Task 5 Flashcards

1
Q

What is structural imaging?

A

based on different types of tissue [skull, white matter, grey matter] having differet physiological properties

-> This information can be used to construct static maps of the brain

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2
Q

What is functional imaging ?

A

based on the assumption that neural activity produces local physiological changes in that region of the brain

-> results in dynamic maps of the moment-to-moment activity of the brain during a task

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3
Q

What is PET?

A
  • based on blood volume (= indirect)
  • involves radioactivity -> tracer
  • participants scanned only once
  • temporal resolution: 30 seconds (-> slower than fMRI)
  • spatial resolution: 10mm (-> bigger than fMRI)
  • must use a blocked design
  • sensitive to the whole brain
  • can use pharmacological tracers
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4
Q

What are advantages of PET?

A
  • less distortion around the air cavities (compared to fMRI)
  • tracers can be used to follow specific pathways
  • sensitive to the whole brain
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5
Q

What are disadvantages of PET?

A
  • MRI is less expensive (+ easier to maintain)
  • invasive -> radioactive tracers
  • individual´s cannot be tested repeatedly
  • low spatial resolution (compared to MRI)
  • poor temporal resolution (compared to ERP)
  • indirect measure
  • interpretation difficulties (correlation ≠ causation)
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6
Q

What is MRI ?

A
  • structurally depicting the brain through magnetic fields caused by spinning protons (of hydrogen nuclei)
  • creating 3D images
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7
Q

What is fMRI?

A
  • exploits the increase of local blood flow in active parts of the brain
  • deoxygenated hemoglobin is paramagnet (weakly magnetic within a magnetic field) -> oxygenated hemoglobin is not
  • detectors measure the BOLD signal
  • an active brain area results in an increase in the ratio of oxygenated to deoxygenated hemoglobin
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8
Q

What are advantages of fMRI ?

A
  • scanners are less expansive (compared to PET)
  • non-invasive -> it is possible to measure participants repeatedly
  • better spatial resolution (than PET and CT)
  • can be adopted for use in detecting the changes in blood oxygenation associated in neural activity
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9
Q

What are disadvantages of fMRI ?

A
  • poor temporal resolution (compared to ERP)
  • indirect measure
  • interpretation difficulties (correlation ≠ causation)
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10
Q

What is BOLD contrast?

A
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11
Q

What is preprocessing?

A
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12
Q

What is BOLD?

A
  • blood oxgen level-dependent
  • ratio of oxygenated and deoxygenated hemoglobin
  • signal increases are proportional to the underlying neuronal activity
  • depends on source: using magnetic field gravity to vary the strength of the magnetic field
  • depends on its strength: the number of spins involved allowing the amount of water to be determined at any point within the body
  • depends on rate at which the signal decays: the number of factors describing the interaction of the spins with their surroundings
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13
Q

What is the hemodynamic response function?

A
  • maps the way that the BOLD signal evolves over time in response to an increase in neural activity
  • Initial dip: as neurons consume oxygen -> small rise in the amount of deoxyhaemoglobin = reduction of BOLD signal
  • Overcompensation: increase in blood flow in response to the increased consumption of oxygen -> increase > increased consumption of oxygen = increase of BOLD (measured in fMRI)
  • undershoot: blood flow and oxygen consumption dip before returing to the original levels -> possibly due to venous system relaxation causing a temporary increase in deoxyhaemoglobin
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14
Q

What are Berman´s fMRI approaches? In what ways can fMRI be used in research?

A
  • studies of localisation: discovering brain behaviour correlations (helps understanding the normal organisation of modules + predicting deficits in case of brain damage)
  • studies of commonalities in brain activation: if two tasks lead to activation of common brain areas, then those tasks are likely to share some process
  • studies of distinctiveness in brain activation:
  • documenting individual differences
  • testing psychological models: testing model predictions
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15
Q

How does PET work?

A
  • a radioactive substace (=tracer) is introduced into the bloodstream
  • the radiation emitted from this tracer is motored
  • radioactive isotopes of the tracer rapidly decay, by emitting a positron from their nuclei
  • when a positron collides with an elextron: two photons (gamma rays) are created
  • those photons move in opposing directions and pass through brain tissue, skull, and scalp
  • PET scaner determines where the collision took place -> gamma ray detector
  • more blood flow = more radiation
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