Module 2
NEUR2201 - Summary Notes (Module 2)
Neuroscience Fundamentals (University of New South Wales)
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Studocu is not sponsored or endorsed by any college or university
REAL-TIME NEURAL MEASUREMENTS
Direct Measures Measures electrical activity of neurons | Indirect Measures Tells us where neurons are active BUT does NOT indicate if neurons are excitatory/inhibitory |
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Explain what a real-time neural measurement is, and provide three examples including the temporal and spatial resolution of each of the measurements.
Real-Time Neural Measurement: measures neural activity at a rate that keeps up with the speed of the activity being monitored
Spatial Resolution: one neuron or less (direct) | Spatial Resolution: groups of neurons (direct) | Spatial Resolution: groups of neurons (indirect) | |
Temporal Resolution: one action potential/less |
- EPSP/IPSP; soma)
|
| - EMG (evaluates condition of muscles and motor neurons which control them) |
Temporal Resolution: several action potentials | - Voltage-sensitive dyes (dye changes its fluorescence as electrical potential inside cell changes) | - Neurochemical measurements (electrochemistry) |
|
Microelectrode Recording: direct, one neuron, one action potential/less, invasive
Determine neural coding strategy
Determine if binding uses gamma waves
EEG Recording: direct, groups of neurons, one action potential/less, non-invasive (awake human subject)
Diagnose conditions - epilepsy, sleep disorders and brain tumours
Locating a sensory brain region
Transduction: stimulus-alerting events wherein a physical stimulus is converted into an action potential, which is transmitted along axons towards the CNS for integration; part of sensory processing
Stimulus
Change in ionic permeability of receptor cell/afferent nerve ending
Change in membrane potential – receptor potential
Generation of action potentials in afferent nerve terminal
Propagation of action potentials to CNS
Ionotropic (ligand-gated) | Metabotropic (G-protein coupled receptors) |
|
|
Briefly explain how photon capture causes a change in membrane potential in the photoreceptor. Photoreceptors: receptor cells that enable transduction; contain opsin and retinal
In vision, retinal captures a photon and dissociates, activating opsin (GPCR)
Activated opsin interacts with phosphodiesterase → reduction in concentration of cGMP
In the dark, transmitter is released | In the light, transmitter release is reduced |
|
|
Neural Code: uncovering the meaning behind the activity of a given neuron → insight into cognition
Time based codes contain MORE information than counting based codes
How to design an experiment that studies neural coding:
Add sensory input, record animal’s perception/behaviour, record neuronal activity
Measure three languages using real-time measurement
Can record at different levels of nervous system
Peripheral afferent neuron synapses in brain stem
Brain stem neuron synapses in thalamus
Thalamic neuron synapses in sensory cortex
Orientation-Selectivity (in cortical neurons): emerges from their convergent inputs
Retinal ganglion cells - respond to spots/rings of light (have concentric visual fields) – NO response that relates to the orientation of a bar of light
ON centre cell: excitatory center, inhibitory surround
OFF centre cell: inhibitory center, excitatory surround
Cortical neurons - sensitive to bar orientation – this is an emergent property of these cortical cells which is NOT present in their input neurons
Brain has a modular organisation – composed of distinct sections defined by function/histology.
