FINAL PSYCH 345A Flashcards

1
Q

SEDATIVE-HYPNOTICS
General Description

A
  • Drugs which slow/reduce/depress nervous system
    activity and behavior
  • Collectively, most widely used class of psychoactive
    drugs
  • Arbitrarily classified into four groups
  • barbituate
  • benzodiazapines
  • non-barbituate …
  • misc compounds (includes alcohol)

similarities w hypnotics
- similar uses (to tread anxiety)
- benzodiazapine to tread anxiety

  • Similarities:
    – Uses
    – Sites of action
    – Ability to induce various levels of behavioral
    depression
  • Differences
    – Individual potency
    – Chemical structures which affect ADME

anxiolytic = tranquilizer ) - used to treat agittion and anxiety disorders

sedative hypnotic used to sadate and air sleep

meprobamate - Miltown
mathaqualone - Quaaludes (widely used in 60s)

z drugs - widely used for insomnia
*** PRIMARY MECAHNISM IS MODULATION OF THE GABAA RECEPTOR - BUT HAVE DIFFERENT BINDING AFFINITIES

fast acting short duration - as sedative hypnotic
longer acting barbituate as anxiolytics
Z drugs can target specific symptoms

have been perscribed for bed wetting, arthritis, anxiety, … by the 90s, benzodiazepines have mostly replaced the barbituates. benzodiasapines are safer
- benzodiazepine - diazapam - Valium

phenobarbital is still prescribed for epileptic seisures - used to antagonize stimulant effects of other drugs given

illicit barbituates - “downers”

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2
Q

SEDATIVE-HYPNOTICS
Sites and Mechanisms of Action

A

effects of these drugs: Their effects are
mediated primarily by their ability to modify transmission
of the inhibitory transmitter GABA, specifically at
the GABAA receptor

(1) Ascending Reticular Activating System - Messaging becomes depressed (role of neurological arousal), causes fogginess and sedation
(2) Diffuse Thalamic Projection System - Role in alertness and responsiveness, so sedatives depress this

(3) GABA Receptor Complex System - Receptors(GABA, benzo, or barb) connected to Cl- ion channel, when Cl- enters produces IPSP, induces behavioral depression and neural activity

(3) GABA Receptor Complex System
- see textbook for GABA receptor, slowing activity .. how this works.
- barbituate can open receptor on its own
- overdose on barbituate is more common than on benzodiazapines

The barbiturates, benzodiazepines, and nonbenzodiazepines
do not modify GABAA receptor activity by
altering levels of GABA or by interacting directly with
GABA’s receptor binding site. Instead, these drugs are
positive allosteric modulators—they have their own
binding sites on the GABAA receptor complex that,
when occupied, enhances the effects of GABA binding.

(4) Cells - Reduce cellular metabolism

(5) Norepinephrine synapses - Decrease activity at NE receptors

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3
Q

SEDATIVE-HYPNOTICS - effects, tolerance, depenencey

A

SEDATIVE-HYPNOTICS
* Effects are additive
* Potentiation can occur
* Inhibitory synapses are depressed slightly before
excitatory synapses
* Dependency can develop
* Tolerance can develop

More severe dependency seen when people have been taking high doses for about 6 months
- Causes extreme withdrawal symptoms

Acute tolerance - very rapidly developing, single dose of benzodiazepines
Chronic tolerance - anticonvulsant and drowsiness effects of benzos or barbs
Cross-tolerance - b/w barbs, benzos, and alcohol

Sedative-hypnotic withdrawal
more severe, tremors, delirium, confusion, hallucination, cramps, convulsions - seen at very high doses for a month, but mostly within 6 months

Low-dose withdrawal
seen w benzos taking a therapeutic dose taken for longer than 6 months - symptoms emerge more slowly and never become as severe - no consistent data showing when withdrawals stop - symptom re-emergence of anxiety or sleep that were present before starting drug - irregular HR, increased BP, sensitivity to light, poor attention, perceptual problems

  • initially, only barbituates were used as sedatives and tranqs
  • brandy used before this
    *** respiratory depression seen with barbituates is similar to depression causes by alchohol.

Similarities w different setadive hypnotics:

  • Similarities: - Uses - Sites of action - Ability to induce various levels of behavioral depression
  • Differences - Individual potency - Chemical structures which affect ADME
  • barbituates can open the Cl- ion channel themselves, without GABA binding co-presence.
  • high levels can depress breathing and autonomic centres in brainstem
  • benzodiazapine in contrast, can cause extreme sedation and grogginess but not life threatening

barbituates have much higher portntial for lethal overdose

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4
Q

ALCOHOL
Absorption

A

Alcohol is completely and rapidly absorbed when
taken orally

  • some absorption in stomach, but majority in
    intestines
  • Rate of absorption modified by a # of factors

Volume of fluid (higher concentrated alcohol more quickly absorbed)
Time it takes for stomach to empty
Amount of food in stomach

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5
Q

ALCOHOL
Distribution

A
  • Alcohol fully and evenly distributed through all body
    fluids and tissues
  • BBB is 90% permeable to alcohol
  • Dissolves more readily in water than in fat, thus:
  • Readily crosses placental
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6
Q

Fetal Alcohol Spectrum Disorders

A
  • Prenatal exposure to alcohol is associated with a
    range of congenital physical and behavioral
    abnormalities categorized under the umbrella
    term of Fetal Alcohol Spectrum Disorders
  • likely underestimated idea of how many ppl have FAS due to underreporting

5 drinks for a setting will increase risk
** third leading cause of birth defects - this is the only preventable one

  • Distinction between conditions is the number
    and/or severity of the symptoms
  • Symptoms include:
    – Facial abnormalities

