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Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors
The entourage effect was a proposed explanation for biological observations that endocannabinoid ligand activities can be modified by other lipids released from cells at the same time. An increasing volume of anecdotal reports and interest in the plant have provoked research into the activity of min...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109307/ https://www.ncbi.nlm.nih.gov/pubmed/32269529 http://dx.doi.org/10.3389/fphar.2020.00359 |
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author | Finlay, David B. Sircombe, Kathleen J. Nimick, Mhairi Jones, Callum Glass, Michelle |
author_facet | Finlay, David B. Sircombe, Kathleen J. Nimick, Mhairi Jones, Callum Glass, Michelle |
author_sort | Finlay, David B. |
collection | PubMed |
description | The entourage effect was a proposed explanation for biological observations that endocannabinoid ligand activities can be modified by other lipids released from cells at the same time. An increasing volume of anecdotal reports and interest in the plant have provoked research into the activity of minor chemical constituents of the plant—including volatile terpenoids such as myrcene, α- and β- pinene, β-caryophyllene, and limonene. However, to date, no clear interaction has been identified. The current study was designed to determine whether terpenes in the cannabis plant have detectable receptor-mediated activity, or modify the activity of Δ(9)-tetrahydrocannabinol, cannabidiol, or the endocannabinoid 2-arachidonylglycerol at the cannabinoid receptors. In addition, we have utilized a standard radioligand binding paradigm with ability to detect orthosteric and allosteric interactions of test compounds. With the possible exception of a weak interaction of β-caryophyllene with CB2, no data were produced to support the hypothesis that any of the five terpenes tested (either alone or in mixtures) have direct interactions with CB1 or CB2, as the binding of radioligand ([(3)H]-CP55,940), Δ(9)-tetrahydrocannabinol, and cannabidiol were unaltered by the presence of terpenes. Similarly, terpene functional effects were also not detected, either alone or in combination with Δ(9)-tetrahydrocannabinol, cannabidiol, or 2-arachidonoylglycerol. This study adds to the evidence that the putative entourage effect cannot be explained by direct effects at CB1 or CB2. |
format | Online Article Text |
id | pubmed-7109307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71093072020-04-08 Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors Finlay, David B. Sircombe, Kathleen J. Nimick, Mhairi Jones, Callum Glass, Michelle Front Pharmacol Pharmacology The entourage effect was a proposed explanation for biological observations that endocannabinoid ligand activities can be modified by other lipids released from cells at the same time. An increasing volume of anecdotal reports and interest in the plant have provoked research into the activity of minor chemical constituents of the plant—including volatile terpenoids such as myrcene, α- and β- pinene, β-caryophyllene, and limonene. However, to date, no clear interaction has been identified. The current study was designed to determine whether terpenes in the cannabis plant have detectable receptor-mediated activity, or modify the activity of Δ(9)-tetrahydrocannabinol, cannabidiol, or the endocannabinoid 2-arachidonylglycerol at the cannabinoid receptors. In addition, we have utilized a standard radioligand binding paradigm with ability to detect orthosteric and allosteric interactions of test compounds. With the possible exception of a weak interaction of β-caryophyllene with CB2, no data were produced to support the hypothesis that any of the five terpenes tested (either alone or in mixtures) have direct interactions with CB1 or CB2, as the binding of radioligand ([(3)H]-CP55,940), Δ(9)-tetrahydrocannabinol, and cannabidiol were unaltered by the presence of terpenes. Similarly, terpene functional effects were also not detected, either alone or in combination with Δ(9)-tetrahydrocannabinol, cannabidiol, or 2-arachidonoylglycerol. This study adds to the evidence that the putative entourage effect cannot be explained by direct effects at CB1 or CB2. Frontiers Media S.A. 2020-03-25 /pmc/articles/PMC7109307/ /pubmed/32269529 http://dx.doi.org/10.3389/fphar.2020.00359 Text en Copyright © 2020 Finlay, Sircombe, Nimick, Jones and Glass http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Finlay, David B. Sircombe, Kathleen J. Nimick, Mhairi Jones, Callum Glass, Michelle Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors |
title | Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors |
title_full | Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors |
title_fullStr | Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors |
title_full_unstemmed | Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors |
title_short | Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors |
title_sort | terpenoids from cannabis do not mediate an entourage effect by acting at cannabinoid receptors |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7109307/ https://www.ncbi.nlm.nih.gov/pubmed/32269529 http://dx.doi.org/10.3389/fphar.2020.00359 |
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