Psychobiology Flashcards
Brains job
-takes in info from outside world, perform computations/processes it and produces effects/outputs/behaviours
Peripheral nervous system
- Automatic:CNS -> motor neurone -> internal environment -> sensory neutron -> CNS
- Somatic: CNS -> motor -> external env. -> sensory -> CNS
- sensory neurones: input from skin, output to spinal cord
- motor neurones: input from brain, output to muscles
- parasympathetic system: rest or digest, conserve energy, slows HR
- sympathetic system: fight or flight, rapid involuntary response to danger/stressful situations, raise HR
Brain regions/brain slicing
Anterior: in front of Posterior: behind Superior: above Inferior: below Medial: towards midline Lateral: towards side Coronal Sagittal Horizontal
Brain structures
Brain stem: midbrain, pons, medulla
Forebrain: central hemisphere, diencephalon (thalamus, hypothalamus)
Cerebellum
Spinal cord
Cerebellum
Layered organised structure
Involved in refining movements and thoughts
Diencephalon
Bilateral structure
Thalamus: information hub, relays info from widespread brain areas
Hypothalamus: regulates homeostatic processes, connects to pituitary gland
Cerebrum
sub cortical structures
Hippocampus
Basal ganglia
Amygdala
Olfactory bulb
Hippocampus
Inputs: mid brain, cortex, projection nuclei
Outputs: cortex, amygdala, thalamus, ventral striatum
Computations: associative learning, spatial memory
Basal ganglia
Inputs: cortex, hippocampus, substantia nigra
Outputs: thalamus, substantia nigra
Computations: coordinating movement and motivated behaviour
Amygdala
Inputs: cortex, hippocampus, thalamus, brainstem
Output: cortex, basal ganglia, hypothalamus, brain stem
Computations: emotional learning
Ventricles
Contain cerebrospinal fluid, produced from ependymal cells lining ventricles
Circulated around brain, meninges, blood vessels and small extracellular space around neurones
Clears brain of unwanted products
Blood supply in brain
Specialised blood supply that’s self regulated
Brains highly vascularised
Functional MRI measures increase in oxygenated blood flow
Brain cell types
Neurones Glia: Astrocytes Oligodendrocytes Microglia
Neurones
Information transmitting brain cell
Transmit and process info using electrical signals
Made up of dendrites, soma, myelin sheath, axon terminal
Different shapes indicate different functions
Glia
Astrocytes: wrap processes around neurones, supportive roles
Oligodendrocytes: wrap myelin sheath around axon to insulate
Microglia: resident immune cell, survey brain for infection and damage, destroy/eat damage or infection
Labelling cell types
-fill with dye by inserting an electrode and allowing dye to diffuse in
-label with antibodies which attach to proteins specific to cell
Genetically modify mice to express fluorescent protein that expresses specific proteins
Electricity and corpses
Galvanic process
Electricity applied to corpse face, muscles contorted
Electricity applied to corpse body result in hand being raised and clenched
Electricity
-flow of charged particles
-current only flows through material that conducts electricity
Ohms law:
-current = potential x conductance
-current = potential / resistance
-potential: voltage difference, stored electrical energy
Concentration gradient across axon membrane
Outside of membrane there is more positive ions eg Na+, Cl+, Ca+
Inside membrane is K+, and negatively charged proteins
Electrochemical gradient created and maintained by Na+/K+ ATPase, pumps 3 Na+ out and 2 K+ in
Membrane potential is set by electrochemical gradient and permeability of membrane to ions
resting potential
outside cell is more sodium and little potassium
inside cell is more potassium, little sodium
electrochemical gradient as there is more positive ions on outside of cell
ATPase pump manages resting potential, pumps out 3 sodium ions, and in 2 potassium ions
action potential is a …
wave of transient depolarisation that travels down axon
measured using voltmeter
key concepts about ion channels
- holes in membrane
- allow ions to pass into and out of cell
- selective ions
- opened by different stimuli
- ions flow down electrochemical gradients
action potentials:
convey …
generated by …
occur when …
- convey fast signals from one place to another
- generated by changes in membrane permeability (opening and closing of voltage gated channels)
- self regenerating
- only occur if reach threshold
action potential events
- threshold reached
- depolarisation of membrane (sodium channels opened)
- repolarisation of membrane (sodium channels close, potassium channels open)
- hyperpolarisation as voltage-gated potassium channels still open
all or nothing principles
-for action potential to occur voltage inside membrane must reach that of threshold otherwise no actin potential
action potential propagation
- same size all along
- as move along, depolarises next section of membrane and opens up the next voltage gated sodium channels
- if enough channels open, reach threshold potential and action potential propagates along
absolute refractory periods
all sodium channels inactivated
one-way transmission
relative refractory period
some sodium channels inactivated
only strong stimuli can re-open channels and generate action potential
saltatory conduction
- only in myelinated axons
- action potential jumps from node of ranvier to the next
- depolarisation only occurs at node of ranvier
- faster and more efficient than unmyelinated actions
synapse events
- action potential arrives at pre synaptic cell, opens calcium voltage gated channels