** check in on FAS facial characteristics - Lip-philtrum guide

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7
Q

FASD video - about child CJ

A

child CJ born w FAS (low birth weight) - very thin upper lip, sometime you dont see this in older age.
- often smaller eyes, flatter nose
- a reason that FASD must be diagnosed at birth (problem is that mothers might not be honest about alcohol use during pregnancy)
- diagnosis before 8yo gives kids better chance

  • gangrene in intestines, multiple severe medical disability)
  • adopted kids
  • ppl see her as a totally normal kid and expect things of her.. however she feels more gullible (easily manipulated)
  • she finds it hard to adapt to new situations
  • come challenges w common sense
  • alcohol effects fetus more than cocaine or heroin
  • biggest impact is on brain, can cause severe cognitive impairments
  • causes improper development of brain cells

FAE - older umbrella term for some effects, but not a lightswitch diagnosis (now we call it FASD because its on a spectrum)

  • as CJ gets older, look for signs of depression. ppl get really stressed and worries.
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8
Q

FASD video - about mother Janet

A
  • mother was addicted to alcohol since 13, drink during pregnancy
  • mother drank during pregnancy to relieve nausea
  • child in school was easily distracted, disruptive, lacked work ethic…child had challenges
  • recovered from alcohol, around grade 10 worries about FASD
  • her doctor doubted that she would be one of the parents that who would drink during pregnancy … she reached out to FAS advocacy group and spoke with Jan
  • more difficult to diagnose FAS in adults - we usually stop looking in adults
  • for adults, if their IQ is too high, they dont qualify for any support like $, meals, support homes … etc.
  • trying to keep kid alive and out of jail …
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9
Q

FASD video mark

A
  • adopted son
  • as adult, lots of criminal activity
  • big challenges, Mark is super easily influenced
  • had 24hr house arrest supervision for 2 years
  • 25 yo, but “maturity of 13yo boy”
  • has a daughter and is always supervised when theyre together
  • emotional plea from Marks dad about disabled people in prison and corrections officers
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10
Q

FASD video - genesis house

A
  • support service, programming for adults with FASD
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11
Q

Burns Lake - FASD video

A
  • fas prevention programming, support for women thru pregnancy
  • healthier babies program
  • FOCUS program - for adults with FASD to gain job skills, life skills, work on challenges theyve dealt with
  • people reflect that FOCUS teachers see potential in them
  • *** importance of proactive services - severity of impacts, knowledge that prevention and proactive services are more important
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12
Q

Fetal Alcohol Spectrum Disorders

A

Symptoms include:
– Facial abnormalities
– Heart defects
– Low intellectual functioning
– Growth retardation
– Learning disabilities
* CDN Prevalence Estimates
– 9 /1000 births FASD
– 1-3/1000 births FAS
FASD Cont’d
* Risk and extent of abnormalities believed to be doserelated
* Type of abnormality believed to be related to timing
of alcohol use
– Feldman et at (2012)

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13
Q

ALCOHOL
Metabolization & Elimination

A
  • 90-98% of alcohol ingested is metabolized is stomach (
    and liver (80-85%) before excreted
  • Excretion can occur thru breath, sweat, tears, urine,
    and feces
  • Metabolization in liver occurs in two steps
  • 1
    st step: slow step, determined by amount of alcohol
    dehydrogenase
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14
Q

process of alcohol elimination

A

ethanol –> alcohol dehydrogenaze->, 1. acetaldehyde –> (antabuse) aldehyde dehydrogenase
2. acetyl coenzyme a –> energy, citric acid cycle, carbon dioxide, water

** the first step (w/ aldehyde dehydrogenase) is rate limiting, changes how fast alcohol is metabolized

aldehyde dehydrogenase causes hangover nausea

antabuse - trade name for a medication that prevents abuse of substance (can stop ppl w substance use disorder from drinking be interfering w enzymes) - ppl get very sick from drinking when n this med

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15
Q

nutrition on alcohol?

A

alcohol does NOT have nutritional value, but it does have caloric value

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16
Q

ALCOHOL
Metabolization & Elimination rates of metabolization

A

ALCOHOL
Metabolization & Elimination
* Rate of metabolization is linear with time (10-20
mg/100 ml of blood per hour)
– 1 to 1.5 hours for
* 30 ml of whiskey (40%)
* 120 ml of wine (11%)
* 360 ml of beer (5%)
* Considerable variability between individuals in
elimination rates

  • Non-drinkers metabolize alcohol at slightly lower
    rates than light to moderate drinkers
    (12-15 mg/100mL)

steady metabolism of alcohol - one drink per hour normally keeps u safe w this

*** only slight increases in likelhood of being intoxicated

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17
Q

Alcohol - MEOS

A

Metabolization & Elimination
* Microsomal Ethanol Oxidizing System (MEOS)
– Handles approximately 5 to 10% of alcohol
metabolization, but activity will increase with
higher BALs (blood alc levels)
- this system substantially increases action when drinking

  • Operation of this system believed to be
    responsible for tolerance seen with heavy
    drinking
    *** can have 30-50% increases
  • Operation of this system believed to be
    responsible for cross tolerance to barbiturates
    and benzodiazepines
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18
Q

ALCOHOL
Mechanisms of Action

A

ALCOHOL
Mechanisms of Action
* Facilitates action at the GABAA
receptor chloride
ionphore complex system
– Binds to an allosteric site
– This affects binding at GABA receptor; opens up Cl- ion channel
*** binds to receptor inside the Cl ion channel

  • At high levels, alcohol can directly open up Cl- channel (same as barbiturates)
  • Antagonist of glutamate at NMDA receptors
  • Impacts production and release of endorphins and
    dynorphins; increases release of DA in nucleus
    accumbens
  • Increase activity in mesolimbic dopamine
    system/levels of DA in nucleus accumbens thru release
    of inhibition

