4.7 Article

Gut microbiome and tissue metabolomics reveal the compatibility effects of Xiaoyaosan on depression based on ?gut-liver-kidney? axis

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PHYTOMEDICINE
卷 111, 期 -, 页码 -

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ELSEVIER GMBH
DOI: 10.1016/j.phymed.2022.154628

关键词

Xiaoyaosan; Compatibility; gut -liver -kidney axis; Efficacy groups; Metabolomics; Microbiome

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This study aimed to reveal the compatibility of Xiaoyaosan (XYS) in anti-depression through the perspective of the gut-liver-kidney axis. Results showed that XYS and its efficacy groups significantly regulated the abnormalities of behaviors, kidney metabolism, and intestinal disorders in depressed rats. XYS exhibited the strongest regulation, followed by the Shugan (SG) and Jianpi (JP) groups. The findings provide innovative insights into the anti-depression effects and compatibility of XYS, as well as a new perspective and methodology for studying complex diseases and traditional Chinese medicine (TCM) compatibility.
Background: Depression affects not only the central nervous system, but also the peripheral system. Xiaoyaosan (XYS), a classical traditional Chinese medicine (TCM) prescription, exhibits definite anti-depression effects demonstrated both clinically and experimentally. However, its compatibility has not been entirely revealed due partly to the complex compositions of herbs contained. Aim: Based on the strategy of Efficacy Group, this study aimed to reveal the compatibility of XYS from the perspective of gut-liver-kidney axis. Methods: Firstly, XYS was divided into two efficacy groups, i.e. Shugan (SG) and Jianpi (JP) groups. Classic behaviors of rats were measured to confirm the anti-depression effects of XYS and its two efficacy groups. On top of this, gut microbiota analysis and kidney metabolomics were performed by 16S rRNA sequencing and 1H NMR, respectively. Results: We found that XYS and its efficacy groups significantly regulated the abnormalities of behaviors and kidney metabolism of depressed rats, as well as intestinal disorders, but to different degrees. The regulatory effects of XYS and its efficacy groups on behaviors and kidney metabolomics of depressed rats had the same order, i.e. XYS > SG > JP, while the order of regulating gut microbiota was XYS > JP > SG. Both XYS and its efficacy groups significantly ameliorated gut microbiota disturbed, especially significant modulation of Peptos-treptococcaceae. XYS significantly regulated nine kidney metabolites, while SG and JP regulated four and five differential metabolites, respectively, indicating that the two efficacy groups synergistically exhibited anti -depression effects, consequently contributing to the overall anti-depression effects of XYS. Conclusion: The current findings not only innovatively demonstrate the anti-depression effects and compatibility of XYS from the perspective of gut-liver-kidney axis, comprehensively using Efficacy Group strategy, macro behavioristics, metabolome and microbiome, and also provide a new perspective, strategy, and methodology for studying complex diseases and the compatibility of TCMs.

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