Lecture 25 - Neuroimaging and Reward Intro Flashcards

1
Q

Diffusion MRI for

A

structural connectivity visualisation

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2
Q

Diffusion MRI process

A

In addition to the general principles of MRI imaging:
In Diffusion MRI local magnetic fields applied to the head at
different angles
Rapid repeated scans

Rapidly repeated at all angles, instead of slow to get anatomical definition you go fast to get the hydrogen atoms to move in all different directions (want to see how and where they are moving so you do not get very good definition from diffusion MRI but you will get movement of water along tracts

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3
Q

Diffusion MRI measures

A

Measure anisotropy:
Degree to which the hydrogen ions travel along white fibre bundles
Measure of white fibre bundle cohesiveness/integrity i.e. how good that white matter bundle is

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4
Q

Diffusion MRI - Isotropic

A

= 0
Hydrogen ions are not constrained (e.g. CSF)

When not constrained by anything the ions are going to move all around in the head in many directions, therefore say they are isotope

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5
Q

Diffusion MRI - Anisotropic

A

=1
Hydrogen ions constrained (e.g. White fibre bundles)

Trying to move water along a white matter bundle, the hydrogen ions are going to very much constrained so when we go in a certain direction even though magnetic field is trying to make it go all around it is going to go in one direction therefore called anisotropic movement

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6
Q

Isotropic =

A

0

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7
Q

Anisotropic =

A

1

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8
Q

Diffusion MRI - Fractional anisotropy

A

(between 0 and 1)
Practical assessment of degree of white matter integrity: axon myelin, diameter and density

Certain degree of movement allowed in certain directions because the bundles are not completely compact all the time, so get a fraction, the fraction is affected by the axon myelin, diameter and density

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9
Q

Fractional anisotropy =

A

between 0 and 1

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10
Q

Application of Diffusion MRI

A

looking at the reward system and its networks

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11
Q

Reward system define

A

Reward system: a group of interconnected brain structures involved in motivation (desire, motivation, craving), associative learning (operant reinforcement (learning something that you did associates with some kind of outcome that makes you want to do this thing more or less) and positive conditioning (associate the reward with the action being done e.g. teaching a dog to sit with a treat)) and in emotions, particularly those associated with pleasure

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12
Q

Reward system

A

look at poster

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13
Q

Reward system circuit

A

Prefrontal cortex is a complex structure in the front of the brain that helps us decide the kind of things we might want to aim towards obtaining (motivation) and perceive something from memory we have experience before and start wanting to work our actions towards that

Nucleus accumbens is part of the basal ganglia which is small but a central component to this reward system

Ventral tegmental area in the midbrain is one area where the cells that make dopamine live and dopamine is a pleasure chemical that reinforces/motivates and tells the brain that we have experienced something that is potentially pleasurable that we may want to do again that is rewarding and reinforcing and these are connected together the VTA delivers the dopamine to the prefrontal cortex and to the nucleus accumbens and other areas as well and this part of the sopamine projection is called the mesolimbic (medial surface of brain)

Prefrontal cortex actually makes its major projects ions onto the nucleus accumbens (red arrow is green on recording), anything that is being remembered/desired/planned about is informing the nucleus accumbens so it is an input pathway if you want to the reward system

Nucleus accumbens then has a projection out (not anatomically correct on this diagram) to the ventral pallidum (globes pallidus is part of the lent information nucleus and this is the ventral part of it) and from here it goes to the thalamus and from the thalamus it goes back to the cortex and back to areas that are often closely aligned to the prefrontal areas where the activity actually started

This is a loop that is responsive for motivation, positive emotions, associative learning (learning about the value of the stimulus)

This is the circuit that is known to be disrupted in addiction

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14
Q

Using diffusion MRI to measure the integrity of a fibre bundle - Diffusion Tensor Imaging (DTI)

A

Map the fractional anisotropy (FA) of a fibre bundle
- Compare FA values (0 = fully isotropic and 1 = fully anisotropic) between individuals and
groups; FA increases during adolescence but at different rates between people ( not all developing at the same rate, as you are getting older, your white matter tracts are getting more myelinated and therefore assume they are getting more organised and constrained therefore an increase in FA as the individual grows)

For reward network specifically lock at connections between nucleus accumbens and ventral tegmental area

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15
Q

Using diffusion MRI to measure the integrity of a fibre bundle - Diffusion Tensor Imaging (DTI) - Study looking at addiction-free 14 to 15 year old boys in Oregon with a parental history of adolescent binge drinking

A

Looked at integrity of white matter between prefrontal cortex, ventral pallidum, VTA and nucleus accumbens (as reward centres) and duration to begin binge drinking (followed to 21 y.o. with three-monthly questionnaires (cohort study type)

Association between pre-existing individual differences in FA and the onset of binge drinking in adolescents - NOT necessarily causal (correlation rather than causal)

The greater the FA, the longer it took them to develop a drinking habit
The less organisation of the fibre bundle the more likely they were to develop binge drinking habits earlier in their lives
Adolescence with lower FA in the medial orbital gyrus white matter display greater activation of nucleus accumbens during decision making involving risk and reward

Can map the FA onto a scan, brighter the tracts are the greater the FA I.e. more organised, impressive fibre connection between frontal areas here and the down in the areas posteriorly that are related to the reward system

Smaller FA, less organised WM, start binge drinking earlier - greater NAcc activation - less regulated reward /risk response

