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Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol

In light of legislative changes and the widespread use of cannabis as a recreational and medicinal drug, delayed effects of cannabis upon brief exposure during embryonic development are of high interest as early pregnancies often go undetected. Here, zebrafish embryos were exposed to cannabidiol (CB...

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Autores principales: Kanyo, Richard, Amin, Md Ruhul, Locskai, Laszlo F., Bouvier, Danika D., Olthuis, Alexandria M., Allison, W. Ted, Ali, Declan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169761/
https://www.ncbi.nlm.nih.gov/pubmed/34075141
http://dx.doi.org/10.1038/s41598-021-90902-3
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author Kanyo, Richard
Amin, Md Ruhul
Locskai, Laszlo F.
Bouvier, Danika D.
Olthuis, Alexandria M.
Allison, W. Ted
Ali, Declan W.
author_facet Kanyo, Richard
Amin, Md Ruhul
Locskai, Laszlo F.
Bouvier, Danika D.
Olthuis, Alexandria M.
Allison, W. Ted
Ali, Declan W.
author_sort Kanyo, Richard
collection PubMed
description In light of legislative changes and the widespread use of cannabis as a recreational and medicinal drug, delayed effects of cannabis upon brief exposure during embryonic development are of high interest as early pregnancies often go undetected. Here, zebrafish embryos were exposed to cannabidiol (CBD) and Δ(9)-tetrahydrocannabinol (THC) until the end of gastrulation (1–10 h post-fertilization) and analyzed later in development (4–5 days post-fertilization). In order to measure neural activity, we implemented Calcium-Modulated Photoactivatable Ratiometric Integrator (CaMPARI) and optimized the protocol for a 96-well format complemented by locomotor analysis. Our results revealed that neural activity was decreased by CBD more than THC. At higher doses, both cannabinoids could dramatically reduce neural activity and locomotor activity. Interestingly, the decrease was more pronounced when CBD and THC were combined. At the receptor level, CBD-mediated reduction of locomotor activity was partially prevented using cannabinoid type 1 and 2 receptor inhibitors. Overall, we report that CBD toxicity occurs via two cannabinoid receptors and is synergistically enhanced by THC exposure to negatively impact neural activity late in larval development. Future studies are warranted to reveal other cannabinoids and their receptors to understand the implications of cannabis consumption on fetal development.
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spelling pubmed-81697612021-06-02 Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol Kanyo, Richard Amin, Md Ruhul Locskai, Laszlo F. Bouvier, Danika D. Olthuis, Alexandria M. Allison, W. Ted Ali, Declan W. Sci Rep Article In light of legislative changes and the widespread use of cannabis as a recreational and medicinal drug, delayed effects of cannabis upon brief exposure during embryonic development are of high interest as early pregnancies often go undetected. Here, zebrafish embryos were exposed to cannabidiol (CBD) and Δ(9)-tetrahydrocannabinol (THC) until the end of gastrulation (1–10 h post-fertilization) and analyzed later in development (4–5 days post-fertilization). In order to measure neural activity, we implemented Calcium-Modulated Photoactivatable Ratiometric Integrator (CaMPARI) and optimized the protocol for a 96-well format complemented by locomotor analysis. Our results revealed that neural activity was decreased by CBD more than THC. At higher doses, both cannabinoids could dramatically reduce neural activity and locomotor activity. Interestingly, the decrease was more pronounced when CBD and THC were combined. At the receptor level, CBD-mediated reduction of locomotor activity was partially prevented using cannabinoid type 1 and 2 receptor inhibitors. Overall, we report that CBD toxicity occurs via two cannabinoid receptors and is synergistically enhanced by THC exposure to negatively impact neural activity late in larval development. Future studies are warranted to reveal other cannabinoids and their receptors to understand the implications of cannabis consumption on fetal development. Nature Publishing Group UK 2021-06-01 /pmc/articles/PMC8169761/ /pubmed/34075141 http://dx.doi.org/10.1038/s41598-021-90902-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kanyo, Richard
Amin, Md Ruhul
Locskai, Laszlo F.
Bouvier, Danika D.
Olthuis, Alexandria M.
Allison, W. Ted
Ali, Declan W.
Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol
title Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol
title_full Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol
title_fullStr Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol
title_full_unstemmed Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol
title_short Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ(9)-tetrahydrocannabinol
title_sort medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and δ(9)-tetrahydrocannabinol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169761/
https://www.ncbi.nlm.nih.gov/pubmed/34075141
http://dx.doi.org/10.1038/s41598-021-90902-3
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