圣约翰草与肠道微生物群的双向相互作用:对肠-脑轴的潜在影响

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Maria-Eleni Grafakou , Eva-Maria Pferschy-Wenzig , Heba Aziz-Kalbhenn , Olaf Kelber , Christine Moissl-Eichinger , Rudolf Bauer
{"title":"圣约翰草与肠道微生物群的双向相互作用:对肠-脑轴的潜在影响","authors":"Maria-Eleni Grafakou ,&nbsp;Eva-Maria Pferschy-Wenzig ,&nbsp;Heba Aziz-Kalbhenn ,&nbsp;Olaf Kelber ,&nbsp;Christine Moissl-Eichinger ,&nbsp;Rudolf Bauer","doi":"10.1016/j.biopha.2025.118111","DOIUrl":null,"url":null,"abstract":"<div><div>Emerging evidence highlights the role of gut microbiome in mental health disorders, including depression, raising the question whether the action of antidepressants could be mediated, at least in part, via the microbiome-gut-brain axis. To explore this, we subjected a St. John's wort extract (STW 3-VI), clinically proven to be effective in mild to moderate depression, to a model of the upper and lower intestinal tract, including static <em>in vitro</em> predigestion followed by <em>ex vivo</em> incubation with human microbiota samples. To cover the interindividual diversity of gut microbiome composition, fecal samples from ten healthy volunteers were used. Although unchanged levels of most annotated compounds were observed during simulated upper intestinal tract digestion, incubation with fecal microbiota led to a significant change of the chemical profile of the extract. While hyperforins remained stable, flavonoids and hypericins were rapidly biotransformed, suggesting that they may act as prodrugs. Several metabolites were formed, many of which are known to be involved in gut-brain communication. Differential abundance analysis revealed significant changes in microbiome composition, particularly for taxa known to be potentially associated with depression. Among others, the <em>Firmicutes</em>/<em>Bacteroidetes</em> ratio, known to be lowered in depressive patients, was increased. Functional profiling revealed modulation of pathways involved in gut-brain communication, such as tyrosine and tryptophan metabolism. These bidirectional interactions suggest for the first time the gut microbiome as a potential mediator of the pharmacological effects of St. John's wort extracts via the microbiome-gut-brain axis.</div></div>","PeriodicalId":8966,"journal":{"name":"Biomedicine & Pharmacotherapy","volume":"187 ","pages":"Article 118111"},"PeriodicalIF":6.9000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bidirectional interactions between St. John´s wort and gut microbiome: Potential implications on gut-brain-axis\",\"authors\":\"Maria-Eleni Grafakou ,&nbsp;Eva-Maria Pferschy-Wenzig ,&nbsp;Heba Aziz-Kalbhenn ,&nbsp;Olaf Kelber ,&nbsp;Christine Moissl-Eichinger ,&nbsp;Rudolf Bauer\",\"doi\":\"10.1016/j.biopha.2025.118111\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Emerging evidence highlights the role of gut microbiome in mental health disorders, including depression, raising the question whether the action of antidepressants could be mediated, at least in part, via the microbiome-gut-brain axis. To explore this, we subjected a St. John's wort extract (STW 3-VI), clinically proven to be effective in mild to moderate depression, to a model of the upper and lower intestinal tract, including static <em>in vitro</em> predigestion followed by <em>ex vivo</em> incubation with human microbiota samples. To cover the interindividual diversity of gut microbiome composition, fecal samples from ten healthy volunteers were used. Although unchanged levels of most annotated compounds were observed during simulated upper intestinal tract digestion, incubation with fecal microbiota led to a significant change of the chemical profile of the extract. While hyperforins remained stable, flavonoids and hypericins were rapidly biotransformed, suggesting that they may act as prodrugs. Several metabolites were formed, many of which are known to be involved in gut-brain communication. Differential abundance analysis revealed significant changes in microbiome composition, particularly for taxa known to be potentially associated with depression. Among others, the <em>Firmicutes</em>/<em>Bacteroidetes</em> ratio, known to be lowered in depressive patients, was increased. Functional profiling revealed modulation of pathways involved in gut-brain communication, such as tyrosine and tryptophan metabolism. These bidirectional interactions suggest for the first time the gut microbiome as a potential mediator of the pharmacological effects of St. John's wort extracts via the microbiome-gut-brain axis.</div></div>\",\"PeriodicalId\":8966,\"journal\":{\"name\":\"Biomedicine & Pharmacotherapy\",\"volume\":\"187 \",\"pages\":\"Article 118111\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-05-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomedicine & Pharmacotherapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0753332225003051\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Pharmacotherapy","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0753332225003051","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

摘要

新出现的证据强调了肠道微生物群在包括抑郁症在内的精神健康障碍中的作用,这就提出了一个问题,即抗抑郁药的作用是否可以至少部分地通过微生物群-肠道-大脑轴来调节。为了探索这一点,我们将临床证明对轻度至中度抑郁症有效的圣约翰草提取物(STW 3-VI)置于上下肠道模型中,包括静态体外预消化,然后与人类微生物群样品进行体外培养。为了覆盖肠道微生物组组成的个体间多样性,使用了10名健康志愿者的粪便样本。虽然在模拟的上消化道消化过程中观察到大多数注释化合物的水平不变,但与粪便微生物群孵育导致提取物的化学特征发生显著变化。虽然金丝桃素保持稳定,但黄酮类和金丝桃素迅速发生生物转化,表明它们可能作为前药。形成了几种代谢物,其中许多已知与肠-脑通讯有关。差异丰度分析揭示了微生物组组成的显著变化,特别是已知可能与抑郁症相关的分类群。其中,已知在抑郁症患者中较低的厚壁菌门/拟杆菌门比率增加。功能分析揭示了肠脑通讯通路的调节,如酪氨酸和色氨酸代谢。这些双向相互作用首次表明肠道微生物组通过微生物组-肠-脑轴作为圣约翰草提取物药理作用的潜在介质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bidirectional interactions between St. John´s wort and gut microbiome: Potential implications on gut-brain-axis
Emerging evidence highlights the role of gut microbiome in mental health disorders, including depression, raising the question whether the action of antidepressants could be mediated, at least in part, via the microbiome-gut-brain axis. To explore this, we subjected a St. John's wort extract (STW 3-VI), clinically proven to be effective in mild to moderate depression, to a model of the upper and lower intestinal tract, including static in vitro predigestion followed by ex vivo incubation with human microbiota samples. To cover the interindividual diversity of gut microbiome composition, fecal samples from ten healthy volunteers were used. Although unchanged levels of most annotated compounds were observed during simulated upper intestinal tract digestion, incubation with fecal microbiota led to a significant change of the chemical profile of the extract. While hyperforins remained stable, flavonoids and hypericins were rapidly biotransformed, suggesting that they may act as prodrugs. Several metabolites were formed, many of which are known to be involved in gut-brain communication. Differential abundance analysis revealed significant changes in microbiome composition, particularly for taxa known to be potentially associated with depression. Among others, the Firmicutes/Bacteroidetes ratio, known to be lowered in depressive patients, was increased. Functional profiling revealed modulation of pathways involved in gut-brain communication, such as tyrosine and tryptophan metabolism. These bidirectional interactions suggest for the first time the gut microbiome as a potential mediator of the pharmacological effects of St. John's wort extracts via the microbiome-gut-brain axis.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信