Final Exam New Material: Chapters 18-20 Flashcards

1
Q

What did Theodule Ribot propose?

In what order do memories disappear?

A

That during diseases of the brain, memories disappear in an orderly fashion.
Recent memories –> Personal memories –> Habits, skills –> Emotional memories

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2
Q

What is Ribot’s law?

A

Old memories are more resistant to disease/disruption than new memories.

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3
Q

What is the Standard Model of Systems Consolidaiton?

A

After initial learning, the memory trace consists of weakly connected neocortical patterns held togehter by their temporary connections with the medial temporal hippocampal (MTH) system. As the memory ages, intrinsic processes result in the consolidation or strengthening of the connections among the neocortical patterns and can therefore be retrieved without the hippocampus.

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4
Q

According to the Standard Model, what are the reasons that old memories are more resistant to disruption?

A
  1. Over time the memory content in the neocortex becomes consolidated and no longer requires the hippocampus for retreival.
  2. The hippocampus is more vulnerable to disruption than neocortical areas.
  3. Since retrieval of recent memories requires the hippocampus, they would be more disrupted by hippocampal dysfunction.
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5
Q

Why might the contextual fear model be inappropriate for evaluating the standard model of systems consolidation?

A

The retrieval of the memory does not require the pattern completion properties provided by the hippocampus.

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6
Q

What is cellular vs. systems consolidation?

A
  • Cellular Consolidation: Consequence of synaptic biochemcial events initiated by the original experience, time frame of hours
  • Systems Consolidation: Conseqeunce of an interaction between the medial temporal hippocampal system and neocortex, time frame days, weeks, months, years
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7
Q

What did Nadel and Moscovitch conclude?

What was the evidence?

A

Both old and new episodic memory always depend on the hippocampus. Patients with almost complete damage to the hippocampus could not recall either new or old episodic memories.

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8
Q

What are the 2 main problems associated with testing people who have damage to the medial temporal lobes?

A
  1. The brain damage extend beyond the regions of interest
  2. There is no way to completely control for the initial strength of the memory.
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9
Q

What is the advantage of animal studies?

A
  1. Provide animals with a known behavioral experience
  2. Vary the exact time between the experience and the occurence of the brain damage
  3. Vary the extent of the brain damage
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10
Q

Did animal studies support the standard model?

A

No support for the standard model, the older 3 and 6-month old memories were still disrupted by hippocampus damage. New memories were also disrupted.

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11
Q

What experiment showed that retrograde but not anterograde damage to the hippocampus produced amnesia?

What did they suggest?

A

Damage to hippocampus prior to contextual fear conditioning does not impair retreival of the memory, but damage to the hippocampus after conditioning prevents subsequent retrieval of the memory.

Without a hippocampus, the memory may be stored extrahippocampal

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12
Q

What experiment showed that new memories can survive hippocampus damage if training is distributed?

A

Contextual fear conditioning produced by several shocks delivered in the same session is impaired by subsequent damage to the hippocampus, but contextual fear produced by the same number of shocks delivered in sepearte sessions is not affected by damage to the hippocampus.

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13
Q

What experiment showed that the extrahippocampal system acquires the memory when the hippocampus is present?

A

Silencing the hippocampus prior to the retrieval test has no effect on retrieval of a contextual fear memory acquired when the hippocampus was funcitoning normally.

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14
Q

What is a fundamental problem with the contextual fear conditioning paradigm?

A

It does not depend on pattern completion processes. There is no need for the animal to pattern complete because all features of the context are present as the animal continuously explores the context.

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15
Q

What is competitive trace theory?

A

As memories age, repetition and replay may consolidate connections among the core overlapping elements of neocortical units to create a semantic memory that may be recalled in the absence of the hippocampus.

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16
Q

What is an instrumental behavior?

A

Studying how a behavior is modified by the outcome it produces

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17
Q

What is Thorndike’s Law of Effect?

A

Outcomes produced by behavior ultimately adapt the animal to the situation by strenghtening and weakening exsisting stimulus-response connections.

Outcomes that reward behavior strengthen S-R connections, while nonrewarding outcomes weaken connections.

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18
Q

What is Tolman’s Cognitive Expectancy Theory?

A

Instrumental behaviors are organized around goals and mediated by expectation of an outcome.

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19
Q

According to Thorndike what is learned and what is the role of the outcome?

A

S-R connections are strengthend or weakend and the role of the outcome determines which

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20
Q

According to Tolman what is learned and what is the role of the outcome?

A

Expectancies are learned and the outcome provides incentive motivation for perfoming the behavior

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21
Q

How do actions and habits differ on what 4 dimensions?

A
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22
Q

What is the reward devalution strategy?

A

The reward devalution strategy centers on changing the value of the outcome after the animal has solved the problem.