Less FA = less organised white matter

Frontal areas are linked in behaviour regulation therefore if you are not connecting to them and have less white matter connection then you are more likely to show risky behaviour

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16
Q

Diffusion MRI - Diffusion Tractography

A

3D representation of fractional anisotropy: build and identify white matter tracts based on the different directionality FAs
Long projection fibres
Short projection fibres - between nucleus accumbens and ventral palladium for example

Multiple scans from different directions then you can see the movement of ions in each orientation and if you do this enough times then you can put it into a 3D representation of the bundles

colour coded to show different connections

c.f. Long association fibres e.g. cingulum bundle
Short association fibres - corticocortical connections

17
Q

Functional MRI for

A

functional connectivity

18
Q

Functional MRI - T2 weighted imaging

A

In addition to the general principles of T2 MRI imaging:

Adjusted scan parameters to be sensitive to
deoxygenated haemoglobin

Rapid repeated scans - measure “Blood-Oxygen-Level-Dependent”
signal = BOLD signal

Rapid repeat scans intend to look at the haemoglobin molecules as they move through vessels, as they are oxygenated they will give up their oxygen to an area that requires it so if you have metabolic activity/a lot of activity going on in a brain area then you will increase your blood flow and it turns out that deoxy haemoglobin (haemoglobin after the oxygen has been removed) is very magnetic and will perturb the magnetic field so if you have an activated brain area where there is lots of blood now flowing in with lots of oxygenated haemoglobin then you have a relative reduction in the concentration of deoxyhaemoglobin = can measure the bold signal

Activated brain regions = increased blood flow = reduced concentration of dHb

Hb = haemoglobin; dHb = deoxygenated haemoglobin

19
Q

Activated brain regions for Functional MRI T2 weighted imaging

A

Activated brain regions = increased blood flow = reduced concentration of dHb

20
Q

Functional MRI T2 weighted imaging and deoxygenated Haemoglobin

A

Deoxygenated haemoglobin is magnetic – disrupts MR signal

Increase in regional brain activity (get relative reduction in dHb) –> Reduced dHb levels in region –> Increased T2 signal –> Map change in T2 signal onto structural T1 (mapping the T2 signal onto a nice high resolution structural T1 scan)

21
Q

Heat map of T2 activity mapped onto a structural T1

A

Red is an increase in activity and blue is a decrease in activity

22
Q

Task functional MRI

A

Participants perform a task while in the scanner - T2 brain activity mapped

Mirror angled so that the participant can see something projected onto a screen without moving from the lying down position

MRI compatible button response panel and joystick - give it this controller in their hand to give answer

23
Q

Application of Task Functional MRI

A

Participants perform a task while in the scanner – T2* brain activity mapped

Had to respond as quickly as possible to light flash knowing that the button press would or would not give reward, depending on the face cue !

Compare the fMRI scans in anticipation of no reward from reward

Greater activation to reward anticipation in nucleus accumbens, midbrain dopamine areas [rewarding stimulus processing], caudate and putamen [action related to reward] (also parts of the frontal gyrus and cerebellum)
Grimm et al, 2020

As quickly as possible after the light had to click the button to indicate what kind of stimulus they were seeing and then got feedback - when they saw a nice smiley face and clicked it in the right amount of time they got money (positive reqard), other condition no reward but still needed to react fast (balance stayed the same)

then can map on to brodmanns area to locate what structures are on the scans

ORANGE

24
Q

Resting Functional MRI

A

Participants rest in scanner without thinking about anything for 10 min – default or resting brain T2* activity mapped (not sleeping, just lying there, not task related)

Map activity during resting, and correlate which brain regions are active at the same time = functional networks

E.g. Other brain regions active at the same time as the right amygdala

  • right hippocampus
  • left amygdala
  • left & right cingulate and subcallosal Cx

Have a start region in these studies to see what is connected to what and so we start with the amygdala on the right hand side which will tell you from there which other brain areas are connected and active at the same time ..

25
Q

Advantages of MRI

A

Detailed anatomical structure

Detect pathology with anatomical precision (because good resolution)

Measure white matter integrity

Ability to assess brain function and functional connectivity at rest and during tasks

Doesn’t involve radiation, relatively safe and individuals can be repeatedly scanned (not worried about the radiation dose)

26
Q

Advantage of MRI compared to CT scanning

A

Compared to CT scanning: CT is anatomically poor contrast, cannot measure white matter integrity, cannot give functional measure

27
Q

Advantage of MRI compared to PET scanning

A

Compared to PET scanning: PET is anatomically poor, less available; MRI does not need a radioactive tracer injected

28
Q

Disadvantages of MRI

A

Susceptibility to magnetic interference

  • Can result in poor signal quality
  • Can be a patient safety issue (e.g. metal in eyes/body such as braces )

Requires significant technical expertise due to the physics, computation and statistical processing (particularly diffusion and functional imaging)

  • Diffusion and functional imaging are approximate, but are not a direct measure of, white matter/functional brain activity, respectively
29
Q

Disadvatnage of MRI compared to CT scanning

A

Compared to CT scanning: cannot visualise bone (marrow only for T1) or acute tissue bleeding; relatively expensive, longer procedure, can be frightening due to confinement

30
Q

Disadvantage of MRI compared to PET scanning

A

Compared to PET: much more difficult to accurately quantify metabolic or molecular processes