Module: brain area in the hierarchy; can be organised into:
Hierarchical – each module performs DIFFERENT task but works on TOTAL scope of job
Parallel – each module performs SIMILAR tasks working on LIMITED scope of total job
Neural Cytoarchitecture: shape of neurons; identifies distinct cortical areas
Neuron density, soma size, spine count, spine density, dendritic tree size
Connection Patterns: determines hierarchies and regions
Sensory inputs arrive at V1 in layer 4 (granular layer)
Feedforward projections terminate in layer 4
Feedback projections originate from layer 5 and 6
Hierarchies - suggest increasingly specialised roles
Regions - identified functionally by reversals in topographic map
Topography: each area on map should only be represented once – the repeat of a mapped feature signals a new cortical region
Explain the difference in the information that flows on the M & P pathways from retina to cortex. Retinal Ganglion Cell: neuron located near inner surface (ganglion cell layer) of retina; receive visual information from photoreceptors via two intermediate neuron types: bipolar cells and amacrine cells
Receptive fields of retinal ganglion neurons have two concentric regions – a center and an antagonistic surround
More photoreceptors that connect to a ganglion cell → larger receptive field
M (magnocellular) Pathway | P (parvocellular) Pathway |
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|
Lateral Geniculate Nucleus (LGN): visual nucleus of thalamus; relay station between retina and visual cortex; multilayered structure (6 layers in humans)
4 layers receiving input from P pathway; 2 layers receiving input from M pathway
Contralateral eye inputs to layers 1, 4 and 6
Ipsilateral eye inputs to layers 2, 3 and 5
Thalamic neurons reflect the properties of their input from retinal ganglion cells (M - large receptive fields, P - small receptive fields)
Visual deficits arising from LGN lesions:
Parallel pathways for different info arriving at V1: V1 separates info coming from LGN about different dimensions → dispatches it to different extrastriate regions each specialised for a particular kind of analysis (features, colour, movement, depth, texture)
WHERE (dorsal – spatial layout and motion, upper) | WHAT (ventral – colour and form, under) |
|
|
NOTE: increasing receptive field sizes beyond V1 reduce acuity but allow generalisability
IT (large receptive field) → V4 → V1
Overlaid Maps: make modules that encode all parameters, spread evenly across cortex
EYE DOMINANCE – encoded by ocular dominance bands in V1
Ocular dominance bands: stripes of neurons across surface of V1 that respond preferentially to input from one eye or the other; span multiple cortical layers
ORIENTATION – orientation preference is encoded by cortical columns in V1
V1 must represent lots of properties including line orientation
Needs to represent each orientation at each retinal location
Ordered distribution of orientations across topographical map – these are swirled together with colour and eye dominance patterns so all properties are represented within every few square mm of cortex
COLOUR – encoded by blobs
Blobs: sections of the visual cortex where groups of neurons that are sensitive to colour assemble in cylindrical shapes
Colour signals to V1 terminate in blobs
Inter-blob zones: where neurons are not sensitive to colour (receive M pathway inputs)
Building Maps. Describe the role of activity on shaping cortical maps. Ocular Dominance Maps: develop in first few weeks after birth
Need visual experience to form maps → drives formation of bands
Activity dependent plasticity – neurons are dependent on trophic (growth) support from their inputs and stabilise their inputs
Neighbouring neurons compete for input synapses → dynamic, ongoing process – disruptions to subset of inputs lead to cortical dominance by remaining subsets
Superior Colliculus: a multisensory midbrain structure that integrates visual, auditory, and somatosensory spatial information
Sensory maps of surrounding space are superimposed in SC
Involved in eye movements and orienting responses
Responsible for blindsight through its input to extrastriate cortex
Blindsight is thought to occur when information can still reach cortex, but the V1/LGN loop is broken. The patient can't "see" but is able to do certain visual tasks.
