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Establishing zebrafish as a model to study the anxiolytic effects of scopolamine
Scopolamine (hyoscine) is a muscarinic acetylcholine receptor antagonist that has traditionally been used to treat motion sickness in humans. However, studies investigating depressed and bipolar populations have found that scopolamine is also effective at reducing depression and anxiety symptoms. Th...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678162/ https://www.ncbi.nlm.nih.gov/pubmed/29118373 http://dx.doi.org/10.1038/s41598-017-15374-w |
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author | Hamilton, Trevor J. Morrill, Adam Lucas, Kayla Gallup, Joshua Harris, Megan Healey, Meghan Pitman, Taylor Schalomon, Melike Digweed, Shannon Tresguerres, Martin |
author_facet | Hamilton, Trevor J. Morrill, Adam Lucas, Kayla Gallup, Joshua Harris, Megan Healey, Meghan Pitman, Taylor Schalomon, Melike Digweed, Shannon Tresguerres, Martin |
author_sort | Hamilton, Trevor J. |
collection | PubMed |
description | Scopolamine (hyoscine) is a muscarinic acetylcholine receptor antagonist that has traditionally been used to treat motion sickness in humans. However, studies investigating depressed and bipolar populations have found that scopolamine is also effective at reducing depression and anxiety symptoms. The potential anxiety-reducing (anxiolytic) effects of scopolamine could have great clinical implications for humans; however, rats and mice administered scopolamine showed increased anxiety in standard behavioural tests. This is in direct contrast to findings in humans, and complicates studies to elucidate the specific mechanisms of scopolamine action. The aim of this study was to assess the suitability of zebrafish as a model system to test anxiety-like compounds using scopolamine. Similar to humans, scopolamine acted as an anxiolytic in individual behavioural tests (novel approach test and novel tank diving test). The anxiolytic effect of scopolamine was dose dependent and biphasic, reaching maximum effect at 800 µM. Scopolamine (800 µM) also had an anxiolytic effect in a group behavioural test, as it significantly decreased their tendency to shoal. These results establish zebrafish as a model organism for studying the anxiolytic effects of scopolamine, its mechanisms of action and side effects. |
format | Online Article Text |
id | pubmed-5678162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56781622017-11-17 Establishing zebrafish as a model to study the anxiolytic effects of scopolamine Hamilton, Trevor J. Morrill, Adam Lucas, Kayla Gallup, Joshua Harris, Megan Healey, Meghan Pitman, Taylor Schalomon, Melike Digweed, Shannon Tresguerres, Martin Sci Rep Article Scopolamine (hyoscine) is a muscarinic acetylcholine receptor antagonist that has traditionally been used to treat motion sickness in humans. However, studies investigating depressed and bipolar populations have found that scopolamine is also effective at reducing depression and anxiety symptoms. The potential anxiety-reducing (anxiolytic) effects of scopolamine could have great clinical implications for humans; however, rats and mice administered scopolamine showed increased anxiety in standard behavioural tests. This is in direct contrast to findings in humans, and complicates studies to elucidate the specific mechanisms of scopolamine action. The aim of this study was to assess the suitability of zebrafish as a model system to test anxiety-like compounds using scopolamine. Similar to humans, scopolamine acted as an anxiolytic in individual behavioural tests (novel approach test and novel tank diving test). The anxiolytic effect of scopolamine was dose dependent and biphasic, reaching maximum effect at 800 µM. Scopolamine (800 µM) also had an anxiolytic effect in a group behavioural test, as it significantly decreased their tendency to shoal. These results establish zebrafish as a model organism for studying the anxiolytic effects of scopolamine, its mechanisms of action and side effects. Nature Publishing Group UK 2017-11-08 /pmc/articles/PMC5678162/ /pubmed/29118373 http://dx.doi.org/10.1038/s41598-017-15374-w Text en © The Author(s) 2017 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 Hamilton, Trevor J. Morrill, Adam Lucas, Kayla Gallup, Joshua Harris, Megan Healey, Meghan Pitman, Taylor Schalomon, Melike Digweed, Shannon Tresguerres, Martin Establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
title | Establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
title_full | Establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
title_fullStr | Establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
title_full_unstemmed | Establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
title_short | Establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
title_sort | establishing zebrafish as a model to study the anxiolytic effects of scopolamine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678162/ https://www.ncbi.nlm.nih.gov/pubmed/29118373 http://dx.doi.org/10.1038/s41598-017-15374-w |
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