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23
Q

What can one conclude if the subsequent test performance is influenced by the devalution?

A

That the behavior was supported by the action system.

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24
Q

What is the progession of control between action and habit systems as training continues?

A

Instrumental behaviors are initially controlled by the action system, but following limited training the animals behavior is reduced following reward devalution. With extensive practice they become habits and reward devaultion has no effect compared to the control condition.

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25
Q

Describe the relationship between action and habit systems.

What happens when you reverse the contingencies?

A

Action and habit systems compete for control. Once an instrumental response is well learned, the two systems can work together to support the same behavior, with the habit system dominating. However, when you reverse the contingencies the action system attempts to rapidly adjust to the system, but the output from the habit system can interfere with adaptation.

Ex: American crossing the street in England has to overcome the habit of looking left before crossing

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26
Q

What was the Pauli experiment?

What happened when the action or habit system was inhibited prior to phase 2?

A

In Phase 1, rats are trained to press levers associated with different outcomes. Rats pressed the lever with the more rewarding outcome more. In Phase 2, the contingencies were reversed.

Inactivating the action system impaired the rat’s learning the new contingency, whereas inactivating the habit system facilitated this learning.

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27
Q

How do psychostimulants and stress affect the balance of action and habit systems?

Why is this?

A
  • Exposure to psychostimulants promotes habitual behaviors.
  • Chronic stress alters the action system leading to more habitual behaviors.

Action systems are more vulnerable to disruption that habit systems.

28
Q

How does the adjacent arm task show that the acquisition of instrumental behaviors depends on the striatum?

A

Rats with damage to the striatum could not learn that immediately turning left or right to enter the adjacent arm would be rewarded.

29
Q

Where does the striatum project too?

What is the rat striatum composed of?

A

Information processed by the striatum projects back to the motor cortex via the thalamus.

Striatum of the rat includes the caudate putamen and nucleus accumbens.

30
Q

What occured in rats with damage to the dorsomedial striatum?

Which system is it involved with?

A

They are not sensitive to reward devalution.

Dorsomedial striatum affects action system.

31
Q

What is the amygdala critical for in the action system?

How do we know this?

A

The amygdala is critical for attaching value to a particular outcome.
- Animals with amygdala damage learn simple discriminations but are insensitive to reward devaluation.

32
Q

What is the prelimbic region critcal for in the action system?

What happens if you damage this region before or after training?

A

The prelimbic region is critical in the acquisition of the associations that support an action.
- If this region is damaged prior to training, reward devalution has no effect.
- If you damage this region after training, there is no impairment since there is no storage here.

33
Q

What is the dorsolateral striatum critical for in the habits system?

How do we know this?

A

The dorsolateral striatum is critical for the development of habits.
- Rats with damage to this region are still sensitive to devaluation and prevent a habit from forming.

34
Q

What is the role of the infralimbic system?

A

With extensive training the infralimbic region suppresses the output of the action system.

35
Q

What happens if you damage the infralimbic region before or after training?

A
  • Damage prior to training prevents instrumental behaviors from becoming habits.
  • Damage after extensive training makes rats sensitive to reward devaluation again.
36
Q

What is the role of the prelimbic region after limited training?

A

The prelimbic region is necessary early in training for building the action system that controls a particular instrumental behavior.

37
Q

What is the role of the prelimbic and infralimbic regions after extensive training?

A

With extensive training, the prelimbic region is no longer necessary to generate an action. The infralimbic region now suppresses the contribution of the action system, and the habit system takes over .

38
Q

What are the storage sites for actions and habits?

A

The dorsal lateral striatum is a storage site for actions and habits.

39
Q

What is the dopamine reinforcement hypothesis?

A

Dopamine at reward supports associations with events preceding it.

40
Q

What is the dopamine incentive salience hypothesis?

A

Dopamine attaches a motivational significance to the stimulus associated with the outcome.

41
Q

What is the mesolimbic dopamine system?

A

The dopamine neurons are located in the VTA and their fibers project into the nucleus accumbens of the striatum.

42
Q

What does the dopamine incentive salience hypothesis assume?

A
  1. The reward activates VTA DA neurons and releases DA in Na
  2. The stimulus not only can associate with the response, it also can get associated with the incentive properties of the outcome.
  3. The stimulus complex itself can elicit strong urges or wants that lead the individual to seek out the outcome/reward
43
Q

What is the concept of fear as a defensive behavioral system?

What can it be activated by?

A

The fear system organizes the expression of a variety of behaviors that have evolved to protect us from danger. It can be activated by innate danger signals or by learned danger signals.

44
Q

What did Robert Bolles develop?

A

Concept of species specific defense responses.
- freezing, flight

45
Q

What did Micheal Fanselow develop?

