Brain imaging & EEG Flashcards

1
Q

Static magnetic field

A

B0 field

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2
Q

Spin-Lattice Relaxation:

A

T1 relaxation: the process where the net magnetization (M) returns to its initial max value (M0) parallel to B0 field

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3
Q

T1:

A

The time required for the z-component (Mz) to reach about 63% of its max value
Rate of recovery (T1 relaxation) is governed by time T1

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4
Q

Spin-Spin Relaxation

A

T2 relaxation –> the process where the transverse magnetization component (Mxy) decays due to the spins’ dephasing

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5
Q

T2:

A

The time required for the signal to fall to approximately 63% of its initial value (when there is only 37% of the signal)
Exponential decay of Mxy is governed by time T2

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6
Q

Inhomogeneity in the B0 field =

A
T2 prime (T2') 
Cause the transverse magnetization (mxy) to decay even faster
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7
Q

T2*

A

The time governing the decay of T2’

T2* = the inverse sum of T2 & T2’

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8
Q

Applications that use T2*

A

fMRI

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9
Q

Brownian Motion

A

Water molecules are in continous motion (Brownian motion)

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10
Q

Rate of motions determines the T1 & T2 relaxations:

A

(1) types of spins
2) distance between spins
3) angle between them
4) relative motion

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11
Q

TR:

A

Repetition time (TR) = the time from one RF pulse to the next RF pulse

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12
Q

TE:

A

Echo Time (TE) = from the RF pulse to the time we receive the strongest MRI signal

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13
Q

T1 weighted image:

A

T1 W = short TR & short TE

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14
Q

T2 weighted image

A

T2 W = long TR & long TE

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15
Q

Proton Density

A

Proton density (PD) = Long TR & Short TE

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16
Q

Diamagnetic

A

All electrons are paired - total magnetic moment = 0

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17
Q

Paramagnetic

A

1 / more unpaired electrons: total magnetic moment = small

18
Q

Ferromagnetic (real magnets)

A

Unpaired electrons all lined up in the same direction: total magnetic moment = large

19
Q

Oxyhaemoglobin is considered what type of magnet

A

diamagnetic

20
Q

Deoxyhaemoglobin is considered what type of magnet

A

Paramagnetic

21
Q

Define EEG

A

EEG (electroencephalography) = the recording of spontaneous electrical activity from the scalp over time (epoch)

22
Q

3 electrodes needed to record EEG:

A
  1. Positive electrode - recording electrode
  2. Negative electrode - reference electrode
  3. Ground/earth electrode - reduces electrical interference
23
Q

What is the montage in an EEG

A

Montage - the design of collecting EEG voltage signals from the scalp

24
Q

Referential Montage:

A

Recording Electrode from reference electrode

25
Q

Bipolar Montage:

A

recording biopotential between 2 electrodes

26
Q

Define an artifact

A

Recorded activity that is not of cerebral origin

27
Q

Factors that change the P300 latency & amplitude:

A

1) habituation to task & repetition of task - decrease in amplitude w repetition of task
2) Task difficulty
3) Mental fatigue - amplitude decreases w time of task

28
Q

Stoke Shift:

A

The energy difference between the peak absorbance & the peak of emission spectrum

29
Q

Components of molecules which absorb light

A

Fluorophores

30
Q

Why are organic dyes used for fluorescence labelling?

A

Organic dyes with aromatic rings - this structure has free electrons able to move around freely allowing fluorescent light to be emitted when excited

31
Q

Uses of Fluorescent dyes:

A

1) analysis of fast, dynamic processes
2) labelling of antibodies
3) organelle labelling
4) Physiological measurements
X - Preparation of specimens w permanent shelf life

32
Q

Fluorescent labelling of cells

A
  • Allows multiple simultaneous labelling
  • Can be used for single-molecule labelling
  • is subject to bleaching
  • CAN be used on living cells
32
Q

Fluorescent labelling of cells

A
  • Allows multiple simultaneous labelling
  • Can be used for single-molecule labelling
  • is subject to bleaching
  • CAN be used on living cells
32
Q

Fluorescent labelling of cells

A
  • Allows multiple simultaneous labelling
  • Can be used for single-molecule labelling
  • is subject to bleaching
  • CAN be used on living cells
33
Q

From which species does green fluorescent protein (GFP) originate:

A

Jellyfish

34
Q

What is an essential requirement for Fluorescence Resonance Transfer (FRET) to occur:

A

The emission spectrum of the donor & the absorption spectrum of the acceptor must overlap

35
Q

What immunohistochemical label can be used to identify newly formed hippocampal neurons?

A

Doublecortin (DCX)

36
Q

Problems with fluorescent techniques:

A

1) Bleed through: broad peaks cross over into 1 another - get false positive labelling
2) Blur: out of focus light decreases resolution
3) Bleaching: excited fluorophores react to become nonfluorescent
4) phototoxicity: light can harm cells
5) Background/Autofluorescence: Cells have fluorophores too

37
Q

Photobleaching definition

A

Defined as irreversible destruction of an excited fluorophore

38
Q

Methods for countering photobleaching:

A

1 - scan for shorter times
2 - use high magnification, high NA objective
3 - Use wide emission filters
4 - Reduce excitation intensity
5 - Use antifade reagents (not compatible w viable cells) - protects against fading

39
Q

Major application of GFP

A

Reporter gene assay of promoter activity

40
Q

what does FRET measure

A

Measurement of molecular interactions