*peripheral vision depressed … due to depression of thalamus, brain step …

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19
Q

action of alcohol on GABAergic neurons (Alpha and Beta)

A

GABAergic neurons (ALPHA) coming from
Nucleus Accumbens ACTIVATE GABAergic
Interneurons (BETA)

GABAergic Interneurons (BETA) INHIBIT dopaminergic neurons in VTA: This is the normal state

INTRODUCE ALCOHOL
GABAergic neurons coming from Nucleus Accumbens (the ALPHAs) increase release of GABA onto the Inhibitory GABAergic interneurons (BETAs) - which decrease the
BETAs activity

Decreased BETA activity, less inhibition of dopaminergic neurons, more DA released in nucleus accumbens

receptor site activiation determines effects

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20
Q

ALCOHOL
Physiological Effects

A
  • Sleep disturbances
  • fall asleep faster, sleep longer
    – Induces SWS and depressed REM
  • effects on RED varies with dosage (REM reduced in first sleep cycle)
  • v high doses, theres no REM sleep at all
  • Affect on REM varies with dose
  • we can dev tolerance to sleep effects
  • Depressed Respiration
  • w very high doses - bc it effects the pons
  • Prevents Seizures
  • Vasodilation
  • causes flushed faces
  • can actually cause loss of body heat and freezing
  • Diuretic effect on kidney (decreases vasopressin and antidiuretic hormones)
  • has nothing to do with breaking the seal, but when the blood levels start to fall, causes constant urination
  • vision / balance problems
  • Immunosuppression -
  • relief from anxiety
  • disinibition
    Euphoria
    **
    these 3 are unpredictable!

disrupted memory function - disrupts long term potentiation
- causes issues w attention (then wouldnt remember)

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21
Q

alcohol - blackout

A

unable to remember effects of being under effects of alcohol
- couldnt remember things youve said or done
- laurie couldnt remember handing out flowers at a party

** does not always mean you LOC

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22
Q

Alcohol Effects and BAL

A

.01-.02 - Slight changes in feeling

.03-.05 - Overt feelings of relaxation,
happiness, skin may flush
- may have tingling

.05-.06 - More noticeable changes in
emotion, slight increase in RT (respond slower)
- noticeable tingling
- cortex effected first

.08-.09 - Moderate increase in RT, possible
numbness in cheeks, lips,
extremities, impaired judgment

.10 Coordination/balance impaired
- cerebellum effects

.20 - approx 14 drinks - Difficulty staying awake, standing,
walking without assistance; sensory
functions impaired
- usually LOC

.30 Confusion and stupor

.40 Typically unconscious, threshold of
coma

.45-60 Typically deep coma, LD50 in humans
due to circulatory and respiratory
depression

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23
Q

Toxic Effects with Chronic Alcohol Use - Liver

A

breaks down rather than fat, liver gets compromised
* Liver Disease
– Fatty Liver
– Alcoholic Hepatitis
– Alcoholic Cirrhosis

if stop drinking, fatty liver can be reversed
** BUT alcoholic hepatitis and alcoholic cirrhosis can be permanently broken down and scarred

progression of scar tissues chokes off blood vessels in liver
- not reverible - only treatment is liver transplant
- high death rate
- most deaths in 40-60 yo men
seen w 5 drinks per day / 5 years

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24
Q

do most alcoholics get liver cirrosis?

A

false, usually get help first

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25
Q

highest rates of heavy drinking age group?

A

young men 20-24

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26
Q

toxic effects chronic alcohol - cancer and heart probs

A
  • Cardiovascular Problems
    – Inflammation of Heart Muscle
    – Irregular Heart Contractions
    – Fatty accumulation in heart and arteries
    – High Blood Pressure
  • Cancer
    – Esophagus, Pharynx, Larynx, Breast
  • breast cancer, 41% of women who had 2-5 drinks/day
  • cancer may be due to immunosuppression effects and carcinogenic effects
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27
Q
  • Wernicke-Korsakoff Syndrome
A
  • Wernicke-Korsakoff Syndrome
    – Permanent diffuse damage to hippocampus and
    cerebral cortex
    – Memory problems
    – Primarily due to malnutrition, but other factors
    may play a role

wernickies encephalopathy - due to efficiency in vitamin B (thiamin)
- can be reveresed w vit therapy
- neuronal death due to vit B deficiency, inability to synthesize glucose. interferes with absorption of vitamin

alcohol will kill off brain cells - can cause irreversible brain damage

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28
Q

Alcohol Tolerance

A
  • Can develop with heavy use re: effects of mood
    and behavior
  • Minimal tolerance re: depressant actions of
    respiration
  • Mechanisms responsible:
    – Increased # of Cytochrome P450 enzymes
    – Increased activity of alcohol dehydrogenase in
    liver and stomach
    – Increased activity of MEOS
    – Down regulation of GABA receptors
    – Upregulation of NMDA receptors
    – Behavioral compensation
  • move more slowly to compensate for loss of coordination

acute tolerance can develop - more pronounced effects when blood alcohol levels are rising

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29
Q

Alcohol dependence

A
  • Psychological and physiological dependency can develop (need to consume lots for months to get physiological dependence)

“hair of the dog” kind of like secondary psychological dependencey

  • Withdrawal can be life-threatening
  • can have heart failure occur

low depressed mood with withdrawal can cause suicide - hallucinations can cause suicides

  • Withdrawal symptoms begin in 6-48 hours
  • after stopping consumption
  • Two clusters of symptoms

person she worked with - head injury, withdrawal, hallucinations … (due to opiates after injury?)

