Research Methods in Biopsychology Flashcards

1
Q

How do C(A)T scans work?

A

They create 2d slice through a 3d object, creating a tomogram
It is a computer assisted X ray procedure in which an x ray scanner is rotated 180 degrees around the body, one degree at a time, therefore making it a non-invasive procedure

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2
Q

How does MRI scanning work?

A

A strong magnetic field causes the protons in tissue to align in a specific orientation to fit with the magnetic field
When a radio frequency is passed through this, the protons are thrown out of equilibrium and strain against the magnetic field
When the radiofrequency is turned off, the MRI protons will move back to the original orientation, and will release electromagnetic energy whilst they do this
When the radiofrequency is turned off, the MRI sensors are able to detect the energy released, and detect what type of tissue it is as different tissues release different signals

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3
Q

What are three advantages of MRI scans over CT scans?

A

CT scans expose people to ionising radiation (health risks)
They have better resolution
They can create a 3d image that you can dissect yourself into coronal, sagittal or horizontal planes

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4
Q

How do fMRIs work?

A

The brain does not store glucose, so the blood will change in flow to supply what areas need glucose the most.
Oxyhaemoglobin can not be magnetised (it has a different magnetic field to deoxyhaemoglobin)
Therefore, when can tell through the magnetisation and tracking proton movement when an area has a lot of deoxyhaemoglobin, so is therefore being stimulated

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5
Q

What is a BOLD signal?

A

Blood-Oxygen- level- dependent signal

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6
Q

What are two drawbacks of EEGs and two positives?

A

Drawbacks:
- poor spatial localisation as the recordings are made from the scalp
- better suited to answering questions of “when” in the brain rather than “where” in the brain
Positives:
- high temporal resolution
- less expensive than fMRI

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7
Q

How does intracellular recording work?

A

We put an electrode into the cell and record the changes in membrane potential

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8
Q

How does extracellular recording work?

A

An electrode sits on the outside of the cell and records the change in potential around the membrane

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9
Q

What are the two most common stimulation techniques?

A

electrical, using electrodes

Optogenetics- stimulating parts of the brain using light

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10
Q

What are three neuropharmacological techniques?

A

microdialysis- a semi permeable probe is inserted into a specific brain site. Fluid is perfused through the probe and chemicals in the fluid across the membrane is collected. Samples are then analysed for chromatography methods, to help us monitor the presence/levels of neurotransmitters

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11
Q

What is immunohistochemistry?

A

We can localise neurotransmitters in different cells by dying specific neurons, with a process of two antibodies (the second antibody binds to a reporter molecule that creates either fluorescence or a black colour)

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12
Q

What is one example of disruptive techniques of studying the brain?

A

chemical lesions- we stop parts of the brain from producing certain neurotransmitters

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13
Q

What are the behaviours we often focus on in animal behaviour paradigms?

A

species common behaviours

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14
Q

Describe the morris water maze?

A

It observes spatial memory
Tank filled with a liquid with a submerged platform that the animal must find by swimming around. The tank also has markers like curtains. The rat is taken out and put back in the water and we then measure how long it takes to find the platform in the water. The rat is put in different start locations (N,S,E and W). Eventually, regardless of location, the rat learns to swim directly to the platform
The main measures in this is: escape latency- how long the rat takes to escape and spatial transfer test.

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15
Q

What is the radial maze and what are the two ways it can test memory?

A

The rat tries to find food in a circular maze.
When the rat goes back to arms of the maze that they have already been to, this indicates weakness in working memory. You can also pick a specific arm to add more and more food to and then track their errors in the maze, now relating to reference/long term memory

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16
Q

What are field observations?

A

They can help study evolution/gene-behaviour relationship

We can study things like polygymy, aggression, how submission can reduce sexual prowess, sexual behaviours etc.

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17
Q

What is the difference between usual x rays and cerebral angiography?

A

Usual x rays can only see things that have significantly different states to the tissue around it (i.e. bone) as it absorbs such a different amount of radiation. in CA, a substance that absorbs less or more radiation than the surrounding tissue is injected into a cerebral artery, so it allows to see the cerebral circulatory system

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18
Q

What does CT scan stand for?

A

Computed Tomography scan

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19
Q

What does PET scan stand for?

A

Positron Emission Tomography

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20
Q

Explain a common version of PET scans involving Fluorodeoxoglucose

A

FDG is injected into a cartoid artery. It is radioactive. Because it has a similar structure to glucose, it is absorbed into the cells that require fuel. It can then detect what brain areas are being activated, as they are the ones that need more fuel, so will have different levels of FDG and radiation picked up by the scan

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21
Q

Why can PET scans be construed as slightly inaccurate?

A

It is just a lot of colours indicating the different levels of radioactivity in the brain. It is therefore often very pixelated and has low resolution, as they are not real images.

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22
Q

Do PET scans detect brain activity or structure?

A

activity

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23
Q

What is diffusion tensor imaging?

A

It is a way of tracking the diffusion of water accross tracts in the brain. As many of these tracts connect brain areas, this allows us to see the connectome

24
Q

Why could MRIs be seen as better than CT scans?

A

they don’t require injections and they allow us to view both structure and function

25
Q

What is transcranial stimulation?

A

It is a way of allowing us to link and determine how brain areas are activated with specific activities, as most activities involve multiple cortices being stimulated, so we can’t directly regard stimulation. We can stimulate the brain area we are investigating (either turn it on or off) and then see how this affects the performance of the activity.

26
Q

What is transcranial magnetic stimulation?

