Neuroscience methods for physiological psychology Flashcards

1
Q

what does MRI stand for?

A

magnetic resonance imaging

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2
Q

what the 2 types of MRI?

A
  • structural MRI
  • functional MRI
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3
Q

what are the goals of structural imaging with non-invasive methods?

A
  • to study anatomy
  • to identify abnormalities (as in brain disease)
  • to follow development (childhood to old age)
  • to show plasticity
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4
Q

what do CT structural MRI scans rely on?

A

contrast between tissue types (for example, between white matter, gray matter and cerebrospinal fluid)

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5
Q

Brain plasticity after motor learning, Draganski et al. (2004)

A
  • healthy ps had to practice a difficult task (juggling) over a series of months
  • ps underwent 3 sessions of structural MRI: one before learning to juggle, one after three months without practice
  • scan 1 show baseline grey matter before learning, san 2 shows and increase in grey matter by 3 % after 3 months of learning, and after three months without practice grey matter is still 2% above baseline.
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6
Q

how do you generate structural MR contrast?

A
  • soft tissue has high water content which has abundant in rotatory motion in random orientation
  • magnetic field produced by the magnet cause the protons to become aligned to the magnetic field
  • when the radiofrequency coil emits a radiofrequency pulse, the net magentisation vector is turned into an orientation perpendicular to the external magnetic field
  • after the radiofrequency pulse the vector of net magnetization returns to the direction of the external magnetic field, during this stage an MR signal is measured
  • MR signal is measured during spin-lattice relaxation at a suitable timepoint,, then structural contrast can be established between tissue and cerebrospinal fluid,
  • MRI protocols that are based on tissue-specific differences in spin-lattice relaxation are referred to as T1-weighted imaging.
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7
Q

what are the goals of fMRI?

A

to identify brain areas that support sensory and cognitive processes, and to derive models of brain function

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8
Q

why is contrast NEEDED for fMRI?

A

separates non-activated from activated tissue

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9
Q

what is T2* contrast in fMRI?

A
  • depends on balance of deoxygenerated to oxygenerated hemoglobin (Hb) within blood in a voxel
  • this in turn depends on local regulation of arterial width
  • during local neuronal activation flow is increased, more oxy-Hb in capillaries
  • oxy-Hb is diamagnetic (does not affect local magnetic field) whereas deoxy-Hb os paramagnetic, making field inhomogeneous
  • in inhomogeneous field, horizontal magnetization decays faster (T2* decay)
  • slower T2* decay: increased MR signal intensity = blood oxygen level dependent (BOLD) effect
  • BOLD signal as an indirect measure of neural activity
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10
Q

what os the BOLD effect?

A

the blood oxygen level dependent effect

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10
Q

what are some advantages of combining activation maps of multiple participants?

A
  • allows for further analysis at a group level, leading ti pattern of activation
  • to label the location of activation by comparison with a brain atlas
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11
Q

what are some disadvantages of fMRI?

A
  • fMRI analysis had low power
  • null results are almost impossible to analyse
  • statistical maps depend on amplitude and noise
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12
Q

What is association?

A

damage to a single brain brain region, but multiple deficits in behavioural tasks

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13
Q

what is dissociation?

A

damage that leads to impaired performance in task A but performance in task B is normal

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14
Q

what is simultanagnosia in Balint’s syndrome?

A

in a visual scene patients can only see one item at a time

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15
Q

what is oculomotor in Balint’s syndrome?

A

a failure to make certain eye movements

16
Q
A