Marijuana Flashcards
1
Q
Cannabis Plant
A
- hemp family
- cannabis sativa: grown in asia
- cannabis indica: smaller plant
- pot, skunk, weed, maryjane, hash, ganja, grass, dope, doobie, bud
- hemp plant: strong in fibre (very low psychoactive)
2
Q
Various psychoactive preparations
A
- marijuana
- hashish
- oil
3
Q
Psychoactive Preparations: Marijuana
A
- herb
- dried flowers and leaves
4
Q
Psychoactive Preparations: Hashish
A
- resin
- resin produced by glands (trichomes) to protect the plant
- separate trichomes from the plant and compressed together
5
Q
Psychoactive Preparations: Oil
A
- concentrated liquid marijuana extract
- thick
- treat with alcohol to extract out the actives and later evaporate the alcohol
6
Q
Potency of Cannabis Preparations
A
- Herb (5%) < Resin (20%) < Oil (70%)
- no probably much higher due to the controlled growth and special breeds
- developing new strains: Marketing
- effects unknown of those very high doses, data only available of the past generation with lower potency
7
Q
History of Cannabis
A
- stone age onwards: hemp fibres
- medical use (china): sedative, pain relief
- hinduism (india): sacred plant: joy
- middle east: 10th century arabs: hashish
- Trade / exploration: europe to south america
- new world: hemp fibre used to make sails
- 1800’s: panacea, medical use (tildens extract)
- 1920: prohibition of alcohol caused increased marijuana smoking
- 1960’s: flower power along with LSD
8
Q
Epidemiology
A
- medical use
- most widely used illicit drug
- medical use in many states
- recreational use in some states legal too
- third most used recreational drug: after alcohol and cigarettes
- 18-24 have highest prevalence
- men more likely than women
- use varies by ethnic group: native americans > blacks > whites > hispanics
9
Q
Active ingredients
A
- > 400 chemical compounds
- about 40 chemicals, cannabinoids (unique to the cannabis plant)
- delta-9-tetrahydrocannabinol: delta-THC: most psychoactive of all
- Cannabidiol (CBD): medical effects, but very little psychoactive effects
- Cannabinol: synergetic effect, much more powerful when all chemicals work together
- very lipidic: not so water soluble (when making space tea, mix with milk)
10
Q
Pharmacokinetics: absorption oral
A
- oral
- chew leaves, liquid, food
- slow onset but long duration (steady absorption) around 46h
- less bioavailability
11
Q
Pharmacokinetics: absorption smoking
A
- most efficient
- joint: herb or resin
- bong/water-pipe
- no enzymes or first-pass-effect
- water pipes are actually the healthier and safer for the lungs since the large harmful particles fall down
12
Q
Pharmacokinetics: distribution
A
- very well distributed due to the high lipidity
- brain, liver
13
Q
Pharmacokinetics: metabolism and excretion
A
- liver (slow)
- high lipid solubility = reservoir effect
- metabolites can be detected for 30 days
14
Q
Mechanism of Marijuana Action: Anandamide
A
- endocannabinoids (remember endorphins)
- naturally occurring lipid neurotransmitters
- anandamide: only one known of all the family of endocannabinoids
- two types of brain receptors or andandamide
1. CB1 (brain): mood, movement, memory, cognition, appetite, pain
2. CB2 (body): immune system - not so much found in the brain, more in the spleen (organ that produced antibodies)
15
Q
Mechanism of Action of Anandamide
A
- anandamide binds post-synaptically to CB1 receptors
- via G protein: trigger opening of potassium channels –> potassium levels of the cell –> hyperpolarization: transduction pathway
- altered neuronal activity (ACh, serotonin, dopamine): stoping neural activities
- very similar to endorphins
- anandamide affect serotonin, serotonin affects appetite and mood