A

Concept of predatory imminence gradient: distance from threat influences fear response.

Ex: When danger is far away the animal will freeze, but if there is imminent danger the animal will fight or flee.

46
Q

What are they key components of the amygdala in supporting fear behaviors?

A

The basolateral amygdala recieves sensory information and the central amygdala regulates the expression of fear.

47
Q

What are intercalated cells (ITCs)?

A

Neurons located between the basolateral complex and the central amygdala that recieve CS information from the BLA and project to the central amygdala. When activated, these cells release GABA and prevent their target neurons from depolarizing and prevent neurons in the central amygdala from generating defensive behavior.

48
Q

What are the 2 types of neurons in the basal nucleus?

When are they active?

A
  1. Fear neurons that are active when fear behaviors are expressed
  2. Extinction neurons that are active when fear has been extinguished.
49
Q

Where do fear neurons project?

A

Fear neurons provide excitatory projections to the central nucleus and to neurons in the prelimbic region of the prefrontal cortex.

50
Q

Where do extinction neurons project?

A

Extinction neurons project to infralimbic projecting ITC-b neurons.

51
Q

What happens inside the amygdala when an aversive event occurs?

Specifically referring to ITC cells

A

The inhibitory influence of ITC-b neurons on central neurons will be removed by ITC-a cells and excitatory drive produced by fear neurons and prelimbic cortex neurons will increase.

52
Q

What is extinction?

A

Extinction is a term that refers to both a procedure - the CS is presented without the US, and to an outcome - the CS loses its ability to evoke a conditioned response.

53
Q

What is the associative loss hypothesis?

A

Assumes that extinction is due to a CS-alone presentation eliminating the original CS-US association.

54
Q

What is the competing memory hypothesis?

A

Assumes that extinction produces a new association called a CS-noUS association, but that the orginal CS-US is still intact but is inhibited by the new association.

55
Q

What 3 finidings show that the associative loss hypothesis is not correct because extinction is not permanent?

A
  1. Spontaneous recovery
  2. Renewal effect
  3. Reinstatement effect
56
Q

What is spontaneous recovery?

A

Spontaneous recovery can occur when there is a long retention interval between extinction and the test.

57
Q

What is the renewal effect?

A

Renewal can occur when the context where extinction trials occurs is different from the context in which training occurs, renewal will occur back in the training context.

58
Q

What is the reinstatement effect?

A

Reinstatment occurs if the US is re-presented without the CS. In all cases, recovery from extinction occurs even though the CS and US are never repaired.

59
Q

What is the neural basis for fear extinction?

A

Extinction training strengthens synaptic connections linking the context and CS input to extinction neurons in the basal nucleus to ITCs and to neurons in the infralimbic prefrontal cortex that also projects to ITCs. Thus, when the CS is presented ITC-b is activated and neurons in the critical amygdala are inhibited.

60
Q

Describe the experiment that showed that the hippocampus is critical for the renewal of fear.

A

In the experiment, rats are conditioned to the CS in context A but extinguished in context B. Normal rats display renewed fear of the CS if they are tested in context A, but display no fear in context B. Rats with damage to the hippocampus do not display renewed fear in context A.

61
Q

Describe the experiment that showed that spontaneous recovery may be due to active forgetting.

A

Rats received fear conditioning, and then extinction training so that the fear behavior was extinguished. Either Glua23Y or a vehicle was injected into the infralimbic cortec to prevent AMPA receptor endocytosis. Rats in the vehicle condition had spontaneous recovery of the fear behavior, while mice with GluA23Y did not.

62
Q

Why is extinction considered new learning and dependent on NMDA receptors?

A

APV antagonizes the glutamate binding site on the NMDAr and interferes with extinction. DCS is an agonist for the glycine binding site on the NMDAr and enhaces the processes that produce extinction.

63
Q

How can extinction erase fear memories in infant rats?

A

When infant rats experience extinction training they do not exhibit either spontaneous recovery or renewal.

64
Q

What is the role of perineuronal nets in the regulation of plasticity?

A

Early in development, immature perineuronal nets surround spines and during this period extinction training can erase a memory. When these nets are mature, extinction training does not erase the fear memory and extinction is due to new learning.

65
Q

What were Ledoux’s 2 proposed systems of fear?

A
  1. A subcortical system for defensive behavior
  2. A neocortical system that generates the subjective feelings of fear.
66
Q

What is the evidence that midbrain subcortical nuclei are responsible for generating fear behaviors?

A

Direct electrical stimulation of these brain regions can elicit fear behaviors, and damage to these regions impairs the expression of fear behaviors.

67
Q

What are the components of the basal ganglia?

A

Caudate nucleus, putamen, globus pallidus, subthalamic nucleus, nucleus accumbens, and substantia nigra.