biopsych Flashcards

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1
Q

the nervous system

A

2 main functions:

  • to collect, process + respond to info in the environment
  • to coordinate the working of different organs + cells in the body

made up of:

  • central nervous system
  • peripheral nervous system
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2
Q

central nervous system

A

made up of the brain + spinal cord:

  • the brain = centre of all conscious awareness
  • the spinal cord = an extension of the brain + responsible for reflex actions
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3
Q

peripheral nervous system

A

made up of neurones that connect the CNS to the rest of the body
further divided into:

  • somatic nervous system: controls conscious activities (eg running)
  • autonomic nervous system: controls vital functions in body (eg breathing, heart rate, digestion etc)
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4
Q

the endocrine system

A
  • works alongside the NS to control vital functions in the body through the action of hormones
  • acts more slowly but has v widespread + powerful effects
  • instructs glands to release hormones directly into the bloodstream to be carried to target organs
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5
Q

glands

A
  • organs in the body that produce hormones
  • pituitary gland (aka master gland) = major endocrine gland located in the brain which controls the release of hormones from all other endocrine glands in the body
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6
Q

hormones

A
  • secreted into the bloodstream + affect any cell in the body that has a receptor for that particular hormone
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7
Q

fight or flight

A

endocrine system + autonomic nervous system work together during stressful events

  • when a stressor is perceived, the hypothalamus triggers activity in the sympathetic NS
  • stress hormone adrenaline is released from the adrenal medulla into the bloodstream
  • adrenaline triggers physiological changes in target organs + causes: increased heart rate, pupil dilation, decreased production of saliva (fight or flight)
  • once the threat has passed, the parasympathetic NS returns the body back to its resting state (rest + digest)
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8
Q

structure of a neurone

A
  • cell body (soma): includes a nucleus which contains the genetic material of the cell
  • dendrites: branch-like structures that protrude from the cell body - carry nerve impulses from neighbouring neurons towards the cell body
  • axons: carries electrical impulse away from the cell body down the length of the neuron
  • myelin sheath: fatty layer that covers the axon + speeds up electric transmission of impulse
  • nodes of Ranvier: gaps in the myelin sheath from/to which impulses jump
  • terminal buttons: at the end of the axon - communicate w the next neuron in the chain across the synapse
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9
Q

firing of a neurone
electric transmission

A

when neurone is at rest:

  • inside of cell is more negatively charged compared to the inside

when neurone is stimulated:

  • inside of cell becomes positively charged for a split second, causing an AP to occur
  • this creates an electrical impulse that travels down the axon toward the end of the neurone
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10
Q

types of neurones

A

sensory

  • carry messages from the PNS to CNS
  • long dendrites and short axons

relay

  • connect sensory neurons to motor neurons
  • short dendrites and short axons

motor

  • connect CNS to effectors e.g. muscles + glands
  • short dendrites and long axons
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11
Q

synaptic transmission

A
  • when the electrical impulse reaches the end of the preSN, it triggers the release of NTs from the synaptic vesicles
  • once NT diffuses across synaptic cleft, it’s taken up by the postsynaptic receptor sites (aka dendrites) of the next neurone
  • chemical message is converted back into an electrical impulse + process of transmission begins again
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12
Q

excitation

A
  • when a NT increases the positive charge inside the postsynaptic neurone (depolarisation)
  • making it more likely to fire an AP
  • eg adrenaline
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13
Q

inhibition

A
  • when a NT increases the negative charge inside the postSN (hyperpolarisation)
  • making it less likely to fire an AP
  • eg serotonin
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14
Q

summation

A
  • accumulation of NTs in the synapse where both excitatory + inhibitory influences are summed
  • net effect of NTs on postSN decides whether an AP is fired or not
  • is only fired if depolarisation reaches the threshold
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15
Q

brain localisation

A

scientists first supported the holistic theory (that all parts of the brain were involved in processing of thought + action

