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Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics
BACKGROUND: Rhynchophylline (RHY) is an alkaloid component of Uncaria, which are plants extensively used in traditional Asian medicines. Uncaria treatments increase sleep time and quality in humans, and RHY induces sleep in rats. However, like many traditional natural treatments, the mechanisms of a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161643/ https://www.ncbi.nlm.nih.gov/pubmed/37143153 http://dx.doi.org/10.1186/s13062-023-00377-7 |
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author | Ballester Roig, Maria Neus Leduc, Tanya Dufort-Gervais, Julien Maghmoul, Yousra Tastet, Olivier Mongrain, Valérie |
author_facet | Ballester Roig, Maria Neus Leduc, Tanya Dufort-Gervais, Julien Maghmoul, Yousra Tastet, Olivier Mongrain, Valérie |
author_sort | Ballester Roig, Maria Neus |
collection | PubMed |
description | BACKGROUND: Rhynchophylline (RHY) is an alkaloid component of Uncaria, which are plants extensively used in traditional Asian medicines. Uncaria treatments increase sleep time and quality in humans, and RHY induces sleep in rats. However, like many traditional natural treatments, the mechanisms of action of RHY and Uncaria remain evasive. Moreover, it is unknown whether RHY modifies key brain oscillations during sleep. We thus aimed at defining the effects of RHY on sleep architecture and oscillations throughout a 24-h cycle, as well as identifying the underlying molecular mechanisms. Mice received systemic RHY injections at two times of the day (beginning and end of the light period), and vigilance states were studied by electrocorticographic recordings. RESULTS: RHY enhanced slow wave sleep (SWS) after both injections, suppressed paradoxical sleep (PS) in the light but enhanced PS in the dark period. Furthermore, RHY modified brain oscillations during both wakefulness and SWS (including delta activity dynamics) in a time-dependent manner. Interestingly, most effects were larger in females. A brain spatial transcriptomic analysis showed that RHY modifies the expression of genes linked to cell movement, apoptosis/necrosis, and transcription/translation in a brain region-independent manner, and changes those linked to sleep regulation (e.g., Hcrt, Pmch) in a brain region-specific manner (e.g., in the hypothalamus). CONCLUSIONS: The findings provide support to the sleep-inducing effect of RHY, expose the relevance to shape wake/sleep oscillations, and highlight its effects on the transcriptome with a high spatial resolution. The exposed molecular mechanisms underlying the effect of a natural compound should benefit sleep- and brain-related medicine. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13062-023-00377-7. |
format | Online Article Text |
id | pubmed-10161643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101616432023-05-06 Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics Ballester Roig, Maria Neus Leduc, Tanya Dufort-Gervais, Julien Maghmoul, Yousra Tastet, Olivier Mongrain, Valérie Biol Direct Research BACKGROUND: Rhynchophylline (RHY) is an alkaloid component of Uncaria, which are plants extensively used in traditional Asian medicines. Uncaria treatments increase sleep time and quality in humans, and RHY induces sleep in rats. However, like many traditional natural treatments, the mechanisms of action of RHY and Uncaria remain evasive. Moreover, it is unknown whether RHY modifies key brain oscillations during sleep. We thus aimed at defining the effects of RHY on sleep architecture and oscillations throughout a 24-h cycle, as well as identifying the underlying molecular mechanisms. Mice received systemic RHY injections at two times of the day (beginning and end of the light period), and vigilance states were studied by electrocorticographic recordings. RESULTS: RHY enhanced slow wave sleep (SWS) after both injections, suppressed paradoxical sleep (PS) in the light but enhanced PS in the dark period. Furthermore, RHY modified brain oscillations during both wakefulness and SWS (including delta activity dynamics) in a time-dependent manner. Interestingly, most effects were larger in females. A brain spatial transcriptomic analysis showed that RHY modifies the expression of genes linked to cell movement, apoptosis/necrosis, and transcription/translation in a brain region-independent manner, and changes those linked to sleep regulation (e.g., Hcrt, Pmch) in a brain region-specific manner (e.g., in the hypothalamus). CONCLUSIONS: The findings provide support to the sleep-inducing effect of RHY, expose the relevance to shape wake/sleep oscillations, and highlight its effects on the transcriptome with a high spatial resolution. The exposed molecular mechanisms underlying the effect of a natural compound should benefit sleep- and brain-related medicine. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13062-023-00377-7. BioMed Central 2023-05-05 /pmc/articles/PMC10161643/ /pubmed/37143153 http://dx.doi.org/10.1186/s13062-023-00377-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ballester Roig, Maria Neus Leduc, Tanya Dufort-Gervais, Julien Maghmoul, Yousra Tastet, Olivier Mongrain, Valérie Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
title | Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
title_full | Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
title_fullStr | Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
title_full_unstemmed | Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
title_short | Probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
title_sort | probing pathways by which rhynchophylline modifies sleep using spatial transcriptomics |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161643/ https://www.ncbi.nlm.nih.gov/pubmed/37143153 http://dx.doi.org/10.1186/s13062-023-00377-7 |
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