ch 9: Drug Misuse and Addiction

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40 Terms

1
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what are recreational drugs + most popular (legal + illegal) (4)

  • psychoactive substances consumed voluntarily

    • have the potential to be used in a problematic way

  • illegal in US → marijuana

  • legal drugs: alcohol, tobacco

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categories of drugs in Canada (5)

  1. prescription drugs: antibiotics, antidepressants, insulin

  2. over-the-counter (OTC): acetaminophen, ibuprofen

  3. controlled substances: opioids, cocaine, amphetamines

  4. natural health products (NHPs): vitamins, herbal remedies

  5. cannabis: dried flower, edibles, oils 

<ol><li><p><strong>prescription drugs:</strong> antibiotics, antidepressants, insulin</p></li><li><p><strong>over-the-counter (OTC):</strong> acetaminophen, ibuprofen</p></li><li><p><strong>controlled substances:</strong> opioids, cocaine, amphetamines</p></li><li><p><strong>natural health products (NHPs):</strong> vitamins, herbal remedies</p></li><li><p><strong>cannabis:</strong> dried flower, edibles, oils&nbsp;</p></li></ol><p></p>
3
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what characterizes a drug addiction (3)

  • considered to be chronic, relapsing behavioural disorder 

  • focus is on compulsive features of drug seeking + use including craving 

  • individuals remain addicted for long periods of time → drug-free periods (remission) often followed by relapses 

4
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substance use vs substance-induced disorders (2)

  • substance use disorders: cognitive, bhvrl and physiological symptoms indicating that the individual continues using the substance despite significant substance-related problems

  • substance-induced disorders: reversible substance-specific syndrome due to recent ingestion of a substance (ie, ↑bp)

5
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substance-related disorders → what do they have in common + what are the 10 classes

  • all substances have the ability to activate the neural circuitry that mediates rewards

  1. alcohol: beer, wine, spirits

  2. caffeine: coffee, tea, energy drinks, pills

  3. cannabis: marijuana, hashish THC concentrates

  4. hallucinogens: LSD, mescaline

  5. inhalants: glue, paint thinners, nitrous oxide 

  6. opioids: heroin, morphine, oxycodone, fentanyl

  7. sedatives, hypnotics, anxiolytics benzodiazepines, barbiturates

  8. stimulants: amphetamine, methamphetamine, cocaine

  9. tobacco (nicotine): cigarettes, vaping, chewing tobacco

  10. other (unknown) substances 

<ul><li><p>all substances have the ability to activate the neural circuitry that mediates rewards</p></li></ul><ol><li><p><strong>alcohol</strong>: beer, wine, spirits</p></li><li><p><strong>caffeine:</strong> coffee, tea, energy drinks, pills</p></li><li><p><strong>cannabis:</strong> marijuana, hashish THC concentrates</p></li><li><p><strong>hallucinogens:</strong> LSD, mescaline</p></li><li><p><strong>inhalants:</strong> glue, paint thinners, nitrous oxide&nbsp;</p></li><li><p><strong>opioids:</strong> heroin, morphine, oxycodone, fentanyl</p></li><li><p><strong>sedatives, hypnotics, anxiolytics</strong> benzodiazepines, barbiturates</p></li><li><p><strong>stimulants:</strong> amphetamine, methamphetamine, cocaine</p></li><li><p><strong>tobacco (nicotine):</strong> cigarettes, vaping, chewing tobacco</p></li><li><p><strong>other (unknown) substances&nbsp;</strong></p></li></ol><p></p>
6
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DSM-5 criteria to diagnose substance use disorder (3)

  1. pattern of use must be problematic + must lead to clinically significant impairment or distress

  2. no single criterion for determining presence of a substance use disorder

  3. severity: mild-severe → depending on how many of the diagnostic criteria are met

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____ is the only compulsive behavioural disorder in the DSM-5 → meets several of the criteria for ______ and shows similar _____ and ______ dysfunctions

  1. gambling

  2. substance abuse disorder

  3. neurobiological 

  4. cognitive

8
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two types of progression in drug use

  1. gateway theory: progress from legal substances like alcohol → marijuana → cocaine/heroin/etc

  2. regular pattern → problematic use (addictive) and many people mature out of it → alcohol/illicit drug use decline w age

9
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schedule of controlled substances + factors that need to be considered (4)

  • 5 classes → based on degree of potential misuse and medicinal value 

  • capture ratio: percent who try a drug and become habitual users

  • considering withdrawal, tolerance, reinforcement, dependence, and intoxication

    • heroin, alcohol, nicotine most addictive → caffeine, hallucinogens, cannabis least addictive

