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Neural Plasticity Lecture 7
36

Neural Plasticity

Dec 31, 2015

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Neural Plasticity. Lecture 7. Neural Plasticity. Nervous System is malleable learning occurs Structural changes increased dendritic branching new synapses Changes in synaptic efficiency Long-term potentiation Long-term depression ~. Neural Mechanism of Memory. Donald Hebb - PowerPoint PPT Presentation
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Page 1: Neural Plasticity

Neural Plasticity

Lecture 7

Page 2: Neural Plasticity

Neural Plasticity

Nervous System is malleable learning occurs

Structural changes increased dendritic branching new synapses

Changes in synaptic efficiency Long-term potentiation Long-term depression ~

Page 3: Neural Plasticity

Neural Mechanism of Memory

Donald Hebb Short-term Memory

Change in neural activity not structural temporary

Reverberatory Circuits - cortical loops of activity ~

Page 4: Neural Plasticity

Reverberating Loops

Maintains neural activity for a period Activity decays ~

Page 5: Neural Plasticity

Hebb’s Postulate

Long-Term Memory required structural change in brain relatively permanent

Hebb Synapse use strengthens synaptic efficiency concurrent activity required

• pre- & postsynaptic neurons ~

Page 6: Neural Plasticity

Long-term Potentiation

According to Hebb rule use strengthens synaptic connection

Synaptic facilitation Structural changes Simultaneous activity

Experimentally produced hippocampal slices associative learning also ~

Page 7: Neural Plasticity

Inducing LTP

Stimulating electrode

Record

DGPerforantPathway

Page 8: Neural Plasticity

-70mv

-

+

Postsynaptic Potential

Single elec. stimulation

100 stim. burst

Single stim.

Page 9: Neural Plasticity

Strong, high frequency stimulation Minimum stimulation

1 + burst of 4 4-7 Hz

• Theta HC: Arousal & REM ~

Pattern Of Stimulation

Page 10: Neural Plasticity

LTP Duration

Experimentally-induced LTP Intact animals

seconds - months HC slice

40 hrs ~

Page 11: Neural Plasticity

LTP: Molecular Mechanisms

Presynaptic & Postsynaptic changes HC ---> Glutamate

excitatory 2 postsynaptic receptor subtypes

AMPA ---> Na+ NMDA ---> Ca++

Glu ligand for both ~

Page 12: Neural Plasticity

NMDA Receptor

N-methyl-D-aspartate Glu binding opens channel?

required, but not sufficient Membrane must be depolarized

before Glu binds ~

Page 13: Neural Plasticity

Single Action Potential

Glu ---> AMPA depolarization

Glu ---> NMDA does not open Mg++ blocks channel no Ca++ into postsynaptic cell

Followed by more APs ~

Page 14: Neural Plasticity

NMDAMg

G

Ca++

GAMPA

Na+

Page 15: Neural Plasticity

NMDAG

Ca++

G

Mg

AMPA

Na+

Page 16: Neural Plasticity

Activation of NMDA-R

Ca++ channel chemically-gated voltage-gated

Mg++ blocks channel Ca++ influx --->post-synaptic changes

strengthens synapse ~

Page 17: Neural Plasticity

LTP: Postsynaptic Changes

Receptor synthesis More synapses Shape of dendritic spines Nitric Oxide synthesis ~

Page 18: Neural Plasticity

PresynapticAxon Terminal

Dendritic Spine

Before LTP

Page 19: Neural Plasticity

PresynapticAxon Terminal

Dendritic Spine

After LTP

less Fodrin

Less resistance

Page 20: Neural Plasticity

Nitric Oxide - NO

Retrograde messenger Hi conc. ---> poisonous gas

Hi lipid solubility storage?

Synthesis on demand Ca++ ---> NO synthase ---> NO

Increases NT synthesis in presynaptic neuron more released during AP ~

Page 21: Neural Plasticity

G Ca++

G

Ca++NOSNO

NO cGMP Glu

Page 22: Neural Plasticity

Cerebellum Motor functions

Coordination of movements Regulation of posture

Indirect control Adjust outputs of descending tracts

Also nonmotor functions memory/language ~

The Cerebellum & Long-term Depression

Page 23: Neural Plasticity

Cerebellum: Anatomy

Folia & lobules analogous to sulci & gyri

Vermis - along midline output ---> ventromedial pathway

Hemispheres output ---> lateral pathway

Deep cerebellar nuclei fastigial, interposed, & dentate Major output structures ~

Page 24: Neural Plasticity

Cerebellum

Programs ballistic movements feed-forward control

no feedback during execution direction, force, & timing long term modification of circuits

Motor learning shift from conscious ---> unconscious ~

Page 25: Neural Plasticity

Cerebellum

Acts as comparator for movements compares intended to actual

performance Correction of ongoing movements

internal & external feedback deviations from intended movement ~

Page 26: Neural Plasticity

Cerebellum: 3 layered cortex

Molecular layer parallel fibers axons of granule cells

runs parallel to long axis of folium Purkinge cell layer

large somas axons to underlying white matter

perpendicular to main axis of folium ~

Page 27: Neural Plasticity

Cerebellum: 3 layered cortex

Purkinge cell layer large somas axons to underlying

white matter perpendicular to

main axis of folium ~

Page 28: Neural Plasticity

Cerebellum: 3 layered cortex

Granular layerinnermost layer

small, densely packed granule cells > # neurons in cerebral cortex ~

Page 29: Neural Plasticity

Cerebellum: 3 layered cortex

Molecular

Purkinje

Granule

Page 30: Neural Plasticity

Cerebellum: & Motor Learning

Purkinje cells only output from cerebellar cortex inhibit deep cerebellar nuclei

Input to Purkinje cells Mossy fibers via parallel fibers

from spinal cord & brainstem nuclei climbing fibers

cerebral cortex & spinal cord

via inferior olivary nucleus ~

Page 31: Neural Plasticity

Cerebellum: & Motor Learning

1 Purkinje cell synapses.. 1 each with 200,000 parallel fibers Many with 1 climbing fiber

strong synaptic connections Climbing fibers effects of mossy fibers

transient ~

Page 32: Neural Plasticity

Cerebellum: 3 layered cortex

Molecular

Purkinje

Granule

Mossy fibersClimbing fibers

Page 33: Neural Plasticity

Cerebellum: & Motor Learning

Long-term depression (LTD) requires concurrent activity climbing & parallel fibers active together in activity of specific Purkinje cells

Climbing fibers may carry error signals corrections ---> parallel fiberinfluence

input specificity only affects active synapses of a parallel fiber ~

Page 34: Neural Plasticity

LTD Mechanisms

Similar to LTP * changes are postsynaptic Glutamate receptors

Page 35: Neural Plasticity

LTD Mechanisms

*Requires concurrent activity Climbing fiber

1. Ca++ *influx - voltage-gated Parallel fibers activate

2. AMPA - Na+ influx

3. mGLUR1 AMPA desensitized

Na+ influx ~

Page 36: Neural Plasticity

LTD Mechanisms

mGluR1 metabotropic cGMP-mediated intracellular Ca++ stores activation of phosphatases

Knockout mice lack mGluR1 loss of motor coordination ~