Neuroimaging techniques Flashcards

1
Q

What is brain imaging?

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

Why is neuroscience research under the spotlight?

A
  1. Neuroscience is a young discipline - imaging techniques have tripled in the last 15 years
  2. Emergence of awake human imaging - first used in the 70s - now how the tools to answer questions
  3. We have the technology - human research, animal research - first picture = diffusion tensor imaging
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3
Q

Name some of the inventions in neuroscience which have changed the field

A

Golgi - Golgi staining - 1890s
Hubel and Wiesal - visual receptive fields 60s
Damadian - inventor of MRI early 70s
Ogawa - inventor of fMRI 1990s

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4
Q

Is there downsides to having such a fast changing field?

A
  • Constant pressure to publish
  • Increasingly sophisticated techniques needed
  • Researchers need to understand the physical and statistical basis of the techniques they use
  • Can lead to bad science
  • Old interpretations of data is not always reliable today
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5
Q

What is an example of bad science?

A

Bennet salmon imaging
- Dead salmon placed in an fMRI scanner and asked to determine the emotion of the individual in the picture
- It appeared that there was activity in the salmon’s brain and they concluded that there must have been some processing in the salmon in response to the question
- In reality, it was random noise in the EPI time series that caused the activation as the salmon was dead
- Crucial to understand the stats behind the imaging to ensure the correct conclusions are made

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6
Q

Why study brain structure?

A
  • Comparisons of clinical/sub-clinical populations
    – size/shape or regions/whole brain
    – expression of specific neurons
  • Localise site of neural insult
    – assess impact on behaviour
  • Imaging white matter tracts/projections
  • Vasculature
    – understanding the link between blood flow and neural activity
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7
Q

What can we use MRI for?

A

Grey matter density and cortical thickness
White matter tract density and location
The sizes, location, and course of blood vessels
The flow of cerebrospinal fluid
Measures related to neural activity (bold fMRI)

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8
Q

Why is fMRI dominant but flawed?

A

DOMINANT
Whole brain awake imaging
Non-invasive

FLAWED
Relatively low spatial resolution (can only accurately measure within a centimetre of the brain)
Moderate temporal resolution (haemodynamic responses are often delayed)
Surrogate measure of neural
Hugely expensive
Fears about replicability

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9
Q

Why are mice a good animal model in neuroimaging research?

A

The mouse genome is entirely mapped - know what every gene does
Allows the insertion or deletion of various genes - assess behaviour

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10
Q

What are the different functional modalities of neuroimaging techniques?

A

Voltage based (visualises a direct indicator of activity by measuring changes in voltage - similar to electrophysiology)
Haemodynamic signalling
Chemical flux

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11
Q

What frequencies are used to obtain electrophysiological data?

A

Low frequency (<300Hz) sampled to obtain the local field potential (LFPs) - detectable at surface and deep brain

High frequency (>300Hz) samples to obtain multiple-unit activity (MUA) - detectable using deep brain recording

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12
Q

What techniques are used to measure electrophysiology?

A

EEG = non-invasive in humans
Electrophysiology in animals = invasive - electrode inserted into the brain

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13
Q

What are some examples of techniques using haemodynamic measures?

A

Laser Doppler flowmetry
Laser speckle imaging
Near infra-red spectroscopy
Optical imaging spectroscopy
BOLD fMRI

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14
Q

What is a major limitation of haemodynamic measures?

A

They are not a direct measure of neural activity - it is an indirect measure of blood oxygenation which represents neural activity
Need to measure neural activity simultaneously to compare haemodynamics to neural

Blood based changes are delayed and extended

Ceiling effect - limited by the vessels and how much blood can flow at a certain time

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15
Q

What are the different blood-based measures?

A

Flow and velocity
Vasodilation/vasoconstriction
Blood oxygenation

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16
Q

When does calcium signalling occur?

A
  • Exocitosis of synaptic vesicles
  • Backpropagation of action potentials
  • Gene transcription
  • Synaptic plasticity
  • Vasodilation

Calcium signalling doesn’t always reflect neural activity

17
Q

How does calcium imaging work?

A

Takes advantage of calcium indicators and fluorescent molecules that respond to the binding of Ca2+ ions by fluorescence properties

Bioluminescent proteins
Binding of Ca2+ causes photon emission

Chemical calcium indicators
Excitable by UV light. Ca2+ binding causes change in fluorescence depending on indicator used (increase or decrease)

Genetically encoded calcium indicators
- FRET based = Ca2+ binding causes shift in colour of fluorescence: blue to yellow
- GCaMP = binding of Ca2+ causes photon emission = increase in fluorescence

18
Q

What are the limitations of calcium imaging?

A

Indirect measures - measuring light not calcium
- Reliance on statistical models and estimation

Imaging depth limited by laser power

Expensive

19
Q

Why is multimodal imaging important?

A

Covers blind spots/weaknesses in single technique e.g., spatio-temporal resolution
Increases certainty in results
Allow for illumination of relation between modalities