Final Flashcards

1
Q

What is the nature of Sensation and Perception?

A
  • Brain receives input solely through action potentials along sensory pathways
  • All sensory systems follow a hierarchical organization
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2
Q

What are sensory receptors?

A
  • Specialized cells that convert sensory energy to neural activity (signal transduction)

– Vision: Light energy produces chemical energy

– Auditory: Air pressure produces mechanical energy

– Somatosensory: Mechanical energy

– Taste and olfaction: Chemical molecules

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3
Q

What are receptive fields?

A

– Region of sensory space in which a stimulus modifies a receptor’s activity

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4
Q

What is receptor density and sensitivity?

A
  • Sensory receptors are not evenly distributed across the body or its organs.
  • Density is essential for determining the sensitivity of a sensory system.
    – Example: More tactile receptors on the fingers than on the arm
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5
Q

What are neural relays?

A
  • Sensory information is encoded by action potentials traveling along peripheral nerves to the central nervous system.
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6
Q

Why is the neocortex important for the sensory field?

A
  • The neocortex represents the sensory field of each modality as a spatially organized neural representation of the external world.
    – In mammals, each sensory system has at least one primary cortical area.

The neocortex contains several key sensory fields: primary visual cortex (V1), primary auditory cortex (A1), and primary somatosensory cortex

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7
Q

Sensation vs. Perception

A
  • Sensation
    – Registration of physical stimuli from the environment by the sensory organs
  • Perception
    – Subjective interpretation of
    – Our visual is a subjective construction of reality manufactured by the brain.
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8
Q

Pathway of visual receptors

A

Visual receptors –> thalamus –> cerebral cortex

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9
Q

Pathway of auditory receptors

A

Auditory receptors –> hindbrain –> midbain –> thalamus –> cerebral cortex

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10
Q

Pathway of somatosensory receptors

A

Somatosensory receptors –> spinal cord –> brainstem –> thalamus –> cerebral cortex

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11
Q

What is the range of visible light for humans?

A
  • Range of electromagnetic energy visible to humans

– About 400 nanometers (violet) to 700 nanometers (red)

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12
Q

Retina and Fovea

A

Retina
– Light-sensitive surface at the back of the eye; consists of neurons and photoreceptor cells

  • Translates light into action potentials
  • Discriminates wavelengths (colors)
  • Works in a wide range of light intensities

Fovea
– Region at the center of the retina that is specialized for high acuity

– Receptive field at the center of the eye’s visual field

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13
Q

Photoreceptors

A
  • Rods
    – Sensitive to low levels of light (dim light)
    – Used mainly for night vision
    – One type of pigment only
  • Cones
    – Highly responsive to bright light
    – Specialized for color and high visual acuity
    – In the fovea only
    – Three types of pigments
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14
Q

What are some types of retinal neurons?

A
  • Bipolar cell: Receives input from photoreceptors.
  • Horizontal cell: Links photoreceptors and bipolar
  • Amacrine cell: Links bipolar cells and ganglion cells.
  • Retinal ganglion cell (RGC): Gives rise to the optic nerve.
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15
Q

What is glaucoma?

A

Series of diseases that cause damage to the optic nerve due to high intraocular pressure
– Risk increases with age
– Genetic component-easier to understand in early-onset forms
– One of the major causes of blindness

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16
Q

What is retinitis pigmentosa?

A

Death of retinal cells
– No light-sensing ability
– Group of rare genetic disorders

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17
Q

What are the two types of ganglion cells?

A
  • Magnocellular cell (M-cell)
    – Magno- means large
    – Receives input primarily from rods
    – Sensitive to light and moving stimuli
  • Parvocellular cell (P-cell)
    – Parvo- means small
    – Receives input primarily from cones
    – Sensitive to colour
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18
Q

What is the optic chiasm?

A
  • Junction of the optic nerves from each eye
  • Information from the left visual field goes to the right side of the brain; information from the right visual field goes to the left side of the brain.
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19
Q

Three Routes to the Visual Brain

A
  1. Geniculostriate system (all P ganglion axons and some M)
    – Projections from the retina to the lateral geniculate nucleus to the visual cortex
  2. Tectopulvinar system (remaining M cells)
    – Projections from the retina to the superior colliculus to the pulvinar (thalamus) to the parietal and temporal visual areas
  3. Retinohypothalamic tract
    – Synapses in the tiny suprachiasmatic nucleus in the hypothalamus
    – Roles in regulating circadian rhythms and in the pupillary reflex
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20
Q

