Van Den Oever - Aim and Procedure

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Last updated 2:28 PM on 10/14/25
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31 Terms

1
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What is the full name of Van den Oever's study?

Van den Oever et al 2008 Prefrontal Cortex AMPA Receptor Plasticity is Crucial for Cue Induced Relapse to Heroin Seeking Behaviour

2
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What was the aim?

to investigate changes in (the) composition and function of synapses in (the) medial prefrontal cortes upon reexposure to heroin cues after long term abstinence

3
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What were the participants?

hundreds (of) male waster rats

4
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What was an advantage of skinners box?

allowed (the) researcher to control all extra variables such as social interaction and situational environmental factors creating a mini laboratory setting to model human experience

5
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Describe the process of self administration of heroin?

light and buzzer, if rat pokes nose through hole, heroin dose through catheter

6
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What were the drug associated cues?

light and buzzer

7
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What was the drug seeking behaviour?

nose poking

8
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What was modelled by the light and buzzer, and nose poking?

drug associated cues and drug seeking behaviour

9
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What is an advantage of using animals in this study?

scientific as allows objective data collection and high control, standardised procedures

10
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What are three examples of standardised procedures?

biological control as all male, same audiovisual cues, same amount of heroin (each time)

11
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What was the focus of the study?

concerned with biological changes in (the) brain linked to heroin addict relapse upon reexposure to drug associated cues

12
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What changes in the brain did van den oever specifically look for?

changes in AMPA receptors on (the) postsynaptic neurones in (the) mPFC

13
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What are AMPA receptors?

receptors for the neurotransmitter glutamate which is linked with reward pathways

14
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What was the name of stage 1?

self( )administration of heroin

15
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What happened to the experimental group during stage 1?

trained to self( )administer heroin upon audiovisual cues

16
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What happened to the control group during stage 1?

trained to self( )administer a sucrose solution

17
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Why was a control group used?

to ensure that any neurobiological changes were due to heroin and not just any reward

18
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What is the name of stage 2?

abstinence and extinction

19
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What happened to the experimental group in stage 2?

split into two groups

20
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What happened to the abstinence group in stage 2?

kept in separate cage for 21 days with no heroin

21
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What happened to the extinction group in stage 2?

left in (the) self administration box for 21 days with no heroin

22
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What difference was found between the abstinence and extinction groups?

none

23
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What is the name of stage 3?

reexposure to drug associated cues

24
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What happened to the abstinence and extinction groups in stage 3?

split into two groups

25
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What happened to group 1 in stage 3?

reexposed to drug associated cues for 60 mins with no heroin

26
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What happened to group 2 in stage 3?

not exposed to drug associated cues for 60 mins with no heroin

27
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Why was group 2 in stage 3 necessary? (not exposed to drug cues)

control to confirm that any synaptic changes were due to (the) drug associated cues

28
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What was the measure of relapse?

nose poking

29
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What was the name of stage 4?

analysis of composition and function of synapses in (the) mPFC

30
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What happened to all rats in stage 4?

decapitated and their brains frozen and analysed using mass spectrometry

31
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What is mass spectrometry?

analytical technique to identify the amount and types of chemicals present in a microscopic sample allowing detection of subtle changes in receptor proteins

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