  • was replaced by the localisation theory
  • Broca & Wernicke discovered specific areas of the brain that are associated w specific functions
  • if an area of the brain is damaged, the function associated w that area is also affected
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16
Q

lobes

A
  • cortex of both hemispheres is subdivided into 4 lobes:
  • frontal, parietal, occipital and temporal
  • each lobe is associated with different functions
  • language, unlike other areas, is restricted to the left hemisphere
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17
Q

motor area

A
  • found at the back of the frontal lobe
  • controls voluntary movement in the opposite side of the body
  • damage may result in loss of control over fine motor movements
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18
Q

somatosensory area

A
  • found at front of parietal lobe
  • processes sensory information from the skin (touch, heat, pressure etc)
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19
Q

visual area

A
  • found at the back of the occipital lobe
  • each eye sends info from right visual field to left visual cortex + vice versa
  • damage to left hemisphere can produce blindness in the right visual field of both eyes
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20
Q

auditory area

A
  • found in the temporal lobe
  • analyses speech-based info
  • damage may produce partial hearing loss
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21
Q

Broca’s area

A
  • found in left frontal lobe
  • responsible for speech production
  • damage results in Broca’s aphasia - characterised by slow, laborious speech, lacking in fluency
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22
Q

Wernicke’s area

A
  • found in the left temporal lobe
  • responsible for language comprehension
  • damage results in Wernicke’s aphasia - produce neologisms (nonsense words) as part of their speech
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23
Q

brain localisation
ao3

A

brain scan evidence

  • Peterson used brain scans to demonstrate how Wernicke’s area was active during a listening task + Broca’s area was active during a reading task, showing that these areas of the brain have different functions
  • Tulving revealed that semantic + episodic memories reside in different parts of the prefrontal cortex

Phineas Gage case study

  • damage to left frontal lobe caused a change in his personality
  • calm + reserved –> quick-tempered + rude
  • suggests frontal lobe is responsible for regulating mood
  • HOWEVER, case studies cannot be generalised

neural plasticity

  • suggests that the rest of the brain is able to reorganise itself to recover lost function, following damage
  • this poses as a challenge to the localisation theory as it suggests that localisation is not as rigid/permanent as made out to be
  • although this doesn’t happen everytime, there are several documented case studies of stroke victims recovering seemingly lost abilities

Lashley’s rats provide counter-evidence

  • Lashley removed between 10-50% of the cortex in rats learning a maze
  • found that no one area was more important than any other in the rats’ ability to learn the maze
  • shows that learning requires every part of the cortex, not just some areas
  • suggests learning is too complex to be localised + requires involvement of the whole brain
  • HOWEVER, can’t generalise rats to humans
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24
Q

hemispheric lateralisation

A
  • brain is divided into 2 halves: left + right hemispheres
  • generally, left side of body is controlled by right hemisphere + vice versa

lateralisation: idea that 2 halves of the brain are functionally different

  • certain mental processes are mainly controlled by a particular hemisphere
  • eg language is controlled by the left hemisphere
  • suggests language is subject to hemispheric lateralisation
  • questions whether other neural processes may be organised this way
  • investigated in series of experiments conducted by Sperry via split brain research
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25
Q

split brain research

A
  • series of studies (began in 60s)
  • involving epileptic pxs who had undergone cerebral commissurotomy (surgical lesioning of the corpus callosum) to control epileptic seizures
  • where info processed by 1 hemisphere can’t be relayed onto the other
  • allowed Sperry to investigate the extent to which brain function is lateralised
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26
Q

split brain research
PROCEDURE

A
  • image/word projected to px’s RVF (processed by LH)
  • and same or different image/word projected to px’s LVF (processed by RH)
  • in the ‘normal’ brain, the corpus callosum would immediately share info between both hemispheres
  • however, in a split brain, info cannot be conveyed between hemispheres
27
Q

split brain research
DESCRIBING WHAT YOU SEE

A
  • when object shown to RVF, they could easily describe what was seen
  • but when same object shown to LVF, they reported that nothing was there

why?