One of the 2 types of transcranial stimulation

A

A magnetic coil is positioned next to the skull, creating a magnetic field next to the brain. This will then “turn off” a specific field of the brain. We can then observe the effect on behaviour and cognition

27
Q

What is transcranial direct current stimulation?

One of the 2 types of transcranial stimulation

A

When we apply a direct current through 2 electrodes on the scalp. We then observe behaviour and cognition.

28
Q

Why can electroencepholagrams be seen as inaccurate?

A

They record action potentials, post-synaptic potentials and electricity from the skin, muscles, blood and eyes, so can not only show neural activity.

29
Q

What are sensory evoked potentials?

A

The change in cortical EEG signal elicited by a sensory stimulus

30
Q

What is the process of signal averaging in recording a SEP?

A

You record the initial EEG before a stimulus many times (say 1000). We then create an average. We then record the EEg as a stimulus happen 1000 times, We then record the eegs 1 millisecond after a stimulus 1000 and create an average, 2 milliseconds after a stimulus 1000 times and create an average etc.

31
Q

What does MEG stand for? What is an MEG?

A

MEG is magnetoencelography. It is when we measure changes in magnetic fields on the scalp and can therefore measure the changes in neural activity underlying these magnetic changes

32
Q

What is EMG?

A

Electromyography
measuring muscle tension
This can indicate psychological arousal as muscles tense when we are stressed/excited
These are recorded through electrodes on the skin

33
Q

What is EOG?

A

Electrooculography
There is a potential between the front of the eye (positive) and the back of the eye (negative). When the eye moves, the potential changes, This can be recorded with electrodes around the eye

34
Q

What are BP measurements made of?

A

The measurement of the pressure in the arteries both during diastole and systole. These are separate measurements. The measuring of changes in this is called plethysmography

35
Q

What is the SCL?

A

Skin conductance level ( how the skin conduct electricity)

36
Q

What is the SCR?

A

Skin conductance response (changes in skin conductance)

37
Q

How do SCL and SCR change with emotion?

A

both can be increased with emotional arousal. This could be because of increased activity of sweat glands

38
Q

What is stereotaxic surgery?

A

When we shove instruments into the brain in order to view brain function

39
Q

What is the stereotaxic atlas?

A

A map of the brain used in stereotaxic surgery, as the brain is very complex and different between animals, it is usually based around a specific point

40
Q

What is the stereotaxic instrument?

A

It is used in stereotaxic surgery and is made of a head holder to keep the skull still and a holder for the electrode

41
Q

What are aspiration lesions?

A

It is a type of lesion that can only be done on areas of cortical tissue. It involves sucking away the tissue from the tougher white matter underneath using a glass pipette.

42
Q

What are radiofrequency lesions?

A

When we pass a radiofrequency current through tissue via an electrode, which then destroys the tissue in a specific neural area

43
Q

What are reversible lesions?

A

When we forcibly stop activity in an area of the brain while we are doing tests. This can be done by cooling the area or using anaesthetic

44
Q

What is are the main differences between bilateral and unilateral lesions?

A

bilateral lesions affect both hemispheres, unilateral affect one. Bilateral tend to have more of an affect on behaviour and function than unilateral.

45
Q

What is a multiple unit recording?

A

an invasive electrical recording method where a large electrode records the APs from multiple neurons and then adds them up to create an average for each neuron

46
Q

How can we do chemical lesions?

A

Neurotoxins can bind to specific areas and stop the release of some neurotransmitters

47
Q

How can we use 2 DG to measure chemical activity in the brain?

A

We inject 2 Deoxy glucose into the brain. As it is a similar structure to glucose, it is taken up by fuel requiring cells. It is not metabolised, so builds up. The subject is then killed, the brain removed and sliced, the slices placed in emulsion in the dark and left to develop for several days. The areas with more 2 DG will show up with black spots. We then colour code this based on the density of the spots.

48
Q

What is immunocytochemistry?

A

When the antibody that we need for a neuroprotein is radioactively marked or marked with fluorescence. They will then also often bind to the neurons that make the neuroprotein

49
Q

What are AEPs?

A

Average Evoked POtentials

50
Q

What are gene knockout techniques?

A

You literally just get rid of a gene for a specific neurochemical and then see how it affects behavious

51
Q

What do we call procedures to observe a particular behavioural phenomena?

A

A behavioural paradigm

52
Q

What is neuropsychology?

A

How neural function affects emotion, cognition and motivation. It can help us test if an issue is just due to psychological factors or is affected by brain dysfunction

53
Q

What is the Common Neuropsychological Test Battery?

A

A battery of tests that allows us to detect if a problem is caused by neural issues. It involves first a basic battery of tests to identify symptoms/issues and then moves on to more specific tests that deeper investigate these issues. It bases the results on cognitive strategy as well as test performance and involves factors such as language, memory, lateral language (when one hemisphere is disabled) and intelligence

54
Q

What is the default mode network?

A

The structures of the brain that are more active when the brain is in “default mode” (i.e. resting) than during cognitive or behavioural activities

55
Q

How can we use the “mean image”

A

When we do a PET or MRI scan, random, accidental stimuli such as little noises can affect the brain’s activity, therefore affecting the results. If we use the image from multiple volunteers when exposed to the same stimulus and sort of combine them, this can give us a better idea of what areas are actually being stimulated.

56
Q

What is the paired image subtraction technique?

A

When a task involves multiple areas being stimulated, we will make the participant do the task and then do different versions of the task and compare these to see what is actually being stimulated.