Binding Problem: concerns how items that are encoded by distinct brain circuits can be combined for perception/decision/action; combining different sensory representations of one object and segregating activity of multiple distinct objects
Activity is NOT processed in parallel
Cannot be solved by spatial location
We represent distinct objects/thoughts by having the involved neurons fire action potentials out- of-phase with different neurons representing another object at ~40 Hz
Registering the maps across different sensory systems is critical to binding outside world into coherent percepts ← achieved by overlaying maps and timing neural activity
Localisation of Sensory Experience: sensory systems use receptors to transduce an environmental signal → signal processed by layers of neurons at successive levels of nervous system
Tactile afferents travel in the ipsilateral dorsal column
Decussate (form X shape) at medulla and form medial lemniscus
From here, they synapse in ventro-basal thalamus
These thalamic neurons project to somatosensory cortex
Axons originating from each eye separate before reaching thalamus → right visual field is sent to left thalamus, and vice versa
Inputs from each eye remain separate until reaching cortex
Example 1: colour adaption after-effect
Adaption occurs at level of retina, thalamus and cortex before binocular convergence
Adaption in peripheral field is weak - no cones in comparison to center field
Example 2: binocular rivalry
Reflects intra-cortical battles for dominance between two stimuli
Perception alternates between different images presented to each eye
Not an after-effect but an unstable percept from a stable stimulus
Occurs at a higher level than level of retina and thalamus – occurs in cortex after convergence
Cerebral cortex contains large numbers of neurons
Activity of these neurons is synchronised in regular firing rhythms (brain waves) to an extent
Electrodes placed on scalp can pick up variations in electrical potential that derive from this underlying cortical activity
EEG signals are affected by state of arousal of cerebral cortex and show characteristic changes in different changes of sleep
Used in diagnosis of epilepsies and of brain death
Records many channels of activity from multiple recording electrodes placed in an array over the head
Phantom Limb: a vivid perception that a limb that has been removed or amputated is still present in the body and performing its normal functions
Amputees usually experience sensations including pain in the phantom limb
Caused by reorganisation of wiring of sensorimotor cortex (processes sensory inputs and executes movements)
Mismatch between movement and perception of that movement
Thalamus: relay motor and sensory signals to the cerebral cortex
Brain stem: acts as a relay center connecting the cerebrum and cerebellum to the spinal cord
Targeted muscle and sensory reinnervation (TMSR): rerouting motor and sensory nerves from residual limb towards intact muscles and skin regions
Skin near or over the targeted muscle is denervated, then reinnervated with afferent fibers of the remaining hand nerves
When this piece of skin is touched, it provides the amputee with a sense of the missing arm or hand being touche
NEUR2201 - Summary Notes (Module 2)
Neuroscience Fundamentals (University of New South Wales)
Scan to open on Studocu
Studocu is not sponsored or endorsed by any college or university
REAL-TIME NEURAL MEASUREMENTS
Direct Measures Measures electrical activity of neurons | Indirect Measures Tells us where neurons are active BUT does NOT indicate if neurons are excitatory/inhibitory |
|
|
Explain what a real-time neural measurement is, and provide three examples including the temporal and spatial resolution of each of the measurements.
Real-Time Neural Measurement: measures neural activity at a rate that keeps up with the speed of the activity being monitored
Spatial Resolution: one neuron or less (direct) | Spatial Resolution: groups of neurons (direct) | Spatial Resolution: groups of neurons (indirect) | |
Temporal Resolution: one action potential/less |
- EPSP/IPSP; soma)
|
| - EMG (evaluates condition of muscles and motor neurons which control them) |
Temporal Resolution: several action potentials | - Voltage-sensitive dyes (dye changes its fluorescence as electrical potential inside cell changes) | - Neurochemical measurements (electrochemistry) |
|
Microelectrode Recording: direct, one neuron, one action potential/less, invasive
Determine neural coding strategy
Determine if binding uses gamma waves
EEG Recording: direct, groups of neurons, one action potential/less, non-invasive (awake human subject)
Diagnose conditions - epilepsy, sleep disorders and brain tumours
Locating a sensory brain region
