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THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior
High doses of the Cannabis constituent Δ9-tetrahydrocannabinol (THC) increase the risk of psychosis in humans. Highly accessible animal models are needed to address underlying mechanisms. Using zebrafish with a conserved endocannabinoid system, this study investigates the acute effects of THC on adu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333334/ https://www.ncbi.nlm.nih.gov/pubmed/34344922 http://dx.doi.org/10.1038/s41598-021-95016-4 |
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author | Dahlén, Amelia Zarei, Mahdi Melgoza, Adam Wagle, Mahendra Guo, Su |
author_facet | Dahlén, Amelia Zarei, Mahdi Melgoza, Adam Wagle, Mahendra Guo, Su |
author_sort | Dahlén, Amelia |
collection | PubMed |
description | High doses of the Cannabis constituent Δ9-tetrahydrocannabinol (THC) increase the risk of psychosis in humans. Highly accessible animal models are needed to address underlying mechanisms. Using zebrafish with a conserved endocannabinoid system, this study investigates the acute effects of THC on adult zebrafish behavior and the mechanisms involved. A concentration-dependent THC-induced behavioral stereotypy akin to THC’s effect in rats and the psychotropics phencyclidine and ketamine in zebrafish was established. Distinctive circular swimming during THC-exposure was measured using a novel analytical method that we developed, which detected an elevated Repetition Index (RI) compared to vehicle controls. This was reduced upon co-administration of N-methyl-D-aspartate (NMDA) receptor agonist NMDA, suggesting that THC exerts its effects via biochemical or neurobiological mechanisms associated with NMDA receptor antagonism. Co-treatment of γ‐aminobutyric acid receptor antagonist pentylenetetrazol also showed signs of reducing the RI. Since THC-induced repetitive behavior remained in co-administrations with cannabinoid receptor 1 inverse agonist AM251, the phenotype may be cannabinoid receptor 1-independent. Conversely, the inverse cannabinoid receptor 2 agonist AM630 significantly reduced THC-induced behavioral stereotypy, indicating cannabinoid receptor 2 as a possible mediator. A significant reduction of the THC-RI was also observed by the antipsychotic sulpiride. Together, these findings highlight this model’s potential for elucidating the mechanistic relationship between Cannabis and psychosis. |
format | Online Article Text |
id | pubmed-8333334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83333342021-08-05 THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior Dahlén, Amelia Zarei, Mahdi Melgoza, Adam Wagle, Mahendra Guo, Su Sci Rep Article High doses of the Cannabis constituent Δ9-tetrahydrocannabinol (THC) increase the risk of psychosis in humans. Highly accessible animal models are needed to address underlying mechanisms. Using zebrafish with a conserved endocannabinoid system, this study investigates the acute effects of THC on adult zebrafish behavior and the mechanisms involved. A concentration-dependent THC-induced behavioral stereotypy akin to THC’s effect in rats and the psychotropics phencyclidine and ketamine in zebrafish was established. Distinctive circular swimming during THC-exposure was measured using a novel analytical method that we developed, which detected an elevated Repetition Index (RI) compared to vehicle controls. This was reduced upon co-administration of N-methyl-D-aspartate (NMDA) receptor agonist NMDA, suggesting that THC exerts its effects via biochemical or neurobiological mechanisms associated with NMDA receptor antagonism. Co-treatment of γ‐aminobutyric acid receptor antagonist pentylenetetrazol also showed signs of reducing the RI. Since THC-induced repetitive behavior remained in co-administrations with cannabinoid receptor 1 inverse agonist AM251, the phenotype may be cannabinoid receptor 1-independent. Conversely, the inverse cannabinoid receptor 2 agonist AM630 significantly reduced THC-induced behavioral stereotypy, indicating cannabinoid receptor 2 as a possible mediator. A significant reduction of the THC-RI was also observed by the antipsychotic sulpiride. Together, these findings highlight this model’s potential for elucidating the mechanistic relationship between Cannabis and psychosis. Nature Publishing Group UK 2021-08-03 /pmc/articles/PMC8333334/ /pubmed/34344922 http://dx.doi.org/10.1038/s41598-021-95016-4 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 Dahlén, Amelia Zarei, Mahdi Melgoza, Adam Wagle, Mahendra Guo, Su THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
title | THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
title_full | THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
title_fullStr | THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
title_full_unstemmed | THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
title_short | THC-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
title_sort | thc-induced behavioral stereotypy in zebrafish as a model of psychosis-like behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333334/ https://www.ncbi.nlm.nih.gov/pubmed/34344922 http://dx.doi.org/10.1038/s41598-021-95016-4 |
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