T3L1 reward and addiction Flashcards

1
Q

addiction/dependence def

A

a persistent order of brain function in which compulsive drug use occurs despite serious negative consequences for the afflicted individual

both physical and psychological

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2
Q

withdrawal symptoms def

A

negative physiological and emotion features that occur when the drug is not taken

generally the opposite effect of the positive that the drug makes

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3
Q

tolerance

A

diminished response to the effects of a given amount of drug following repeated exposures to the drug

larger dose for same effect

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4
Q

where do drugs act on the brain

A

the reward system:

the mesocorticolimbic pathway is formed of:

  1. mesolimbic system
  2. mesocortical system

also involves

  • amygdala
  • prefrontal cortex
  • hippocampus
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5
Q

anticipation of reward involves the __

A

nucelus accumbens (NAcc)

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6
Q

neurotransmitter of reward

A

dopamine - DA

  • has an error signal
  • the reinforcement system is activated by unexpected stimuli, and by presence of reward relative to prediction

anticipation releases more dopamine than actual reward
unexpected reward also releases a lot

unpredictable - nucleus accumbens (needs to be learned)
predictable - temporal lobe (has been learned)

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7
Q

function of reinforcement system

A

detect reinforcing stimulus:

  • recognise something good has happened
  • learning

strengthen neural connections:

  • between neurons that detect stimulus and neurons that produce response
  • LTP
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8
Q

drug induced synaptic plasticity

A
  • in NAcc (early reinforcement)
  • dorsal striatum (caudate, putamen- instrumental conditioning)

consolidate:

  • drug wanting
  • drug seeking
  • drug taking
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9
Q

mesocorticolimbic dopamine system - natural

A
  • pathway for reward and reinforcement
    s15

natural reinforcers eg sex, food cause extracellular DA release into NAcc (into synapse)

  • the behaviours activating system is reinforced, so more likely to be repeated
  • addictive drugs cause more powerful and reliable activation than natural stimuli
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10
Q

effects of drugs on DA system

pshycostimulants

opiates

alcohol

nicotine

A

psychostimulants - direct action on dopaminergic neurons in NAcc

opiates- indirectly inhibit GABAergic interneurons in VTA (disinhibition of VTA DA neurons)

alcohol - disinhibition of VTA DA neurons

nicotine- increases NACC DA, stimulates nicotinic cholinergic receptors on mesocorticolimbic DA neurons

maybe check out s20 that pretty cool huh B)

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11
Q

cocaine and amphetamines -

A

DA AGONISTS
- potentiate monoaminergic transmission by inhibition of DA, 5HT, NA reuptake inhibitors

(coke inhibits reuptake transporter, amphetamine reverses it)

coke:

  • psychotic behaviour
  • long term decrease in DA transporters and receptors
  • hypofrontality
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12
Q

all drugs of abuse cause

A

increase in AMPA/NMDA ratio

- increase in basal excitatory synaptic strength

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13
Q

associative learning

A

cells that fire together wire together

coincidence firing between sensory pathways and mesocorticolimbic pathway induce LTP
- thus sensory information, people, places, emotions etc. present at the time when drug induced DA release occurs will become associated with taking the drug

DOPAMINE ENHANCES LTP:

  • modifies glutamatergic transmission in LTP
  • synaptic remodelling- more spines and dendritic branches
  • long term changes even after months of absetenance

ie higher risk of doing coke at a club if you’ve done it there before, even years later

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14
Q

opiates

A

action:

  • on endogenous opioid receptors
  • inhibitory
  • many receptors (m, k, d)
  • morphine works on mu receptors

reward:

  • disinhibition of DA neurons in VTA
  • action at opiate receptors in NAcc independent of DA release

see s35 for mechanism

physical dependence to opiates:
- chronic activation of opiate receptors leads to homeostatic mechanism that compensates for changes leading to physical dependence

acute morphine: inhibits LC firing
chronic treatment: LC neurons return to normal firing rate
withdrawal: dramatic increase in LC firing s38,39

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15
Q

alcohol

A
  1. GABAa agonist (inhibitory)
  2. NMDA antagonist (blocks excitation)

large doses inhibit functioning of most voltage gated channels

increase DA release in NAcc

opiate system also involved: naltrexons (an opiate antagonist) stops craving in alcohols

physical dependence:
chronic alcohol leads to downregulation of GABAa receptors, upregulation of NMDA
- in presence of alcohol, firing balance returns to normal
- in withdrawal, balance shifts to excitation
s40

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16
Q

nicotine

A

acts as nicotinic acetylcholine receptors (nAChRs) (ligand gated ion channels)

  • release DA into NAcc

due to:

  • activation of receptors on cell body to increase firing in VTA
  • facilitation of DA release by presynaptic receptors in NAcc

opiate involvement system
- both opiate and DA antagonists can block nicotine induced behaviours and self administration