Week 6 Flashcards

1
Q

What do lesion studies tell us about behaviour

A

Lesion studies help to understand the functions of particular brain areas through observing behaviour changes after a site is damaged.

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2
Q

What is experimental ablation

A

Experimental ablation is the removal or destruction of a portion of the brain of a laboratory animal.

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3
Q

What is a brain lesion

A

A brain lesion refers explicitly to a wound or injury of the brain.

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4
Q

Who is phineas gage

A

He was a construction worker who set off an explosion that sent an iron rod shooting through his cheek and head.

He had a complete personality change after experiencing damage to his frontal lobe.

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5
Q

Who was Tan

A

He was someone with language difficulties. He was able to understand and follow commands however the only word he could say was Tan.

Broca performed an autopsy which found a lesion on the left frontal lobe of his left cerebral hemisphere, in an area now known as “Broca’s Area”.

His condition was termed “Aphasia” (the inability to produce words that were meaningful, but being able to understand language perfectly).

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6
Q

Who was HM

A

He suffered a bicycle accident at a young age that left him with severe seizures (epilepsy). At 26 he was operated on and it was successful.

The doctors realised the seizures were originating from the left and right medial temporal lobes which include; the hippocampus, amygdala and part of the entorhinal cortex. They removed the related brain tissue.

After the surgery his long term memory formation was impaired.

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7
Q

How does a researcher produce a subcortical lesion

A

Radio frequency lesions and excitotoxic lesions

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8
Q

What is a radio frequency lesion.

A

Electrical current is passed through a stainless steel wire (electrode)

Researchers guide the electrode to a very specific location in the brain

Activate a lesion making device that produces an alternating current of very high frequency - a radio frequency

Passing current through brain tissue produces heat that kills cells surrounding the tip of the electrode.

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9
Q

What is an excitotoxic lesion

A

Excitatory amino acid is injected via a cannula into a brain region.

The amino acid kills neuron cell bodies by stimulating them to death

Axons nearby are spared = selectivity.

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10
Q

What are sham lesions

A

Researchers insert an electrode or a cannula into the brain region of an animal, but do not activate the RF current, or inject the amino acid.

This is to account for possible damage to brain tissue along the way of a cannula or electrode being put in the brain.

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11
Q

How can brain lesions be made temporarily

A

Injecting a local anaesthetic into the part of the brain you want to lesion. This anaesthetic blocks action potentials in axons entering or leaving to produce a temporary lesion.

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12
Q

What are the 3 types of non invasive brain structure imaging

A
  1. Computerised tomography (CT)
  2. Magnetic Resonance Imaging (MRI)
  3. Diffusion Tensor Imaging (DTI)
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13
Q

What is Computerised tomography (CT Scan)

A

The use of a device that employs a computer to analyse data obtained by a scanning a beam of X-rays to produce a two-dimensional picture of a “slice” through the body

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14
Q

What is Magnetic Resonance Imaging (MRI)

A

A technique whereby the interior of the body can be accurately imaged; involves the interaction between radio waves and a strong magnetic field.

The magnet causes protons in the brain tissue to line up in parallel (normally they are in random orientations)

Protons are knocked over by a powerful pulse of radio waves. When the pulse is turned off, the protons go back to their original configuration, emitting radio waves as they do.
Scanner picks up the radio frequency energy being emitted.

A powerful computer compiles the density based information to generate a detailed cross sectional view of the brain

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15
Q

Where are protons found and where are they mostly found in the brain.

A

In the nuclei of atoms, and most protons in the brain are hydrogen atoms

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16
Q

What is Diffusion Tensor Imaging (DTI)

A

An imaging method that uses a modified MRI scanner to reveal bundles of myelinated axons in the living human brain.
Molecules move in random directions because of thermal agitation, and the higher temperature, the faster the movement.
DTI takes advantage of this.

Movement of water molecules in bundles of white matter will not be random, but will tend to be in a direction parallel to the axons that make up the bundles

The MRI scanner uses information about the movement of the water molecules to determine the location and orientation of bundles of axons in white matter.

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17
Q

What is Fractional Anisotropy (FA)

A

It measures the freedom of movement of water around the tissues.

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18
Q

Where are FA values high and low

A

White matter is higher FA values and grey matter is lower FA values

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19
Q

What are the 3 ways electrical events can be recorded

A
  1. Recording with microelectrodes
  2. Recording with macroelectrodes (EEG)
  3. Magnetoencephalography (MEG)
20
Q

Explain recording with microelectrodes

A

It is the recording of the electrical activity of a single nueron.

They are made of very thin wires and have a very fine top that can be used for single unit recording

21
Q

Explain recording with macroelectrodes (EEG)

A

They record the summed electrical activity of many neurons.

An EEG is an electrical brain potential recorded by placing electrodes on the scalp.

