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Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis

Ganoderma resinaceum is a valuable Chinese medicine. This study aimed to investigate whether a G. resinaceum alcohol extract (GRAE) improves sleep, and analyze the potential mechanism. After 30 days of continuous administration of GRAE at various doses, GRAE (1,000 mg/kg.bw) prolonged pentobarbital...

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Autores principales: Chen, Tianci, Zhang, Fangyi, Chen, Juanqin, Zhong, Qiangui, Hu, Yuxin, Wu, Ruru, Xie, Baogui, Jiang, Yuji, Chen, Bingzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837518/
https://www.ncbi.nlm.nih.gov/pubmed/35165654
http://dx.doi.org/10.3389/fnut.2022.745624
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author Chen, Tianci
Zhang, Fangyi
Chen, Juanqin
Zhong, Qiangui
Hu, Yuxin
Wu, Ruru
Xie, Baogui
Jiang, Yuji
Chen, Bingzhi
author_facet Chen, Tianci
Zhang, Fangyi
Chen, Juanqin
Zhong, Qiangui
Hu, Yuxin
Wu, Ruru
Xie, Baogui
Jiang, Yuji
Chen, Bingzhi
author_sort Chen, Tianci
collection PubMed
description Ganoderma resinaceum is a valuable Chinese medicine. This study aimed to investigate whether a G. resinaceum alcohol extract (GRAE) improves sleep, and analyze the potential mechanism. After 30 days of continuous administration of GRAE at various doses, GRAE (1,000 mg/kg.bw) prolonged pentobarbital sodium-induced sleep, increased the rate of sleeping in mice treated with a subthreshold dose of pentobarbital sodium, and shortened sleep latency. The mice brain was analyzed using UPLC-MS/MS and RNA-sequencing. Metabolomics analysis revealed that 73 metabolites in the high-dose (HD) group had changed significantly, mainly in amino acids and their derivatives, especially the accumulation of L-glutamine and PGJ2 (11-oxo-15S-hydroxy-prosta-5Z, 9, 13E-trien-1-oic acid). Transcriptome analysis revealed 500 differential genes between HD and control groups, mainly enriched in neuroactive ligand-receptor interaction, amphetamine addiction, and cocaine addiction pathways. The conjoint analysis of the transcriptome and metabolome showed that the biosynthesis of L-glutamine might be regulated by Homer1, Homer3, and Grin3b. This suggests that GRAE may affect L-glutamine accumulation by regulating the expression of these genes. This study showed that GRAE may prolong the sleep time of mice by reducing the accumulation of L-glutamine and deepens our understanding of the regulatory network between certain genes and L-glutamine.
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spelling pubmed-88375182022-02-13 Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis Chen, Tianci Zhang, Fangyi Chen, Juanqin Zhong, Qiangui Hu, Yuxin Wu, Ruru Xie, Baogui Jiang, Yuji Chen, Bingzhi Front Nutr Nutrition Ganoderma resinaceum is a valuable Chinese medicine. This study aimed to investigate whether a G. resinaceum alcohol extract (GRAE) improves sleep, and analyze the potential mechanism. After 30 days of continuous administration of GRAE at various doses, GRAE (1,000 mg/kg.bw) prolonged pentobarbital sodium-induced sleep, increased the rate of sleeping in mice treated with a subthreshold dose of pentobarbital sodium, and shortened sleep latency. The mice brain was analyzed using UPLC-MS/MS and RNA-sequencing. Metabolomics analysis revealed that 73 metabolites in the high-dose (HD) group had changed significantly, mainly in amino acids and their derivatives, especially the accumulation of L-glutamine and PGJ2 (11-oxo-15S-hydroxy-prosta-5Z, 9, 13E-trien-1-oic acid). Transcriptome analysis revealed 500 differential genes between HD and control groups, mainly enriched in neuroactive ligand-receptor interaction, amphetamine addiction, and cocaine addiction pathways. The conjoint analysis of the transcriptome and metabolome showed that the biosynthesis of L-glutamine might be regulated by Homer1, Homer3, and Grin3b. This suggests that GRAE may affect L-glutamine accumulation by regulating the expression of these genes. This study showed that GRAE may prolong the sleep time of mice by reducing the accumulation of L-glutamine and deepens our understanding of the regulatory network between certain genes and L-glutamine. Frontiers Media S.A. 2022-01-28 /pmc/articles/PMC8837518/ /pubmed/35165654 http://dx.doi.org/10.3389/fnut.2022.745624 Text en Copyright © 2022 Chen, Zhang, Chen, Zhong, Hu, Wu, Xie, Jiang and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Chen, Tianci
Zhang, Fangyi
Chen, Juanqin
Zhong, Qiangui
Hu, Yuxin
Wu, Ruru
Xie, Baogui
Jiang, Yuji
Chen, Bingzhi
Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis
title Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis
title_full Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis
title_fullStr Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis
title_full_unstemmed Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis
title_short Effects of Alcohol Extracts From Ganoderma resinaceum on Sleep in Mice Using Combined Transcriptome and Metabolome Analysis
title_sort effects of alcohol extracts from ganoderma resinaceum on sleep in mice using combined transcriptome and metabolome analysis
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837518/
https://www.ncbi.nlm.nih.gov/pubmed/35165654
http://dx.doi.org/10.3389/fnut.2022.745624
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