Primary Visual Cortex

A
  • AKA V1 or striate cortex
  • Two paths emerge from this area
    – parietal lobe.
    – temporal lobe
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21
Q

Dorsal and Ventral Visual Streams

A
  • Dorsal visual stream
    – projects to the parietal cortex
    – The how pathway (how action is to be guided toward objects)
  • Ventral visual stream
    – Projects to the temporal cortex
    – The what pathway (identifies an object)
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22
Q

Geniculostriate Pathway

A
  • Lateral geniculate nucleus (LGN)
    – Right LGN: input from the right half of each retina
    – Left LGN: input from the left half of each retina
  • P and M retinal ganglion cells send separate pathways to the thalamus.
    – Segregation continues in the striate cortex.
  • Left and right eyes also send separate pathways to the thalamus.
    – Pathways remain segregated in the striate cortex.
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23
Q

Tectopulvinar Pathway

A
  • Magnocellular cells superior colliculus thalamus (pulvinar region)
    – Medial pulvinar
  • Sends info to the parietal lobe
    – Lateral pulvinar
  • Sends info to the temporal lobe
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24
Q

Occipital Cortex

A
  • Primary visual cortex (V1; striate cortex)
    – receives input from the LGN
  • Secondary visual cortex (V2−V5; extrastriate cortex) – cortical areas outside the striate cortex
  • Extrastriate (secondary visual) cortex
    – Remaining occipital visual areas
    – Each region processes specific features of visual information.
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25
Heterogeneous Layering
* Blob (V1) – Region in the visual cortex that contains color-sensitive neurons – Revealed by staining for cytochrome oxidase * Interblob (V1) – Region that separates blobs – Participates in the perception of form and motion
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Coding Location in the Retina
* Each retinal ganglion cell (RGC) responds to stimulation on just a small circular patch of the retina—the cell’s receptive field. * Coding location – Light falling on one place on the retina will activate one ganglion cell, and light falling on another place will activate a different ganglion cell.
27
Location in the LGN and Region V1
* Cells in the lateral geniculate nucleus (LGN) also have visual fields. * Each LGN cell represents a particular place. * Projects to V1, forming a topographic map – Receptive fields of cells in the cortex are typically larger than those of retinal ganglion cells. – More cortical tissue is devoted to cells in the fovea than in the periphery.
28
Receptive-Field Hierarchy
- The receptive fields of many retinal ganglion cells .... - combine to form the receptive field of a single lateral geniculate nucleus (LGN) cell ... - the receptive fields of many LGN cells combine to form the receptive field of a single V1 cell
29
Callosal Connections: Corpus Callosum
* The corpus callosum connects the two hemispheres but only specific brain structures. – Most of the frontal lobes are connected. – The occipital lobes have almost no connections * Exception: Cells that lie along the midline of the visual field are connected so that their receptive fields overlap.
30
Processing in Retinal Ganglion Cells (RGCs)
– Respond only to the presence or absence of light, not to shape (job of the cortex) – Concentric circle arrangement * Center and surround (periphery) * Luminance contrast - The amount of light reflected by an object relative to its surroundings - This allows input from RGCs to tell the brain about shape.
31
Overlapping Receptive Fields
* Neighbouring retinal ganglion cells receive their inputs from an overlapping set of photoreceptors. – Receptive fields overlap. * A small spot of light shining on the retina is likely to produce activity in both on-center and off-center ganglion cells.
32
Processing Shape in the Primary Visual Cortex (V1)
* V1 neurons receive input from multiple RGCs. * V1 neurons have a much larger receptive field than RGCs. * Cells behave like orientation detectors. – Excited by bars of light oriented in particular directions * Simple cells – Receptive field with a rectangular on-off arrangement * Complex cells – Are maximally excited by bars of light moving in a particular direction through the receptive field. * Hypercomplex cells – Are like complex cells, maximally responsive to moving bars. – Have strong inhibitory area at one end of the receptive field.
33
Neural Circuit in a Column in the Visual Cortex
* Sensory inputs enter the cortical column at layer VI (bottom) and terminate on stellate cells in layer IV that synapse with pyramidal cells in layers III and V. * The information flow is vertical. * Axons of the pyramidal cells leave the column to join other columns or structures.
34
Intrinsically Photosensitive Melanopsin Ganglion Cells (ipRGCs)
▪Represent a very small portion (2-3 %) of ganglion cells in the mammalian retina ▪In response to light, ipRGCs are capable of depolarizing without any synaptic input from other photoreceptors (intrinsically photosensitive) * M1-M5 subtypes * Differences in morphology and projections * Circadian brain areas predominantly innervated by M1 subtype * Brn3 family of transcription factors regulates the differentiation of RGCs
