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What are the ways of studying the Brain
fMRI (functional magnetic resonance imaging)
EEGs (electroencephalogram)
ERPs (event-related potentials)
post-mortem examinations
What does a fMRI (functional magnetic resonance imaging) do
measures oxygenated blood flow in brain (brain activity)
active areas can be compared with areas lower in activity
indicated on fMRI scan image via degree of bright colour
How does a fMRI (functional magnetic resonance imaging) work
oxygenated blood has different resonance
more active areas of brain receive more oxygenated blood
fMRI use magnets to detect oxygenated haemoglobin blood flow
mapped using voxels (thousands of neurons)
Scientific strength of fMRI’s
fMRI has good spatial resolution of 1mm
enables researcher to precisely identify (below)
active brain region and patterns of activation over time
lead to increased insight on how brain works
e.g. dopamine in addiction
Ethical strength of fMRI’s
non-invasive procedure
participants are protected from injection of potentially harmful substances
PET involves radioactive tracer
fMRI has good ethical validity
Delay criticism of fMRI’s
fMRI is slow (5 second delay)
between brain activity and measurement
important information could be not detected due to delay
fMRI cannot prove a theory
only indicate biological correlates to behaviour
External Validity criticism of fMRI’s
fMRI is expensive
technical specialist equipment and skilled personnel
use is limited to countries/regions/institutions that afford purchase and maintenance
economic considerations mean sample sizes in fMRI are small
limits external validity and reliability of data
What does an EEGs (electroencephalogram) do
show brain activity
via brain waves
presents as series of lines
has distinct pattern
How do EEGs (electroencephalogram) work
EEG involves placing electrodes on scalp
to record brain activity
22-34 electrodes used but can be from 2-100
depends on age, size of participant and aim of research
electrodes fitted to cap placed on scalp with conductive gel
electrode measure activity of cells directly below
more electrodes = more detailed info
What does Amplitude show
brain intensity
What does Frequency show
speed of activation
What is an EEG used to investigate
sleep disorders
seizures
memory problems
Useful strength of EEG
historically important understanding sleep patterns
e.g. used to determine 5 different sleep stages
key find was eye movement linked to dreaming phases
REM = rapid eye movement
REM reflected type of dream
only possible due to EEG
Standardised strength of EEG
systematic timetable for waking participants
and collecting dream reports
objective measure like EEG makes study replicable
consistency of results can be checked over time
increased reliability
Limited criticism of EEG
only detects surface activity in brain
cannot provide insight to deeper regions of brain
e.g. amygdala
EEG limited to what it can achieve (in measuring brain activity)
Issues with Attaching Cap criticism of EEG
electrode may be placed inaccurately or move during
each head is unique in shape and size
hasn’t got a ‘one size fits all’ basis
some electrodes may not work or need replacing
leads to unrepresentative findings
What does a ERPs(event-related potentials) do
records when there is activity in response to stimulus
can be stimulated by sensory, cognitive or motor events
ERPs are tiny voltages generated in brains structures
in response to specific events or stimuli
How does an ERPs(event-related potentials) work
uses same apparatus and technique as EEG
original EEG recording used
white noise is filtered out to leave only what investigating
using statistical averaging technique
waveform peaks and dips when specific cognitive process happens
e.g. language
Cost strength of ERPs
cheaper than fMRI
more utilised more readily and widely
conditions like epilepsy easier to diagnose
Accuracy strength of ERPs
ERP records brain activity in real time
measurements every millisecond of brain activity
results in accurate measurement
of electrical activity when specific task performed
Comfort criticism of ERPs
electrode cap participants find uncomfortable
leads to subject attrition
therefore lower sample size and robust data
participants may wriggle, scratch or pull
altering validity of findings
Precision criticism of ERP
ERP signal cannot pinpoint with 100% accuracy
exact source of specific brain activity
more than one electrode may pick up activity’s signal
lead to confusion what signal is and from which part brain originates
What does a Post-Mortem Examination do
determine the cause of behaviour or dysfunction
experienced when patient was alive
investigate structure of brain
cannot detect brain activity
How do Post-Mortem Examinations work
examine the brain after death
usually cut into slices
findings used to infer a correlation with behaviour
may involve comparing damaged brain to non-damaged brain
to assess which region are implicated in behaviour observed when alive
Why were Post-Mortem Examinations used
early days of biopsychology
no sophisticated tech available to look at brain
When are Post-Mortem Examinations used today
if no alternatives available
alzheimer’s disease can only be determined by PME
How was Post-Mortem Examination used for HM
alongside other techniques to investigate damage in HM
helped determine link between hippocampus and formation of new memories
after HM died his preserved brain sent to Uni of Cal
