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Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures

There can be a fine line between therapeutic intervention and substance abuse, and this point is clearly exemplified in herbal cannabis and its products. Therapies involving cannabis have been the treatment of last resort for some cases of refractory epilepsy, and this has been among the strongest m...

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Autores principales: Mascal, Mark, Hafezi, Nema, Wang, Deping, Hu, Yuhan, Serra, Gessica, Dallas, Mark L., Spencer, Jeremy P. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533278/
https://www.ncbi.nlm.nih.gov/pubmed/31123271
http://dx.doi.org/10.1038/s41598-019-44056-y
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author Mascal, Mark
Hafezi, Nema
Wang, Deping
Hu, Yuhan
Serra, Gessica
Dallas, Mark L.
Spencer, Jeremy P. E.
author_facet Mascal, Mark
Hafezi, Nema
Wang, Deping
Hu, Yuhan
Serra, Gessica
Dallas, Mark L.
Spencer, Jeremy P. E.
author_sort Mascal, Mark
collection PubMed
description There can be a fine line between therapeutic intervention and substance abuse, and this point is clearly exemplified in herbal cannabis and its products. Therapies involving cannabis have been the treatment of last resort for some cases of refractory epilepsy, and this has been among the strongest medical justifications for legalization of marijuana. In order to circumvent the narcotic effects of Δ(9)-tetrahydrocannabinol (THC), many studies have concentrated on its less intoxicating isomer cannabidiol (CBD). However, CBD, like all natural cannabinoids, is a controlled substance in most countries, and its conversion into THC can be easily performed using common chemicals. We describe here the anticonvulsant properties of 8,9-dihydrocannibidiol (H2CBD), a fully synthetic analogue of CBD that is prepared from inexpensive, non-cannabis derived precursors. H2CBD was found to have effectiveness comparable to CBD both for decreasing the number and reducing the severity of pentylenetetrazole-induced seizures in rats. Finally, H2CBD cannot be converted by any reasonable synthetic route into THC, and thus has the potential to act as a safe, noncontroversial drug for seizure mitigation.
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spelling pubmed-65332782019-06-03 Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures Mascal, Mark Hafezi, Nema Wang, Deping Hu, Yuhan Serra, Gessica Dallas, Mark L. Spencer, Jeremy P. E. Sci Rep Article There can be a fine line between therapeutic intervention and substance abuse, and this point is clearly exemplified in herbal cannabis and its products. Therapies involving cannabis have been the treatment of last resort for some cases of refractory epilepsy, and this has been among the strongest medical justifications for legalization of marijuana. In order to circumvent the narcotic effects of Δ(9)-tetrahydrocannabinol (THC), many studies have concentrated on its less intoxicating isomer cannabidiol (CBD). However, CBD, like all natural cannabinoids, is a controlled substance in most countries, and its conversion into THC can be easily performed using common chemicals. We describe here the anticonvulsant properties of 8,9-dihydrocannibidiol (H2CBD), a fully synthetic analogue of CBD that is prepared from inexpensive, non-cannabis derived precursors. H2CBD was found to have effectiveness comparable to CBD both for decreasing the number and reducing the severity of pentylenetetrazole-induced seizures in rats. Finally, H2CBD cannot be converted by any reasonable synthetic route into THC, and thus has the potential to act as a safe, noncontroversial drug for seizure mitigation. Nature Publishing Group UK 2019-05-23 /pmc/articles/PMC6533278/ /pubmed/31123271 http://dx.doi.org/10.1038/s41598-019-44056-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mascal, Mark
Hafezi, Nema
Wang, Deping
Hu, Yuhan
Serra, Gessica
Dallas, Mark L.
Spencer, Jeremy P. E.
Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
title Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
title_full Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
title_fullStr Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
title_full_unstemmed Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
title_short Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
title_sort synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533278/
https://www.ncbi.nlm.nih.gov/pubmed/31123271
http://dx.doi.org/10.1038/s41598-019-44056-y
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