Ch 2 Flashcards

1
Q

research methods in cognitive neuroscience can be divided into 2 methods

A

a. Perturbational methods
b. Monitoring methods

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2
Q

Perturbational methods

A

change the workings in the brain, then measures cognition = shows causal relationship

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3
Q

monitoring methods

A

measures brain activity = showing correlational relationship between behaviour and brain activity

manipulates cognitive process, then measures the brain

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4
Q

Perturbational methods

A

a. brain lesions
b. pharmacological perturbations
c. intracranial brain stimulation
d. extracranial brain stimulation

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5
Q

PM: brain lesions

A

observing the effect of damage to the brain resulting from stroke, tumor, trauma

Can be natural or directed (in animals)

Major limitation for natural
- not under control
- lesion isn’t focal
- no 2 patients are the same, therefore can’t generalise
solution is to group patients together and look at the overlap

Disadvantages for directed
- ethical issues
- diaschisis

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6
Q

Natural brain lesions: advantages/ disadvantages

A

Advantages: naturally occurring,

Disadvantages:
- no control
- no temporal resolution
- damage is not focal (it impacts many areas of the brain)
- complex effects of recovery
- difficult to generalise as no 2 patients are the same
solution: use fMRI to look at the overlap of multiple patients with similar lesions

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7
Q

Directed brain lesions in animals

A

Advantages:
- control
- temporal resolution

Disadvantages
- difficulty in training animals to perform a particular task
- ethical reasons
- animals are different from humans
- Diaschisis: the brain is very interconnected, therefore damage to one area may affect another due to the lack of input for example

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8
Q

Diaschisis

A

damage to one area may cause damage to another due the brain’s interconnectedness

= decrease activity in surviving neurons after damage to other neurons

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9
Q

PM: pharmacological perturbations

A

involves interfering with neurotransmitters and their signalling

2 methods:
Method I: measuring the effects of chronic drug on cognition

Method II: controlled pharmacological experimentation

Disadvantages:
- very unspecific (drugs affect the whole brain)
solution: drugs can be injected directly to an area of an animal’s brain

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10
Q

Agonist drugs

A

drugs that activate receptors, identical to neurotransmitters (such as nicotine for acéthylcoline)

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11
Q

Antagonist drugs

A

drugs that bind and block receptors ex: antipsychotic drugs

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12
Q

PM: Intracranial Brain Stimulation

A

electrical stimulation works to perturb the brain with chronically implanted electrodes

— > mostly done in animals but also in patients with severe Parkinson’s disease

Wilder Penfield mapped the somatosensory and motor cortex with this method

Advantages: we can map brain regions, it is very specific

Disadvantages: invasive method, limited to animals

recently developed technique: optogenetics

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13
Q

Somatotropic organisation

A

adjacent body parts have adjacent cortical representations proportional to sensitivity of the body part

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14
Q

Optogenetics

A

only in animals, a virus with genetic material to make light-gated ion channels is injected into a targeted brain area

light-gated ion channels: channels that open or close in response to light. when a laser is targeted at the ‘infected’ area, this causes an influx of ions, which can inhibit or excite neurons

advantages: very specific, high temporal resolution
disadvantage: expensive, can only be done with animals

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15
Q

Extracranial brain stimulation

A

2 methods:
a. TMS: Transcranial Magnetic Stimulation
b. TES: Transcranial Electrical Stimulation or tDCS

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16
Q

TMS

A

a strong magnetic field creates a changing electric field in the underlying brain areas, which can activate neurons

2 types:
a. single pulse TMS: pulse is delivered at each trial, when a stimulus is presented
b. repetitive TMS: series of pulses that change underlying brain areas for a longer period of time

Advantages: non-invade, high temporal resolution

Disadvantages: limited to outer cortex, non-specific areas of the brain are affect: LOW SPATIAL RESOLUTION, can cause seizures

17
Q

TES (or tDCS)

A

A constant but weak electrical current directly on the scalp to either increase or decrease excitability
used to treat depression

Anodal (positive) stimulation: increases excitability of the stimulated area

Cathodal stimulation: decreases excitability of the stimulated area

Advantages; higher temporal resolution

Disadvantages: low spatial resolution, can’t target deep areas, pulses cause unpleasant scalp and head muscle contractions, can cause seizures

