Tetrahydrocannabinol (THC)
THC
Tetrahydrocannabinol (THC), or more specifically, ∆9-THC, is the primary psychoactive compound found in the cannabis plant. It is the neutral form of the plant's raw compound, Tetrahydrocannabinolic Acid (THCA). As the flower cures, THCA will slowly decarboxylate into THC. However, this process happens very quickly when heat is applied. Decarboxylation can occur when heat is applied during extraction or consumption, such as smoking a flower. THC oxidizes to Cannabinol (CBN).
When THC is consumed, it binds to receptors within the endocannabinoid system, which can lead to a variety of effects on the body and mind. The intensity and duration of these effects can vary depending on factors such as the dose consumed, the method of consumption, and the individual's tolerance and metabolism.
Isomers: ∆8-THC, ∆10-THC, ∆11-THC
Vaporization Point: 314℉
Indications
Depression
Anxiety
PTSD
Multiple Sclerosis
Parkinson's Disease
Muscular Dystrophy
Seizures
Cancer
Chronic Pain
Functions
Neuroprotection
Cardioprotection
Ocular protection
Metabolic regulation
Anti-inflammation
Antiproliferation/antitumor
Anticonvulsive
Antispasmodic
Desirable Effects
Psychoactivity
Analgesia
Relaxation / Sedation
Antiemetic / Appetite stimulation
Common Adverse Effects
Psychoactivity / Confusion
Dry Mouth
Red eyes
Appetite stimulation
Serious Adverse Effects
Fatigue / Somnolence
Tachycardia
Amotivaional Syndrome
Cannabinoid Hyperemesis Syndrome
Dosing
Dosing THC can vary depending on the individual and the condition being treated, and it is always recommended to consult a cannabis healthcare professional before using THC.
Many effects are dose-dependent, meaning low doses and high doses will elicit different experiences. This is usually noticed with energy/clarity at lower doses and relaxation at higher doses.
In general:
Micro Dose = 5 mg and below
Fatigue and mood stabilizing
ADHD
Metabolic disorders
Low Dose = 5 - 10 mg
Mild pains and aches
PTSD, anxiety, and depression
Nausea
Standard Dose = 10 - 25 mg
Mild to moderate pain and muscle relaxation
PTSD, anxiety, and depression
Appetite stimulation
High Dose = 25 - 100 mg
Moderate to severe pain and muscle spasms
Insomnia
Macro Dose = 100 - 1000 mg
Severe pain and muscle spasms
Cancer, epilepsy
Pharmacokinetics: ADME
Absorption
The bioavailability of ∆9-THC is greatly influenced by the method of consumption:
Inhalation = 5-55%
Highly variable depending on the inhalation method
Smoking: 30% lost to pyrolysis during combustion
Vaping: 20% increase in bioavailability
Sublingual = 10-50%
Depends on formulation and duration
Oral = 10-20%
Highly variable depending on individual factors
Increased if taken with food
4-12% conversion in the liver to 11-hydroxy-∆9-THC (active metabolite)
Topical = low systemic absorption
Used locally for peripheral effects
The onset of ∆9-THC effects varies depending on the consumption method:
Inhalation = Seconds < 1 minute
Sublingual = 15-30 min
Oral = 45-90 min
Food delays onset but increases bioavailability
Topical = 5-30 min
Depends on formulation
The time to peak levels depends on the method of consumption and metabolism:
Inhalation = Seconds < 1 minute
∆9-THC = 8 mins
11-hydroxy-∆9-THC (active metabolite) = 15 mins
Sublingual = 30-60 min
Oral = 60-120 min
It can be extended by up to 100% in some cases
Dual peaks from ∆9-THC and 11-hydroxy-∆9-THC (active metabolite)
Distribution
∆9-THC is distributed very well into fatty tissues and organs in a manner proportional to blood flow. The distribution half-life depends on the frequency of use:
Infrequent users = 1.3 days
Daily users = 5-13 days
Metabolism
The metabolism of ∆9-THC is unique because it is metabolized in the liver to a more potent, active metabolite before being metabolized to an inactive metabolite. When inhaled, ∆9-THC enters the blood, and 11-hydroxy-∆9-THC is made by the liver and then dispersed in the blood. When ∆9-THC is ingested, it is metabolized by the liver before it enters the blood, which is partly why edibles may have a longer onset but can feel more potent.
Phase 1: hydroxylation of THC to the primary (active) metabolite, 11-hydroxy-∆9-THC (11-OH-THC)
50-100% more active than ∆9-THC on CB1 receptors
Phase 2: oxidation of 11-hydroxy-∆9-THC to the secondary (inactive) metabolite, 11-nor-9-carboxy-THC (THC-COOH)
Glucuronidation to excrete in feces, urine, and sweat
Elimination
The inactive metabolite, 11-nor-9-carboxy-THC, is excreted mainly through the feces and secondarily through urine and sweat—urinary drug tests screen for this marker.