helveticus乳杆菌HY7801及其胞外囊泡在经前综合征中的作用机制研究:肠道微生物群和激素调节的作用。

IF 3.1 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Hyeonji Kim, Hyeonjun Gwon, Ji-Woong Jeong, Joo-Yun Kim, Jae-Jung Shim, Jae-Hwan Lee
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引用次数: 0

摘要

经前综合征(PMS)的特点是育龄妇女在月经周期中出现周期性的生理和心理症状。本研究旨在探讨helveticus乳杆菌HY7801 (HY7801)对pms相关激素和炎症反应的影响,特别关注其对肠道微生物群组成的影响以及HY7801衍生的细胞外囊泡(EVs)的功能作用。来自甲氧氯普胺(MCP)诱导的高催乳素血症小鼠模型的数据显示,口服HY7801可显著降低血清催乳素和促炎细胞因子水平,同时恢复MCP引起的激素失衡。HY7801还改变了肠道微生物群的组成,降低了与精神健康障碍相关的细菌科——Desulfovibrionaceae、Staphylococcaceae和Bacteroidaceae的相对丰度。这些类群的丰度与泌乳素和细胞因子水平呈正相关。此外,hy7801衍生的ev被鉴定为功能性生物活性成分,在雌二醇刺激的GH3细胞中发挥细胞保护作用,显著抑制催乳素分泌。这些发现表明,HY7801不仅通过调节肠道微生物群,而且通过其ev介导的直接细胞机制缓解PMS症状。综上所述,这些双重机制表明HY7801及其分泌成分代表了一种有希望的方法来管理经前症候群症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Mechanistic Study of <i>Lactobacillus helveticus</i> HY7801 and Its Extracellular Vesicles in Premenstrual Syndrome: Role of Gut Microbiota and Hormonal Modulation.

A Mechanistic Study of <i>Lactobacillus helveticus</i> HY7801 and Its Extracellular Vesicles in Premenstrual Syndrome: Role of Gut Microbiota and Hormonal Modulation.

A Mechanistic Study of <i>Lactobacillus helveticus</i> HY7801 and Its Extracellular Vesicles in Premenstrual Syndrome: Role of Gut Microbiota and Hormonal Modulation.

A Mechanistic Study of Lactobacillus helveticus HY7801 and Its Extracellular Vesicles in Premenstrual Syndrome: Role of Gut Microbiota and Hormonal Modulation.

Premenstrual syndrome (PMS) is characterized by periodic physical and psychological symptoms during the menstrual cycle of women of reproductive age. This study aimed to investigate the effects of Lactobacillus helveticus HY7801 (HY7801) on PMS-related hormonal and inflammatory responses, with a specific focus on its influence on the composition of the gut microbiota and the functional role of HY7801-derived extracellular vesicles (EVs). Data from a metoclopramide (MCP)-induced hyperprolactinemia mouse model showed that oral administration of HY7801 reduced serum levels of prolactin and pro-inflammatory cytokines significantly, while restoring hormone imbalances caused by MCP. HY7801 also altered the composition of the gut microbiota by decreasing the relative abundance of Desulfovibrionaceae, Staphylococcaceae, and Bacteroidaceae, which are bacterial families associated with mental health disorders. The abundance of these taxa correlated positively with prolactin and cytokine levels. Furthermore, HY7801-derived EVs were identified as functional bioactive components that exert cytoprotective effects and suppress prolactin secretion significantly in estradiol-stimulated GH3 cells. These findings indicate that HY7801 alleviates PMS symptoms, not only by modulating gut microbiota but also through direct cellular mechanisms mediated by its EVs. Taken together, these dual mechanisms suggest that HY7801 and its secreted components represent a promising approach to management of PMS symptoms.

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来源期刊
Journal of microbiology and biotechnology
Journal of microbiology and biotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-MICROBIOLOGY
CiteScore
5.50
自引率
3.60%
发文量
151
审稿时长
2 months
期刊介绍: The Journal of Microbiology and Biotechnology (JMB) is a monthly international journal devoted to the advancement and dissemination of scientific knowledge pertaining to microbiology, biotechnology, and related academic disciplines. It covers various scientific and technological aspects of Molecular and Cellular Microbiology, Environmental Microbiology and Biotechnology, Food Biotechnology, and Biotechnology and Bioengineering (subcategories are listed below). Launched in March 1991, the JMB is published by the Korean Society for Microbiology and Biotechnology (KMB) and distributed worldwide.
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