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What are the divisions of the Nervous System
human nervous system: Body wide system of nerve cells that collect information from the world, processes then takes action by directing organs and muscles via transmission of electro chemical messages.
Central nervous system: Complex processing
Spinal cord: receives and transmits, reflex processing
Sympathetic: increased heart rate, sweat breathing noradrenaline release, activates fight/flight
Homeostasis: Internal environment is balanced between sympathetic and parasympathetic systems.
Peripheral nervous system (PNS): Messenger Nerones: Sensory (afferent) and motor (efferent)
Autonomic (ANS): Controls actions of internal glands, involuntary system
Somatic (SNS): Controls skeletal muscles, voluntary system
Parasympathetic: decreased heart rate, sweat, breathing, Acetylcholine release, activates rest/digest
Structure and function of neurones
The sensory neurone detects sensations at sensory receptors, an action potential travels along the myelinated axon.
The electrical signal is converted into a chemical signal at the synapse.
The relay neurone detects the signal and forms a new action potential, sending signals to both the CNS and motor neurone.
The motor neurone detects the signal from the relay neuron (synaptic transmission) and this signal travels down its own myelinated axon
The signal reaches an effector, this could be a muscle group in an arm (moving it away from the source of pain)
Synaptic transmission
The synapse: located at the end of a nerve cell (neurone), it allows communication between neuron’s by transmitting chemical signals.
Neurotransmitters: The chemical messengers released from neurones. These either make the development of an action potential in the post synaptic cell more likely to form (excitatory) or less (inhibitory).
Process: Action potential travels down the axon of the presynaptic neuron. Vesicles release neurotransmitters into the synaptic cleft, they are detected by receptors on the post synaptic neurones membrane. Summation is the combined effect of excitatory/ post-synaptic neurone and the message has been passed on. The neurotransmitters detach from the receptors and transport proteins return the neurotransmitters to the presynaptic cell via reuptake.
The Endocrine system
collection of glands that release hormones that regulate bodily functions and psychological factors.
Pituitary (master gland): ACTH: controls the release of other hormones.
Pineal: Melatonin: modulates sleep
Pancreas: insulin: regulates sugar levels
Testis: testosterone: secondary s*xual characteristics and linked to aggression.
Adrenal: see fight or flight
fight or flight response
evolutionary survival threat response
Stressor is detected by hypothalamus, triggers the endocrine system releasing cortisol and the sympathetic ANS releasing adrenaline.
Psychological effects of adrenaline: increased anxiety, attention and alertness. Physical: increased blood flow to brain and muscles (quick thinking/reactions), dilated pupils, increased breathing rate. decreased blood flow to skin and digestive and immune systems.
Maladaptive to demands of the modern world.
Localisation of function in the brain
Localisation of the function is the belief that functions of the brain are performed in distinct areas
Hemispheric lateralisation: each hemisphere is specialised. E.g. language centres in the left and visuospatial tasks are best performed by right.
Motor cortex: voluntary muscle movements contralateral. Damage = on opposite side… if mild: muscle weakness, if severe: paralysis on opposite side.
Somatosensory cortex: receives sensations from opposite side of body, damage leads to a loss of sensation/numbness.
Broca’s area: left frontal lobe only, for speech production, damage can lead to expressive apashia (difficulty producing fluent speech)
Wernickes area: left temporal lobe only. Speech comprehension, damage can lead to receptive aphasia (difficulty understanding speech)
Auditory cortex: In both hemispheres. Contralateral, receives and processes sound info. Damage on one side can lead to difficulty isolating locating sound, damage on both sides can lead to cortical deafness
Visual cortex: Occipital lobe, both sides. visual processing of opposite visual field
Localisation of function in the brain AO3
Large numbers of clinical case studies demonstrate loss of functions if damage to a particular brain location. E.g. Broca and Wernickes case studies (aphasia) and Clive Wearing (amnesia = severe damage to hippocampus)
Modern FMRI studies support case studies using healthy brains
The historical use of case studies in location of function research Is seen as unscientific as damage often covers multiple areas.
There are many brain functions that appear not to be localised like consciousness and memory storage
Plasticity and functional recovery
Plasticity: the brain adapts in function and structure due to change in the environment. Damage/learning
Functional recovery: undamaged areas take over functions that used to be performed by damaged areas.
Synaptic pruning: Synapses that are used frequently get stronger, unused synaptic connections are lost.
Denervation super sensitivityL Remaining axons in a pathway become more sensitivity: Remaining axons in a pathway become more sensitive to compensate for lost axons.
Factors affecting recovery, children and women recover better.
