging

A

fMRI is a functional imaging method that permits the measurement of regional metabolisim in the brain by detecting changes in blood oxygen level

fMRI has excellent spatial resolution - we know exactly where activity in the brain is occuring. However, one limitation of fMRI is that it has poor temporal resolution. It takes a while for blood to travel to different parts of the brain, so you aren’t able to tell exactly when changes in neural activity are occurring

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11
Q

How functional Magnetic Resonance Imaging works

A
  • Modifications are made to MRI machines to measure neural activity, by looking at blood flow and oxygen levels in the brain.
  • > Blood flows to the brain.
  • > Cells in the brain get oxygen via red blood cells.
  • > More energy needed by the brain = more oxygen use.
  • For fMRI, a large, very strong magnet is placed around participants head that measures changes in magnetic field strength with different concentrations of oxygenated and deoxygenated blood.
  • Measured differences in concentration are called the BOLD Response (Blood Oxygen Level Dependent Response)
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12
Q

Stimulating neural activity

A
  • Electrical stimulation
  • Chemical stimulation
  • Transcranial magnetic stimulation (TMS)
  • Optogenetic Methods
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13
Q

Electrical stimulation

A
  • passes electrical current through wire inserted into brain. Activates neurons near the electrode (cell bodies and axons).

Advantage: relatively simple
Disadvantage: not very localised

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14
Q

Chemical stimulation

A

injects small amount of excitatory amino acid into brain

Advantage: more localised
Disadvantage: relatively complex

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15
Q

Transcranial Magnetic Stimulation (TMS)

A
  • stimulation of cerebral cortex by magnetic fields produced by passing pulses of electricity through a coil of wire placed next to skull.
  • Interferes with functions of brain region that is stimulated.
  • Treats symptoms of neurological and mental disorders.
  • Can be used to create virtual lesions.
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16
Q

Optogenetic Stimulation

A
  • What if you could control neural activity with light?
  • The use of a genetically modified virus to insert light-sensitive ion channels into the membrane of particular neurons in brain
  • Can depolarize or hyperpolarize neurons with lights of appropriate wavelength is applied
  • Used to study functions of particular neural circuits in brain