Week 20 Flashcards
Phrenology
- correlation of a person’s brain anatomy and skull shape with their behaviour/personality
- dividing the skull into sections of different psychological traits that are said to correlate to the brain + depending on the size of that region that determines how much of that trait you have as an individual
Modern methods for investigating the brain
- examining the effects of brain damage (brain injury/lesions or simulations in the lab, e.g. stimulating electrodes/TMS)
- physiology (recording electromagnetic activity of single of populations of neurons - EEG and MEG)
- imaging (visualising the structure and/or activity of neurons on the whole brain - neuronal staining techniques, MRI, CT/PET scans)
Natural brain injuries and lesions
- used to determine the correlation of the loss of a specific cognitive function with the area of brain damage
- e.g. Phineas Gage (frontal lobe damage); corpus callosotomy (split brain patients); Broca’s aphasia (link with Broca’s area to sentence structure processing)
Stimulating localised brain activity (invasive)
- in lab animals or open-brain surgery
- stimulating electrodes used to pierce the skull to activate certain areas of the brain
Stimulating localised brain activity (non-invasive)
- in healthy patients
- transcranial magnetic stimulation (TMS) can be used to excite/inhibit neurons by externally applying time-varying electromagnetic fields generated by a coil located above the head
- used to induce a temporary “lesion” to see the outcome in a patient (e.g. see if inhibiting a certain brain region specifically inhibits a certain activity in a patient)
Single-cell recordings
- single neuron behaviour can be examined through the use of microelectrodes which impale the cells of interest
- a nano lead (a submicron scale electrode) is implanted into an intracellular axon or extracellular axon membrane
- records neural activity of a single neuron but doesn’t stimulate it
- e.g. single-cell recordings in hippocampus to see if cells respond to one single stimulus (such as a specific person)
Electroencephalography (EEG)
- used to measure electrical brain activity on the scalp (recording the electromagnetic activity of a population of neurons rather than just single ones)
- sensitive to postsynaptic dendritic currents generated by populations of neurons that are active in synchrony
- placement of electrodes on the scalp is frontal (F), central (C), parietal (P), occipital (O) and temporal (T)
- very strong time-based resolution (less than 1 ms) but a rather poor spatial resolution (as it is difficult to tell specifically where the sources of signals are within the brain)
- useful for diagnosing epilepsy (characterised by an abnormal spike and wave discharge)
- can also use EEGs to assess brain waves during a specific repeated cognitive task to assess event-related potentials to assign different cognitive domains to activities
EEG Rhythms (delta)
- 0.5-4 Hz
- most prominent frontally in adults and posteriorly in babies
- seen normally in babies and in sleeping adults
EEG Rhythms (theta)
- 4-7 Hz
- seen normally in young children
- in adults, seen in drowsiness or sleep arousal or meditation
- excess theta waves for your age represents abnormal activity (e.g. due to focal subcortical lesions)
EEG Rhythms (alpha)
- 8-12 Hz
- bilaterally in the posterior regions but higher on the dominant side
- emerges with closing of the eyes and with relaxation
- attenuates with eye opening or mental exertion
- abnormally diffused and not responsive to external stimuli alpha waves in a coma
EEG Rhythms (beta)
- 12-30 Hz
- most evident frontally
- linked to motor behaviour, attenuated during active movements
- absent or reduced in areas of cortical damage
- dominant rhythm in patients who are alert or anxious or who have their eyes open
EEG Rhythms (gamma)
- 30-100 Hz
- represent binding of different populations of neurons together into a network for the purpose of carrying out a certain cognitive or motor function
Magnetoencephalography (MEG)
- recording of the magnetic fields produced by electrical currents in the brain using arrays of SQUIDs (superconducting quantum interference devices)
- it is much more expensive but can be more reliably localised to sources within the brain (due to signal being unaffected by the skull, meninges etc. like EEGs are)
- also more sensitive to activity at sulci, whereas EEGs are sensitive to both sulci and gyri activity alike
Neuronal staining techniques
- in order to stain a slice, the brain cannot be alive (not useful for dynamic imaging)
- e.g. Golgi stain method: randomly stains 5% of neurons, making them visible against the background of neural “chaos”