18
Q

Monitoring methods

A

a. Direct electrophysiological recordings
b. EEG
c. MEG
d. PET
e. fMRI

19
Q

Direct Electrophysiological Recordings (Single Cell Recordings)

A

electrical recordings directly in the brain

a. intracellular: recordings in the cells, single neurons are penetrated with an electrode tip, provides insights on how neurons behave while the brain carries out a function

b. extracellular: monitoring electrical activity of neurons near the tip of the electrode, provides info on how groups of neurons behave

Peristimulus time histogram
Tuning curves

Advantages: HIGH TEMPORAL AND HIGH SPATIAL RESOLUTION, control, specific

Disadvantages: very invasive, cannot identify networks

20
Q

Peristimulus time histogram

A

compilation of spikes = when a neuron has an action potential from all trials when a stimulus is presented. This illustrates how responsive a neuron is to the stimulus

21
Q

Tuning curve

A

measuring the response time of a neuron when a stimulus is varied, for example orientation
If a neuron is tunes to a specific orientation, it will fire the most for that type of stimulus

22
Q

EEG

A

measures electrical recordings outside the skull

a cap with 28-128 electrodes is placed on a participant’s scalp and can measure changes in electrical potential

Advantages: temporal resolution, non-invasive, rapid

Disadvantages:
- inverse problem: patterns observed could have been cause by something else
- low spatial resolution
- not sensitive to deep brain structure or sulci

23
Q

How and what do we measure with EEG

A

HOW: LFP: local field potential is produced when many neurons at the same location have similar changes in potential

If LFP strong enough, EEG will pick it up

WHAT:
- summed dendritic field potentials
- extracellular return current
- electrical fields in gyri
= electrical potential at the level of electrodes, not the brain

IT DOES NOT MEASURE:
- individual action potentials
- intracellular current
- electrical fields in sulci (cause must be perpendicular to the electrodes
- activity in deep bain structures

24
Q

How is the information extracted with EEG

A

a. Oscilllations
h. ERPs : even related potentials: voltage differences that are triggered by something

—> epoch: EEG data is ‘cut’ in portions, then averaged so the most frequent signal of a certain time remains

  • topographic maps show the spatial-temporal patterns of ERPs, we can observe how activity at the electrodes dynamically change over time and space
25
Q

MEG: magnetoencephalography

A

an electrical current produces a circular magnetic field
it detects ERFs : event-related magnetic-field responses over space and time

Advantages:
- no obstruction from skull, non-invasive, can reach deep brain structure, sensitive to sulci, HIGHER SPATIAL RESOLUTION than EEG

Disadvantages: more expensive than EEG, restricts movement, inverse problem

26
Q

PET: positron Emission Tomography

A

a tracer = radioactive substance, is injected into the blood
since active brain areas require more oxygen and therefore more blood = detection of active brain areas

related to metabolic activity: activity related to the supply of energy

Disadvantages:
- scary; very expensive, slow process: uptake in blood, transport to brain, time required to get a clear signal, blocked design only

27
Q

fMRI: functional magnetic Resonance Imaging

A

Oxyhemoglobin vs deoxyhemoglobine

active brain areas require more oxygen, resulting in a local increase of oxyhémoglobine
an fMRI scanner can detect active brain areas by picking up BOLD signals (Blood Oxygenation Level Dependant signals)

uses event-related design : switching between 2 conditions can be done without the need to wait 10 minutes as in PET

fmri adaptation: helps the understanding of brain areas by making use of repetitive suppression

advantages: HIGH SPATIAL RESOLUTION
- better temporal resolution than PET
- even-related design, non invasive

Disadvantages
- expensive

28
Q

MR scanner

A

used for DTI: diffusion tensor imaging -, which reveals white matter tracts of the brain (such as axons)

29
Q

Analysing activation patterns in a brain area in fMRI

A

most fMRI research is concerned with the activation of different bran areas in response to a manipulated variable

researchers use multivoxel pattern analysis for this: machine learning techniques are used to make sense of activation patterns in brain areas

or principal and independent component analysis: where data is being decomposed to find brain areas that behave similarity

  • structural equation modelling: incorporates anatomical connections
  • dynamic causal modelling: incorporates functional connections