Tetrahydrocannabinol

Tetrahydrocannabinol (THC) is one of at least 113 cannabinoids identified in cannabis. THC is the principal psychoactive constituent of cannabis. With chemical name (−)-trans-Δ⁹-tetrahydrocannabinol, the term THC also refers to cannabinoid isomers. Like most pharmacologically active secondary metabolites of plants, THC is a lipid found in cannabis,[9] assumed to be involved in the plant's self-defense, putatively against insect predation, ultraviolet light, and environmental stress.[10][11][12]

"THC" redirects here. For other uses, see THC (disambiguation).
Tetrahydrocannabinol
INN: dronabinol
Clinical data
Trade namesMarinol
Other names(6aR,10aR)-delta-9-Tetrahydrocannabinol; (−)-trans-Δ⁹-Tetrahydrocannabinol; THC
License data
Pregnancy
category
  • US: C (Risk not ruled out)
    Dependence
    liability    		8–10% (Relatively low risk of tolerance)[1]
    Routes of
    administration    		Oral, local/topical, transdermal, sublingual, inhaled
    ATC code
    Legal status
    Legal status
    • AU: Unscheduled: ACT Schedule 8 (Federal)
    • CA: Unscheduled
    • DE: Dronabinol: Anlage III, Δ9-THC: II, other isomers and their stereochemical variants: I. (Does not apply to THC as part of cannabis, which is regulated separately, see Cannabis (drug))
    • UK: Class B
    • US: Schedule II as Syndros, and Schedule III as Marinol[2]
    Pharmacokinetic data
    Bioavailability10–35% (inhalation), 6–20% (oral)[3]
    Protein binding97–99%[3][4][5]
    MetabolismMostly hepatic by CYP2C[3]
    Elimination half-life1.6–59 h,[3] 25–36 h (orally administered dronabinol)
    Excretion65–80% (feces), 20–35% (urine) as acid metabolites[3]
    Identifiers
    CAS Number
    PubChem CID
    IUPHAR/BPS
    DrugBank
    ChemSpider
    UNII
    ChEBI
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.153.676
    Chemical and physical data
    FormulaC21H30O2
    Molar mass314.469 g·mol−1
    3D model (JSmol)
    Specific rotation−152° (ethanol)
    Boiling point155-157°C @ 0.05mmHg,[6] 157-160°C @ 0.05mmHg[7]
    Solubility in water0.0028,[8] (23 °C) mg/mL (20 °C)
     NY (what is this?)  (verify)

    THC, along with its double bond isomers and their stereoisomers,[13] is one of only three cannabinoids scheduled by the UN Convention on Psychotropic Substances (the other two are dimethylheptylpyran and parahexyl). It was listed under Schedule I in 1971, but reclassified to Schedule II in 1991 following a recommendation from the WHO. Based on subsequent studies, the WHO has recommended the reclassification to the less-stringent Schedule III.[14] Cannabis as a plant is scheduled by the Single Convention on Narcotic Drugs (Schedule I and IV). It is specifically still listed under Schedule I by US federal law[15] under the Controlled Substances Act for having "no accepted medical use" and "lack of accepted safety". However, dronabinol, a pharmaceutical form of THC, has been approved by the FDA as an appetite stimulant for people with AIDS and an antiemetic for people receiving chemotherapy under the trade names Marinol and Syndros.[16] The pharmaceutical formulation dronabinol is an oily and viscous resin provided in capsules available by prescription in the United States, Canada, Germany, and New Zealand.

    Medical uses
    Further information: Dronabinol
    Not to be confused with Droperidol.

    THC is an active ingredient in Nabiximols, a specific extract of Cannabis that was approved as a botanical drug in the United Kingdom in 2010 as a mouth spray for people with multiple sclerosis to alleviate neuropathic pain, spasticity, overactive bladder, and other symptoms.[17][18] Nabiximols (as Sativex) is available as a prescription drug in Canada.[19]

    Pharmacology
    See also: Effects of cannabis, Long-term effects of cannabis, and Cannabis in pregnancy

    Mechanism of action
    For a review of the mechanisms behind endocannabinoid synaptic transmission, see Endocannabinoid system.

