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Cannabinoids are a group of chemicals which activate the body's cannabinoid receptors. Before other types were discovered, the term referred to a unique group of chemical compounds found in the cannabis plant, which are responsible for the plant's physiological effects. Currently, there are three general types of cannabinoids: herbal cannabinoids occur uniquely in the cannabis plant; endogenous cannabinoids are produced in the bodies of humans and other animals; and synthetic cannabinoids are similar compounds produced in the laboratory.
1 Cannabinoid Receptors
1.1 Cannabinoid Antagonists
2 Herbal Cannabinoids
3 Endogenous Cannabinoids
4 Synthetic Cannabinoids
5 External Links and References
A cannabinoid receptor is a tissue that receives and responds to cannabinoids, sending signals to other parts of the body. Before the 1980s, it was unknown whether cannabinoids produced their effects by acting on cell membranes, like alcohol, or by acting on a specific receptor. The discovery of the first cannabinoid receptors in the 1980s helped resolve this debate. They are common in animals, as they have been been found in mammals, birds, fish, and reptiles. There are currently two known types of cannabinoid receptors, called CB-1 and CB-2.
CB-1 receptors are found primarily in the brain, specifically in the basal ganglia and in the limbic system, including the hippocampus. They are also found in the cerebellum and in both male and female reproductive systems. CB-1 receptors are essentially absent in the medulla oblongata, the part of the brain that is responsible for respiratory and cardiovascular functions. Thus, there is not a risk of respiratory or cardiovascular failure as there is with many other drugs. CB-1 receptors appear to be responsible for the euphoric and anticonvulsive effects of cannabis.
CB-2 receptors are found only in the immune system, with the greatest density in the spleen. CB-2 receptors appear to be responsible for the anti-inflammatory and possible other therapeutic effects of cannabis.
The protein sequences of these two receptors are about 45% similar. In addition, minor variations in each receptor have been identified. There is some indication that other receptors exist, but none have been confirmed. Cannabinoids bind reversibly and stereo-selectively to the cannabinoid receptors. The affinity of an individual cannabinoid to each receptor determines the effect of that cannabinoid. Cannabinoids that bind more selectively to certain receptors are more desirable for medical usage.
Cannabinoids are generally cannabinoid receptor agonists, which means that they dock with a cannabinoid receptor and activate it. Research has also been conducted on compounds that prevent the activation of the receptor. Such receptor antagonists have potential in medicine.
Herbal cannabinoids (sometimes called classical cannabinoids) are organic compounds that are insoluble in water but soluble in lipids, alcohols and other organic solvents. They occur naturally only in the cannabis plant, and are concentrated in a viscous resin that is produced in glandular structures known as trichomes. In addition to cannabinoids, the resin is rich in terpenes, which are largely responsible for the odor of the cannabis plant.
There are over sixty known herbal cannabinoids. Of these, tetrahydrocannabinol (THC), cannabidiol (CBD) and cannabinol (CBN) are the most prevalent and have received the most study. Other common ones are listed below:
CBG Cannabigerol CBC Cannabichromene CBL Cannabicyclol THCV Tetrahydrocannabivarin CBDV Cannabidivarin CBCV Cannabichromevarin CBGV Cannabigerovarin CBGM Cannabigerol Monoethyl Ether
THC is the primary psychoactive component of the plant. Medically, it appears to mediate pain and to be neuroprotective. THC has a greater affinity for the CB-1 receptor than for the CB-2 receptors. Its effects are perceived to be more cerebral.
CBD is not psychoactive, and appears to mediate the euphoric effect of THC. It may decrease the rate of THC clearance from the body, perhaps by interfering with the metabolism of THC in the liver. Medically it appears to relieve convulsion, inflammation, anxiety, and nausea. CBD has a greater affinity for the CB-2 receptor than for the CB-1 receptor. It is perceived to have more effect on the body.
CBN is the primary product of THC degradation, and there is usually little of it in a fresh plant. CBN content increases as THC degrades in storage, and with exposure to light and air. It is only mildly psychoactive, and is perceived to be sedative or stupefying.
These compounds may be in different forms depending on the position of the double bond in the alicyclic carbon ring. There is potential for confusion because there are different numbering systems used to describe the position of this double bond. The dibenzopyram numbering system is most widely used today. Under this system, the major form of THC is called Delta-9-THC, while the minor form is called Delta-8-THC. Under the alternate terpene numbering system, these same compounds are called Delta-1-THC and Delta-6-THC, respectively.
Most herbal cannabinoid compounds are 21 carbon compounds. However some do not follow this rule, primarily because of variation in the length of the side chain attached to the aromatic ring. In THC, CBD, and CBN, this side chain is a pentyl (5 carbon) chain. In the most common homologue, the pentyl chain is replaced with a propyl (3 carbon) chain. Cannabinoids with the propyl side chain are named using the suffix "varin", and are designated, for example, THCV, CBDV, or CBNV. It appears that shorter chains increase the intensity and decrease the duration of the activity of the chemicals.
Cannabinoids were first discovered in the 1940s, when CBD and CBN were identified. The structure of THC was first determined in 1964. Due to molecular similarity and ease of synthetic conversion, it was originally believed that CBD was a natural precursor to THC. However it is now known that CBD and THC are produced independently in the cannabis plant. Cannabinoid production starts when an enzyme causes geranyl-pyrophosphate and olivetolic acid to combine and form CBG. Next, CBG is independently converted to THC, CBD or CBC, each of which is formed by action of a separate synthase enzyme. For the propyl homologues (THCV, CBDV and CBNV), there is a similar pathway that is based on CBGV.