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30
Q

first cluster - alcohol withdrawal syndrome

A
  • More common cluster
  • significant rem sleep
    (rem-rebound, agressive sleep_
  • Characterized by:
    – Insomnia, vivid dreaming
    – Tremors, sweating, agitation, n/v, increased hr and bp

could have sroke due to increased BP

  • Peak in 24-36 hours, typically over in 48
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31
Q

second withdrawal cluster - delirium tremens

A

Delirium Tremens
* less common cluster
* More dangerous

  • Characterized by:
    – Extreme disorientation
    – Fever, profuse sweating
    – Periods of hallucinations
  • see small animals, insects
  • antipsychotics might be given to deal with
  • Fever, sweating can lead to heart failure and
    dehydration
  • Suicide sometimes seen
  • agitation and tenseness remains. loss of pleasure
  • dsyphoria, low mood
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32
Q

excessive consumption of ancohol can cause death by overstimulation of nerve cells?

A

FALSE
- nerve cells die by vitamin deficienceies

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33
Q

it is difficult to consume a lethal dose of alcohol

A

FALSE - its easy ish to do this (17 shots in a row …)

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34
Q

new canadian drinking guidelines?

A

2 drinks per week

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35
Q

alcohol has no medicinal value?

A
  • some (less that 3) reduces risk of diabetes t2
  • prevents blood clotting, prevents stroke
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36
Q

The opiates

A

THE OPIATES
Definitional Issues
▪ Naturally occurring, derived, and synthetic
compunds with analagesic properites
▪ Often referred to as “narcotic analgesics”

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37
Q

Naturally Occuring Opiates

A

▪ Morphine, codeine, and
thebaine found in opium
▪ Opium is the sap from
seedpods of opium poppy
(white milky oooze)
▪ Morphine – 10%
▪ Codeine - .75 to 2.5 %
▪ Thebaine - <1%

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38
Q

Opiate Derivatives/Semi-Synthetics

A

Heroin
- derived from **

▪ Other examples
▪ Hydromorphone (derived from morphine),
Oxycodone (derived from _thebane___,
Oxymorphone (can be derived from codnine)
Hydrocodone can be derived from thebaine

adding acetyle groups makes heroin more lipid soluble and more potent than morphine

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39
Q

THE OPIATES
Synthetic

A

▪ Meperdine
- very common, less potent painkiller than morphine

▪ Methadone
- to treat chronic pain & for opioid dependencey (less potent)
- as potent as morphine for pain, less potent euphoric effects

▪ Other examples

▪ Fentanyl - first used for chronic pain

(needed to put ppl under for surgeries, marketed in tablets for chronic pain w cancer, also marketed as a slow release patch) later used on streets. in 2005, many deaths associated w fentanyl use… 30-50 times more potent than heroin (ppl think theyre buying heroin, but laced w fentanyl

LAMM
- for chronic pain

, buprenorphine,

tramadol - synthetic opitate. laurie mentioned that this dosent work for her - she thinks it might have to do with her alcohol use (cross tolerance w opiates and alcohol)

40
Q

Opiate Antagonists

A

▪ Useful in treating overdoses
▪ Naloxone (brand name/trade name, Narcan)
▪ Nalorphine

  • reverse depressed breathing within minutes
  • effects dont last long - will need another dose
41
Q

Dilaudid

A

synthetic opioid - sometimes used recreationally
- new brunswick - call it “hillbilly heroin”

42
Q

Uses of Opioids

A

Uses
▪ Medical uses include
▪ Treatment of pain
▪ Treatment of diarrhea
▪ Treatment of cough

43
Q

History Opioids

A

▪ Medical use dates back hundreds of years
▪ Documented in Egyptian medical scrolls dating
back to 1550 BC
▪ In second century AD, Galen recommended it for
practically everything

children crying

▪ Medical use dates back hundreds of years
▪ Documented in Egyptian medical scrolls dating
back to 1550 BC
▪ In second century AD, Galen recommended it for
practically everything

women for menstrual pain, melancholy

▪ In 1520, medicinal drink called laudanum
introduced
- w alcohol, up to 46-45% alcohol … plus opium
- marketed as “mrs. winslow soothing syrup_ - given names that are misleading, for kids… a fix all

(opioids abused and over prescribed)

▪ Recreational use dates back hundreds of years (at least!)
▪ 2nd Century AD: Galen noted that opium cakes
and candy sold everywhere on the street
- popular, socially acceptable

▪ 18th Century: Opium Dens Appear in China, and elsewhere (e.g, North America, Asia, France) With Chinese “Invention” of Opium Smoking
- heating and inhaling the opium
- ppl are given the drug and the paraphernalia needed in these dens
- very long pipes, reclined while smoking

▪ Up until early to mid 1800s, opium use was
widely socially accepted and not perceived
as a social or medical problem
– despite large number of individuals being
addicted
▪ Mid to late 1800s saw some governmental
efforts in US and Britain to regulate use
and selling of drug
- Due to concern about negative consequences
of chronic opium use or anti-Chinese
prejudice?
- ** problem w drug, or racism?

