Lecture 5- Cannabis Flashcards

1
Q

What are the background uses of cannabis?

A

-Produced from weedlike plant (Cannabis Sativa (Hemp) -Uses such as Rope, cloth, paper, seed for oil
-Over 70 other non-psychoactive agents incl Cannabidiol

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2
Q

What is the psychoactive agent ∆9Tetrahydocannabinol (THC)

A

Found in all parts of the plant but concentrated in sticky resin secreted the flowering tops of female plants.

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3
Q

What are the 4 forms of Cannabis?

A

Marijuana
Sinsemilla
Hashish (solid)
Hash oil

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4
Q

What is Marijuana

A

-Dried and crumbled leaves, small stems, flowering tops of the plant -Usually smoked in joints, pipes, bongs. -THC content varies

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5
Q

What is Sinsemilla?

A

-pollination prevented -↑ potency

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6
Q

What is Hashish?

A

-Prepared from resin -Potency varies with concentration

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7
Q

What is Hash oil?

A

-Reduced alcoholic extract -Single drop placed in a joint

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8
Q

What is the THC content of Cannabis?

A

-Typical joint contains approx. 0.5-1g of cannabis. -A joint w/ 1g of cannabis, 4% THC content, contains 40mg of THC
-THC content of samples in 1995 contain 4% THC compared to average 15% in 2015.

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9
Q

How does smoking Cannabis affect consumption?

A

-Burning marihuana results in vaporisation of THC
-THC readily absorbed through the lungs into blood plasma but only 20% of original THC is absorbed into lungs.

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10
Q

What is a potential way THC absorption can be increased w/ smoking?

A

-Absorption can be increased by breath holding eg Black et al (1998) found increased high w/ 15s hold vs 7s.

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11
Q

What is the half-life of cannabis?

A

-Half-life of 20/30 hrs, metabolism in liver and fat storage.

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12
Q

How does oral consumption of cannabis affect?

A

-Slower/delayed effects relative to smoking (smoking bypasses liver metabolism, goes straight from lungs to blood plasma).

-Effect is more sustained, due to slower metabolism and absorption into blood plasma.

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13
Q

What is the process of oral consumption of Cannabis?

A

Ingestion > Metabolism in liver > Absorbed into blood plasma.

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14
Q

What are Cannabinoid receptors?

A

Cannabis receptor = CB1 Agonist = THC Antagonist = SR141716

-Cannabis receptors active in areas consistent w/ behavioural effects eg hippocampus associated w/ spacial memory

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15
Q

Describe the study of Huestis et al (2001) for antagnoist effects

A

-Effects of marijuana attenuated by treatment of CB1 antagonist -Two groups : placebo control, SR141716 group -Responses recorded over next hour of rating of drug effect, increase in HR.

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16
Q

What is the Endocannabinoid system?

A

Given the presence of natural (endo)cannabinoids, is there a normal regulatory function of the system.

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17
Q

What are the effects of the CB1 antagonist from the Richardson et al (1988) study

A

-SR 141716 induces hyperalgesia (↑ pain sensitivity) -endocannabinoids ↓ responsiveness to pain.

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18
Q

What are the 3 types of behavioural effects (Iverson, 2000)?

A

The Buzz
The High
Being Stoned

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19
Q

What is ‘The buzz’ in the Iverson (2000) study

A

The buzz- Brief perception of dizziness, tingling sensations in extremities

20
Q

What is ‘The high’ in Iverson (2000) study?

A

The high- Feelings of euphoria, exhilaration, disinhibition eg the giggles

21
Q

What is ‘Being stoned’ in the Iverson (2000) study?

A

Being stoned- Reached w/ signif amount of marijuana, feelings of being calm, dreamlike. Sensations of floating and enhanced visual/auditory perception. Slowing of perception of time, changes in sociability

22
Q

What is Psychopathology?

A

Paranoia, anxiety, panic (more likely in 1st time)

23
Q

What are the physiological effects of Cannabis?

A

-Increased blood flow to skin (warmth sensation) -Increase in heart rate (pounding pulse) -Increase in hunger (munchies)

24
Q

What is Hyperphagia?

A

Increased appetite and consumption

25
Q

What are the cognitive deficits of Cannabis?