    The actions of THC result from its partial agonist activity at the cannabinoid receptor CB1 (Ki = 10 nM[20]), located mainly in the central nervous system, and the CB2 receptor (Ki = 24 nM[20]), mainly expressed in cells of the immune system.[21] The psychoactive effects of THC are primarily mediated by the activation of cannabinoid receptors, which result in a decrease in the concentration of the second messenger molecule cAMP through inhibition of adenylate cyclase.[22]

    The presence of these specialized cannabinoid receptors in the brain led researchers to the discovery of endocannabinoids, such as anandamide and 2-arachidonoyl glyceride (2-AG). THC targets receptors in a manner far less selective than endocannabinoid molecules released during retrograde signaling, as the drug has a relatively low cannabinoid receptor efficacy and affinity. In populations of low cannabinoid receptor density, THC may act to antagonize endogenous agonists that possess greater receptor efficacy.[23] THC is a lipophilic molecule[24] and may bind non-specifically to a variety of entities in the brain and body, such as adipose tissue (fat).[25][26]

    Due to its partial agonistic activity, THC appears to result in greater downregulation of cannabinoid receptors than endocannabinoids, further limiting its efficacy over other cannabinoids. While tolerance may limit the maximal effects of certain drugs, evidence suggests that tolerance develops irregularly for different effects with greater resistance for primary over side-effects, and may actually serve to enhance the drug's therapeutic window.[23] However, this form of tolerance appears to be irregular throughout mouse brain areas. THC, as well as other cannabinoids that contain a phenol group, possesses mild antioxidant activity sufficient to protect neurons against oxidative stress, such as that produced by glutamate-induced excitotoxicity.[21]

    Pharmacokinetics

    THC is metabolized mainly to 11-OH-THC by the body. This metabolite is still psychoactive and is further oxidized to 11-nor-9-carboxy-THC (THC-COOH). In humans and animals, more than 100 metabolites could be identified, but 11-OH-THC and THC-COOH are the dominating metabolites.[27] Metabolism occurs mainly in the liver by cytochrome P450 enzymes CYP2C9, CYP2C19, CYP2D6, and CYP3A4.[28][29] More than 55% of THC is excreted in the feces and ≈20% in the urine. The main metabolite in urine is the ester of glucuronic acid and THC-COOH and free THC-COOH. In the feces, mainly 11-OH-THC was detected.[30]

    Physical and chemical properties

    Discovery and structure identification

    Cannabidiol was isolated and identified from Cannabis sativa in 1940,[31] and THC was isolated and its structure elucidated by synthesis in 1964.[32][33]

    Solubility

    As with many aromatic terpenoids, THC has a very low solubility in water, but good solubility in most organic solvents, specifically lipids and alcohols.[8]

    Total synthesis

    A total synthesis of the compound was reported in 1965; that procedure called for the intramolecular alkyl lithium attack on a starting carbonyl to form the fused rings, and a tosyl chloride mediated formation of the ether.[34]

    Biosynthesis
    Biosynthesis of THCA

    In the Cannabis plant, THC occurs mainly as tetrahydrocannabinolic acid (THCA, 2-COOH-THC, THC-COOH). Geranyl pyrophosphate and olivetolic acid react, catalysed by an enzyme to produce cannabigerolic acid,[35] which is cyclized by the enzyme THC acid synthase to give THCA. Over time, or when heated, THCA is decarboxylated, producing THC. The pathway for THCA biosynthesis is similar to that which produces the bitter acid humulone in hops.[36][37]

    No known lethal dose

    The Median lethal dose of THC in humans is not known because no human has ever been known to have died from it. A 1972 study gave up to 9000 mg/kg of THC to dogs and monkeys without any lethal effects. Some rats died within 72 hours after a dose of up to 3600 mg/kg.[38]

    Detection in body fluids
    Main article: Cannabis drug testing

    THC and its 11-OH-THC and THC-COOH metabolites can be detected and quantified in blood, urine, hair, oral fluid or sweat using a combination of immunoassay and chromatographic techniques as part of a drug use testing program or in a forensic investigation.[39][40][41]

    Detection in breath

    Recreational use of cannabis is legal in many parts of North America, increasing the demand for THC monitoring methods in both personal and law enforcement uses.[42] Breath sampling as a noninvasive method is in development to detect THC, which is difficult to quantify in breath samples.[42] Scientists and industry are commercializing various types of breath analyzers to monitor THC in breath.[43]

    History
    Further information: Removal of cannabis from Schedule I of the Controlled Substances Act