35
Biological clocks
* Anticipate rhythmic changes in the environment – Anticipate vs. respond to event * Temporal organization of behaviour – Avoid predators and competitors * Biological rhythms – Daily or seasonal changes in physiology and behaviour – Related to: * Earth’s rotation about its axis * Earth’s progression around the sun
36
Biological Rhythms in Humans
* Our biology is most closely tied to daily variations, rather than seasonal cycles * Dominated by rhythm of daytime activity and nighttime sleep – We don’t migrate, we’re not seasonal breeders * Rhythms in more than activity/rest – Pulse, blood pressure, body temperature, cell division, blood cell count, alertness, metabolic rate, sexual drive, response to medication, hormone levels ... Examples of human rhythms: * Physiological parameters – Hormones * Cortisol, melatonin – Body temperature * Psychological parameters – Alertness – Reaction time
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Biological rhythms
* Wide variety of biological rhythm * Infradian – more than daily – Estrus or menstrual cycles * Ultradian – less than daily – BRAC (basic-rest activity cycle) – Respiration – Eating
38
Studying rhythms
* Usually use a running wheel connected to computer * Can use other measures too – Perch hopping – Physiological measures Rhythms in time-free environments * Test humans in bunkers or caves * Note that period is >24h – 1h later each day * “Freerunning” rhythm
39
Synchronization
* A clock isn’t much good if it doesn’t predict something – Don’t just generate rhythms – Also need to synchronize to the environmental cycles * Even though our circadian clock runs a little slow, we exhibit 24h patterns in behavior and physiology * Like a cheap watch, our clock needs to be reset each day.
40
Why doesn’t the clock run at exactly 24 hours?
* Permits it to track changing dawn / dusk – Unless you live near the equator, day length can change quite a bit over the year
41
What kinds of cues reset the clock?
* Sunrise / sunset * Socialinteraction * Exercise * Food * Each of these gives information about time – Zeitgeber (German for time-giver) * Zeitgebers synchronize the circadian clock through entrainment
42
What is the best zeitgeber?
* Light is the most potent zeitgeber – Most obvious cue as to if it is day or night – Can synchronize and reset the circadian clock * Light in the early morning or late evening is the best cue – Nudges the clock ahead or back respectively * The deeper light falls into the night, the bigger the effect – Maximal around body temperature minimum
43
Implications of the circadian clock
* Edison’s Curse: – The light bulb has allowed people to be active at times of the day when we normally wouldn’t be – Shift workers working at times when the body would normally be sleeping – Rotating shift workers constantly jumping to new shifts * Increase rates – On the job accidents – Disease
44
What is the role of the suprachiasmatic nucleus in biological rhythms?
- When SCN is removed, mice become completely arrhythmic, they have “broken clocks”, no temporal organization - Important experiment to determine function of SCN: tau mutant hamsters with fast clocks, lesioned SCN, complete arythmancy as a result, then took SCN from animal with regular clock (24 hour) and implanted into tau hamster, restored rhythm and now the period followed the donor’s clock (regular 24 hour), showed that SCN sets rhythm - SCN looked at outside of animal, each cell is ticking on its own, SCN cells are rhythmic on their own - SCN at the base of hypothalamus, main clock that sets the rhythm of other body cloths
45
How does the clock tick?
* Transcription- translation feedback loop – A gene is activated – mRNA is produced – protein being produced cytoplasm – The protein feeds back into the nucleus and turns off its own transcription
46
Period genes
* There are three “period” genes (Period 1, 2, 3) * Mutations in period 2 and 3 have been associated with human sleep disorders – Advance sleep phase syndrome (Period 2) – Delayed sleep phase syndrome (Period 3) * Similar to the hamster Tau mutation * Hamster has a mutant enzyme (casein kinase 1 epsilon), humans have a mutant site on the period gene where the same enzyme acts
47
SCN as a pacemaker
* The SCN may not drive behaviours directly * SCN lesioned animals still eat, drink and sleep, they just do it haphazardly – The SCN is controlled by light – The SCN controls rhythms target neural structures – These targets regulate the behaviour * May be an oscillator for each
48
Sleep
* We break our 24 hour day into bouts of wake and sleep – Spend about 1/3rd of our lives asleep * “Wake” is a complex state that includes a wide variety of behaviours – Eating, drinking, thinking, exercising, sex * “Sleep” is often thought of as “not wake” * Sleep is also a complex state with many distinct parts – Resting, napping, deep sleep, snoring, dreaming, sleepwalking
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Sleep patterns
* Sleep trends are highly variable and change throughout life. * Typically sleep quality and quantity decreases as you age. * Average adult should get between 7-8 hours of sleep – Some get much less or much more
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Measuring sleep