A

-Oral THC administration impairs verbal memory (Curran et al, 2002) Psychomotor functions affected eg makes driving dangerous

26
Q

How is cognitive tolerance affected by cannabis?
(Hart et al, 2001)

A

Dose dependent=Low doses have relatively few effects (esp in heavy users)

Task dependent= If task demands are high creates impaired performance

27
Q

What does the Tanda et al (2000) study suggests about rewarding effects of cannabinoids?

A

Phase 0: intravenous cocaine → lever press
Phase 1: extinguished with saline
Phase 2: intravenous THC → lever press
Phase 3: Effect abolished with CB1 antagonist
Phase 4: intravenous THC → lever press

28
Q

What does Valjent & Maldonado (2000) say about conditioned place preference?

A

-Conditioned place preference w/ THC in mice -Only works if mice pre-exposed to THC in home cages (before being introduced to experimental apparatus -First experience is aversive then becomes rewarding

29
Q

What is the age of initiation of Cannabis?

A

-Most widely used illicit drug in UK and US
-Most common in 18-21yrs

30
Q

What is the definition of Tolerance?

A

Needing a greater dose to achieve same effect

31
Q

What do human studies say about Cannabis tolerance?

Mixed result

A

Crompton et al (1990)- Tolerance observed following repeated administration of marijuana/pure THC.

Kirk & de Wit (1999)- Same ‘high’ in light users relative to heavy users

32
Q

What do animal studies say about Cannabis use?

Consistent results

A

Breivogel et al (1999) w/ rats- Daily injection of THC over 3 wks and found progressive reduction in CB1 receptor density and activity and some brain areas were totally desensitised in 3wks.

33
Q

What is the definition of Dependence?

A

Difficulty stopping taking, cravings, withdrawal symptoms.

34
Q

What does the Buddy et al (2003) say about Dependence?

A

Found abstinence triggers irritability, anxiety, depression which resembles nicotine withdrawal symptoms. Found to be worst in first 2wks but can last for over a month.

35
Q

What do animal studies say about Cannabis Dependence?

A

-Early studies found no effect of drug withdrawal but THC has a long half-life, so may still be in system.

36
Q

What does Aceto (1996) animal study suggest about Precipitated withdrawal?

A

Rats given THC injections twice a day then given SR141716, symptoms of hyperactivity eg shaking, scratching. However, possible consequence of rats being stressed as it caused increased Corticotrophin releasing hormone (CRH)

37
Q

How does CBT treat cannabis-use disorder?

A

Ppts rewarded w/vouchers for providing cannabis free urine sample.

-Moore & Budney (2003) found signif relapse. -Haney et al (2004) found withdrawal symptoms may be eased by oral THC consumption.

38
Q

What were the conclusions of CBT treatment efficiency in the Haney (2004) study?

A

-Useful in ST but difficult to achieve in LT abstinence as only 30% had not relapsed after 180 days.

39
Q

What does the Lynsky & Hall (2000) study say about Cannabis behavioural effects?

A

Chronic cannabis use associated w/ poor education performance eg neg attitudes, poor grades, absent from lessons.

Amotivational syndrome= Apathy, aimlessness, lack of productivity in ST and LT.

40
Q

What does Fergusson et al (2003) say about Cannabis behavioural effects?

A

Found regular cannabis use in early life predicts poor school performance and dropout rates.

41
Q

What does Solowij et al (2002) say about Cannabis cognitive effects?

A

Found cognitive deficits in LT users, standardised tests of learning, memory, attention. LT user deficient 1 and 7 days after exposure.

42
Q

What does Pope et al (2001) say about Cannabis cognitive effects?

A

No difference found between heavy user and control after 28days of abstinence. Cognitive deficits linked to recent use but reversible over time.

43
Q

What are the health considerations of Cannabis?

A

-Higher concentrations of carcinogens in cannabis smoke than tobacco
-More tar and Carbon monoxide in joint than cigarette.

44
Q

What are the clinical applications of Cannabis?

A

-Can be tracked back thousands of years but identification of THC led to manufacture of synthetic compounds.
-Can be used for chronic pain treatment eg spinal cord injuries
-Limited widespread use due to side effects

45
Q

What is the definition of Dronabinol and Nabilone?

A

Dronabinol: Antiemetic for chemotherapy patients
Nabilone: Appetite stimulant on AIDS patients