▪ San Franciso Newspaper Quote
“…many women and young girls, as wellas
young men of respectable family, were being
induced to visit the dens, where they were
ruined morally and otherwise”
- newspaper expresses concerns about opioid use - no mention of alcohol

▪ Canada: Opium Act, 1908: prohibited the
- “importation, manufacture, and sale of
opium for other than medicinal purposes”

▪ Canada: Opium and Narcotic Act, 1911:
prohibited the
- “improper use of Opium and other drugs

44
Q

DeQuincy - english opium eater quote

A
  • depresses, ate opium in a cake
  • felt a resurrection, pains vanished
  • finds happiness, its portable ecstacy, peace of mind …
45
Q

MOA opioids

A

MOA
Opiates will be administered
▪ Orally (cake, tablets)
▪ Parenterally
▪ Via inhalation
▪ Transdermally (slow release for chronic pain)

46
Q

Opioids Distribution

A

Distribution
▪ High concentrations in lungs, liver, spleen
▪ Readily passes thru placental barrier
- baby can experience withdrawal

▪ In brain, concentrated in limbic system, basal
ganglia, nucleus acumbens, ventral tegmental
areas, periaqueductal gray area (pain area), brain
stem

47
Q

Metabolization Opioates

A

Metabolization
▪ Codeine and much of heroin inactive until
metabolized
▪ Metabolization is rapid
▪ Exception is some of the synthetic compounds (e.g., methadone (8-10 hrs 1/2 life), LAAM (48hrs))
these synthetic have longer half life
- this makes them helpful for dependencey

heroin becomes morphine, coedine becomes morphine and other stuff

48
Q

Pharmacological Actions
Opioids

A

Pharmacological Actions
▪ Mimic endorphins
▪ Agonist action at six types of receptors: mu, kappa, delta most understood
- also sigma, epsalon, landa receptors …

▪ Decrease rate of neuronal firing via two
mechanisms:
▪ Inhibiting Ca influx
▪ Enhance flow of K
hyperpolarizes the neuron - decreases NTs released and decreased release of NE and dopamine and ACh

▪ Increase firing in some neurons by preventing
inhibition of those neurons (inhibition prevented by
depressing/inhibiting “inhibitory “synapses)

  • decreased firing causes release of dopamine
49
Q

CNS effects

A

analgesic effects activated thru Mu (respiratory in brain step) , delta (cough) , and chemoreceptor (vomiting centre)

increased activity in periaqueductal grey area, released serotonin in raphe nuclei - synapse with interneurons at spinal cord
- when synpaseing here, serotonin binds to …release of encephalons , bind to opioid receptors on interneurons axons carrying pain signals .. reduce release of substance P

1 neuron activates another

▪ Depress respiratory center
▪ Suppress cough center
▪ Depress vomitting center
▪ Drowsiness
▪ Decrease levels of sex hormones
- reduces sex drive, stops menses (18th century, prostitutes would use as birth control)
- muscle mass inhibited

50
Q

opioids effect on eyes

A

▪ Constriction of pupil
▪ Mechanism unknown

51
Q

GI effects of opioids

A

Gastrointestinal Effects
▪ Diminish Peristalsis in Intestine
▪ Increase muscle tone in Intestine
▪ Above two effects lead to constipation

leads to fecal dehydration

52
Q

Opioids Psychological Effects

A

(1) Euphoria
(2) Dysphoria
- can have delusions, anger,
(3) Decreased Concentration
- secondary to drowsiness
(4) Dulling of Emotional Pain
- mediated thru limbic system and frontal lobe receptors
-

53
Q

Tolerance to opioids

A

tolerance in 8-10 days of daily use - consumption will increase 10X for same effects

▪ Develops to:
▪ Respiratory depression
▪ Analgesic
▪ Sedation
▪ Euphoria

▪ May develop to:
▪ Pupil constriction

▪ Does NOT develop to:
▪ Constipation

▪ Develops rapidly
▪ Three types:
pharmakokinetic - increase enymes
pharmacodynamic - decreaae in sensitivieity of receptors, changes in concentration
cross tolerance - w alcohol

little tolerance to intermittent use
takes about a year for development if not regular

54
Q

Opioids Physical Dependence

A
  • craving 4-6 hrs after last use
  • 8-12 hrs after drug used youll see withdrawal effects

▪ Characteristic withdrawal
- like a wicked case of the flu
▪ Restlessness and agitation
▪ Yawning appears
▪ Fever and chills
▪ Deep sleep
- yen sleep - during sleep, theres often profuse sweating
▪ Cramps, v/d
▪ Twitching of limbs - kicking habit
▪ Profuse sweating

▪ Symptoms intensify to a peak (36 to 72
hours); over in 5 to10 days
▪ Withdrawal not typically life-threatening

sometimes mild symptoms for up to a year - HR changes …

craving, wanting drug to avoid withdrawal

55
Q

Psychological Dependence Opioids

A

Psychological Dependence
▪ More difficult to treat than physical
dependence

▪ Some success seen with Methadone and
other synthetic opiates (e.g.,LAAM,
buprenorphine)
-there is no euphiora with these

56
Q

Methadone Treatment

A

Methadone Treatment
▪ Factors contributing to potential
effectiveness include

▪ Oral admin - in a juice - this takes away the potentially reinforcing effects … they are changing the environment of that drug
-n encourages compliance .. going in every 2-3 days

▪ Long acting effect
▪ Antagonistic action - removes pleasurable effects of heroine (takes away the euphoria of the other drugs)

▪ Are advantages to terminate use
- gives person freedom (no need to plan life around going to clinic to get methadone)
- recude likelihood of being discriminated for this use (trouble getting life insurance)
- effects on sex drive and relationships

57
Q

PSYCHEDELICS - Definitional Issues

A

Definitional Issues
* Heterogenous group of compounds which:
– Can induce hallucinations
– Separate individuals from reality
– Can induce psychotic-like behavior
* No one single term comprehensively classifies
these drugs

58
Q

PSYCHEDELICS - history / types

A
  • Naturally occurring agents used for thousands
    of years – as most derived from plants
    – Ascribed magical/spirtual properties (e.g., Aztecs and psilocybin (for ritual practices), Native Americans and mescaline in peyote(sacred, spiritual practices)

most from plants

Harmine (tropical plant in south america, in a beverage, drink and go into a trance),