  • language is processed in LH
  • so px’s inability to describe objects in LVF is due to the lack of language centres in the RH
  • info couldn’t be relayed to LF via corpus callosum
28
Q

split brain research
RECOGNITION BY TOUCH

A
  • when objects shown to LVF
  • pxs couldn’t name them but could select a matching object using left hand

why?

  • LH is needed to verbally identify the objects
  • but could understand what the object was using the RH
29
Q

split brain research
COMPOSITE WORDS

A
  • when 2 words presented simultaneously, 1 to either VF
  • eg, key on the left + ring on right
  • px would select key with their left hand
  • and they would say the word ‘ring’

why?

  • LVF goes to RH which controls left hand
  • RVF goes to LH which controls language
30
Q

split brain research
MATCHING FACES

A
  • when composite picture made of 2 halves of a face presented
  • the LH dominated verbal description
  • RH for selecting matching picture

why?

  • RH = dominant in recognising faces
  • LH
31
Q

split brain research
AO3

A

theoretical basis for discussion

  • Sperry’s work triggered a theoretical + philosophical debate regarding the** nature of consciousness** + the degree of communication between the 2 hemispheres in everday functioning
  • Pucetti suggested the hemispheres are so functionally different, they represent a form of duality in the brain, implying we are 2 minds
  • others argued the hemispheres are highly integrated + work together

strengths of methodology

  • use of highly specialised + standardised procedures
  • to present visual info to 1 hemispheric field at a time
  • ppts asked to stared at fixation point w 1 eye + image flashed for 0.1s
  • so ppts had no time to move their eye across the image + spread info to both sides of the visual field
  • this allowed Sperry to vary aspects of the basic procedure + ensure only 1 hemisphere received info at a time

clearly demonstrates lateralised brain function

  • Sperry’s work has produced an impressive body of research findings
  • has been pivotal in establishing difference in function of the 2 hemispheres
  • and also opposing the holistic theory of brain function
  • concludes that LH is analytical + verbal (analyser) whilst the RH is adept at spatial tasks + music (synthesiser)
  • HOWEVER, recent research suggests that this distinction may be oversimplified
  • many behaviours associated w 1 hemisphere can also be carried out by the other when situations require
  • suggests that Sperry may have overstated differences between the 2 hemispheres

issues w generalisation

  • split-brain patients constitute such an unusual sample of people
  • there were only 11 individuals who took part in all variations of the procedure + they all were epileptic patients w a history of seizures
  • this may have caused unique changes to the brain that may have influenced findings
  • limits the extent to which finding can be generalised to the wider population
  • lowers validity
32
Q

brain plasticity

A

brain’s tendency to change + adapt as a result of experience + new learning

  • during infancy, brain experiences rapid growth in no of synaptic connections
  • synaptic pruning: as we age, rarely used connections are deleted + frequently used ones are strengthened
  • originally thought that synaptic pruning was restricted within childhood + adult brain would remain fixed in terms of function + structure
  • however, more recent studies suggest that at any time in life, existing neural connections can change or new ones can be formed
33
Q

brain plasticity research
Maguire

A
  • studied brains of London taxi drivers
  • found significantly more volume of grey matter in posterior hippocampus than in matched control group
  • this part of the brain is associated w development of spatial + navigational skills
  • they require these skills because as part of their training, taxi drivers have to take the Knowledge test, which assesses their recall of city streets
  • found a positive correlation between an increase in grey matter volume + the amount of time they had been a taxi driver
34
Q

brain plasticity research
Draganski

A
  • imaged brains of medical students 3 months before + after their final exams
  • learning-induced changes seen in posterior hippocampus + parietal cortex as a result of the exams
35
Q

brain plasticity research
Michell

A
  • found a larger parietal cortex in brains of people who were bilingual compared to matched monolingual controls
36
Q

functional recovery

A
  • form of plasticity, following damage through trauma
  • brain’s ability to redistribute functions usually performed by a damaged area to other unaffected areas
  • can happen quickly after trauma - spontaneous recovery - and then slow down after several weeks/months
  • may need rehabilitative therapy at this point to further their recovery

what happens in the brain during recovery?