- e.g. Myelin stains: taken up by fatty myelin that wraps around neurons and thus identifies neural pathways (by visualising white matter)
- e.g. Nissl stains: identify cell bodies of neurons (visualising gray matter)
Structural imaging
- uses the fact that different types of tissue (e.g. skull, gray matter etc.) have different physical properties in order to construct detailed static maps of the brain
- used to scan alive human brains to view dynamic images
- used to see what is going on in the brain but not too much is revealed about the specific function of different regions
CT (computerized tomography) scans
- contrast dye is injected into the blood with a series of X-rays sent out from different angles
- the X-rays are combined into a series of horizontal sections of the brain
- X-ray absorption varies with tissue density (bone absorbs most = white; CSF absorbs least = black; gray/white matter = grey)
MRI (magnetic resonance imaging) scans
- a strong magnetic impulse is applied, with energy released by molecules in the tissue released as a result of the pulse being measured
- differently charged molecules respond differently to the pulses, hence the energy signals reveal brain structures with different molecular compositions (e.g. showing haemorrhage or tumour)
- brain images plotted with such measurements so more precise and detailed than CT scans
Functional imaging
measures neuronal activity (e.g. brain activity associated with cognitive processing)
fMRI (functional magnetic resonance imaging) scans
- measures activation by detecting the increase in oxygen levels (active neurons consume more oxygen)
- also measures the ratio of deoxyhaemoglobin and oxyhaemoglobin in the blood in different areas (BOLD/blood oxygen level dependent contrast response)
- change in BOLD response over time is known as the haemodynamic response function so you can localise active points (high spatial resolution)
- peaks 6-8 seconds after the stimulus event and is extended over time (limits the temporal resolution of fMRI for pinpointing the exact time of the activity)
- useful for cognitive research to pinpoint exact locations for brain activity (indicating active regions in a specific activitiy)
PET (positron emission tomography) scans
- measures local bloodflow into a brain region, measuring levels of glucose/fuel to the brain
- radioactive tracer injected into bloodstream
- slow technique with very imprecise temporal resolution (tracer takes up to 30 seconds to peak) but has good spatial resolution
- fMRI is better as it does not require radioactive tracer and PET scans have worse temporal and spatial resolution
- but PET is faster and sensitive to the whole brain (whereas fMRI such as near sinuses are harder to image)
Internal rhythms
- circannual (yearly) and circadian (daily) rhythms are endogenously generated, although can be modulated by external cues/zeitgebers like sunlight and temperature but also keep existing without these
- e.g. Mimosa plants still open and close their leaves in the same cycle as it does in darkness as it does in sunlight - suggesting rhythms are generated internally
- human body generates its own circadian cycles of activity and inactivity (including clear patterns of brain wave activity, hormone production, cell regeneration etc.)
Mechanisms of the biological clock
- when the brain is awake: neurons in the upper pons produce acetylcholine –> passed onto the thalamus (relay station) –> signals to cortex to maintain the brain in the conscious/awake state; also neurons in the pons produce noradrenlaine/dopamine etc. –> signals to hypothalamus –> signals distributed across cortical areas
- when the brain is tired: SCN in hypothalamus signals to activate VLPL neurons in thalamus –> GABA released and sent to hypothalamus and pons –> inhibits excitatory signals to the cortex –> cortex shuts down and loses consciousness (i.e. is asleep)
Suprachiasmatic nucleus (SCN)
- present in the hypothalamus and termed the master clock
- main control centre of the circadian rhythms of sleep and temperature
- generates circadian rhythms even when disconnected from the rest of the brain/body
- modified donor rhythms persevere in the recipient’s brain (SCN by itself is sufficient to perserve its own properties)
- the SCN’s zeitgeber is light (provided by neurons in the retina) so that when a light stimulus is present this resets the body’s biological clock
- also SCN corresponds to pineal gland that secretes melatonin (that is also influenced by light hitting retinal neurons)
Polysomnography
- used to study the stages of sleep
- EEG (brain wave activity) + eye tracking + breathing rate + amount of oxygen in the blood
Awake brain wave activity
dominated by beta waves
Drowsy/relaxed brain wave activity
dominated by alpha waves