Entourage effect
The entourage effect is a proposed mechanism by which cannabis compounds other than tetrahydrocannabinol (THC) act synergistically with it to modulate the overall psychoactive effects of the plant.[1][2]
Compounds
Cannabinoids
Cannabidiol (CBD) is under preliminary research for its potential to modify the effects of THC, possibly mitigating some of the negative,[3] psychosis-like effects of THC.
Terpenes
There are numerous terpenes present in the cannabis plant and variation between strains. Some of the different terpenes have known pharmacological effects and have been studied.[4][5][2]
One supported hypothesis is that myrcene is a prominent sedative terpenoid in cannabis, and combined with THC, may produce the ‘couch-lock’ phenomenon.[2]
Difference between C. indica and C. sativa
There are several key differences between Cannabis indica and Cannabis sativa. These include height and stature, internodal length, leaf size and structure, buds size and density, flowering time, odour, smoke and effects.[6] Indica plants tend to grow shorter and bushier than the sativa plants. Indica strains tend to have wide, short leaves with short wide blades, whereas sativa strains have long leaves with thin long blades. The buds of indica strains tend to be wide, dense and bulky, while sativa strains are likely to be long, sausage shaped flowers.[7]
During the 1970s, Cannabis indica strains from Afghanistan and Northern Pakistan particularly from the Hindu Kush mountain range were brought to the United States, where the first hybrids with Cannabis sativa plants from equatorial areas were developed, widely spreading marijuana cultivation throughout the States.[8]
The name indica originally referred to the geographical area in which the plant was grown, leading to widespread public taxonomic misconceptions.[9]
Human intervention has produced variation within the species and some authorities only recognize one species in the genus that has had divergent selective pressure to either produce plants with more fiber or plants with greater THC content.[10] Large variability exists within either species, and there is an expanding discussion whether the existing paradigm used to differentiate species adequately represents the variability found within the genus Cannabis.[11][12][13] There are five chemotaxonomic types of Cannabis: one with high levels of THC, one which is more fibrous and has higher levels of CBD, one that is an intermediate between the two, another one with high levels of cannabigerol (CBG), and the last one almost without cannabinoids.[14]
Cannabis strains with relatively high CBD:THC ratios are less likely to induce anxiety than vice versa.[15] This may be due to CBD's antagonistic effects at the cannabinoid receptors, compared to THC's partial agonist effect.[16] CBD is also a 5-HT1A receptor (serotonin) agonist, which may also contribute to an anxiolytic-content effect.[17] The effects of sativa are well known for its cerebral high, while indica is well known for its sedative effects which some prefer for night time use.[17] Both types are used as medical cannabis. Indica plants are normally shorter and stockier than sativas.[18] Indicas have broader, deeply serrated leaves and a compact and dense flower cluster.[citation needed]
- Cannabinoids
On average, Cannabis indica has higher levels of THC compared to CBD, whereas Cannabis sativa has lower levels of THC to CBD.[19] However, huge variability exists within either species. A 2015 study shows the average THC content of the most popular herbal cannabis products in the Netherlands has decreased slightly since 2005.[20]
In the recent era of cannabis breeding higher-ratio CBD strains are being developed from Indica origins that may test out as 1:1 (CBD-THC balanced) or even as high as a 22:1 (CBD dominant).
There are three chemotaxonomic types of Cannabis: one with high levels of THC, one which is more fibrous and has higher levels of CBD, and one that is an intermediate between the two.[19][18]
Cannabis strains with CBD:THC ratios above 5:2 are likely to be more relaxing and produce less anxiety than vice versa. This may be due to CBD's antagonistic effects at the cannabinoid receptors, compared to THC's partial agonist effect.[citation needed][dubious – discuss] CBD is also a 5-HT1A receptor (serotonin) agonist, which may also contribute to an anxiolytic-content effect.[17] The effects of sativa are well known for its cerebral high. Users can expect a more vivid and uplifting high, while indica is well known for its sedative effects which some prefer for night time use. Indica possesses a more calming, soothing, and numbing experience in which can be used to relax or relieve pain. Both types are used as medical cannabis.
