Neuroimaging Intro/Techniques Flashcards

1
Q

Define Neuroimaging

A

Any technique used to obtain and integrate single or multiple measures of brain structure or function into a picture or series of pictures of the brain

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2
Q

Overview the history of neuroimaging

A

late 19th/early 20th century- Cajal and Golgi- first silver staining of neurons/ angelo mossi- using the balance table to exhibit blood travelling to brain during cognitive tasks
1910-50s- early electrophysiology- giant axon of squid recordings
1960s- Hubel and Weisel- alive animal electrophysiological recordings in cats looking at primary visual cortex
1970s/80- CT scans - first time seeing inside brain of living human non-invasively/ dalmidian invention leading to MRI/ PET scans
1990s- fMRI- looking at functional changes caused by external stimuli- disruptive technology
2000s/2010s- multimodal imaging in cognitive neuroscience fmri plus another imaging technique e.g. PET
2020s- still multimodal/ AI/ optogenetics/ smaller chipboards allowing electrophysiology in alive awake animals/ calcium imaging/ CLARIFY

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3
Q

what are the trade offs of different imaging techniques?

A

spatial resolution/ temporal resolution/ scope (whole brain to single cell)/ invasiveness/ limitations of imaging/statistical hardware

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4
Q

why study brain structure?

A
  • compare between healthy and disease groups to better understand disease
  • localise lesion - can be combined with functional study
  • image white matter tracts- brain systems
  • look at vasculature to link it with neural activity
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5
Q

describe the versatility of MRI

A

it can image a number of components of the brain- grey matter density/ cortical thickness, white matter density/location, blood vessels, CSF
links to function in fMRI

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6
Q

what are the pros of fmri/why is it so dominant in cognitive neuroscience?

A

it can study the whole brain in an awake individual doing cognitive tasks in a non-invasive manner
there is a lot of pressure to use it as it has a publishing bias

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7
Q

what are the cons of fMRI?

A

low spatial resolution
moderate temporal resolution
neurovascular coupling not fully understood- can’t always apply blood flow to neural activity
expensive
issues in replication

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8
Q

which animal model is used most in neuroscience research?

A

mice

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9
Q

what are the 3 broad categories of functional imaging modalities?

A

voltage-based (e.g. electrophysiology)
haemodynamic signaling (e.g. fMRI BOLD signals)
chemical flux (e.g. calcium imaging)

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10
Q

overview the relationship between voltage-based imaging and frequency

A

neuronal events occur at a range of frequencies
low frequency events are <300 Hz and are measured as local field potentials (LFPs), which can be mostly measured at a surface level (with some deep brain)
high frequency events are >300Hz and are measured to obtain multiple unit activity (MUA)- measuring action potentials in deep brain

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11
Q

flow chart overview of how sensory event effects haemodynamics

A

sensory event-> neural activity-> vasodilation (or constriction) -> increased (or decreased) blood flow velocity-> change in deoxyhaemoglobin (fast)-> change in oxyhaemoglibin (slow)

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12
Q

which elements of haemodynamics are measured?

A

blood flow velocity, vasodilation/constriction, blood oxygenation

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13
Q

name 5 haemodynamic measurement techniques

A

laser doppler flowmetry (measures blood flow velocity)
laser speckle imaging
near infrared spectroscopy
optical imaging spectroscopy (OIS)
BOLD fMRI

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14
Q

what has greater flexibility- haemodynamic-based or voltage-based imaging?

A

haemodynamic based

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15
Q

what is the key issue with haemodynamic-based imaging?

A

it is not a direct measurement of neural activity and we still have many unknowns regarding our understanding of neurovascular coupling

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16
Q

why can we not compare different brain regions/structures using fMRI BOLD signals?

A

different regions have different nv coupling and different metabolic needs

17
Q

compare voltage-based imaging against blood-based imaging

A

blood based have lower temporal resolution (seconds), whereas voltage based has higher (miliseconds)
BOLD is seen as a single peak response, whereas voltage-based tends to have more different responses
haemodynamics can have a cieling effect- where a vessel can only dilation so wide/blood can only flow so fast/ can reach a maximum oxygenated level.

18
Q

what are the 2 main measures using chemical flux techiques?

A

measuring neurotransmitter levels using microdialysis
measuring calcium signalling

19
Q

which processes is calcium signalling involved in?

A

exocitosis of synaptic vesicles containing NTs
backpropogation of APs
gene transcription
synaptic plasticity
vasodilation

20
Q

how is calcium signalling imaged?

A

inserting calcium imagers (genetically encoded indicators) into the animal with a molecule which gives off light when bound to calcium

21
Q

what are 2 key genetically encoded calcium indicators?

A

FRET-based and GCaMP

22
Q

how does FRET-based calcium imaging work?

A

when bound to Calcium, there’s a shift in fluorescence from blue to yellow wavelengths

23
Q

how does GCaMP calcium imaging work?

A

when bound to calcium is increases photon emission- increased intensity of fluorescence seen

24
Q

does calcium imaging tend to have a high or low temporal resolution?

A

high because changes in calcium are transcient and measured as they happen in real time

25
Q

what are the cons of calcium imaging?

A
  • it’s an indirect measure- you are measuring light fluorescence, rather than ca2+ directly hence relying on statical models and estimation
  • imaging depth is limited by laser power- can only penetrate to shallow layers currently
  • expensive
26
Q

what is the advantage of using multimodal imaging techniques?

A

it reduces the weaknesses in single technique and increases the certainty in the results