    THC was first isolated and elucidated in 1969 by Raphael Mechoulam and Yechiel Gaoni at the Weizmann Institute of Science in Israel.[32][44][45]

    At its 33rd meeting, in 2003, the World Health Organization Expert Committee on Drug Dependence recommended transferring THC to Schedule IV of the Convention, citing its medical uses and low abuse and addiction potential.[46] In 2018 the federal farm bill was passed allowing any hemp derived product not exceeding 0.3% Δ-9 THC to be sold legally. Since the law currently only counts for Δ-9 THC , Δ-8 THC is considered legal to sell under the farm bill and is currently being sold online. [47]

    Society and culture

    Comparisons with medical cannabis
    Further information: Medical cannabis
    Part of a series on
    Cannabis
    • Cannabis portal
    • Medicine portal
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    Female cannabis plants contain at least 113 cannabinoids,[48] including cannabidiol (CBD), thought to be the major anticonvulsant that helps people with multiple sclerosis;[49] and cannabichromene (CBC), an anti-inflammatory which may contribute to the pain-killing effect of cannabis.[50]

    Regulation in Canada

    As of October 2018 when recreational use of cannabis was legalized in Canada, some 220 dietary supplements and 19 veterinary health products containing not more than 10 parts per million of THC extract were approved with general health claims for treating minor conditions.[19]

    Research

    The status of THC as an illegal drug in most countries imposes restrictions on research material supply and funding, such as in the United States where the National Institute on Drug Abuse and Drug Enforcement Administration continue to control the sole federally-legal source of cannabis for researchers. Despite an August 2016 announcement that licenses would be provided to growers for supplies of medical marijuana, no such licenses were ever issued, despite dozens of applications.[51] Although cannabis is legalized for medical uses in more than half of the states of the United States, no products have been approved for federal commerce by the Food and Drug Administration, a status that limits cultivation, manufacture, distribution, clinical research, and therapeutic applications.[52]

    In April 2014, the American Academy of Neurology found evidence supporting the effectiveness of the cannabis extracts in treating certain symptoms of multiple sclerosis and pain, but there was insufficient evidence to determine effectiveness for treating several other neurological diseases.[53] A 2015 review confirmed that medical marijuana was effective for treating spasticity and chronic pain, but caused numerous short-lasting adverse events, such as dizziness.[54]

    Multiple sclerosis symptoms
    • Spasticity. Based on the results of 3 high quality trials and 5 of lower quality, oral cannabis extract was rated as effective, and THC as probably effective, for improving people's subjective experience of spasticity. Oral cannabis extract and THC both were rated as possibly effective for improving objective measures of spasticity.[53][54]
    • Centrally mediated pain and painful spasms. Based on the results of 4 high quality trials and 4 low quality trials, oral cannabis extract was rated as effective, and THC as probably effective in treating central pain and painful spasms.[53]
    • Bladder dysfunction. Based on a single high quality study, oral cannabis extract and THC were rated as probably ineffective for controlling bladder complaints in multiple sclerosis[53]

    Neurodegenerative disorders
    • Huntington disease. No reliable conclusions could be drawn regarding the effectiveness of THC or oral cannabis extract in treating the symptoms of Huntington disease as the available trials were too small to reliably detect any difference[53]
    • Parkinson's disease. Based on a single study, oral CBD extract was rated probably ineffective in treating levodopa-induced dyskinesia in Parkinson's disease.[53]
    • Alzheimer's disease. A 2009 Cochrane Review found insufficient evidence to conclude whether cannabis products have any utility in the treatment of Alzheimer's disease.[55]

    Other neurological disorders
    • Tourette syndrome. The available data was determined to be insufficient to allow reliable conclusions to be drawn regarding the effectiveness of oral cannabis extract or THC in controlling tics.[53]
    • Cervical dystonia. Insufficient data was available to assess the effectiveness of oral cannabis extract of THC in treating cervical dystonia.[53]
    gollark: It is inevitable.
    gollark: Edge is basically just Chromium now anywya.
    gollark: They like backward compatibility so obviously there'll just be some sort of extreme WINE thing.
    gollark: See, MS likely doesn't want to maintain their own kernel and stuff. The implications are obviously obvious: MS is looking to port Windows to run on the Linux kernel, and thingying Edge is a test.
    gollark: Or a test for the confusing future of Windows for Linux™.

    See also

    References
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