 fMRI: functional (nuclear) magnetic resonance imaging  Neuroimaging: get the structure of the brain Want to know how it works: connection brain parts.

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Presentation transcript:

 fMRI: functional (nuclear) magnetic resonance imaging  Neuroimaging: get the structure of the brain Want to know how it works: connection brain parts and brain functions Aim: measure the local „thinking activity”  Usage (criticism): Lie detector Neural- and psychological-modell checking (think/know experiment)

How we use it  Human attempts frequent  Well-planned tasks or questions  Measures: order of minutes One measure: order of 5 seconds Measure with and without tasks or question, further investigation based on the difference  Overlap the intensity map and brain image

The basics of fMRI  MRI: interaction between spins and magnetic field  QM based phenomena Classical view is almost satisfactory  Find a „think-activity”-sensitive MRI measureable quantity, measure it, and then reflect to think activity

Get the signal - BOLD  Blood-oxygen-level dependence  Hemoglobin: Fe 2+ can absorb O 2 Hemoglobin + O 2 : diamagnetic molecule Hemoglobin – O 2 : paramagnetic (S=2)  Measure the oxygen-flow differencies in vein  Determine the connection between BOLD singal and toughts

Get the signal – O 2 flow  The oxygen flow depends on the communicating intenstiy  Communication needs energy Neuron cells don’t have repository Increased activity needs more energy BOLD signal decreasing and then increasing

Time, accuracy and resolution  Time: depends on the BOLD signal, about less than half a minute Do experiments with the same patient, same time  Accuracy: easily detect maximum of BOLD  Space: resolution: in order of mm×mm×mm Problem: the motion of the patient

Increasing space resolution  No new information with increasing resolution  Signal comes from multiple capillars  Solution: BOLD signal minimum: more localised  Longer time or  Bigger magnetic field  No (?) news: cerebral tasks are not well localised

Temporal resolution   Increasing time resolution does count  (more details) usable image  Two tricks to improve: Spin echo – gradient echo EPI: echo planar imaging

Measurement: EOM  First: apply  Short RF pulse: 

Measurement: relaxation and decoherence  Solutions after „excitation”:  We can measure  Important:  New rotating cylindrical coordinates with frequency:

Measurement: spin-echo

Measurement: slice-excitation

Measurement: slice-excitation and spin-echo  Find for the desired excitation- distribution:

Measurement: another way, the gradient echo

Measurement: EPI  Echo Planar Imaging: increase time resolution even more!

What we get: images

An experiment: caffeine  caffeine as a contrast booster

Limits  We cannot answer any why question – only answer the question where  The brain is 3D – the image is 2D, so more experiments needed  We can measure only the neurons firing, but not the real actyvity (block or stimulate?)  High degree of cerebral plasticity: places may vary

Mind reading  The map of optic nerves to vissual cortex is so „localised”, „continous”  Training set: known videos and those fMRI signal  Unknown video: fMRI signal → video images  Ability to guess what patient think  Numerical problem  Further aim: movement of implants  Success: camera-eye

 /publications /publications