Methods (part 1) Flashcards

1
Q

Why do we need to measure the behaviour of a whole organism

A

treatments and cures need to be tested on organism to check for therapeutic value and unwanted side effects

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2
Q

Clinical relevance of measuring behaviours

A
  • fear (PTSD, phobias)
  • anxiety (product of condition)
  • attention (schizophrenia, ADHD)
  • depression (bipolar disorder)
  • locomotor activity (PD)
  • locomotor coordination (Huntington’s Chorea)
  • learning (autism spectrum disorder)
  • memory (Alzhimer’s disease)
  • sensory perception (pain sensitivity, chronic pain)
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3
Q

How can we measure fear

A

cued or contextual fear conditioning

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4
Q

How can we measure anxiety

A

elevated plus maze/light-dark maze

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5
Q

How can we measure attention

A

attentional set-shifting task

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6
Q

How can we measure depression

A

learned helplessness

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7
Q

How can we measure locomotor activity

A

activity box

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8
Q

How can we measure locomotor coordination

A

rotarod, skilled reaching, balance beam

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9
Q

How can we measure learning

A

morris water maze, radial arm maze, paired associate learning

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10
Q

How can we measure memory

A

memory: spontaneous alternation, novel object recognition

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11
Q

How can we measure sensory perception

A

Von Frey test, temperature sensitivity

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12
Q

What are the 3 validity criteria for animal models

A
  • construct validity
  • predictive validity
  • face validity
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13
Q

Describe construct validity

A

similar cause of pathophysiology between the human condition and the animal model

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14
Q

Describe predictive validity

A

treatments that are effective in animal models are also effective in human patients, and vice versa

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15
Q

Describe face validity

A

the symptoms of the animal model mimic the symptoms of the human condition

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16
Q

Describe the simplified duel coding for behavioral tasks

A
  • translational: train an animal to mimic a human test
  • naturalistic: use a relevant intrinsic or innate skill or preference of the animal
17
Q

Describe classical conditioning

A
  • e.g. Pavlov’s dog
  • stimulus triggers biological response is paired with a new stimulus that results in the same reaction
  • cannot create new behaviour, but instead triggers involuntary biological responses
  • conditioning can be undone through extinction
18
Q

Clinical relevance of classical conditioning

A
  • e.g. addiction
  • contextual cues of drug taking/smoking/drinking
  • can be positive/negative
  • conditioned stimulus affect physiological response, so might compensate for “missing” conditioned stimulus
19
Q

What is an unconditioned stimulus

A

intrinsic response (e.g. dog salivating)

20
Q

Cued fear conditioning

A
  • unlearned sound = shock (unconditioned stimulus) = freeze (jump/run)
  • learned sound (conditioned stimulus) = freeze
21
Q

Contextual fear conditioning

A
  • dining room when sound and no shock = no freeze
  • bedroom with sound and shock = freeze
  • bedroom with sound and no shock = freeze
22
Q

Parts of the brain involved in cued fear conditioning

A

amygdala

23
Q

Parts of the brain involved in contextual fear conditioning

A

amygdala and hippocampus

24
Q

Role of the hippocampus

A
  • store and remember information
  • ‘tags’ memories with information about where and when they occurred
  • when ‘threat system’ is active, the hippocampus doesnt work as well and can forget to tag the memories with time and place information, meaning they sometimes get stores in the wrong place
  • when we remember it can feel like it is happening again
25
Q

Role of the amygdala

A
  • threat system
  • set off fight or flight response
  • not good at discriminating between real dangers and percieved dangers
  • can trigger FoF by just thinking about unpleasant memory or danger that has passed
26
Q

Regulatory relationships between the mPFC, hippocampus and amygdala

A
  • mPFC inhibits amygdala and stimulates hippocampus
  • amygdala inhibits mPFC and hippocampus
  • hippocampus inhibits amygdala and stimulates mPFC
27
Q

Lateral hypothalamus in panic response

A
  • increased HR
  • increased BP
28
Q

Dorsal vagal nerve in panic response

A
  • bradycardia
  • ulcer disease
29
Q

Parabrachial nerve in panic response

A
  • panting
  • respiratory diseases
30
Q

Basal forebrain in panic response

A
  • arousal
  • hypervigilance
  • attention
31
Q

Nucleus reticularis pontis caudalis in panic response

A

increased startle response

32
Q

Central grey area in panic response

A
  • freezing
  • decreased social interaction
33
Q

Paraventricular nerve in panic response

A

corticosteroid release

34
Q

What is active place avoidance

A
  • “sophisticated” version of fear conditioning
  • tests accurate spatial learning and spatial strategies
  • using negative reinforcer (shock)
  • creates angry/anxious/ fearful mice
35
Q

Describe active place avoidance

A
36
Q

Measuring anxiety

A
  • elevated plus maze / light-dark maze
  • measure time spent in oven (aversive) vs closed (safe) arms
  • no certain stimulation
  • prefer dark environment
  • more anxious they are, longer it would take to come into open arms
  • uses natural animal behaviour
37
Q

Measuring attention

A
  • attentional set-shifting task
  • rat/mouse pay attention to either odour of bowl, texture of digging medium, or texture of bowl covering
  • correct strategy is switched frequently
  • test attention to different types of sitmuli
  • wisconsin card shifting task
38
Q

Measuring depression

A