l3- methods for studying teh brain Flashcards

1
Q

particpant population

clinical populations

A
  • ppts w brain injuries or nuerological disorders
  • eg parkinsons disease affecting basal ganglia
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2
Q

ppt populations

neurologically intact ppl

A
  • ppts w no brain damage; used to study how the brain functions under normal conditions using non invasive methods
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3
Q

ppt population

animal models

A
  • non-human subjects used in neuroscience
  • allow for invasive techniques n more control
  • ethical issues+ limit study of complex cognition
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4
Q

lesion method

lesion method

A

studying brain function by observing deficits after damage to specific brain regions

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5
Q

lesion method

brocas area lesion example

A
  • damage to brocas area (BA 37) in Left hemisphere impairs speech production but not comprehension
  • suggests brocas area is necessary for speech production (reverse inference)
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6
Q

lesion method

lesion causes

A
  • can be accidental (eg stroke/trauma) or surgical (eg epilepsy treatment)
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7
Q

lesion method

lesion localisation methods

A
  • autoposy (limited by brain reorganisation)
  • known neurosurgery
  • brian imaging (eg MRI,CT)
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8
Q

lesion method

single case vs group studies

A
  • single case: in depth, hard to generlise
  • group: confirms brain behvaiour links, variability in lesion locations=challenge
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9
Q

lesion method

strengths

A
  • shows casual links between brain regions n specific functions
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10
Q

lesion method

limitations

A
  • identifies only 1 region
  • variability in lesion location
  • brain reogranisation or compensation may occur
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11
Q

animal lesion studies

animal lesion studies

A
  • surgical removal of brain regions in trained animals to assess behavioural changes
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12
Q

animal lesion studies

advantages

A
  • controlled lesion location
  • compare before vs after, or to sham group
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13
Q

animal lesion studies

disadvantages

A
  • ethical concerns
  • animal human brain differences
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14
Q

anatomical imaging

anatomical imaging

A
  • originally for locating lesions; now also used to correlate anatomy w behaviour
  • eg brain size w traits
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15
Q

anatomical imaging

computerized tomography (CT)

A
  • uses xrays- creates 3d images
  • measures tissue density- diff in skull, brain n blood but little diff in white n grey matter
  • spatial resolution ~ 1cm per voxel
  • invasive (ionising radiation)
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16
Q

anatomical imaging

magnetic resonance imaging MRI

A
  • uses radiofrequcny waves to excite hydrogen atoms
  • captures emitted signals to create images
  • fine spatial resoltion (~1mm)
  • non-invasive
17
Q

anatomical imaging

diffusion weighted MRI

A
  • measures water diffusion direction
  • it diffuses along axon in white matter
  • used to map white matter structure
18
Q

anatomical imaging

diffusion tractography

A
  • maps white matter connections by following water diffusion paths
  • identifies brain fascicles between regions
19
Q

functional techniques

functional techniques

A
  • measure brain activity during tasks either elctrophysiological (direct) or neuroimaging (indirect) methods
20
Q

functional techniques

electrophysiological techniques
(EP)

A
  • record electrical activity like APs or PSPs
21
Q

functional techniques

neuroimaging techniques

A
  • measure metabolic activity (blood flow, glucose/oxygen use) linked to neural activity
22
Q

functional techniques- EP methods

single-neuron recordings

A
  • microelectrodes record electrical activity from individual neurons
  • highly invasive, mainly in animals
  • reveals receptive fields n stimulus preferences
23
Q

functional techniques- EP methods

EEG

A
  • records electrical potentials from scalp
  • measure PSPs from neuron populations
  • good temporal but poor spatial resolution
24
Q

functional techniques- EP methods

event related potentials (ERPs)

A
  • averaged EEG responses to repeated stimuli
  • reveal stages of sensory n cognitive processing
  • eg emotional pictures elicit stronger erp 400 ms after stimulus
25
ERP example study schupp et al 2000
- ppts presented w neautral, pleasant n unpleasant pictures - erps r more positive for pleasant n unpleasant pics then neutral pics, 400ms post stimulus
26
# functional techniques- ep methods MEG (magnetoencephalography)
- measures magnetic fields from brain activity - uses squid sensors - slightly better spatial resolution than EEG - still non-invasive
27
# functional techniques- NI methods PET
- inject radioactive tracer - measures blood flow, glucose or NT use - invasive n poor temporal resolution (~1min) - spatial resolution ~1cm per voxel
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# functional techniques -NI methods fMRI
- measures oxygenated vs deoxygenetaed blood - reflects hemodynamic reponse not direct activity - good spatial (~3mm) poor temporal (1-10s) - eg memory encoding activites LIFG n temporal regions
29
fMRI eg study wagner et al 1998
- ltm n brain areas study - ppts lie in mri scanner - shown words to remember - asked to recall later - some regions respond more to words that were later remembered: - the LIFG and parahippocampal n fusiform gyri (in temp lobe)
30
# functional techniques- NI methods Functional near-infared spectroscopy
- NRI light measures blood flow in superficial cortex - also reflects hemodynamic response not neuronal activity directly - non-invasive, portable, but limited to outer brain regions - temporal resolution ~ 1-10s - spatial res= few cms, only records from superficial cortex between light source n sensor
31
# non- invasive brain stimulation methods why use brain stimulation?
- recording shows correlation - stimulation shows causation (if altering activity changes behaviour)
32
# non- invasive brain stimulation methods example study
- letters presented on screen - TMS applied to visual cortex at diff times before/after presentation - ppt reports letter presented - result: accuracy decreases if TMS applied 80 to 120 ms after letter
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# non- invasive brain stimulation methods transcranial direct current stimulation
- applies weak electrical current between electrodes - anode+: excess (depolarises); cathode-: inhibts (hyperpolarises) - poor spatial resolution - superfical cortical regions
34
# non- invasive brain stimulation methods transcranial ultrasound stimulation
- uses ultrasound pressure waves to affect deep brain activity - more precise than TMS/TDCS - very new method w unknown mechanisms
35
# non- invasive brain stimulation methods transcranial magnetic stimulation
- magnetic pulses disrupt activity in specific brain areas - eg visual cortex TMS affects letter recognition if applied 80-120 ms after stimulus