Lecture 3 Haemodynamics Flashcards

1
Q

describe briefly the chain of events from sensory event occurring (flow chart)

A

sensory event–> neural activity–>metabolite recruitment–> increased blood flow–> deoxyhaemoglobin (short)–> oxyhaemoglobin (long)

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2
Q

explain the importance of metabolite recruitment to the brain

A

neural activity is metabolically expensive, despite only being 2% of body weight, the brain uses ~20% of the O2, blood flow and glucose.
the majority of these are used to produce ATP as the brain, unlike muscles, cannot store much energy so needs this constant fresh supply

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3
Q

briefly outline ATP synthesis/krebs cycle (flow chart)

A

glucose from blood is transported into cells–> glycolysis produces 2ATP+pyruvate –> in absence of O2 pyruvate is reduced to lactate, in presence of O2, pyruvate enters TCA cycle where 36 ADP are recycled to produce 36 ATP–> ATP diffuses into blood to supply energy to neural cells

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4
Q

how does ATP produce energy

A

it is hydrolysed when reacting with water in order to produce phosphate which binds and alters/activates proteins e.g. ATPase ion pumps

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5
Q

what neural processes is ATP involved in?

A

synaptic transmission, housekeeping, maintaining resting potential, allowing APs

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6
Q

what are the 3 exploitable physical properties of haemodynamics

A

blood flow
vasodilation
blood oxygen charges

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7
Q

briefly overview the vasculature of neural tissue

A

energy demands are chiefly met by dense capillary network- cells at cortical level are 1-2 cells away from capillary

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8
Q

describe blood flow

A

a robust physiological change associated with cellular activity, closely linked to vasodilation

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9
Q

describe vasodilation

A

capillaries increase diameter up to 11% increasing metabolite transit

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10
Q

describe blood oxygen changes

A

red blood cells are packed with haemoglobin, a complex protein that binds and changes with O2. It is in one of 2 states- oxygenation and deoxygenated.
haemoglobin oxygenation changes magnetic, chemical and optical properties
following a neural events, after 10-15 second delay, there’s a large peak in HBO2 and a drop in HBr

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11
Q

neurovascular coupling

A

a link between neural activity and blood flow/oxygenation are well-established, however, not well understood

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12
Q

doppler shift

A

change in frequency imparted upon waves as a source moves

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13
Q

when light is shone on tissue what happens

A

it is either absorbed, reflected or scattered

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14
Q

describe light/photon scatter

A

the directionally random scattering of photons independent of blood flow by moving RBCs

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15
Q

how does more RBCs affect doppler shifted photons

A

more doppler shifted photons

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16
Q

describe the technique used for laser doppler perfusion monitoring

A

a fibre optic probe passes laser light into an area of tissues, photons are scattered by static and dynamic particles, imparting doppler shift and light is return to a photoreceptor in a mixture of original frequency and doppler shifted frequencies
it is measured as arbitrary voltage

17
Q

describe how different wavelengths are utilised

A

red wavelengths can penetrate deeper, so used to measure blood flow- laser doppler flowmetry
green light is more sensitive to changes in blood flow velocity due to vasodilation/constriction as it measures rate of RBC flow in the periphery of vessel- laser doppler velocimetry

18
Q

what are the pros of laser-doppler measurements

A

non-invasive measurement of flow and velocity for peripheral activity

sensitive to high frequency perfusion changes

measurable in real time

19
Q

what are the cons of laser-doppler methods

A

surrogate measure of neural activity (indirect)
sensitive to movement (artefacts)
invasive surgery for neural recordings
lacking quantitative units
difficulty localising depth

20
Q

describe functional near infrared spectroscopy (fNIRS)

A
  • human tissue has high penetration of NIR wavelengths
  • oxy- and deoxyhaemoglobin have different chromophore properties, absorbing differening wavelengths preferentially (830nm HBO2 and 692nm HBr)
  • when neural activity occurs, NIR at varying wavelengths shone through cap and detectors detect light- which will vary depending on the ratio of HBO2 and HBr
  • banana shaped photon paths
    -proportional- no set units
21
Q

pros of fNIRS

A
  • Biochemical specificity is high (good understanding of chromophores and wavelengths absorbed)
  • high temporal resolution (for a blood-based measurement)
  • transportable
  • easy for use with children
22
Q

cons of fNIRS

A
  • same limitations of BOLD fMRI- surrogate measure/ delay/ ceiling effect
  • limited to cortex (superficial penetration)
  • issues with machine differences
23
Q
A