DMT - compound in >50 plants, as well as insects and amphibians, can be made synthetically - this is whats in ayahuasca
N,N-dimethyltryptamine (DMT) found in ayahuasca

Myristine/Elmycin

Salvinorum A - salvia - from a mint plant, in a native plant in mexico

Ibotinic Acid - the red with white dots mushroom (looks like the mushroom in disney)

59
Q

Sytnetic Psychidelics

A

LSD, ketamine, PCP
marketed as a halucinacetic and analgesic

ketamine is used by vets

60
Q

history –> present times … with psychedelics

A

Late 60s and 70s “discovered” as agents to:
– Enhance and expand reality, promote personal awareness, stimulate understanding of spirtual world

quote:

During the next five hours, I was whirled
through an experience which could be
described in many elegant metaphors but
which was above all and without question
the deepest religious experience of my life

  • Present times:
    – Primarily used recreationally
    – Used in lower doses
    ** now being explored as drugs to be used in therapy and to treat pain … widely explored therapeutic use

much lower doses now compared to 60s

61
Q

Psychedelic Nature of Hallucinations

A
  • Hallucinations will occur in stages:
    – Stage 1: visual images (e.g., spirals, grids,
    geometric patterns)
    recognized as not being real
    ; first seen with eyes closed than projected
    on surfaces when eyes opened
  • dots, squiggles, phospense (little balls of light)
  • seen on wall
  • eyes staring back

– Stage 2: meaningful images of people,
animals, places
* Images can change rapidly; and changes
will typically have a pattern

weight images, turn into other ones

  • Colours shift from blues to reds as drugs effects
    intensify
  • At high doses, people will get swept up into
    hallucination
  • ppl start to interact with what they are seeing
62
Q

Psychedelics - Hallucinations and Other Sensory
Distortions

A
  • Visual
  • Colour, Contrast, Size Changes
  • more sharply defined, the objects are popping out at you
  • ppl see hands as gigantic!
  • object move around - larger objects do not move as much
  • Auditory
  • Sounds amplified, but not always clearer
  • Smell
  • More acute, but recognition can be impaired
  • Taste
  • Tastes linger, but recognition can be impaired
  • Touch
  • Tactile sensations more intense
  • Synesthesia
  • fusing of senses - sounds might have specific colours
63
Q

Psychedelics Video in class

A
  • about creation and use of LSD
  • steve jobs use
  • oliver sacks - neuroscientists - LSD changed their lives (altering what they think the mind is capable of)
  • credit LSD for profound insights, life changing insights

michael polland how to change your mind - 900 year old mushroom use

  • early research changed use… LSD had high potential for treating psychological disorders

media in early 70s?? Nixon (drug bill..) stopped research 9war on drugs) - controlled substances act in 1970 - however, LSD does not have high change or abuse

ALbert Hoffman - drug company in switzerland - injests LSD - realized this is the first acid trip (bikes home, hes separating from his body, has this magical experiences)

Send LSD 25 for free to scientists across the world
- LSD supported research of neurotransmitters and psychoactive drugs for theraputic purposese

50% success rate for using LSD to stop alcohol use

Military - thought they could weponize LSD, put in water supply … use as a truth serum or mind control agent

Timothy Learey - promoted LSD as a free for all …

64
Q

BIOLOGY OF HALLUCINATIONS

A
  • Brain areas believed to be involved in
    hallucinations are
    – Thalamus
  • Traffic officer for incoming sensory information
  • Activity modulated by glutamate, GABA, dopamine, and
    serotonin
  • does some filtering of what needs to be processed or not
  • most are excititory - EPSE

– Cerebral Cortex
* Primary and secondary cortex
- - sensory - for recognition and perception of sensory information
- prefrontal cortex, decreases in EPSP s

– Default Mode Network
* Connected brain areas in the frontal and parietal lobes
that are active when someone is not focused on outside
world

Psychedelics alter neurotransmitter activity in
thalamus
– Changes in the overall balance between excitatory
and inhibitory
– Disrupted activity in thalamus leads to poor filtering
of sensory information
- more sensory info going up than is typical

  • Disrupted activity in thalamus leads to
    disruption in the connections to the cortical
    areas
    – Release of control on the Default Mode Network
    such that it becomes more active and more topdown processing of incoming sensory information
  • default mode network becomes much more active
  • theres more top-down processing
  • top down is emotions influencing what you are seeing
    expectations / knowledge effects what we are seeing
  • Over and above effects on neurotransmitter
    activity in the thalamus, psychedelics alter
    neurotransmitter activity in prefrontal cortex,
    limbic system, and temporal parietal cortex.
  • effecting the locus coeruleus - effects how novel experiences impact
  • increased activity
  • ## fear response, emotions
65
Q

BIOLOGY OF HALLUCINATIONS - senses

A

Imaging studies have shown that
– There is increased/overactivity from normal states in
primary and secondary cortex

– Auditory hallucinations associated with disrupted
activity in middle and superior temporal lobes

– Visual hallucinations associated with disrupted
activity in occipital lobe

– Tactile hallucinations – disrupted activity in primary
somatosensory cortex and posterior parietal cortex

most psychedelics effect serotonin and type 2 a receptors

66
Q

LSD General Description

A

– First use in therapy
– In 60s, recreational use began
– Very potent drug
* Effective dose can be only 10 micrograms, with only one hundreth of a percent being absorbed into brain

  • Rapidly absorbed into bloodstream, an
    distributed (most ends up in liver)
  • Extensively metabolized (excreted in feces)
  • Effects can last up to 12 hours
    – peak effects: 90 min to 5 hours
67
Q

LSD Administration

A

LSD

  • Odorless, tasteless, no colour
  • Usually consumed orally as “hits”
  • Forms include:
  • powder pellets
  • Gelatin chips
  • liquid
  • blotters (papers)
68
Q