  • brain is able to rewire + recover by forming new synaptic connections
  • and secondary neural pathways that aren’t typically used are activated, enabling functioning to continue

this process is supported by a no. of structural changes in the brain:

  • axonal sprouting - growth of new nerve endings which connect w other undamaged nerve cells to form new neural pathways
  • reformation of blood vessels
  • recruitment of similar areas - on opposite side of brain to perform specific tasks
37
Q

brain plasticity
ao3

A

practical application

  • understanding processes involved in plasticity has contributed to the field of neurorehabilitation
  • techniques including movement therapy + electrical stimulation of the brain are used to counter deficits to cognitive functioning following a stroke

research support in animal studies

  • when 1 eye of a kitten was sewn shut
  • analysis of brain’s cortical response found area of visual cortex, associated w the shut eye, was not idle but continued to process info from open eye
  • shows how loss of function leads to compensatory activity in the brain
  • provides evidence for neural plasticity
  • HOWEVER, can’t generalise cats to humans

negative plasticity

  • brain’s ability to rewire itself can have maladaptive behavioural consequences
  • eg prolonged drug use has been shown to result in poorer cognitive functioning + increased risk of dementia
  • and a lot of amputees experience phantom limb syndrome which is often painful + unpleasant
38
Q

investigating the brain
fMRI

A
  • works by detecting changes in blood oxygenation + flow that occur as a result of neural activity in specific parts of brain
  • when brain area is more active, it consumes more oxygen
  • so to meet this increased demand, blood flow is directed to active area - haemodynamic response
  • produces 3D images (activation maps) showing which parts of the brain are involved in particular mental process
  • has important implications for understanding of localisation of function
39
Q

fMRI
ao3

A

doesn’t’ rely on radiation

risk-free, non-invasive + straightforward

✔ produces images w a high spatial resolution
- details by the mm

expensive compared to other neuroimaging techniques

poor temporal resolution
- 5 second time lag between initial firing of neuronal activity and the image on the screen

✘ person has to be perfectly still to capture clear image

can only measure blood flow
- can’t hone in on activity of individual neurones so difficult to tell what Kind of brain activity is being represented

40
Q

investigating the brain
EEGs

A
  • record of electrical impulses produced by brain’s activity
  • measures electrical activity within brain via electrodes that are fixed to a person’s scalp using a skull cap
  • scan recording represents brainwave patterns generated from the action of millions of neurons
  • providing overall account of brain activity
  • often used by clinicians as a diagnostic tool as unusual arrhythmic patterns of activity may indicate neurological abnormalities e.g. epilepsy, tumours, sleep disorders
41
Q

EEGs
ao3

A

✔ extremely high temporal resolution
- accurately detects brain activity at a resolution of a single millisecond

✔ contributed to understanding of sleep stages

✘ generalised nature of info received
- EEG signal not useful for pinpointing exact source of neural activity - poor spatial resolution
- doesn’t allow researchers to distinguish between activities originating in different but adjaecent locations

42
Q

investigating the brain
ERPs

A
  • event-related potentials
  • EEG data contain all the neural responses associated w/ specific sensory, cognitive + motor events
  • these responses are isolated using a statistical averaging technique
  • ERPs are what is left when all extraneous brain activity from an EEG recording is filtered out
  • leaving only those responses that relate to the presentation of a specific stimulus or performance of a certain task
  • research has revealed many different forms of ERP + their link to cognitive processes
43
Q

ERPs
ao3

A
44
Q

investigating the brain
post-mortem examinations

A
  • analysis of a person’s brain following their death
  • usually those w a rare disorder + have experienced unusual deficits in mental processes or behaviour during their lifetime
  • areas of damage in the brain are examined after death as a means to establish the likely cause
  • may involve comparison w a neurotypical brain to see extent of difference
45
Q

post-mortem examinations
ao3

A
46
Q

biological rhythms

A
  • all living organisms are subject to bio rhythms
  • these are changes in body processes or behaviour in response to cyclical changes within the environment

all rhythms governed by 2 things:

  • endogenous pacemakers: body’s internal biological clock
  • exogenous zeitgebers: external changes in environment
47
Q

bio rhythms
CIRCADIAN

A
  • last around 24 hours
  • eg sleep wake cycle
48
Q

circadian rhythms
SLEEP-WAKE CYCLE

A
  • feel drowsy when it’s night
  • alert during day
  • demonstrates effect of daylight - exogenous zeitgeber
49
Q

sleep-wake cycle
SIFFRE

A
  • spent extended periods underground to study the effects on his own bio rhythms
  • deprived of exposure to natural light + sound
  • spent 2 months underground before resurfacing
  • a decade later, he spent 6 months underground
  • in each case, his rhythm settled to one that was around 25 hours
  • he did have a regular sleep-wake cycle
50
Q

sleep-wake cycle
ASCHOFF & WEVER

A
  • got a group of ppts to spend 4 weeks in a WWII bunker
  • deprived of natural light
  • all but 1 ppt displayed a circadian rhythm between 24-25 hours

both studies suggest that the ‘natural’ sleep-wake cycle may be slightly longer than 24 hours but is entrained by EZs associated w our 24 hour day
(eg no of daylight hours, typical meal times)

51
Q

sleep-wake cycle
FOLKARD

A
  • got a group of people to spend 3 weeks in a dark cave, going to bed and waking up at certain times
  • over course of study, researchers gradually sped up the clock, without the ppts knowing
  • so 24 hour day eventually only lasted 22 hours
  • only 1 ppt was able to comfortably adjust to this new regime
  • suggests the existence of a strong free-running circadian rhythm that can’t be easily overridden by changes in the environment
52
Q

circadian rhythms
AO3

A

✔ practical application

✘ use of case studies + small samples

✘ poor control in studies

-

53
Q

bio rhythms
INFRADIAN

A
  • last longer than 24 hours
  • eg menstrual cycle, SAD
54
Q

infradian rhythms
MENSTRUAL CYCLE

A
  • lasts about 28 days
  • rising levels of oestrogen cause the ovary to develop + release an egg (ovulation)
  • then, progesterone helps womb lining to thicken, preparing body for pregnancy
  • if pregnancy doesn’t occur, egg is absorbed into body + womb lining comes away + leaves the body (menstrual flow)
55
Q

menstrual cycle
STERN & MCCLINTOCK

A
  • studied group of women w irregular periods
  • phermones were taken from some at different stages of their cycle via a cotton pad under their armpits
  • these pads were cleaned w alcohol + later rubbed on upper lips of other ppts
  • 68% of women experienced changes to their cycle that brought them closer to the cycle of their ‘odour donor’
56
Q

infradian rhythms
SAD

A
  • circannual cycle
  • depressive disorder w a seasonal pattern
  • symptoms triggered during winter months when no. of daylight hours becomes shorter
  • during the night, the pineal gland secretes melatonin until dawn when there is an increase in light
  • during winter, lack of light in morning means secretion goes on for longer
  • has a knock-on effect on production of serotonin in the brain
  • low levels of serotonin associated w low mood
57
Q

infradian rhythms
AO3

A

✔✘

58
Q

bio rhythms
ULTRADIAN

A
  • last less than 24 hours
  • eg stages of sleep
59
Q

ultradian rhythms
STAGES OF SLEEP

A
  • psychologists identified 5 distinct stages of sleep
  • each stage characterised by diff level of brainwave activity
  • monitored using EEG

stage 1 + 2:

  • light sleep, person is easily woken
  • beginning → brainwave patterns start to become slower and more rhythmic (alpha waves)
  • becoming even slower as sleep becomes deeper (theta waves)

stage 3 + 4:

  • delta waves → slower + have greater amplitude
  • deep sleep or slow wave sleep
  • difficult to rouse someone

Stage 5 REM:

  • body = paralysed yet brain activity speeds up, resembling awake brain
  • REM activity correlates w/ dreams
60
Q

ultradian rhythms
AO3

A
61
Q

endogenous pacemakers

A
62
Q

exogenous zeitgebers

A
63
Q
A