All summary questions- classical conditioning Flashcards

1
Q

Strategy for studying neural basis of memory?

A

– Need to pick a simple task to start with

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

– Suitable simple task?

A

– Eyeblink conditioning has been well studied.

– Simplest version: delay conditioning of nictitating membrane response (NMR)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Where in brain are the plastic synapses that mediate this conditioning?

A

– In people, medial temporal lobe damage prevents formation of new long-term memories, but has little effect on eyeblink conditioning
– In rabbits the forebrain not needed for delay NMR conditioning
– But both electrophysiological and lesion studies implicate the cerebellum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How to establish circuitry underlying delay NMR conditioning?

A

– Use standard neuroscience techniques
• Anatomy
• Electrophysiology
• Manipulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Circuitry can be broken down into 5 parts

A

– Unconditioned reflex pathway
– Output of anterior interpositus nucleus controlling the conditioned response
– Output of eyeblink region of cerebellar cortex controlling the anterior interpositus nucleus
– Eyeblink region receives information about conditioned stimulus via mossy fibres
– Eyeblink region receives information about unconditioned stimulus via climbing fibres

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the main cell types in cerebellar cortex?

A

– Purkinje, granule, Golgi, stellate, basket.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How are they connected?

A

– See circuit diagram

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Where are the potential sites of plasticity?

A

– Purkinje cell dendrites receive information about the CS from parallel fibres, and about the US from climbing fibres
– Cells in anterior interpositus nucleus also receive these inputs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How is eyeblink conditioning related to other ‘cerebellar’ tasks?

A

– They are all mediated by the same basic neural circuit

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

General theories of cerebellar function: what task do they model?

A

– Making sure movements are accurate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What methods (algorithms) have been proposed?

A

– Supervised learning: an error signal makes movements bigger or smaller as required

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How does learning theory work in cerebellum?

A

– Mossy fibres convey input information
– Climbing fibres convey error information
– Latter used to depress synapses contributing to error (LTD)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Can this general theory be applied to eyeblink conditioning?

A

– In principle yes. In practice?

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Where are the plastic synapses in NMR conditioning?

A

– Modelling predicts the synapses between granule cells and Purkinje cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Evidence: are plastic synapses in cerebellum or brainstem?

A

– Several lines of evidence strongly point to the cerebellum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Are plastic synapses in cerebellar cortex, or the deep cerebellar nuclei

A

– Evidence increasingly indicates that the cerebellar cortex mediates initial learning

17
Q

Is there any plasticity in the deep nuclei?

A

– Perhaps with extended training

18
Q

What kind of synaptic plasticity was predicted to underlie eyeblink conditioning?

A

– LTD at the synapses between parallel fibres and Purkinje cells

19
Q

What is evidence for LTD at these synapses?

A

– Generally agreed that in slices LTD can be demonstrated reliably

20
Q

How does it work?

A

– Unclear: one suggestion is activation of mGluR1 receptors (in conjunction with climbing fibre input)

21
Q

Does this apply to actual conditioning in vivo?

A

– A quite different mechanism involving mGluR7 receptors has been implicated
– What (if any) role LTD plays is unclear