Plants with elevated levels of propyl cannabinoids, including tetrahydrocannabivarin (THCV), have been found in populations of Cannabis indica from India, Nepal, Thailand, Afghanistan, and Pakistan, as well as southern and western Africa. THCV levels up to 53.7% of total cannabinoids have been reported[19][21]
- Terpenes
Sativa ancestry is associated with farnesene and bergamotene, while Indica ancestry is associated with myrcene, elemene, and sesquiterpene alcohols.[22]
Background
The phrase entourage effect was introduced in 1999.[23][24] While originally identified as a novel method of endocannabinoid regulation by which multiple endogenous chemical species display a cooperative effect in eliciting a cellular response, the term has evolved to describe the polypharmacy effects of combined cannabis phytochemicals or whole plant extracts.[25] The phrase now commonly refers to the compounds present in cannabis supposedly working in concert to create “the sum of all the parts that leads to the magic or power of cannabis”.[4] Other cannabinoids, terpenoids, and flavonoids may be part of an entourage effect.[24] The entourage effect is considered a possible cannabinoid system modulator and is achieved in pain management.[1][24][26]
Criticism
A 2020 review of research found no entourage effect in most studies, while other reports claimed mixed results, including the possibility of increased adverse effects.[27] The review concluded that the term, "entourage effect", is unfounded and used mainly for marketing.[27]
References
- ^ a b Grof CP (November 2018). "Cannabis, from plant to pill". British Journal of Clinical Pharmacology. 84 (11): 2463–2467. doi:10.1111/bcp.13618. PMC 6177712. PMID 29701252.
- ^ a b c Russo EB (August 2011). "Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects". British Journal of Pharmacology. 163 (7): 1344–64. doi:10.1111/j.1476-5381.2011.01238.x. PMC 3165946. PMID 21749363.
- ^ Hudson R, Renard J, Norris C, Rushlow WJ, Laviolette SR (October 2019). "Cannabidiol Counteracts the Psychotropic Side-Effects of Δ-9-Tetrahydrocannabinol in the Ventral Hippocampus through Bidirectional Control of ERK1-2 Phosphorylation". The Journal of Neuroscience. 39 (44): 8762–8777. doi:10.1523/JNEUROSCI.0708-19.2019. PMC 6820200. PMID 31570536.
{{cite journal}}
: External link in
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ignored (help) - ^ a b Chen A (20 April 2017). "Some of the Parts: Is Marijuana's "Entourage Effect" Scientifically Valid?". Scientific American. Retrieved 2017-12-31.
- ^ Fine PG, Rosenfeld MJ (2013-10-29). "The endocannabinoid system, cannabinoids, and pain". Rambam Maimonides Medical Journal. 4 (4): e0022. doi:10.5041/RMMJ.10129. PMC 3820295. PMID 24228165.
- ^ "Indica vs Sativa – Differences". Freedom Seeds. Archived from the original on 2014-09-09. Retrieved 2014-09-09.
- ^ Rosenthal E (2010). Marijuana Grower's Handbook (Ask ed.). Oakland, California: Quick American Publishing. p. 40. ISBN 978-0-932551-46-7.
- ^ Flowers T (1997). Marijuana flower forcing : secrets of designer growing. Berkeley, CA. p. 48. ISBN 978-0-9647946-1-0.
{{cite book}}
: CS1 maint: location missing publisher (link) - ^ Nakamura G (1973). "The forensic identification of marijuana: some questions and answers". Journal of Police Science and Administration. 1 (1): 102–112.
- ^ Chandra S, Lata H, El Sohly JA (23 May 2017). Cannabis sativa L. - Botany and Biotechnology. Springer. pp. 54–. ISBN 978-3-319-54564-6.
- ^ Piomelli D, Russo EB (2016-01-14). "The Cannabis sativa Versus Cannabis indica Debate: An Interview with Ethan Russo, MD". Cannabis and Cannabinoid Research. 1 (1): 44–46. doi:10.1089/can.2015.29003.ebr. PMC 5576603. PMID 28861479.
- ^ Aizpurua-Olaizola O, Omar J, Navarro P, Olivares M, Etxebarria N, Usobiaga A (November 2014). "Identification and quantification of cannabinoids in Cannabis sativa L. plants by high performance liquid chromatography-mass spectrometry". Analytical and Bioanalytical Chemistry. 406 (29): 7549–60. doi:10.1007/s00216-014-8177-x. PMID 25338935. S2CID 206916401.
