Method Flashcards
The development of human neuroimaging techniques
1930: Electroencephalography (EEG) was discovered
1970: First radiographic methods available
1980-1990: Positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) became available
1990-2000: U.S. president George H. W. Bush declared the “Decade of the Brain”
Ap recap
Post-synaptic potential is determined by integrating input of many synapses at the dendrites.
Action potential travels along the axon to all terminals.
-resting at -70mv, stimulus over threshold lead to depolarisation. follow by repolarisation also hyper polarisation
- We rarely get the chance to measure activity of neurons directly in humans
- We rely on techniques that measure activity “indirectly” and from ”the outside”
How can we measure neuron activity
- We (mostly) rely on methods that are non-invasive, meaning that we do not open the skull (or interfere with brain function)
- One class of neuroimaging methods available for human research detects frequencies in neural signals (i.e. the rate of change of the signal over time)
- 1 Hertz (Hz) = completing a full cycle (up and down) in one second
- Biological signals never contain just one frequency (as in artificial signals)
- Complex signals can be decomposed into frequency components, each has a particular frequency (e.g., 1 Hz, 2 Hz, 3 Hz, …)
- The amplitude describes how much it goes up and down
- The phase describes when it goes up and down
Methods that measure fast-changing electrical activity from outside the scalp
oMagnetoencephalography (MEG): Measures electrical activity through the magnetic fields produced by the electrical activity of neurons
oElectroencephalography (EEG): Measures small voltage fluctuations
picked up by sensitive scalp electrodes
hemodynamics
- The changes at the cell membrane leading up to the generation of action potentials and the neurotransmitter release at the synapse all require energy
- For this, oxygenated blood is transported to “active” brain regions, because oxygen is used there to produce the necessary energy
o functional Near-Infrared Spectroscopy (fNIRS): Optical imaging technique that uses light to study blood oxygenation through the skull
o Positron Emission Tomography (PET): Can measure the distribution of specific molecules in the blood (by radioactive labelling)
o functional Magnetic Resonance Imaging (fMRI): Measures local changes in blood oxygenation with high spatial resolution
How does neuron packing arragement affect signal mesurement
- Luckily for us, neurons with similar “interests” tend to “cluster” together
- This clustering happens at the level of small “columns” but also in larger “areas”, which serve (roughly) the same functions
The trade off
- We have to trade-off methods that have a high spatial resolution (e.g., fMRI) vs. methods that have a high temporal resolution (e.g., EEG)
- Finally, there are methods that are “causal”, because they rely on direct stimulation of the brain, meaning that we can study what effects this might have
- The most commonly used method is Transcranial Magnetic Stimulation (TMS)
Transcranial Magnetic Stimulation
transcranial Magnetic Stimulation is a “non-invasive” technique used to create “virtual cortical lesions”
- Studies on patients with real lesions have informed cognitive science for a long time as they allow studying what patients can’t do anymore
- E.g., Phineas Gage (1823-1860), an American railroad construction worker, who suffered a serious injury by an iron rod piercing his head and frontal cortex
- This led to severe changes in his personality
- Lesions can therefore tell us a lot about the functions of specific brain region
Why don’t we just rely on patients with natural lesions?
- Removing most parts of his hippocampus, parahippocampal gyrus and amygdala in famous patient H.M. led to severe anterograde amnesia
- In the same way, lesions in Broca and Wernicke areas have been linked to impairments of speech production and language comprehension, respectively
- However, there might not be enough patients with circumscribed lesions to study all cognitive functions
- Lesions in single, specialised areas are rare
- Recovery and brain plasticity might compensate for lesions over time è patients might become quite ‘special’ over time
How TMS work
TMS is a method to create a small, short-lived virtual lesion that is reversible
- TMS can be applied externally, using a coil placed on the scalp that produces a rapidly changing magnetic field to induce electrical currents in the brain
- These currents can depolarise neurons in a small, circumscribed area of cortex
- TMS-induced current causes neurons to fire randomly, acting as “neural noise”, thereby masking the neurons that are firing correctly
- In order to create the current pulse, which is required to generate the magnetic field, a capacitor is charged and then suddenly discharged
- In order to create a magnetic field strong enough for stimulation, very fast loading times (~100-200 μs) and short discharge durations (<1 ms) are required.