Transduction: stimulus-alerting events wherein a physical stimulus is converted into an action potential, which is transmitted along axons towards the CNS for integration; part of sensory processing
Stimulus
Change in ionic permeability of receptor cell/afferent nerve ending
Change in membrane potential – receptor potential
Generation of action potentials in afferent nerve terminal
Propagation of action potentials to CNS
Ionotropic (ligand-gated) | Metabotropic (G-protein coupled receptors) |
|
|
Briefly explain how photon capture causes a change in membrane potential in the photoreceptor. Photoreceptors: receptor cells that enable transduction; contain opsin and retinal
In vision, retinal captures a photon and dissociates, activating opsin (GPCR)
Activated opsin interacts with phosphodiesterase → reduction in concentration of cGMP
In the dark, transmitter is released | In the light, transmitter release is reduced |
|
|
Neural Code: uncovering the meaning behind the activity of a given neuron → insight into cognition
Time based codes contain MORE information than counting based codes
How to design an experiment that studies neural coding:
Add sensory input, record animal’s perception/behaviour, record neuronal activity
Measure three languages using real-time measurement
Can record at different levels of nervous system
Peripheral afferent neuron synapses in brain stem
Brain stem neuron synapses in thalamus
Thalamic neuron synapses in sensory cortex
Orientation-Selectivity (in cortical neurons): emerges from their convergent inputs
Retinal ganglion cells - respond to spots/rings of light (have concentric visual fields) – NO response that relates to the orientation of a bar of light
ON centre cell: excitatory center, inhibitory surround
OFF centre cell: inhibitory center, excitatory surround
Cortical neurons - sensitive to bar orientation – this is an emergent property of these cortical cells which is NOT present in their input neurons
Brain has a modular organisation – composed of distinct sections defined by function/histology.
Module: brain area in the hierarchy; can be organised into:
Hierarchical – each module performs DIFFERENT task but works on TOTAL scope of job
Parallel – each module performs SIMILAR tasks working on LIMITED scope of total job
Neural Cytoarchitecture: shape of neurons; identifies distinct cortical areas
Neuron density, soma size, spine count, spine density, dendritic tree size
Connection Patterns: determines hierarchies and regions
Sensory inputs arrive at V1 in layer 4 (granular layer)
Feedforward projections terminate in layer 4
Feedback projections originate from layer 5 and 6
Hierarchies - suggest increasingly specialised roles
Regions - identified functionally by reversals in topographic map
Topography: each area on map should only be represented once – the repeat of a mapped feature signals a new cortical region
Explain the difference in the information that flows on the M & P pathways from retina to cortex. Retinal Ganglion Cell: neuron located near inner surface (ganglion cell layer) of retina; receive visual information from photoreceptors via two intermediate neuron types: bipolar cells and amacrine cells
Receptive fields of retinal ganglion neurons have two concentric regions – a center and an antagonistic surround
More photoreceptors that connect to a ganglion cell → larger receptive field
M (magnocellular) Pathway | P (parvocellular) Pathway |
|
|
Lateral Geniculate Nucleus (LGN): visual nucleus of thalamus; relay station between retina and visual cortex; multilayered structure (6 layers in humans)
4 layers receiving input from P pathway; 2 layers receiving input from M pathway
Contralateral eye inputs to layers 1, 4 and 6
Ipsilateral eye inputs to layers 2, 3 and 5
Thalamic neurons reflect the properties of their input from retinal ganglion cells (M - large receptive fields, P - small receptive fields)
Visual deficits arising from LGN lesions:
Parallel pathways for different info arriving at V1: V1 separates info coming from LGN about different dimensions → dispatches it to different extrastriate regions each specialised for a particular kind of analysis (features, colour, movement, depth, texture)
WHERE (dorsal – spatial layout and motion, upper) | WHAT (ventral – colour and form, under) |
|
|
NOTE: increasing receptive field sizes beyond V1 reduce acuity but allow generalisability
IT (large receptive field) → V4 → V1
Overlaid Maps: make modules that encode all parameters, spread evenly across cortex
EYE DOMINANCE – encoded by ocular dominance bands in V1
Ocular dominance bands: stripes of neurons across surface of V1 that respond preferentially to input from one eye or the other; span multiple cortical layers
ORIENTATION – orientation preference is encoded by cortical columns in V1