LSD Mechanism of Action

A

Mechanism of Action

(1) Agonist of serotonin: activates 5-HT2A
receptors
- (1) Suppresses activity/output of locus coeruleus (LC)
- (2) Enhances response of the LC to novelty

(2) Affects activity in the medial prefrontal cortex via glutaminergic neurons

(3) Inhibits firing and release of serotonin by
raphe nuclei, which may be responsbile for LC
suppression

69
Q

LSD Effects First Phase

A
  • First Phase
    – Begins within 30 min
    – Minor physiological effects
    – Sensation of release of inner tension
70
Q

LSD effects second phase

A
  • Second Phase
    – Occurs within 30 min and 2 hours
    – Characterized by 4 different effects
  1. Images seen with the eyes closed
  2. Synthesia
  3. Perception of a multilevel reality
  4. Strange and exaggerated appearances of
    objects or experiences
71
Q

LSD effects third phase

A
  • Third Phase
    –Begins within approx 3 – 5 hours
    –Characterized by:
    1. Great swings in emotions or panic
    2. Feeling of timelessness
    3. Feeling of ego disintegration, or
    separation of one’s mind from one’s
    body
72
Q

other LSD effects

A

(1) Euphoria
(2) Development of Insight
(3) Impaired Cognition (e.g., confusion)
(4) Bizarre thoughts or feelings (e.g., can fly)

73
Q

Toxicity of LSD?

A
  • Low level of “physiological toxicity”
  • Harmful consequences of sensory/psychological alterations
  • Other consequences include:
    (1) Flashbacks aka Hallucination Persisting
    Perception Disorder (HPPD)
74
Q

Flashbacks with LSD

A
  • Reexperiencing of LSD trip or spontaneous
    memories of a trip complete with images,
    sensations, and emotions
  • Typically only last a few seconds
  • Tend to occur within first few days after a trip,
    then decrease in frequency, eventually
    disappear (caveat: some reports of years after
    drug taken)
  • Triggered by darkness, stress, fatigue, acute
    alcohol or cannabis intoxication, idiosyncratic
    factors
  • Unknown mechanism
75
Q

LSD Related HPPD

A

Hallucination Persisting
Perception Disorder

Re-experiencing of the perceptual disturbances
causing significant distress in social,
occupational and other areas of functioning

  • Occurs primarily after LSD use, but not
    exclusively
  • Can last for weeks, months, or years
  • No strong correlation between occurrence and
    frequency of hallucinogen use
  • Prevalence is approx. 4.2%
  • Possible genetic factors re: risk of developing
76
Q

LSD Tolerance

A

Tolerance to both psychological and physical
effects develops

  • Tolerance due to down regulation of 5-HT2A
    receptors
  • Disappears within approx. a week
  • Cross tolerance with other psychedelics
  • mushrooms and mescaline
77
Q

LSD Dependence

A
  • No physiological dependence
  • Some psychological dependence in some
    people
78
Q

Mescaline History

A
  • Active ingredient in peyote cactus, San Pedro
    cactus, and Peruvian Torch cactus
  • Isolated and named in 1897 by Heffler
  • Synthesized in 1919 by Spath
  • Used to treat illness and in religious and cultural ceremonies dating back to the Aztecs
  • Only psychedelic sanctioned for open use by US government (Native American Church)
  • Entered Mainstream culture in the 1950s with
    publication of Huxley’s “The Doors of Perception”
  • Widespread use in universities until LSD and laws introduced to control all psychedelics
79
Q

Mescaline Administration

A
  • Consumed orally
  • Mescal buttons have nauseous odor and
    bitter taste
  • Typical dose 200-500 mg/5-15 buttons
  • Rapidly and completely absorbed
  • Relatively long acting (4-12 hours)
  • Structurally similar to norepinephrine but it
    acts on serotonin, type 2A receptors (agonist)

locus coeruleus
(LC) causes that feeling of “seeing things for the first time”

Cross-tolerance has been observed between LSD,
psilocybin, and mescaline but not between LSD and damphetamine
or THC

80
Q

Mescaline Effects

A

Mescaline
Effects
* Similar effects as LSD but 1/2000th as potent

  • 1st symptoms are:
    – Nausea, vomitting, tremors, incoordination
  • After approx 1 hour:
    – Vivid hallucinations
81
Q

Mescaline - Tolerance and Dependence

A

Mescaline
Tolerance and Dependence
* Tolerance develops rapidly
* Tolerance dissipates within approx. 7 days
* No physical dependence
* Minimal to no psychological dependence

82
Q

Phencyclidine (PCP)
General Info

A

Phencyclidine (PCP)
General Info
* Synthetic
* Developed and marketed in 1963 as an
analgesic and anesthetic
* Use discontinued in humans due to adverse
reactions in recovery
* When medical use halted, it appeared on
street under a variety of names e.g., crystal,
angel dust, hob

83
Q

PCP Administration

A
  • Comes in various forms
  • Administered orally, intra-nasally, intravenously, and via inhalation
  • Long half life
  • Many psychoactive metabolites
  • Effects typically last 4-6 hours
  • Effects followed by partial or total amnesia
84
Q

PCP Mechanism of Action

A
  • Antagonist of glutamate and aspartate at
    NMDA receptors
  • Inhibit serotonin re-uptake
  • Agonistic action at opiate and adenosine
    receptors
85
Q