- ^ Hazekamp A, Fischedick JT (2012-07-01). "Cannabis - from cultivar to chemovar". Drug Testing and Analysis. 4 (7–8): 660–7. doi:10.1002/dta.407. PMID 22362625.
- ^ Mandolino G, Bagatta M, Carboni A, Ranalli P, de Meijer E (2003-03-01). "Qualitative and Quantitative Aspects of the Inheritance of Chemical Phenotype in Cannabis". Journal of Industrial Hemp. 8 (2): 51–72. doi:10.1300/J237v08n02_04. ISSN 1537-7881. S2CID 84817948.
- ^ Russo EB, Tyler VM (22 December 2015). Handbook of Psychotropic Herbs: A Scientific Analysis of Herbal Remedies for Psychiatric Conditions. Routledge. pp. 233–. ISBN 978-1-136-38607-7.
- ^ "Marijuana Chemicals Cannabinoids, Terpenes, Flavonoids (THC and CBD)". Howtogrowmarijuana.com. 2015.
- ^ a b c Joy JE, Watson Jr SJ, Benson Jr JA (1999). Marijuana and Medicine: Assessing The Science Base. Washington D.C: National Academy of Sciences Press. ISBN 978-0-585-05800-9.
- ^ a b Fischedick JT, Hazekamp A, Erkelens T, Choi YH, Verpoorte R (December 2010). "Metabolic fingerprinting of Cannabis sativa L., cannabinoids and terpenoids for chemotaxonomic and drug standardization purposes". Phytochemistry. 71 (17–18): 2058–73. doi:10.1016/j.phytochem.2010.10.001. PMID 21040939.
- ^ a b c Hillig KW, Mahlberg PG (June 2004). "A chemotaxonomic analysis of cannabinoid variation in Cannabis (Cannabaceae)". American Journal of Botany. 91 (6): 966–75. doi:10.3732/ajb.91.6.966. PMID 21653452.
- ^ Niesink RJ, Rigter S, Koeter MW, Brunt TM (December 2015). "Potency trends of Δ9-tetrahydrocannabinol, cannabidiol and cannabinol in cannabis in the Netherlands: 2005-15". Addiction. 110 (12): 1941–50. doi:10.1111/add.13082. PMID 26234170.
- ^ Turner CE, Hadley K, Fetterman PS (October 1973). "Constituents of Cannabis sativa L. VI. Propyl homologs in samples of known geographical origin". Journal of Pharmaceutical Sciences. 62 (10): 1739–41. doi:10.1002/jps.2600621045. PMID 4752132.
- ^ McElroy M, Maassen H, Hazekamp A, Myles S (June 2018). Cannabis Reclassified: Redefining ‘Indica’ and ‘Sativa’ by Genetics and Chemistry (PDF). 28th Annual Symposium of the International Cannabinoid Research Society. Leiden, Netherlands.
- ^ Cite error: The named reference
Ben-Shabat_1998
was invoked but never defined (see the help page). - ^ a b c Gupta S (11 March 2014). "Medical marijuana and 'the entourage effect'". CNN. Retrieved 31 December 2017.
- ^ Russo EB (2019-01-09). "The Case for the Entourage Effect and Conventional Breeding of Clinical Cannabis: No "Strain," No Gain". Frontiers in Plant Science. 9: 1969. doi:10.3389/fpls.2018.01969. PMC 6334252. PMID 30687364.
{{cite journal}}
: CS1 maint: unflagged free DOI (link) - ^ Bouaziz J, Bar On A, Seidman DS, Soriano D (April 1, 2017). "The Clinical Significance of Endocannabinoids in Endometriosis Pain Management". Cannabis and Cannabinoid Research. 2 (1): 72–80. doi:10.1089/can.2016.0035. PMC 5436335. PMID 28861506.
- ^ a b Cogan PS (August 2020). "The 'entourage effect' or 'hodge-podge hashish': the questionable rebranding, marketing, and expectations of cannabis polypharmacy". Expert Review of Clinical Pharmacology. 13 (8): 835–845. doi:10.1080/17512433.2020.1721281. PMID 32116073. S2CID 211726166.