A03 Plasticity and functional recovery
Maguire: MRI 16 taxi drivers who took “the knowledge” had significantly larger posterior hippocampi than controls.
Danelli: Case study: at 2 yo, EB has a left side hemispherectomy removing Broca and Wernickes. EB recovered language ability in 2 yrs.
Practical applications: Constraint induced therapy stopping clients using coping strategies makes them improve (functional reorganisation)
Mathia meta analysis, not everyone has high levels of plasticity, some P’s have high levels of cognitive reserve (TQ and education are correlated)
Split brain research
The brain is contralateral, each hemisphere controls the opposite side of the body. The hemispheres are connected by the corpus collosum. 200-300 million nerve fibres. Cutting this was a treatment for epilepsy.
Sperry studied 11 “split brain” P’s who had a corpus callosotomy. Showing a different image to each visual. (sending info to opposite hemisphere.) P’s were asked to say what they had seen/draw/select.
Sperry FOUND only info presented to left hemisphere could be spoken (location of the speech centre) right hemisphere could select items.
This suggests both hemispheres are capable of independent awareness and action. Additionally language centres are on left Hem.
Gazzanigas’s split-brain research each hemisphere shown faces. FOUND right hemisphere is specialised for facial recognition.
Split brain research AO3
Small sample size: P’s had varying amount of connection cut and had all taken drug therapy and the control group were not epileptic.
Experimental procedure was unusual the p’s lived normal lives, moving their heads from side to side so both hemispheres had the same visual info
This research has had a large impact on psychology and philosophy as it challenges ideas about the unity of consciousness and identity.
Ways of studying the brain + AO3
FMRI: detects blood flow in the brain, as more active areas need more blood they can be compared to low activation areas when P’s are doing tasks.
Good spatial resolution (1mm), non invasive and safe
Poor temporal resolution, one image every few seconds.
EEG: 22-34 electrodes attached to a cap. Read out is sum of activation under the electrode. Displays brain waves
Good temporal resolution 9ms), cheaper than FMRI
Poor spatial resolution and can’t see deep activation
Event-related potentials (ERP): same equipment as EEG, but presents stimulus multiple times, creating smooth curve of activation by statistical averaging (removing background noise
Can isolate and study individual cognitive processes, good temporal resolution
Poor spatial resolution, some processes cannot be presented multiple times.
Post mortem examinations: Brains are precisely cut after treatment (to give firm texture). The structure of unusual brains (trauma/mental illness) are compared to healthy brains. E.g. Brocas area was identified by post mortem,
High spatial resolution, down to microscopic brain structures/ neuronal level.
Not on living brain so no activation, damage and behaviour is correlational
Biological rhythms - Circadian rhythms
Circadian rhythm lasts around 24 hours (e.g. sleep/wake, release of hormones, body temperature and blood pressure) Endogenous pacemakers are internal body clocks that keep biological processes to time. Exogenous zeitgebers (EZ) are external cues that set internal body clocks.
In the sleep wake cycle, the EP is the suprachiasmatic nucleus, when it detects light it sends a signal to the pineal gland, stopping the production of melatonin.
Social cues and clocks may also be EZ’s.
Siffre: lived in a cave for 6 months (no natural light). Body clock maintained a cycle of around 25 hours. Evidence for EP
Vetter FOUND workers exposed to blue light shifted the timing of their CR, this could lead to practical applications, understanding blue lights could help
Lights may have acted as an EZ, disrupting the EP, studies that controlled for articial light found 24 hour cycle
Biological rhythms - Infradian rhythm
Infradian rhythm lasts longer than 24 hours (e.g. Seasonal affective disorder and the menstrual cycle.
In the 28 day menstrual cycle the levels of hormones, oestrogen and progesterone act as EP’s. It is argued the pheromones of other women can act as EZ’s
Stern and McClintock 20 women wiped pads from armpits of other women on their top lip (daily), lengthened/shortened their cycles to match, supporting pheromones as EZ’s.
Trevathan: co-habiting lesbians didn’t match cycles.
Biological rhythms - Ultradian rhythm
Ultradian rhythms last less than 24 hours.
The stages of sleep: 90 mins /3-5 times per night. N1 easy to wake and sudden body movements, N2 harder to wake, body relaxed heart rate body temp decreased. N3 deepest, very difficult to wake, REM = dreams, body is paralysed (brain EEG is very active)
Dermot and Kleitman: EEG of 33 P’s while sleeping. Brain waves followed cyclic pattern, body relaxed in low wave sleep (N3) and high activation in REM. Supports stages
Significant individual differences newborns spend 80% of sleep in REM
Longest part of REM sleep matches lowest point of circadian body temp cycle, they may not be different cycles but use the same EP the SCN.