- influx of calcium causes vesicles containing neurotransmitters to fuse with membrane and release them into synaptic cleft
- neurotransmitters bind to post synaptic ligand-gated channels
- ligand gated channels open and sodium ions diffuse into post synaptic neurone
- depolarisation creating new impulse
excitatory and inhibitory action potentials
excitatory: makes action potential more likely to happen by allowing positive charged ions to diffuse into post-synaptic neuron
inhibitory: makes action potentials less likely to happen by allowing negatively charged ions to diffuse into post-synaptic neuron
excitation in post-synaptic membrane
- depolarisation of dendrites
- glutamate binds to AMPA receptor causing it to open allowing sodium ions to diffuse through
- generates excitatory post synaptic potential
summation
- temporal summation: many action potentials from one neuron, increases the amount of neurotransmitter in synaptic cleft
- spatial summation: many neurons active at same time, combine to reach threshold
post synaptic membrane inhibition
- GABA is main inhibitory neurotransmitter in brain
- opens chloride channels allowing negative charge into cell, hyperpolarising membrane making ti harder to reach threshold
- generates inhibitory post-synaptic potential
anxiety: clinical aspects
- feeling of fear or dread
- psychiatric literature: term anxiety used in situations where there is ‘no reasonable’ external cause fro anxiety and fear
- clinical anxiety refers to anxiety that’s ‘pathologically’ interfering with other activities and priorities
- symptoms: fear (panic/phobia), worry (anxious misery, apprehensive expectations, obsessions)
drug treatments of anxiety
- alcohol (self medicated)
- barbiturates, mepobromate: low therapeutic index, induces tolerance and dependence
- benzodiazepine: anxiolytic effect, induce dependence
- selective seratonin reuptake inhibitors: first line pharmacological treatment, delayed onset of action
expectations of psychopharmacological treatments
- disease centred: suggests drug restores normal function
- symptom centred: suggests drug produces specific change in aspects of mood, motivation, cognition and makes condition less disabling
GABA synapse and benzodiazepine
- GABA binds to receptor causing chloride ion pore to open, inhibiting action potential
- GABA receptor: separate binding sites for alcohol, barbiturates and benzodiazepine
- benzodiazepine enhances effect of GABA
- benzodiazepine sensitive receptors are selectively expressed in specific brain areas such as hippocampus and amygdala (mouse brain)
GABA receptor subtypes
- made up of 5 subunits, each coded for by different genes
- variety in structure alters sensitivity to benzodiazepine
- GABA a receptor is ionotrophic (ligand gated channel)
- GABA b receptor is metobotrophic (g protein coupled receptor)
fear and amygdala
fear conditioning
-tone played creates small increase in blood pressure and brief startle response
-tone preceded by mild footshock, larger increase in blood pressure and freeze response
-tone elicits increase in blood pressure and freezing
-condition process greatly reduced in rats with damage to amygdala
PET imaging
-subjects given stroop test with fear related words
-fear related words produce greater activation of amygdala (suggest structure involved with processing linguistic coded threat stimuli)
fear circuit
-output from amygdala can modulate aspects of fear including processing fear stimuli, hormonal changes and autonomic symptoms
noradrenaline and fear circuits
- peripheral stress hormone and central neurotransmitter
- hindbrain contains noradrenergic cell bodies that project forwards to cortex and subcortical structures eg amygdala
- selective chemogentic stimulation of cell bodies delays extinction of simple response in rats
- effect blocked by propanolol, noradrenergic beta receptor antagonist
worry circuits
- complex neural loops run between cortex, striatrum and thalamus
- responsible for modulation of motor output and cognition
- dorsolateral prefrontal cortex important in worry and anxiety
benzodiazepine and modulation
- may modulate GABA-ergic inputs to amygdala
- may modulate GABA-ergic inputs in CSTC worry loop
overlap of anxiety and depression
- many of the same symptoms present in anxiety and depression
- overlap in drugs that are effective at treating anxiety and depression
non-benzodiazepine anxiolytics
- selective seratonin reuptake inhibitors: enhance sertonergic inhibition in the amygdala
- buspirane: serotonergic drug with different mechanism
- modulators of voltage gated calcium channels: reduce excitatory glutamate transmission
- noradrenergic antagonists: reduces inputs taht enhance vigilance in hippocampus and amygdala
recreational drugs
varied groups of compounds:
- nicotine, alcohol, hallucinogens, cannabis, psychostimulants, opiates
- widespread use in human cultures
- use frequently associated with addiction, tolerance, dependence and withdrawal
addictive behaviour
definition: “loss of control over form of behaviour pleasurable to most” “excessive appetite”
- suggests separation of liking and wanting; basis of some psychological theories of addiction
drugs and their neurotransmitter receptors
nicotine -> subtype of acetylcholine receptor
alcohol -> modulates GABA receptors, opioid receptors
opiates -> opioid receptors
MDMA -> seratonin 2A receptors and seratonin transporter
cocaine -> dopamine receptor
amphetamine -> releases dopamine
barbiturates -> modulate GABA a receptor