V1 must represent lots of properties including line orientation
Needs to represent each orientation at each retinal location
Ordered distribution of orientations across topographical map – these are swirled together with colour and eye dominance patterns so all properties are represented within every few square mm of cortex
COLOUR – encoded by blobs
Blobs: sections of the visual cortex where groups of neurons that are sensitive to colour assemble in cylindrical shapes
Colour signals to V1 terminate in blobs
Inter-blob zones: where neurons are not sensitive to colour (receive M pathway inputs)
Building Maps. Describe the role of activity on shaping cortical maps. Ocular Dominance Maps: develop in first few weeks after birth
Need visual experience to form maps → drives formation of bands
Activity dependent plasticity – neurons are dependent on trophic (growth) support from their inputs and stabilise their inputs
Neighbouring neurons compete for input synapses → dynamic, ongoing process – disruptions to subset of inputs lead to cortical dominance by remaining subsets
Superior Colliculus: a multisensory midbrain structure that integrates visual, auditory, and somatosensory spatial information
Sensory maps of surrounding space are superimposed in SC
Involved in eye movements and orienting responses
Responsible for blindsight through its input to extrastriate cortex
Blindsight is thought to occur when information can still reach cortex, but the V1/LGN loop is broken. The patient can't "see" but is able to do certain visual tasks.
Binding Problem: concerns how items that are encoded by distinct brain circuits can be combined for perception/decision/action; combining different sensory representations of one object and segregating activity of multiple distinct objects
Activity is NOT processed in parallel
Cannot be solved by spatial location
We represent distinct objects/thoughts by having the involved neurons fire action potentials out- of-phase with different neurons representing another object at ~40 Hz
Registering the maps across different sensory systems is critical to binding outside world into coherent percepts ← achieved by overlaying maps and timing neural activity
Localisation of Sensory Experience: sensory systems use receptors to transduce an environmental signal → signal processed by layers of neurons at successive levels of nervous system
Tactile afferents travel in the ipsilateral dorsal column
Decussate (form X shape) at medulla and form medial lemniscus
From here, they synapse in ventro-basal thalamus
These thalamic neurons project to somatosensory cortex
Axons originating from each eye separate before reaching thalamus → right visual field is sent to left thalamus, and vice versa
Inputs from each eye remain separate until reaching cortex
Example 1: colour adaption after-effect
Adaption occurs at level of retina, thalamus and cortex before binocular convergence
Adaption in peripheral field is weak - no cones in comparison to center field
Example 2: binocular rivalry
Reflects intra-cortical battles for dominance between two stimuli
Perception alternates between different images presented to each eye
Not an after-effect but an unstable percept from a stable stimulus
Occurs at a higher level than level of retina and thalamus – occurs in cortex after convergence
Cerebral cortex contains large numbers of neurons
Activity of these neurons is synchronised in regular firing rhythms (brain waves) to an extent
Electrodes placed on scalp can pick up variations in electrical potential that derive from this underlying cortical activity
EEG signals are affected by state of arousal of cerebral cortex and show characteristic changes in different changes of sleep
Used in diagnosis of epilepsies and of brain death
Records many channels of activity from multiple recording electrodes placed in an array over the head
Phantom Limb: a vivid perception that a limb that has been removed or amputated is still present in the body and performing its normal functions
Amputees usually experience sensations including pain in the phantom limb
Caused by reorganisation of wiring of sensorimotor cortex (processes sensory inputs and executes movements)
Mismatch between movement and perception of that movement
Thalamus: relay motor and sensory signals to the cerebral cortex
Brain stem: acts as a relay center connecting the cerebrum and cerebellum to the spinal cord
Targeted muscle and sensory reinnervation (TMSR): rerouting motor and sensory nerves from residual limb towards intact muscles and skin regions
Skin near or over the targeted muscle is denervated, then reinnervated with afferent fibers of the remaining hand nerves
When this piece of skin is touched, it provides the amputee with a sense of the missing arm or hand being touche