sliced into 2401 sections and scanned on slides
as permanent neurological research resource
How was Post-Mortem Examination used for Tan
Broca’s patient was scientific breakthrough
in locating language area of brain in left hemisphere
Tan only could say tan
but understood conversation
Harm Free strength of PME
enables research to study brain without inflicting harm on person
as long as consent is given
ethical way to investigate brain structure/abnormality
Conformation strength of PME
patient suspected of alzheimer’s
PET scans conducted indicating it present
but scan itself could not diagnose with 100% confidence
PME determines conclusively that patient suffers from alzheimer
Ecological criticism of PME
difficult to compare post-mortem slices of brain
with actual brain functioning before death
lacks ecological validity as the ‘real’ living brain of person is not reflected
Consent criticism of PME
may not always be possible for researchers to obtain fully informed consent
from prospective PME participant
particularly true if ability to consent is severely compromised by disorder
e.g. HM has amnesia so consent by proxy only
limits ethics of PME
What is Neuroplasticity
brain’s ability to adapt to change
due to injury, damage from illness
or change due to learning and experience
What is Structural Plasticity
changes within brain structures
e.g. increased grey matter built up in posterior hippocampus
due to learning experienced over time
not immediate, developed slowly
in response to either degree of damage or extent of learning experience
What is the buildup of grey matter due to
increased synaptic connectedness in brain regions involved
What does Plasticity mean
brain is not static concrete mass
brain is flexible organ
responds and adapts to environmental stressors
Examples of Neuroplasticity
london black cap taxi drivers years long learning routes through central
brains adapt by increasing grey matter
juggling routine learnt increased grey matter
once juggling ceased for 3 months the grey matter linked to juggling decreased
jugglers brain showed evidence of neural pruning
mindfulness practised increased grey matter in prefrontal cortex
mindfulness practised decreased grey matter in amygdala
What is Functional Plasticity
brain’s ability to replace lost or damaged functions
using existing brain regions
e.g. mobility, memory and language taken over by healthy brain regions
capable of replacing lost functionality stand in but not 100%
What is an example of Functional Plasticity
child had half of brain removed
(hemispherectomy)
to control epilepsy
can now function almost normally after surgery
remaining hemisphere takes over the tasks of removed hemisphere
What are the Key Structural Changes
axonal sprouting
reformation of blood vessels
recruitment of homologous areas
neural pruning
What is Axonal Sprouting
new growth of nerve endings
from surviving neurons
fibres link up with other undamaged cells
to form alternative neural circuits
What is Reformation of Blood Vessels
damaged tissue stimulates angiogenesis
restoring oxygen and nutrient supply
to recovering areas
What is Recruitment of Homologous Areas
regions in opposite hemisphere adopt functions of injured zones
e.g. broca area damaged so right hemisphere equivalent compensate over time
What is Neural Pruning
use-dependent refinement - synapses used frequently grow stronger
unused ones are cleared out
pruning makes network leaner and more efficient
structurally and functionally
Draganski’s study - learning-induced growth
followed by selective pruning of excess connections
Case Study of Functional Plasticity/Recovery
danelli et al conducted a case study of EB
14yo boy with brain damage
at 2 EB had hemispherectomy on left side to remove tumour
language centres removed (incl. Broca and Wernicke)
immediately after EB lost all language functions
after 2 years EB recovered his language ability even without left side
fMRI scans showed right side was acting as if it was the left
in terms of language functions
What does the case of EB demonstrate
functional recovery
brain can adapt and recover after trauma
Why does Functional Recovery have a Time Stamp
recovery early in life has chance of full recovery
older people less likely
brain ageing and decrease in synaptic activity
How should Rehabilitative Therapy be altered for Functional Recovery
begins with rapid growth spurt
slows down
eventual plateau after some time
reflected in therapy
Research Support strength of Plasticity & Functional Recovery
impressive body of research into neuroplasticity
findings supporting idea that brain adapts to change
good internal validity (different studies same conclusion)
researchers can exclude other explanations for findings
Practical strength of Plasticity & Functional Recovery
understand brain’s capacity to compensate for loss
being aware of slowing-down phase
key to informing therapy (physical and cognitive)
for patients with brain damage
Not Universal criticism of Neuroplasticity
not always happened when needed
HM removed hippocampus at 27
anterograde amnesia
never recovered any functionality
short-term memory affected permanently
does not apply in every case, casting doubt
Correlational criticism of Plasticity & Functional Recovery
research in field is correlational only
cause-effect cannot be established
leaves too many unanswered questions
e.g. why does grey matter build up in specific brain regions
e.g. what other factors could account for grey matter
sample sizes used are generally small