22
Q

What is EEG output

A

It is continuous voltage fluctuations across time

23
Q

Why do we use EEG?

A

It is non-invasive “on-line” recording of neural activity in real time.

It is also clinically valuable as it can be used to diagnose epilepsy and seizure disorder and detect abnormal brain states and classify sleep stages.

24
Q

What is a “event related potential”

A

The changes in electrical activity following an event.

25
Q

What are advantages and disadvantages of EEG recordings

A

A: Excellent temporal resolution

D: Poor spatial resolution

26
Q

Explain Magnetoencephalography (MEG)

A

It is a procedure that detects groups of synchronously activated neurons by means of the magnetic field induce by their electrical activity.

They use special detectors called “SQUIDS” as the magnetic fiels that are produced are so tiny.

27
Q

What are the clinical applications of MEG’s

A

Finding the source of seizures so that they can be removed surgically.

28
Q

Explain Functional Imaging

A

The computerised method of detecting metabolic or chemical changes within the brain.

29
Q

What is Positron Emission Tomography (PET)

A

PET uses a radioactive tracer to localise activity within the brain. It studies the function of the human brain.

30
Q

What are the 6 steps involved with Positron Emission Tomography (PET)

A
  1. The person is injected with a radioactive tracer that is specifically created in a lab fit for purpose (e.g., 2-DG - a sugar). The tracer dose is harmless.
  2. The person is then placed into a machine that is similar to a CT scanner.
  3. When the radioactive molecules of 2-DG decay, they emit subatomic particles called positrons.
  4. The Positrons meet nearby electrons, and they destroy each other. This leads to the emission of gamma rays, which travel in opposite directions.
  5. Sensors around the head pick up the gamma rays.
  6. This information is used to produce images of slices of the brain that show variations in activity.
31
Q

What is the downside of PET scans

A

They are really expensive and don’t have good spatial or temporal resolution.

32
Q

Explain Functional Magnetic Resonance Imaging (fMRI)

A

fMRI is a functional imaging method that permits the measurement of regional metabolism in the brain by detecting changes in blood oxygen levels.

33
Q

How are fMRI’s conducted

A

A large, very strong magnet is placed around the participant’s head that measures changes in magnetic field strength with different concentrations of oxygenated and deoxygenated blood.

34
Q

What are measured differences in concentration called?

A

BOLD Response (Blood oxygen level dependent response)

35
Q

What are the positives and negatives of fMRI

A

It has excellent spatial resolution.

It has poor temporal resolution.

36
Q

What are the 4 ways of stimulating neural activity.

A
  1. Electrical stimulation
  2. Chemical Stimulation
  3. Transcranial magnetic stimulation (TMS)
  4. Optogenetic Methods
37
Q

Explain electrical stimulation.

A

It passes electrical current through wire inserted into the brain and activates neurons near the electrode

Ad: Relatively simple
Dis: Not very localised

38
Q

Explain chemical stimulation

A

Injects a small amount of excitatory amino acid into the brain.

Ad: more localised
Dis: relatively complex

39
Q

Explain Transcranial magnetic stimulation (TMS)

A

It is the stimulation of cerebral cortex by magnetic field produced by passing pulses of electricity through a coil of wire (in a figure 8) placed next to skull.

Treats symptoms of neurological and mental disorders.

Can be used to create virtual lesions.

40
Q

Explain Optogentic Methods

A

The use of a genetically modified virus to insert light-sensitive ion channels into the membrane of particular neurons in brain.

It can depolarize or hyperpolarize neurons with lights of appropriate wavelength is applied

Used to study functions of particular neural circuits in brain.

41
Q

What is a genome

A

Complete set of genes that compose DNA of particular species.

42
Q

What is an Allele

A

The particular form of an individual gene

43
Q

What are linkage studies

A

They identify families whose members vary in a particular trait (E.G., presence/absence of Huntington’s disease)

Markers = sequences of DNA whose locations are already known

Compare markers across members of the family

44
Q

What are genome-wide association studies

A

They compare all or portions of the genomes of different individuals to determine where the differences in the People’s genome’s correlate with the presence or absence of diseases (or other traits)

45
Q

What are the benefits of GWAS

A

Identify novel variant – trait associations (E.g. anorexia nervosa, major depressive disorder) which might have important clinical applications.

Led to the discovery of novel biological mechanisms (E.g. GWAS discovered that autophagy (house sells degrade and recycle components) plays a role in Crohn’s).

GWAS data is easy to share, and publicly available data allows for further discoveries and advancement.

46
Q

What are the limitations of GWAS

A

GWAS usually only estimates a modest amount of the heritability of a given trait, meaning it can have limited clinical predictive value.

Correlation does not equal causation - GWAS do not necessarily pinpoint causal variants and genes.