PCP Effects

A
  • Dose of 5 mg
    – Euphoria
    – Slurred speech
    – Motor incoordination
    – Drowsiness
    – Numbness of extremities
  • Dose of 10 mg or more
    – Increased hr and bp
    – Sweating, nausea
    – Pupil dilation
    – Analgesia
    – Changes in Body Image
    – Prolonged visual stare
    – Nystagmus
    – Blurred or double vision
    – Feeling detached from others/surroundings or their own body
    – Amnesia
    – Frenzied motor activity or Catatonic Stupor
    – Sudden mood changes
    – Disorientation, confusion
    – Delusional thought
    – Repetitive stereotyped movements
  • Psychotic behavior disappears as drug levels
    decline but sometimes requires
    hospitalization
86
Q

PCP Toxic Effects

A
  • With high doses (20 mg)
    – Respiratory Depression
    – Generalized Seizures
    – Pulmonary Edema
  • Fetal Effects
    – Use in pregnancy slows growth, precipates labor and causes fetal distress
    – Infants show muscle stiffness, tremor, irritability, and attention problems (latter can last several years)
    – Animal studies: widespread brain cell death
87
Q

PCP Tolerance and Dependance

A
  • With daily use, develops within 2-3 weeks
  • Psychological dependence develops
  • No clear evidence of withdrawal syndrome in
    humans
88
Q

Salvinorin A
General Info

A

Salvinorin A
General Info

  • Psychoactive compound found in the mint
    plant “Salvia divinorum” (leaves contain about
    .18% Salvinorin A)
  • Plant is indigenous in a region in Oaxaca,
    Mexico
  • Traditionally used by Mazatec shamans for
    health purposes and spiritual healing
    purposes
  • First reported in 1930s and psychoactive
    compounded identified in 1990
  • Recreational use saw a rise in popularity in the
    21st century
  • It is a Schedule IV drug in Canada
  • Usage is relatively low, with highest rates in
    teens and young adults
    – 2009: 1.6 % aged 15 or older (7.3% in ages 15 to 24)
    – 2019: 2.2 % aged 15 or older (4.8% ages 20 to 24 vs 2.1 % ages 25+)
89
Q

Salvinorin Administration

A
  • Administration

– Oral
* Leaves chewed; held in mouth for 20 to 30 min
* Tinctures: drops into cheek
* Typical dose: 30 grams of fresh leaves

– Smoked/Inhalation
* Dried leaves burned
* Dried leaves vaporized and aerosol mixture inhaled
* Typical dose: 250 to 750 milligrams

  • Rapidly distributed throughout body and
    quickly eliminated
  • With oral admin
    – Effects felt within 5 – 10 minutes, build and
    plateau over another hour, and then begin to
    slowly decline after 60 minutes
  • With smoking
    – Effects experienced within 30 seconds, peak in 5 to 10 minutes (2 minutes with vaporization) then gradually decline over 20 to 30 minutes
  • Cleared from the brain with an active
    transport mechanism
  • Metabolized by the liver and gallbladder
  • Principle metabolite is inactive
90
Q

Salvinorin A
Pharmacology

A

Salvinorin A
Pharmacology

  • Opioid Agonist at kappa receptors
  • Animal studies suggest that it indirectly affects
    other neurotransmitter systems
    – Inhibiting release of dopamine in striatum,
    prefrontal cortex, and nucleus acumbens
    – Inhibiting release of serotonin in hippocampus
    – Stimulates release of NE in hippocampus
91
Q

Salvinorin A
Some Effects

A
  • Physiological effects
    – Increased sweating
    – Body feeling warm/hot or “chills”
    – Dizziness
    – Nausea
    – Intense drooling
    – Decreased heart rate
    – Experiences of rotation
  • Behavioral
    – Impaired coordination
    – Uncontrollable laughter
  • Psychological
    – Feeling calm, dreamy like state
    – Improved mood and self-confidence
    – Increased insight and creativity
    – Mind racing
    – Time distortions
    – Spirtual experiences
  • Psychedelic
    – Colourful visions of objects and designs
    – Perception of becoming an object
    – Changes in bodily form
    – Revisiting places from the past
    – Overlapping realities
    – “Salvia Winds”: feeling of intense sideways or
    downwards pressure
  • Effects not always pleasant
  • Some adverse effects are
    – Headaches
    – Drowsiness
    – Dysphoria
    – Feeling of terror and panic attacks
92
Q

Salvia * Physiological effects

A
  • Physiological effects
    – Increased sweating
    – Body feeling warm/hot or “chills”
    – Dizziness
    – Nausea
    – Intense drooling
    – Decreased heart rate
    – Experiences of rotation
93
Q

salvia behavioural and psychological effects

A
  • Behavioral
    – Impaired coordination
    – Uncontrollable laughter
  • Psychological
    – Feeling calm, dreamy like state
    – Improved mood and self-confidence
    – Increased insight and creativity
    – Mind racing
    – Time distortions
    – Spirtual experiences
94
Q

salvia psychedelic effects

A
  • Psychedelic
    – Colourful visions of objects and designs
    – Perception of becoming an object
    – Changes in bodily form
    – Revisiting places from the past
    – Overlapping realities
    – “Salvia Winds”: feeling of intense sideways or
    downwards pressure
95
Q

Correctional Services of Canada (2021 Report) on crime and alcohol

A

Study to look at crime and alcohol in inmates
Computerized assessment of substance abuse
Asked individuals if drug they were on when being arrested was a contributing factor and if they committed the crime in order to get a drug
Found alcohol and other substances involved in 42% of attributable offenses
Alcohol associated w more violent (20%) than non-violent crime (7%)

96
Q

Canadian Centre on Substance Abuse (2002)

A

Nationally alcohol intoxication at time of crime in 24% of offenders
Assault offenders: 39%
Homicides: 34%
Attempted murder: 30%
Thefts: 16%
Breaking and entering: 22%
Number one crime under influence of alcohol is intoxicated driving