1) EEG: electroencephalograph – Cortical electrical activity – Primary measure of sleep – Described in terms of frequency and amplitude of waves 2) EMG: Electromyograph – Muscle tone 3) EOG: Electrooculograph – Eye movements
51
Wake states
* Wake: – Small amplitutde, high frequency EEG (15-30Hz) – EEG pattern: Beta * Relaxed wakefulness, eyes closed – Alpha – Amplitude a little higher, frequency a little lower * (7-11 Hz) – Sign that the membrane potentials of cortical neurons are becoming more synchronized
52
Divisions of sleep
* There are 2 main divisions of sleep * Slow Wave sleep (SWS) (Non-REM sleep, N-sleep) – EEG activity has increasing amplitude and decreasing frequency – 3 stages: progressive changes in EEG * Paradoxical Sleep (REM sleep, R-Sleep) – Wake-like EEG
53
Sleep stages
* All Non-REM sleep is characterized by: – Some muscle tone/activity – Slow rolling eye movements – Drop in body temperature, heart rate, breathing * Progresses from low amplitude / high frequency to high amplitude / low frequency
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Stage N1
* Transition from wake into sleep * Lasts several minutes * low amplitude, mixed frequency – Includes 4-7Hz Theta Waves * Muscles have tone and eyes can be rolling
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Stage N2
* EEG gets a little slower and higher amplitude * Also shows: – Sleep spindles (11-16Hz) – K Complexes (Very high amplitude)
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Slow Wave Sleep – NREM Stage 3+4
* Slow wave sleep or deep sleep (in humans) * High amplitude low frequency (0.5-2Hz) – Delta waves * Muscle tone
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REM sleep (R-Sleep)
* Low amplitude, high frequency * Resembles wake EEG with beta waves – Called paradoxical sleep * Rapid eye movements (REMs) * Dreams!!! * Muscle atonia – Antigravity muscles shut off – Some muscle movements: eye muscles, muscles in the middle ear, diaphragm * Some twitching in postural muscles
58
Sleep Progression
* 1st half of night predominated by slow wave sleep – Little REM * Last half predominated by REM – Little or no Stage 3 or 4 * Drift between slow wave and REM in about a 90-minute cycle
59
Cognition During Sleep
* Slow wave sleep – Little dreaming – Lack of content, more like vague images – Night terrors * REM – Rich dreams, occur in real time – Nightmares – More frequent and longer dreams as night progresses – Memory function is impaired, so dreams are difficult to remember the next day * Actually, anything that occurs during sleep is hard to remember
60
Why do we sleep?
1) Biological adaptation (energy conservation) * Inactivity * Low brain activity during NREM * Body temperature drops * But... don’t save that much more than you would just resting, where vigilance would be higher – Also, what about REM? 2) Sleep as a restorative process – At the end of the day, you feel tired – After a nights sleep you feel refreshed – Irritable, decreased attention after not enough sleep – World record of no sleep is about 11 days – Little effect on person – SWS made up first, followed by a rebound in REM * Total sleep loss: – Rats will die in about 4 weeks without sleep – Metabolism gets totally messed up – Rest helps physical fatigue – Sleep necessary to relieve mental fatigue 3) Memory storage – Theory: Sleep facilitates the storage of memories - Best theory!! - During REM, circuits become activated that were active during training - Birds learning a new song will show activation in auditory areas during REM sleep - Sleep deprivation decreases performance on learned tasks
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Sleep and memory
* NREM sleep seems to be most important for explicit/declarative memories – Word learning in humans – Spatial learning in rodents * REM sleep seems to be most important for implicit, non-declarative memories
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Brain control of sleep / wake
* Acetylcholine from the brainstem Reticular Activating System and basal forebrain are important for wake * RAS stimulation leads to wake-like EEG * RAS lesion = persistent coma
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Other Wake active systems
Raphe(serotonin) and Locus coeruleus (Norepinephrine) * All project widely in cortex * All are active during wake * Silent during REM sleep – Antidepressants suppress REM – Antidepressants promote 5-HT and NE
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Hypocretin (AKA Orexin) and Sleep
* Found in the dorsolateral hypothalamus * Project to many of the wake centers – Activates them * Projects to the cortex too, promotes arousal * These cells die in narcolepsy – The sleep/wake and REM system become deregulated.
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Learning and Memory
* Learning: permanent change in behaviour as a result of experience * Memory: ability to recall or recognize previous experience – A product of a physical trace or engram – Two categories: Implicit memory (unconscious) and explicit memory (conscious) * Can also be discussed in terms of procedural memory and declarative memory
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Classification of Memory
Short term memory: stores sensory, motor, and cognitive memory Long term memory: divided into explicit (CONSCIOUS personal, autobiograohical, facts) implicit (UNCONCSIOUS skills, habits, priming), and emotional memory (attraction, fear...)