cannabis -> cannabinoid CB1 receptor
recreationally used drugs are likely to …
interact with specific neurotransmission systems, often by mimicking a natural neurotransmitter
place preference task
- one compartment associated with drug administration (morphine or control)
- other compartment had no association
- rat moves freely between
- transgenic mouse without opioid receptors fail to learn task
- normal mouse shows preference for morphine compartment
cocaine
obtained from leaves of coca shrub
blocks dopamine transporter
-increase levels at synapse
-local anaesthetic resemblances lidocaine
amphetamine
- first synthesised in 1887
- psychotrophic effects not discovered until 1920
- clinical uses eg narcolepsy
- used recreationally at higher doses
- widely used as decongestant
- enhances dopamine release, reduces reuptake
psychostimulants and dopamine receptor
- dopamine is released into synaptic cleft, taken up by transporter, reincorporated into vesicles by vesicular monoamine transporter
- cocaine and amphetamine block dopamine transporters preventing reuptake
- amphetamine stimulates release of dopamine by displacing vesicles
cannabis: components, mechanisms and mimics
components:
-∆9-tetrahydrocannabidol (THC) (major psychoactive component)
-cannabidiol (diff pharmacological properties)
-canabigerol (precursor with own activity)
mechanisms:
-CB1 mostly CNS
-CB2 mosty peripheral
-TRPV1 capsacin acts here also
mimics:
endogenous neurotransmitters: anadamide, 2-arachidonoglycerol
synthetic cannabinoids
- originated from work of huffman
- ∆9-THC high affinity, low efficacy, partial agonsit
- full agonist, max stimulation, high efficacy
- partial agonist, smaller effect at larger doses, compete with full agonist and reduce effect-moderate efficacy
- antagonist, negligible effect, by competition at receptor reduce effect of partial and full agonists
dopamine and reward
- many abused drugs lead to activation of brain dopamine systems
- natural rewards such as palatable food, may also lead to activation of same systems
cocaine craving and brain receptors
- neutral or cocaine associated images rate their craving, craving significant when seeing cocaine associated images
- blood flow to prefrontal cortex and medial temporal lobe increased
- activation of ventral striatum and other structures of basal ganglia
mesolimbic dopamine system activation
- activated by range of natural rewards even those with cognitive elements
- imaging study and laughter activated motor areas and other cortical areas
treating drug addiction
- substitute one drug for another thats less rewarding
- block effects of drug with antagonist or partial agonist
- naltrexone helpful is reducing heavy drinking
- variety of behavioural strategies
psychoactive drugs
acts to alter mood, thought or behaviour, used to manage neuropsychological illness and/or is abused
Analysing visual scene
- cornea and lens focus inverted image on retina
- specialised cells in refine transducer physical energy of light into depolarisation of retinal ganglion cells resulting in action potentials in optic nerve
- retinal circuitry is complex, rod and cones hyperpolarised by light and have resting potential closer to 0mV
Optic nerve projects to lateral geniculate nucleus
- optic nerve fibres from nasal half of retina cross midline, projecting contralaterally but those from temporal half of retina project ipsilaterally and do not cross at optic chiasm
- animals with laterally places eyes have minimal crossing over
- damage to optic nerve on right side lead to loss vision of eye
- damage to optic tract on right side lead loss peripheral vision
Dorsal and ventral stream
Dorsal stream goes to posterior parietal cortex
Ventral stream goes to inferior temporal cortex
Identifying an object and remembering where it came from
Projections from brainstem to cortex are important in maintaining attention and arousal-like processes
Moving the eyes
-making a saccade (rapid movement of eye between fixation points)
supplementary area is rostral to motor cortex (involved in planning of movement)
-frontal eye fields have role in voluntary control of gaze distribution
How a Saccade occurs
Critical structures : caudate nucleus, putamen, globes pallidus, substantia nigra
- substantia nigra cells firing away until there’s a pause where cells in caudate and superior colliculus fire
- the disinhibition of superior colliculus by pause of firing of cells within substantia nigra leads to saccade
Cortico striato thalamo cortical loops
- Motor loop and oculomotor loop both have additional cortical output to brainstem motor control areas
- three further loops connect cortical area involved in cognition and emotion with basal ganglia
Parts of motor loop
Cortical input: motor, premotor, somatosensory cortex
Striatum: putamen
Pallidum: lateral globes pallidus, internal segment
Thalamus: ventral lateral and ventral anterior nuclei
Parts of oculomotor loop
Cortical input: posterior parietal, prefrontal cortex
Striatum: caudate (body)
Pallidum: globes pallidus, internal segment, pars reticulata (sub nig)
Thalamus: mediodorsal and ventral anterior nuclei
Function of basal ganglia in relation to motor control
Initiation and termination of actions
Selection of actions
Relating actions to reward or reinforce value
Penfields ‘motor homunculus’
map of brain involved with motor processing- electrical stimulation of human motor cortex
Area lies at back of frontal cortex, adjacent to central sulcus
Some areas such as for hand movement are larger