Cannabis plants can exhibit wide variation in the quantity and type of cannabinoids they produce. The mixture of cannabinoids produced by a plant is known as the plant's cannabinoid profile. Selective breeding has been used to control the genetics of plants and modify the cannabinoid profile. For example, strains of hemp, which are used as fiber, are bred such that they are low in psychoactive chemicals like THC. Strains used in medicine are often bred for high CBD content, and strains used for recreational purposes are usually bred for high THC content, or for a specific chemical balance. Some strains of more than 20% THC have been created.
Quantitative analysis of a plant's cannabinoid profile is usually determined by gas chromatography (GC), or more reliably by gas chromatography combined with mass spectroscopy (GC/MS). Liquid chromatography (LC) techniques are also possible, although these are often only semi-quantitative or qualitative. There have been systematic attempts to monitor the cannabinoid profile of cannabis over time, but their accuracy is impeded by the illegal status of the plant.
Herbal cannabinoids were originally thought to be phenolic compounds, but were later demonstrated to be to be predominantly carboxylic acids, which readily decarboxilate with heat and alkaline conditions. Cannabinoids can be administered by smoking, vaporizing, oral ingestion, transdermal patch, intravenous injection, sublingual absorption, or rectal suppository. Once in the body, most cannabinoids are metabolized in the liver, although some is stored in fat. Delta-9-THC is metabolized to 11-Hydroxy-Delta-9-THC, which is then metabolized to 9-Carboxy-THC. Some cannabis metabolites are can be detected in the body after several weeks.
Cannabinoids can be separated from the plant with solvent extraction. Hydrocarbon or alcohol solvents are often used. However, these solvents are flammable and many are toxic. Supercritical solvent extraction with carbon dioxide is an alternative technique. Although this process requires high pressures, there is minimal risk of fire or toxicity, solvent removal is simple and efficient, and extract quality can be well-controlled. Once extracted, cannabinoid blends can be separated into individual components using wiped film vacuum distillation or other distillation techniques. However, to produce high purity cannabinoids, chemical synthesis is generally required.
Endocannabinoids are naturally produced in the bodies of animals. After cannabinoid receptors were first discovered in the 1980s, scientists began searching for natural compounds that activate these receptors.
In the early 1990s, the first such compound was identified as arachidonyl ethanolamine and named anandamide, the Sanskrit word for bliss. Anandamide is a polyunsaturated fatty acid with pharmacology similar to THC, although its chemical structure is different. Anandamide bonds primarily to the CB-1 receptor, and is found in a wide range of animals. It is about half as potent as THC. Two analogs of anandamide, docosatetraenylethanolamide and Homo-γ-linoenylethanolamide, have similar pharmacology.
Another endocannabinoid, 2-arachidonyl glycerol, binds to both the CB-1 and CB-2 receptors, and is more abundant and less active than anandamide. Little is known about two other discovered endocannabinoids, palmitoyl ethanolamide and oleamide.
Synthetic cannabinoids are produced in the laboratory with organic synthesis and do not occur naturally. Generally, this synthesis is based on the structure of herbal cannabinoids, although some synthetic cannabinoids have been based on the structure of endogenous cannabinoids. Synthesis techniques based on herbal cannabinoids have been known for some time and a large number have been produced and tested.
Synthetic cannabinoids are particularly useful in experiments to determine the relationship between the structure and activity of cannabinoid compounds, by making systematic, incremental modifications of cannabinoid molecule.
Notable synthetic cannabinoids include:
CP-55940 Produced in 1974; 40-60 times as potent as THC HU-210 100-800 times as potent as THC SR-144526 Distinguishes between CB1 and CB2 receptors Nabilone Used as an anti-emetic in chemotherapy
External Links and References
- Chemical Ecology of Cannabis (J. Intl. Hemp Assn. - 1994) (http://www.hempfood.com/IHA/iha01201.html)
- Structure Activity Relationships of the Cannabinoids (NIDA Monograph 79 - 1987) (http://220.127.116.11/pdf/monographs/download79.html)
- Marijuana and Medicine - Assessing the Science Base (Institute of Medicine - 1999) (http://books.nap.edu/html/marimed/)
- Marijuana - THC and Analogs (Rhodium) (http://www.rhodium.ws/chemistry/psychedelicchemistry/chapter2.html)
- THC Synthesis Overview (Rhodium) (http://www.rhodium.ws/chemistry/thc/index.html)
- What Every Doctor Should Know About Cannabinoids (http://www.ccrmg.org/journal/03sum/doctorshouldknow.html)
- Therapeutic Potential in Spotlight at Cannabinoid Researchers' Meeting (http://www.ccrmg.org/journal/04spr/potential.html)
- Cannabis 2002 Report (Ministry of Public Health of Belgium) (http://www.trimbos.nl/Downloads/English_General/Cannabis2002_Report.pdf)
- The Health and Psychological Effects of Cannabis Use (Australia - Monograph 44 - 2001) (http://www.health.gov.au/pubhlth/publicat/document/mono44.pdf)
- House of Lords Report - Cannabis (United Kingdom - 1998) (http://www.parliament.the-stationery-office.co.uk/pa/ld199798/ldselect/ldsctech/151/15101.htm)
- Inheritance of Chemical Phenotype in Cannabis Sativa (Genetics) (http://www.genetics.org/cgi/reprint/163/1/335.pdf)
- Cannabis: A Health Perspective and Research Agenda (World Health Organization - 1997) (http://whqlibdoc.who.int/hq/1997/WHO_MSA_PSA_97.4.pdf)
- Canadian Senate Report on Cannabis - 2002 (http://www.parl.gc.ca/common/Committee_SenRep.asp?Language=E&Parl=37&Ses=1&comm_id=85)
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