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Effects of tenuifolin on rest/wake behaviour in zebrafish

Insomnia is a common sleep disorder with a high prevalence and substantial adverse consequences. There is growing interest in identifying novel therapeutics from herbal medicine. Tenuifolin is a major constituent of the well-known anti-insomnia herb Radix Polygala. The present study investigated the...

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Autores principales: Chen, Zi-Wen, Peng, Chao-Bao, Pei, Zhong, Zhang, Meng-Ruo, Yun, Tian-Chan, Yang, Zhi-Min, Xu, Fu-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027208/
https://www.ncbi.nlm.nih.gov/pubmed/32104301
http://dx.doi.org/10.3892/etm.2020.8476
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author Chen, Zi-Wen
Peng, Chao-Bao
Pei, Zhong
Zhang, Meng-Ruo
Yun, Tian-Chan
Yang, Zhi-Min
Xu, Fu-Ping
author_facet Chen, Zi-Wen
Peng, Chao-Bao
Pei, Zhong
Zhang, Meng-Ruo
Yun, Tian-Chan
Yang, Zhi-Min
Xu, Fu-Ping
author_sort Chen, Zi-Wen
collection PubMed
description Insomnia is a common sleep disorder with a high prevalence and substantial adverse consequences. There is growing interest in identifying novel therapeutics from herbal medicine. Tenuifolin is a major constituent of the well-known anti-insomnia herb Radix Polygala. The present study investigated the neural activity in response to tenuifolin during rest/wake behaviour in zebrafish and identified the potential biological signalling pathways involved. An automatic video tracking system was used to monitor the behavioural response of zebrafish larvae for 24 h after treatment with tenuifolin. In total, six rest/wake parameters were measured and visualized with a behavioural fingerprint. Time series analysis was conducted by averaging the total rest and waking activity in 10 min intervals. A correlation analysis was performed between tenuifolin and well-known compounds to analyse the underlying biological signalling pathways. Reverse transcription-quantitative PCR was also performed to detect the effects of tenuifolin on the transcription of interesting genes associated with the signalling pathways that were potentially involved. The present results suggested tenuifolin significantly increased the total rest time during the dark phase, with a slight effect on the waking activity in zebrafish larvae. This behavioural phenotype induced by tenuifolin is similar to that of selective serotonin reuptake inhibitors and gamma-aminobutyric acid (GABA) agonists. Furthermore, the expression levels of GABA transporter 1 were significantly increased after tenuifolin treatment. No significant difference was determined in other associated genes in untreated control and tenuifolin-treated larvae. The present results suggested that tenuifolin caused sleep-promoting activity in zebrafish and that these effects may be mediated by the serotoninergic systems and the GABAergic systems.
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spelling pubmed-70272082020-02-26 Effects of tenuifolin on rest/wake behaviour in zebrafish Chen, Zi-Wen Peng, Chao-Bao Pei, Zhong Zhang, Meng-Ruo Yun, Tian-Chan Yang, Zhi-Min Xu, Fu-Ping Exp Ther Med Articles Insomnia is a common sleep disorder with a high prevalence and substantial adverse consequences. There is growing interest in identifying novel therapeutics from herbal medicine. Tenuifolin is a major constituent of the well-known anti-insomnia herb Radix Polygala. The present study investigated the neural activity in response to tenuifolin during rest/wake behaviour in zebrafish and identified the potential biological signalling pathways involved. An automatic video tracking system was used to monitor the behavioural response of zebrafish larvae for 24 h after treatment with tenuifolin. In total, six rest/wake parameters were measured and visualized with a behavioural fingerprint. Time series analysis was conducted by averaging the total rest and waking activity in 10 min intervals. A correlation analysis was performed between tenuifolin and well-known compounds to analyse the underlying biological signalling pathways. Reverse transcription-quantitative PCR was also performed to detect the effects of tenuifolin on the transcription of interesting genes associated with the signalling pathways that were potentially involved. The present results suggested tenuifolin significantly increased the total rest time during the dark phase, with a slight effect on the waking activity in zebrafish larvae. This behavioural phenotype induced by tenuifolin is similar to that of selective serotonin reuptake inhibitors and gamma-aminobutyric acid (GABA) agonists. Furthermore, the expression levels of GABA transporter 1 were significantly increased after tenuifolin treatment. No significant difference was determined in other associated genes in untreated control and tenuifolin-treated larvae. The present results suggested that tenuifolin caused sleep-promoting activity in zebrafish and that these effects may be mediated by the serotoninergic systems and the GABAergic systems. D.A. Spandidos 2020-03 2020-01-28 /pmc/articles/PMC7027208/ /pubmed/32104301 http://dx.doi.org/10.3892/etm.2020.8476 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Chen, Zi-Wen
Peng, Chao-Bao
Pei, Zhong
Zhang, Meng-Ruo
Yun, Tian-Chan
Yang, Zhi-Min
Xu, Fu-Ping
Effects of tenuifolin on rest/wake behaviour in zebrafish
title Effects of tenuifolin on rest/wake behaviour in zebrafish
title_full Effects of tenuifolin on rest/wake behaviour in zebrafish
title_fullStr Effects of tenuifolin on rest/wake behaviour in zebrafish
title_full_unstemmed Effects of tenuifolin on rest/wake behaviour in zebrafish
title_short Effects of tenuifolin on rest/wake behaviour in zebrafish
title_sort effects of tenuifolin on rest/wake behaviour in zebrafish
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027208/
https://www.ncbi.nlm.nih.gov/pubmed/32104301
http://dx.doi.org/10.3892/etm.2020.8476
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