History of TMS
- Fritsch & Hitzig (1870) were the first to electrically stimulate the cortex of animals
- D’Arsonval (1896) discovered that the magnetic stimulation of the visual cortex can elicit “phosphenes”
- Magnusson & Stevens (1911) developed the first “head coil” covering the entire head
Barker, Jalinous & Freestone (1985) developed the current TMS technique, which had the great advantage of not being painful (mostly…)
rTMS
fast sequence of pulses instead of a single pulse (called: “repetitive TMS”, or rTMS in short)
coils
Different coils have been used, but the most common one is the ‘figure-eight’ coil
- The figure-eight coil generates magnetic fields generating offset current loops that circulate in opposite directions, allowing for high precision in the stimulation
- A more focal area of the cortex is stimulated using the figure-eight coil compared to the round coil (usually 3-4 mm radius, but up to 1 mm possible)
- The advantage is that the researcher knows which part of the cortex was affected
Applications of TMS in Biological Psychology Research
1) The injection of “neural noise” approach using single-pulse TMS
2) The “virtual lesion” approach using repetitive TMS
3) The “probing excitability” approach using single-pulse TMS
4) The “probing information transfer” approach using paired-pulse TMS
5) Using paired-pulse TMS to test for the decay of activity
6) Clinical applications of TMS
injection of “neural noise” approach
Using single-pulse TMS to disrupt cognitive processing
- If a single TMS pulse to a specific region of the cortex disrupts a cognitive function, this is a powerful demonstration of its causal involvement in this process
- Testing for causality is impossible using most other neuroimaging techniques, which usually rely on correlations
- One way of doing this is to interfere with the process of interest at exactly the time window during which the regions is required; e.g., to delay movements or to disrupt visual processing
- Regions do not stop working completely, but “neural noise” interferes with normal functioning
classical study of injection of “neural noise” approach
the researchers used 3 alphabetical letters as stimuli presented under difficult viewing conditions using illuminated frames/background Amassian et al., 1989
- Magnetic stimulation (i.e. TMS) was applied ~ 2 cm above the inion over visual cortex
- Effects on letter perception were investigated when varying the interval between visual stimuli and time point of TMS stimulation
It was found that during a critical period (40 – 120 ms) stimulation affected
detection performance
When shifting the stimulation site from left to right, perception of letters in
the contra-lateral visual field was predominantly impaired
- When moving the TMS stimulation from top to bottom at midline, and letters were displayed vertically, stimulation above the reference line suppressed
letters at the bottom of the display
- Stimulating below the centre was not possible (the bone was in the way)
The “virtual lesion” approach
repetitive TMS (rTMS) is used to interrupt or enhance cognitive processing
- It is also possible to inhibit cognitive functions for a longer period of time by applying repetitive TMS (rTMS)
- It can then be measured whether (and for how long) a specific cognitive task is impaired (usually slowing instead of total loss of function)
- There are strict safety guidelines for rTMS (Wassermann, 1998)
“probing excitability” approach using
single-pulse TMS
(usually over the motor system)
- For the motor system in particular, one option is to test how responsive (or “excitable”) the motor cortex is during a cognitive task
- The idea is that if the motor cortex is required for a cognitive task, then it should already be activated when single-pulse TMS is delivered
- The measure of interest is how strongly the motor cortex “reacts” to the pulse itself (any “disruption” is ignored), i.e. how strong its output is after being stimulated
- The excitability of the primary motor cortex can be measured by recording “motor evoked potentials” (MEPs) using the electromyogram (EMG) – the electrical activity of muscles
- One can then measure MEPs for each stimulation and compare average
MEPs between experimental conditions