<ul><li><p><strong>5 classes</strong>&nbsp;→ based on degree of potential misuse and medicinal value&nbsp;</p></li><li><p><strong>capture ratio: </strong>percent who try a drug and become habitual users</p></li><li><p>considering withdrawal, tolerance, reinforcement, dependence, and intoxication</p><ul><li><p>heroin, alcohol, nicotine most addictive → caffeine, hallucinogens, cannabis least addictive</p></li></ul></li></ul><img src="https://knowt-user-attachments.s3.amazonaws.com/a0a1a7fc-1d39-4792-a30f-b96e16aef276.png" data-width="100%" data-align="center"><p></p>
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11
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about ___% of Canadians (____million people) will meet the criteria for a substance use disorder at some point in their life → many struggle from _____ (AUD) → ___% of males and % of females of the age of ___

  1. 21.6%

  2. 6 million ppl

  3. alcohol use disorder (AUD)

  4. 5% of males

  5. 2% of females

  6. 15

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how does addiction correlate w race in Canada? (3)

  • significant negative impacts on indigenous communities → solvent abuse 

    • alcohol deaths are twice as high + illegal drug deaths three times as high in indigenous communities vs general population

  • also high in African, Caribbean, and Black Canadians 

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how does addiction correlate w age in Canada? (4)

  • 20-24 year old Canadians are most likely to exceed Canada’s low-risk drinking guidelines 

  • age 55 and older tend to use alcohol + other drugs less frequently than younger Canadians

    • alcohol _ prescription drug abuse increases 

    • substance abuse symptoms can mimic other medical/bhvrl conditions

<ul><li><p>20-24 year old Canadians are most likely to exceed Canada’s low-risk drinking guidelines&nbsp;</p></li><li><p>age 55 and older tend to use alcohol + other drugs less frequently than younger Canadians</p><ul><li><p>alcohol _ prescription drug abuse increases&nbsp;</p></li><li><p>substance abuse symptoms can mimic other medical/bhvrl conditions</p></li></ul></li></ul><p></p>
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how does addiction correlate w gender in Canada? (4)

  • sex differences linked to female reproductive hormones/differences in stress responding

  • men are 70% more likely to be dependent on drugs/alcohol

    • men more likely to begin abusing drugs as a part of a pattern of risky bhvr or to enhance social bhvr

    • women: more likely to use drugs to reduce stress, anxiety, loneliness, depression → progress faster from first use to problematic use (telescoping)

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how is addiction co-diagnosed with a psychiatric disorder in men vs women (2)

  • women: depression, anxiety, phobias

  • men: ADHD and antisocial personality disorder

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how does the route of administration affect the addictive potential of a substance?

  • routes that cause fast onset of drug action have the greatest addiction potential → produce strongest euphoric effects + shortest latency

  • shorter latency btw response + reinforcement would lead to stronger + faster drug conditioning

    • IV/inhalation: rapid drug entry + fast onset of drug action → shorter duration

    • oral/transdermal: relatively slow absorption → slow drug availability to the brain

<ul><li><p>routes that cause fast onset of drug action have the greatest addiction potential → produce strongest euphoric effects + shortest latency</p></li><li><p>shorter latency btw response + reinforcement would lead to stronger + faster drug conditioning</p><ul><li><p><strong>IV/inhalation:</strong> rapid drug entry + fast onset of drug action → shorter duration</p></li><li><p><strong>oral/transdermal: </strong>relatively slow absorption → slow drug availability to the brain</p></li></ul></li></ul><p></p>
17
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In IV self-administration, how do fixed-ratio and progressive-ratio schedules differ, and what does breakpoint index? (2)

  • FR: same number of presses per infusion; yields U-shaped dose–response for reinforcers (low dose = weak effect; mid = peak; high dose = aversion/sedation ↓ responding).

  • PR: response requirement escalates each infusion; the breakpoint (last ratio achieved) indexes motivation/reinforcing strength of the drug.

<ul><li><p><strong>FR:</strong> same number of presses per infusion; yields <strong>U-shaped</strong> dose–response for reinforcers (low dose = weak effect; mid = peak; high dose = aversion/sedation ↓ responding). </p></li><li><p><strong>PR:</strong> response requirement escalates each infusion; the <strong>breakpoint</strong> (last ratio achieved) indexes <strong>motivation/reinforcing strength</strong> of the drug.</p></li></ul><p></p>
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Why do many drugs show a U-shaped self-administration curve under fixed-ratio (FR) schedules? (2)

  • Low doses are sub-threshold (not rewarding enough) → low responding; moderate doses maximize reward with tolerable side effects → peak responding;

  • high doses produce aversive/sedating/toxic effects or rapid satiation → reduced responding.

