Lecture 10 - Neuroimaging and Map Plasticity in Humans Flashcards

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1
Q

What is diagnostic neuroimaging?

A
  • X-ray
  • 3D image & good bone contrast
  • Uses radiation
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2
Q

What is MRI

A
  • Using magnetism
  • Patient within large static magnet
  • Smaller magnets change fields in different directions at right angles to one another
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3
Q

Are all brain contrasts the same in MRI?

A
  • No, diff contrasts provide diff info
  • Used to build up fuller picture
  • No one contrast is best for all injuries
  • e.g static MRI = T1/T2/Proton density
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4
Q

What is BOLD contrast (fMRI)

A
  • Blood Oxygenation Level Dependent
  • Brain cannot perform anaerobic respiration
  • Can map what areas are working harder depending on how much blood travels there
  • Increase local flow = Increased ratio between de/oxygenated blood = increased MR signal
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5
Q

What is a voxhall?

A
  • Volume element (3d location)
  • Makes fMRI imaging
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6
Q

What is the summary of MRI

A
  • Brains contain high conc of hydrogen (in water)
  • Protons will orientate magnetic fields when you put them in a bigger magnetic field
  • Arrangement is disrupted when radio-frequency waves are applied
  • As protons go back to normal magnetic field, they emit signal that is detected by MR scanner
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7
Q

What does the difference in magnetic properties between de/oxygenated blood signify?

A
  • Special MR contrast holds info of ratios of blood
  • BOLD can be used to track what neurons consume more blood & therefore involved in certain tasks
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8
Q

What is the problem with vascular imaging?

A
  • Inferring that relationship is using up energy is static = measuring what the neurons need to work
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9
Q

What is MEG?

A
  • Current generated by single neuron is too weak to be detected
  • MEG detects a change in overall magnetic field caused by lot of neurons working together
  • Cannot go deep into the brain
  • Has to be kept in a sep room to avoid disruptions and needs to have a tank for hydrogen = expensive
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10
Q

What was a brief history of vibration?

A
  • Stimulator that would go up and down its in a magnetic field
  • Claw = tubing = cannot go fast
  • Turning electrical signal into vibrations to study touch
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11
Q

What is the cutaneous rabbit illusion?

A
  • 3 diff vibrotactile stimulators on arms
  • Filling in when people tap you = dissociates subjective experience with objective stimulation
  • Mapped areas in somatosensory cortex and ran the sequence of taps. One condition was that they would feel the tap in the middle because they had a tap, second condition was the feeling of jumping between taps
  • Area mapped was not getting stimulation, there was activation in brain = not reflecting objective reality
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12
Q

How did they investigate spatial resolution?

A
  • (How fine can you differentiate between textures)
  • Present domes to fingers and ppts have to work out orientation
  • Very hard to get both calipers on (have to put domes on with calipers) at the same time so person also measure time
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13
Q

How did they try to get over the temporal resolution with the domes?

A
  • Pet scan contrasting how fine gaps are and orientation of dome
  • Found no diff activity in somatosensory areas
  • Significant blob between parietal/occiptal lobe that was prev active in visual discrimination of gratings
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14
Q

How do we know the blob is doing the job?

A
  • Using TMS
  • Experiment design: delivered a disruptive pulse to area located in ppts when they did different tactile tasks
  • Dropped domes onto fingertip, send signal to TMS coil to fire at given delay (clear temporal resolution)
  • Ppts either had to work out if something was there (control)/ orientation/ pure spatial discrimination
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15
Q

What were the TMS results?

A
  • Middle and left electrodes were closest to blob and showed temporal & spatial specificity.
  • Blasting there would disrupt orientation task only after a specific time
  • Non-classical areas in somatosensory discrimination that involves visual imagery components
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