Introduction in Neuropsychology Flashcards

(41 cards)

1
Q

Cognitive Neurpsychology

A

The study of the relation between structure and function of the brain and specific cognitive functions (e.g., language, memory, attention etc.)

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2
Q

How do we research cognitive neuropsycholgy

A
  • By investigating these cognitive processes in normal healthy people
  • By investigating the breakdown of these processes in brain-damaged individuals (as a result of acquired brain damage or as a result of a developmental disorder
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3
Q

Enthusiasm about Neuropsychology

A

Neuroscience information affects people’s judgement
–> How much are individuals ready to blieve when encountering improbable information through the guise of neuroscience
- they are very ready!

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4
Q

Example brain enthusiasm Verbeke

A

Said that in 2009 that 5 years from then, brain scans would be used in application processes for jobs.
–> People are very interested in the brain and the future in this science

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5
Q

Brain scans as evidence in court of law

A
  • Personality assessment
  • Lie detection
  • Control of actions (‘don’t blame me, blame my brain.
    –> Neuroscientific evidence impacts juror’s perception of responsibility and judgement of self-control
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6
Q

Using brain imaging techniques for diagnosing

A

For neurological syndromes is works really well (think of tumors, dementia, strokes etc.)
For psychiatric and mental syndromes you can’t really use brain imaging methods
- Depression and anxiety
- You can see on group level, but in individuals it is not clear enough for diagnosis

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7
Q

Neurons

A

Nerve cells that you can see as white and grey matter:
- White matter: axons, the endings of the neuron
- Grey matter: the cell bodies of the neuron

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8
Q

Action potential

A

At rest the cell membrane of the neuron has a -70 mV difference
With the help of neurotransmitters this potential changes and can be pushed over the threshold of -55 mV, which causes the signal to go to the next neuron

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9
Q

Schematics of the action potential

A
  • -70 mV is rest
  • -55 mV is threshold for potential
  • depolarization until about 40 mV
  • action reaches 40 mV
  • Repolarization back to the negatives
  • Hyperpolarization goes a little below -70 mV
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10
Q

Neural communication

A

Imput neurons thruogh the neurotransmitters
- depolarization and hypoerpolarization, cause the signal

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11
Q

Inhibitory and excitatory input

A

Inhibitory: neurotransmitters that hyperpolarize, which results into the action potential to not happen
Excitatory: neurotransmitters that depolarize, which result into the action potential

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12
Q

Sinusoidal oscillation

A

The simplest signal
- One wave of up and down in 1 second (1Hz)

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13
Q

Frequency

A

Rate of change of signal, e.g. in the time dimension
- 1 Hz = completing a full cycle in one second
- Biological signals never contain just one frequency

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14
Q

Complex signals

A

Signals that have multiple frequencies -> they can be decomposed into frequency components

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15
Q

Parts of a frequency component

A
  • each one has a particular frequency
  • Amplitude: how high it goes up and down
  • Phase: when it goed up and down (interval)
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16
Q

Frequency spectrum

A

Measured range of frequency (we cannot measure all)
- Highest frequency
- Lowest frequency
-> filtering

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17
Q

Highest frequency

A
  • Limited by sampling frequency (how msny waves are in one second)
  • 1/2 * sampling frequency (Nyquist sampling theorem)
    -> if you measure 100 waves per second, the highest frequency is 50 Hz
18
Q

Lowest frequency

A
  • Limited by how long the signal is measured
  • 1 / number of seconds measured
    -> if you measure for 2 seconds, the lowest frequency is 0.5 Hz
19
Q

Filtering

A

Attenuating or excluding certain part of measured frequency spectrum
- low-pass (everything below a threshold -> low Hz)
- high-pass (everything above a threshold -> high Hz)
- band-pass (everything within 2 limits -> middle Hz)

20
Q

Spectogram

A

Strength of each signal component at each moment in time
- shows different amplitudes of the signals

21
Q

Molecular signals

A

Movement of chemical substances and molecules can cause changes in EEG’s
- depolarization and repolarization
- calciu concentration in active neurons
-> hemodynamics on larger scale

22
Q

Hemodynamics

A

Blood supply is adjusted to current energy needs
-> blood brings glucose to the neurons to stay alive

23
Q

Energy consumption
- not entirely clear on the relation

A

Electrophysiological events require energy
-> Amplitude of potential changes is not the best predictor of energy consumption, because it is a passive chain of events
–> restoring the potential requires the energy, so energy consumption could correlate with number of potentials

24
Q

Clustering

A

Noninvasive methods cannot achieve single neuron resolution
–> neurons of similar functional properties are clustered together
- more clustering, the more the averaged signal corresponds to the individual neuron
- clustering on different levels are measurable by different methods

25
Different levels in sensitivity of clustering
- Neuron level - Column level: neurons that face the same way - Topology level: neurons that correspond on motoric level in motor region - Area level: motorics for example - System level: area's that work together
26
Orientation columns
Containing neurons with similar preference for line orientation -> not in all species
27
Temporal resolution
The samllest unit of time that can be differentiated by a method
28
Spatial resolution
The sammelst unit of space which can be resolved
29
Invasiveness
Majority of methods are either fully invasive (penetration of skull) or not invasive at all -> we focus on the noninvasive methods that can be used on humans
30
Histology
Measuring brain structure -> Cutting brain in pieces (very invasive) - process checmically for visualization of specific structure (chemicals interact with neurons and color a specific way depending on the region)
31
Structural magnetic resonsance imaging (MRI)
Measuring brain structure - > Investigation of anatomy in individuals - Anatomical localization of functional findings - Relate anatomical structure to differences between participants in e.g. behavior, disease classification
32
Measuring hemodynamics
Changes in blood and tissue oxygenation, blood flow, and blood volume - temporal resolution of hemodynamic imaging is poorer compared to electrical imaging (because it is slower) - Spatial resolution varies strongly (optical imaging (column) or fNIRS (several cm))
33
Electrophysiological activity -> spatial resolution is affected by
- distance electrode and source of the signal - intermediate tissue (skull etc.) - noninvasiveness highest frequencies cannot be picked up -> Different frequency bands contain very different information
34
Spatial resolution in electrophysiological measured
From 0 tot multiple cm's - Patch-clamp recordings (clamped to the area) - Single-unit recording - Multi-unit recording - Local field potentials - Human intra-cranial even related potentions * above are invasive, below are noninvasive - Magneto-encephalography - Electro-encephalography and scalp ERP's
35
EEG study in differentiating faces from chairs
You can see which cells/neurons are used to process faces and which ones for chairs, but due to low spation resolution of EEG you cannot make it specific faces for example - anatomical localization is poor
36
Peripheral measures
Autonomic nervous system - Sympathetic (fight or flight) SNS - Parasympathetic (rest and digest) PNS * Heart tells most about parasymp. * Sweat glands tells only about symp. * Pupil size tells both about para and symp.
37
Skin conductance - peripheral measures
Index of sympathetic arousal intensity in affective or cognitive processing - conductor of electricity
38
Heart activity - peripheral measures
Heart rate - Heart rate variability: measures influence of Parasympathetic NS on heart - Blood pressure: measure of stress
39
Pupil dilation - peripheral measures
Indictive of intense emotional arousal toward both pleasant and unpleasant stimuli and experiences - Pupil dilation reflects SNS and pupil constriction reflects PNS
40
Eye movements - peripheral measures
Good measure of visual attention - Saccades = blink so there is a moment of no information - Fixations = information acquisition occurs during fixation
41
Muscle activity - peripheral measures
Facial electromyography (EMG) as a tool for inferring affective status