<ul><li><p><strong>Low doses</strong> are sub-threshold (not rewarding enough) → low responding; <strong>moderate doses</strong> maximize reward with tolerable side effects → peak responding; </p></li><li><p><strong>high doses</strong> produce <strong>aversive/sedating/toxic</strong> effects or rapid satiation → <strong>reduced</strong> responding.</p></li></ul><p></p>
19
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In the reinstatement model, what 3 triggers can restore extinguished drug seeking, and what do they represent clinically? (4)

  • Drug priming,

  • stress, and

  • drug-paired cues.

  • Clinically map to drug exposure, stressful events, and environmental reminders, respectively—key drivers of relapse in humans.

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____ plays a key role in establishing and maintaining drug addiction → withdrawal symptoms (______) motivates users to take the drug again → (_____) 

  1. physical dependence 

  2. abstinence syndrome 

  3. negative reinforcement 

21
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what do the experimental results from heroin studies support in the treatment of opioid-dependence? (2)

  • support the use of agonist replacement theory in the treatment of opioid-dependence

    • ie. methadone or buprenorphine

22
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drug-taking behaviour progresses from _____ → ______. this process may be due to _____ system in the brain (_____)

  1. impulsive stage

  2. compulsive stage 

  3. gradual recruitment of an antireward system

  4. neuroadapted state

<ol><li><p>impulsive stage</p></li><li><p>compulsive stage&nbsp;</p></li><li><p>gradual recruitment of an antireward system</p></li><li><p>neuroadapted state</p></li></ol><p></p>
23
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how do genetic factors contribute to the risk for addiction? (3)

  • heritability of substance use disorders is in the range of 40-60%

  • remaining variability is due to environmental factors → epigenetic and gene-by-environment interactions

    • genetic component is only expressed in ppl w specific life events ie. stressful events 

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Name key psychosocial risk factors for developing SUD, especially in adolescence. (10)

  1. Younger age;

  2. less education;

  3. minority status (contextual inequities);

  4. unemployment;

  5. conduct problems;

  6. high stress load & poor coping;

  7. family conflict/violence;

  8. inadequate parental monitoring;

  9. childhood maltreatment;

  10. psychiatric comorbidity (anxiety, mood, personality disorders). 🧠

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Contrast the self-medication and shared etiology hypotheses for SUD–psychopathology comorbidity. What’s the current evidence? (3)

  • Self-medication: people use drugs to relieve symptoms (e.g., anxiety → sedatives).

  • Shared etiology: common genetic/environmental vulnerabilities raise risk for both disorders.

  • Evidence: not mutually exclusive—both likely operate; varies by person and drug. 🔁

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How can social environment raise or lower addiction risk? Give risk and protective examples. (2)

  • Risk: social facilitation and drug-using peer groups, subculture norms, loss of conventional roles/responsibilities, family instability.

  • Protective: supportive network, stable lifestyle/structure, alternative reinforcers (work, hobbies, sports), and coping-skills training for stress. 🛡

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natural recovery from substance misuse + addiction (2)

  • transitioning from substance misuse/addiction → non-problematic use → nonuse without assistance

  • may be facilitated by transitional life events and/or negative consequences of continuing drug use

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what helps the maintenance of abstinence (5)

  • avoiding drug-associated cues,

  • non-drug sources of reinforcement,

  • new social support networks,

  • financial stability

  • achieving a general structure to the individual’s life

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biopsychosocial model of addiction (2)

  • includes the full range of pharmacological, biological, and psychological/sociocultural factors that influence addiction risk

  • some factors promote the likelihood of substance misuse + addiction → others reduce it

<ul><li><p>includes the full range of pharmacological, biological, and psychological/sociocultural factors that influence addiction risk</p></li><li><p>some factors promote the likelihood of substance misuse + addiction → others reduce it</p></li></ul><p></p>
30
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development of addiction has been conceptualized as a repeating cycle of 3 stages:

  1. preoccupation with + anticipation of obtaining + using the substance

  2. escalating use → drug binges + intoxication

  3. withdrawal + associated negative effects 

<ol><li><p><strong>preoccupation</strong> with + anticipation of obtaining + using the substance</p></li><li><p><strong>escalating use</strong> → drug binges + intoxication</p></li><li><p><strong>withdrawal</strong> + associated negative effects&nbsp;</p></li></ol><p></p>
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how do most recreational drugs affect the reward circuit in the brain? (5)

  • all recreational drugs activate the mesolimbic DA pathway from the VTA → NAcc

  • psycho-stimulants: directly elevate synaptic DA lvls

  • opioids/alcohol/nicotine/cannabinoids indirectly ↑ NAc DA

    • opioids: u-opioid disinhibits VTA neurons

    • nicotine excites VTA

    • alcohol/cannabinoids modulate network that increases net DA

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_____ important bc early use is dominated by _____ → the drug ___ the probability of ___ bc it feels good/strongly wanted 

  1. the mesolimbic DA pathway from the VTA → NAcc

  2. positive reinforcement

  3. increasing

  4. re-use

33
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incentive sensitization theory (4)

  • distinction btw liking vs wanting a reward

  • drug reward declines due to tolerance

  • liking peaks early then declines → wanting increases + stays high

  • positive → negative reinforcement

<ul><li><p>distinction btw liking vs wanting a reward</p></li><li><p>drug reward declines due to tolerance </p></li><li><p>liking peaks early then declines → wanting increases + stays high</p></li><li><p>positive → negative reinforcement </p></li></ul><p></p>
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What neural changes drive the preoccupation/anticipation stage of addiction, and how do they bias behavior? (3)

PFC dysregulation (dlPFC/ACC: control↓; vmPFC/OFC: over-valuation of drug cues) ➜ corticostriatal shift from goal-directed (DMS) to habit (DLS)cue-triggered seeking and poor impulse control → relapse.

<p><strong>PFC dysregulation</strong> (dlPFC/ACC: control↓; vmPFC/OFC: over-valuation of drug cues) ➜ <strong>corticostriatal shift</strong> from <strong>goal-directed (DMS)</strong> to <strong>habit (DLS)</strong> ➜ <strong>cue-triggered seeking</strong> and poor impulse control → relapse.</p>
35
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In the binge/intoxication stage, distinguish reward (“liking”) from incentive salience (“wanting”) and name the core circuit. (4)

  • Liking = hedonic pleasure; wanting = motivational pull of drug/cues.

  • Core circuit: mesolimbic DA, VTA → nucleus accumbens (NAc).

  • Stimulants ↑ DA directly (DAT effects);

  • opioids, nicotine, alcohol, cannabinoids ↑ DA indirectly (e.g., μ disinhibition of VTA).

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How do liking and wanting change with repeated use, and what signals stamp in cue–drug learning? (4)

  • Liking ↓ (tolerance);

  • wanting ↑/persists (incentive sensitization to cues).

  • Phasic DA reward-prediction-error signals strengthen cue–drug associations.

    • Opioid & endocannabinoid systems also reinforce.

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Which systems mediate the withdrawal/negative affect stage, and how does motivation shift? (2)

  • CRF, NE, dynorphin in the extended amygdalahyperkatifeia (dysphoria, anxiety) and anhedonia.

  • Motivation flips from positive (“use to feel good”) to negative reinforcement (“use to stop feeling bad”).

<ul><li><p><strong>CRF, NE, dynorphin</strong> in the <strong>extended amygdala</strong> → <strong>hyperkatifeia</strong> (dysphoria, anxiety) and <strong>anhedonia</strong>. </p></li><li><p>Motivation flips from <strong>positive</strong> (“use to feel good”) to <strong>negative reinforcement</strong> (“use to stop feeling bad”).</p></li></ul><p></p>
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Why can craving reappear long after abstinence? What neural substrates are implicated? (2)

  • Long-lasting plasticity in reward (VTA→NAc) and anti-reward (extended amygdala) circuits;

  • gene/epigenetic changes and altered synaptic strength sustain vulnerability to cue-induced craving.

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Summarize the brain disease vs choice/motivational models of addiction and the testable prediction each makes. (3)

  • Brain disease: pathological circuit dysregulation; predicts persistent vulnerability despite intentions.

  • Choice/motivational: drug use serves functions (relief, scarce alternatives); predicts changing contingencies (access to non-drug rewards) reduces use. Best view integrates both.

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What is contingency management, and why does it work? (2)

  • Behavioral treatment delivering immediate, certain non-drug rewards for verified abstinence.

  • It reallocates behavior toward alternative reinforcers, countering delay discounting and competing with drug reward.