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Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors
Introduction: Compounds present in Cannabis sativa such as phytocannabinoids and terpenoids may act in concert to elicit therapeutic effects. Cannabinoids such as Δ(9)-tetrahydrocannabinol (Δ(9)-THC) directly activate cannabinoid receptor 1 (CB(1)) and cannabinoid receptor 2 (CB(2)); however, it is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Mary Ann Liebert, Inc., publishers
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757242/ https://www.ncbi.nlm.nih.gov/pubmed/31559333 http://dx.doi.org/10.1089/can.2019.0016 |
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author | Santiago, Marina Sachdev, Shivani Arnold, Jonathon C. McGregor, Iain S. Connor, Mark |
author_facet | Santiago, Marina Sachdev, Shivani Arnold, Jonathon C. McGregor, Iain S. Connor, Mark |
author_sort | Santiago, Marina |
collection | PubMed |
description | Introduction: Compounds present in Cannabis sativa such as phytocannabinoids and terpenoids may act in concert to elicit therapeutic effects. Cannabinoids such as Δ(9)-tetrahydrocannabinol (Δ(9)-THC) directly activate cannabinoid receptor 1 (CB(1)) and cannabinoid receptor 2 (CB(2)); however, it is not known if terpenoids present in Cannabis also affect cannabinoid receptor signaling. Therefore, we examined six common terpenoids alone, and in combination with cannabinoid receptor agonists, on CB(1) and CB(2) signaling in vitro. Materials and Methods: Potassium channel activity in AtT20 FlpIn cells transfected with human CB(1) or CB(2) receptors was measured in real time using FLIPR(®) membrane potential dye in a FlexStation 3 plate reader. Terpenoids were tested individually and in combination for periods up to 30 min. Endogenous somatostatin receptors served as a control for direct effects of drugs on potassium channels. Results: α-Pinene, β-pinene, β-caryophyllene, linalool, limonene, and β-myrcene (up to 30–100 μM) did not change membrane potential in AtT20 cells expressing CB(1) or CB(2), or affect the response to a maximally effective concentration of the synthetic cannabinoid CP55,940. The presence of individual or a combination of terpenoids did not affect the hyperpolarization produced by Δ(9)-THC (10 μM): (CB(1): control, 59%±7%; with terpenoids (10 μM each) 55%±4%; CB(2): Δ(9)-THC 16%±5%, with terpenoids (10 μM each) 17%±4%). To investigate possible effect on desensitization of CB(1) responses, all six terpenoids were added together with Δ(9)-THC and signaling measured continuously over 30 min. Terpenoids did not affect desensitization, after 30 min the control hyperpolarization recovered by 63%±6% in the presence of the terpenoids recovery was 61%±5%. Discussion: None of the six of the most common terpenoids in Cannabis directly activated CB(1) or CB(2), or modulated the signaling of the phytocannabinoid agonist Δ(9)-THC. These results suggest that if a phytocannabinoid–terpenoid entourage effect exists, it is not at the CB(1) or CB(2) receptor level. It remains possible that terpenoids activate CB(1) and CB(2) signaling pathways that do not involve potassium channels; however, it seems more likely that they may act at different molecular target(s) in the neuronal circuits important for the behavioral effect of Cannabis. |
format | Online Article Text |
id | pubmed-6757242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-67572422019-09-26 Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors Santiago, Marina Sachdev, Shivani Arnold, Jonathon C. McGregor, Iain S. Connor, Mark Cannabis Cannabinoid Res Original Research Introduction: Compounds present in Cannabis sativa such as phytocannabinoids and terpenoids may act in concert to elicit therapeutic effects. Cannabinoids such as Δ(9)-tetrahydrocannabinol (Δ(9)-THC) directly activate cannabinoid receptor 1 (CB(1)) and cannabinoid receptor 2 (CB(2)); however, it is not known if terpenoids present in Cannabis also affect cannabinoid receptor signaling. Therefore, we examined six common terpenoids alone, and in combination with cannabinoid receptor agonists, on CB(1) and CB(2) signaling in vitro. Materials and Methods: Potassium channel activity in AtT20 FlpIn cells transfected with human CB(1) or CB(2) receptors was measured in real time using FLIPR(®) membrane potential dye in a FlexStation 3 plate reader. Terpenoids were tested individually and in combination for periods up to 30 min. Endogenous somatostatin receptors served as a control for direct effects of drugs on potassium channels. Results: α-Pinene, β-pinene, β-caryophyllene, linalool, limonene, and β-myrcene (up to 30–100 μM) did not change membrane potential in AtT20 cells expressing CB(1) or CB(2), or affect the response to a maximally effective concentration of the synthetic cannabinoid CP55,940. The presence of individual or a combination of terpenoids did not affect the hyperpolarization produced by Δ(9)-THC (10 μM): (CB(1): control, 59%±7%; with terpenoids (10 μM each) 55%±4%; CB(2): Δ(9)-THC 16%±5%, with terpenoids (10 μM each) 17%±4%). To investigate possible effect on desensitization of CB(1) responses, all six terpenoids were added together with Δ(9)-THC and signaling measured continuously over 30 min. Terpenoids did not affect desensitization, after 30 min the control hyperpolarization recovered by 63%±6% in the presence of the terpenoids recovery was 61%±5%. Discussion: None of the six of the most common terpenoids in Cannabis directly activated CB(1) or CB(2), or modulated the signaling of the phytocannabinoid agonist Δ(9)-THC. These results suggest that if a phytocannabinoid–terpenoid entourage effect exists, it is not at the CB(1) or CB(2) receptor level. It remains possible that terpenoids activate CB(1) and CB(2) signaling pathways that do not involve potassium channels; however, it seems more likely that they may act at different molecular target(s) in the neuronal circuits important for the behavioral effect of Cannabis. Mary Ann Liebert, Inc., publishers 2019-09-23 /pmc/articles/PMC6757242/ /pubmed/31559333 http://dx.doi.org/10.1089/can.2019.0016 Text en © Marina Santiago et al. 2019; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Santiago, Marina Sachdev, Shivani Arnold, Jonathon C. McGregor, Iain S. Connor, Mark Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors |
title | Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors |
title_full | Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors |
title_fullStr | Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors |
title_full_unstemmed | Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors |
title_short | Absence of Entourage: Terpenoids Commonly Found in Cannabis sativa Do Not Modulate the Functional Activity of Δ(9)-THC at Human CB(1) and CB(2) Receptors |
title_sort | absence of entourage: terpenoids commonly found in cannabis sativa do not modulate the functional activity of δ(9)-thc at human cb(1) and cb(2) receptors |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757242/ https://www.ncbi.nlm.nih.gov/pubmed/31559333 http://dx.doi.org/10.1089/can.2019.0016 |
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