W2L1 - Fear Conditioning and Extinction Flashcards

1.) What is Fear Conditioning and Extinction 2.) Fear Conditioning in Brain 3.) Fear Extinciton in Brain 4.) Psychiatric Disorders (Anxiety and PTSD)

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1
Q

What is fear conditioning a form of and what does it involve?

A
  • Associative Learning or Classical conditioning
    • Pairing aversive stimulus (US; Shock) with neutral stimulus (CS; Light)
    • Original neutral stimulus (CS; Light) leads to fear response (CR)
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2
Q

What is classical and operant condiioning. Similarity/Differences

A

Classical:

  • Associating automatic involuntary behaviour and stimulus
  • Neutral stimulus before reflex

Operant:

  • Associating voluntary behaviour and consequence
  • Apply reinforcement or punishment to strengthen or weaken behaviour
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3
Q

What is fear extinction?

A

Gradual reduction of fear response when the conditioned stimulus is repeatedly presented without aversive outcome

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4
Q

What are three properties of fear extinction?

A
  • Fear extinction requires extensive traning and fragile, unlike fear conditioning (rapid and robust)
    • Spontaneous Recovery: Time
    • Renewal: Context
    • Reinstatement: Re-exposed to original US
  • Fear extinction is context-dependent
    • Learning to reduce fear in one context may not translate to another
  • Fear extinction produces new memory trace (CS without aversive outcome), inhibiting original CS-US fear association
    • Not erase, but inhibit
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5
Q

What are typical procedures in animal studies of fear conditioning/extinction

A
  1. ) Conditiong acquisiton phase
    * Light/tone is paired with shock
  2. ) Extinction phase (Different chamber for context)
    * Presented with repeated trials of light without shock
  3. ) Test Phase
    * Subsequent day to assess retention of extinction
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6
Q

From Rodent Studies, How is fear conditioned in the brain (Neurologically)?

A
  1. Sensory input (CS) from auditory/visual cortex pairs with pain signals (US) from somatosensory cortex in basolateral nucleus of amygdala
  2. Conditioned association from BLA activates central nucleus of amygdala
  3. Central nucelus of amydala sends afferent to hypothalamic and midbrain regions controlling arousal, freezing, hormonal response.
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7
Q

Difference between low and high road

A

Low Road:

  • Autonmatic, rapid, reflexive fear response
  • Senory input > thalamus > amygdala

High Road:

  • Slower cortical inhibitory response.
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8
Q

What are the key areas in fear in RODENTS

A

Prelimbic Cortex (PL)

  • Stimulation increase fear and inactivation reduces fear
  • Activity predicts poor extinction
    • dACC equivalent
    • Fear conditioning

Infralimbic Cortex (IL)

  • Stimulation reduces fear and inactivation impairs extinction
  • Activity predicts good extinction
    • vmPFC equivalent
    • Fear extinction
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9
Q

What does human neuroimaging found in regions for fear conditioning and extinction

A

Conditioning

  • dACC
    • Threat appraisal
  • Bilateral anterior insula
    • Introspective awareness of fear

Extinction

  • vmPFC
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10
Q

What are 3 explanations as to a lack of amygdala activity in human fear conditioning studies?

A
  • Resolution of fMRI
    • Can’t image subnucleii of amygdala
  • Amygdala only recruited with intense threat as part of defence-circuitry response (mild anxiety in human studies)
  • Amygdala response habitutate after repeated trials
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11
Q

According to meta-analysis of fear extinction studies, what is the difference between humans and rodents neurologically

A

Compared to rodents, humans have

  • Less robust vmPFC activation
  • More robust dACC and anterior insula (similar to fear conditioning)
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12
Q

Why are there similar activation in fear conditioning and extinction

A
  1. dACC and anterior insula involved in threat appraisal and experience of anxiety, but they perform different functions
  2. Networks might be activated but no behavioural experience of conditioning (dissociation in fear measures)
  3. Role of vmPFC in extinction is debated, could be contextual processing
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13
Q

Why are three explanations fear conditioning and extinction involved in etiology of anxiety disorders

A
  • Greater conditionability of CS + of anxetiy disorders
  • Greater stimulus generalization
    • Greater Reactivity to CS+ and Generalization to CS-
  • Impaired capacity to inhibt fear to CS+
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14
Q

When compared healthy and anxious participants, what were the results

A
  • Greater conditionability of CS + of anxetiy disorders
    • No Difference
  • Greater stimulus generalization
    • Greater Reactivity to CS+ and Generalization to CS-
    • Overgeneralization in anxious patients
  • Impaired capacity to inhibt fear to CS+
    • Reduced Capacity
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15
Q

What are results of fear extinction and PTSD

A

Compared to Trauma-exposed controls,

  • No greater conditionability in PTSD
  • Evidence of impaired fear extinction in PTSD
    • Increased amygdala activitng during extinction recall
    • Reduced vmPFC activity during extinction recall
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16
Q

What is the link between PTSD symptoms and extinction

A
  • Long-term PTSD have impaired extinction post-trauma (and pre-trauma)
  • Deficits in extinction networks (reduced vmPFC) and increase amygdala activity to threat is normalized after exposure therapy for PTSD (i.e. increase vmPFC; decrease amygdala activity)