Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.

In this study, we investigated locomotor activity and responses to repeated light and dark stimuli to assess cannabinoid-induced abnormal behavior in zebrafish larvae (Danio rerio), as an alternative to standard rodent models. To induce the desired responses, we used cannabidiol and WIN55,212-2, two...

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Main Authors: Akihiro Hasumi, Hideyuki Maeda, Ken-Ichi Yoshida
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0236606
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author Akihiro Hasumi
Hideyuki Maeda
Ken-Ichi Yoshida
author_facet Akihiro Hasumi
Hideyuki Maeda
Ken-Ichi Yoshida
author_sort Akihiro Hasumi
collection DOAJ
description In this study, we investigated locomotor activity and responses to repeated light and dark stimuli to assess cannabinoid-induced abnormal behavior in zebrafish larvae (Danio rerio), as an alternative to standard rodent models. To induce the desired responses, we used cannabidiol and WIN55,212-2, two major cannabinoid components. A repeated light and dark test was used to assess how drug exposure influences locomotory responses. Larvae were examined after moderate cannabidiol and WIN55,212-2 exposure and at 24 h after transfer to untreated water. We found that cannabidiol did not produce a dose-dependent inhibitory effect on locomotor activity, with both 0.5 and 10 μg/mL concentrations reducing movement velocity and the total distance moved. However, 10 μg/mL cannabidiol was observed to attenuate the responses of larvae exposed to darkness. No differences were detected between the control and cannabidiol-treated groups after 24 h in fresh water. Fish treated with WIN55,212-2 at 0.5 and 1 μg/mL showed virtually no activity, even in darkness, whereas a concentration of 10 μg/mL induced mortality. A 24-h period in fresh water had the effect of reversing most of the drug-induced immobilization, even in the WIN55,212-2-treated groups. Larvae were also evaluated for their responses to cannabidiol subsequent to an initial exposure to WIN55,212-2, and it was accordingly found that treatment with cannabidiol could attenuate WIN55,212-2-induced abnormal immobilization, whereas equivalent doses of cannabidiol and WIN55,212-2 produced a mixed response. In conclusion, the behavioral effects of the two cannabinoids cannabidiol and WIN55,212-2 appear to be ratio dependent. Furthermore, the repeated light and dark test could serve as a suitable method for assaying drug-induced behavior.
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spelling doaj.art-5620248174cc40f18fee4d016436b00c2022-12-21T19:18:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-011510e023660610.1371/journal.pone.0236606Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.Akihiro HasumiHideyuki MaedaKen-Ichi YoshidaIn this study, we investigated locomotor activity and responses to repeated light and dark stimuli to assess cannabinoid-induced abnormal behavior in zebrafish larvae (Danio rerio), as an alternative to standard rodent models. To induce the desired responses, we used cannabidiol and WIN55,212-2, two major cannabinoid components. A repeated light and dark test was used to assess how drug exposure influences locomotory responses. Larvae were examined after moderate cannabidiol and WIN55,212-2 exposure and at 24 h after transfer to untreated water. We found that cannabidiol did not produce a dose-dependent inhibitory effect on locomotor activity, with both 0.5 and 10 μg/mL concentrations reducing movement velocity and the total distance moved. However, 10 μg/mL cannabidiol was observed to attenuate the responses of larvae exposed to darkness. No differences were detected between the control and cannabidiol-treated groups after 24 h in fresh water. Fish treated with WIN55,212-2 at 0.5 and 1 μg/mL showed virtually no activity, even in darkness, whereas a concentration of 10 μg/mL induced mortality. A 24-h period in fresh water had the effect of reversing most of the drug-induced immobilization, even in the WIN55,212-2-treated groups. Larvae were also evaluated for their responses to cannabidiol subsequent to an initial exposure to WIN55,212-2, and it was accordingly found that treatment with cannabidiol could attenuate WIN55,212-2-induced abnormal immobilization, whereas equivalent doses of cannabidiol and WIN55,212-2 produced a mixed response. In conclusion, the behavioral effects of the two cannabinoids cannabidiol and WIN55,212-2 appear to be ratio dependent. Furthermore, the repeated light and dark test could serve as a suitable method for assaying drug-induced behavior.https://doi.org/10.1371/journal.pone.0236606
spellingShingle Akihiro Hasumi
Hideyuki Maeda
Ken-Ichi Yoshida
Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.
PLoS ONE
title Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.
title_full Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.
title_fullStr Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.
title_full_unstemmed Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.
title_short Analyzing cannabinoid-induced abnormal behavior in a zebrafish model.
title_sort analyzing cannabinoid induced abnormal behavior in a zebrafish model
url https://doi.org/10.1371/journal.pone.0236606
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