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Encoding and processing memories
* Encoding is the process by which information is stored in the brain – Implicit memories: data-driven or bottom-up processing – Explicit memories: conceptually driven or top-down processing * All memory is fallible! * Learning and memory is not localized to one brain region!
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Studying Learning and Memory in the Laboratory
Pavlovian conditioning – Learning procedure whereby a neutral stimulus such as a tone (CS) comes to elicit a response (CR) because of its repeated pairing with some event such as the delivery of food (UCS) Operant Conditioning – Learning procedure in which the consequences (such as obtaining a reward) of a particular behaviour (such as pressing a bar) increase or decrease the probability of the behavior occurring again (Edward Thorndike, 1898) – Thorndike's Puzzle Box: A cat gradually learned that its actions had consequences (The cat touched the releasing mechanism by chance on the initial trials as it paced inside box, cat learned that something it did opened the door, and it tended to repeat its behaviours from just before the door opened)
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Neural circuit for explicit memories
* Medial temporal region -entorhinal cortex -parahippocampal cortex -perirhinal cortex * Prefrontal cortex
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Dissociating Memory Circuit
* William Scoville performed a bilateral medial temporal lobe resection on a young man, Henry Molaison (H. M.). – Seizures originated in the region of the amygdala, hippocampal formation, and associated subcortical structures, so Scoville removed them bilaterally. * After the surgery, H. M. had severe amnesia, lacking explicit memory. – He could not recall anything that happened after the surgery. * H. M.’s performance on implicit memory tests was left intact.
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Disrupting Implicit Memory
* Patient J. K. – Impaired implicit memory with intact explicit memory * Developed Parkinson disease in his mid-70s and started to have memory problems at 78 – Damage to basal ganglia * Impaired ability to perform tasks that he had done all his life – Example: turning off the radio * Could still recall explicit events
72
Neural circuit for implicit memories
Mishkin et al. 1987, 1997, proposed: 1. The neocortex receives sensory and motor info 2. The basal ganglia receives inputs from the neocortex and substantia nigra 3. The basal ganglia projects to the ventral thalamus 4. Ventral thalamus projects to premotor cortex
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What evidence supports the idea that the hippocampus is critical for spatial memory?
- Primate study: trained them to displace objects to get food, recognition phase with certain objects involving memory, lesioned the hippocampus and then they were unable to do this - Study on drivers in London: larger parts of the hippocampus in those with better navigational abilities
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Hippocampal cells
Code spatial information * Place cells: fire when organism is in a spatial location, regardless of orientation * Grid cells: fire at many locations, forming a virtual grid of the environment
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Neuroplasticity
* Versatility at the synaptic level provides a mechanism for learning – a relatively permanent change in behaviour that results from experience. “Cells that fire together, wire together!” Two general types of behaviour have been studied in Aplysia: * Habituation: learning behaviour in which a response to a stimulus weakens with repeated presentations. * Sensitization: learning behaviour in which a response to a stimulus strengthens with repeated presentations, because the stimulus is novel or stronger than normal.
76
Long-term potentiation (LTP)
* Long term potentiation (LTP): Long-lasting increase in synaptic effectiveness after high- frequency stimulation (e.g., 100 Hz) - Long lasting permanent increase in synaptic effectiveness, example of neuroplasticity 1) Weak electrical stimulation: because the NDMA receptor is blocked by a magnesium ion, release of glutamate by a weak electrical stimulation activates only the AMPA receptor 2) Strong electrical stimulation (depolarizing EPSP): a strong electrical stimulation can depolarize the postsynaptic membrane sufficiently that the magnesium ion is removed from the NMDA receptor pore 3) Weak electrical stimulation: now glutamate, released by weak stimulation, can activate the NMDA receptor to allow CA2+ influx, which through a second messenger, increases the function or number of AMPA receptors or both
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Long-term depression (LTD)
Long term depression (LTD): Long- lasting decrease in synaptic effectiveness after low-frequency stimulation (e.g., 5 Hz)
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Individual differences in neuroplasticity
May influence how memory circuits are strengthened. Some individuals may naturally have higher neuroplasticity, allowing for more efficient memory formation.