多酚抗艰难梭菌的生物机制:系统综述。

Mohammad Darvishi, Seyed Mahmoud Reza Hashemi Rafsanjani, Majid Nouri, Saber Abbaszadeh, Saeid Heidari-Soureshjani, Karamali Kasiri, Ghorbanali Rahimian
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引用次数: 0

摘要

背景:艰难梭菌是一种机会性感染,可导致抗生素相关性腹泻和中毒性巨结肠:艰难梭菌是一种机会性感染,可导致抗生素相关性腹泻和中毒性巨结肠症:本系统综述研究旨在调查多酚的抗菌和抗毒素特性及其对减少艰难梭菌感染(CDI)相关并发症的作用:本系统性综述是按照《PRISMA 2020》指南进行的。对多个数据库(包括 Web of Science、PubMed、Cochrane Library、EMBASE 和 Scopus)中的现有文献进行了全面检索。在考虑了综述的纳入和排除标准后,共纳入了 18 篇文章。数据被收集并登记到 Excel 文件中,以便进一步调查和得出结论:多酚可降低活性氧(ROS)水平,增加炎症因子白细胞介素 10(IL-10),减少核因子卡巴 B(NF-κB)和肿瘤坏死因子-α(TNF-α)、IL-6、IL-1α、IL-1β、α(TNF-κB)、IL-6、IL-1α、IL-1β、粒细胞集落刺激因子(G-CSF)、单核细胞趋化蛋白-1(MCP-1)和巨噬细胞炎症蛋白-1α(MIP-1α)的水平,并调节 Bcl-2 和 Bax 的表达,从而使艰难梭菌的生长和复制条件变得更加困难,并阻止其生长。多酚能使艰难梭菌更难生长和复制,并阻止其产生毒素。此外,多酚还能抑制益生元特性,促进有益的双歧杆菌和乳酸杆菌的生长,从而调节肠道微生物群,对艰难梭菌发挥抗菌作用。它们还能通过抑制艰难梭菌 TcdA 和 TcdB 的产生而产生有益效果:结论:在临床前研究中,多酚通过多种机制抑制艰难梭菌的生长和毒素的产生。然而,还需要更多的临床研究来调查它们对人体的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biological Mechanisms of Polyphenols against Clostridium Difficile: A Systematic Review.

Background: Clostridium difficile is an opportunistic infection that can lead to antibi-otic-associated diarrhea and toxic megacolon.

Objective: This systematic review study aimed to investigate polyphenols' antibacterial and anti-toxin properties and their effects on reducing complications related to C. difficile Infections (CDI).

Methods: This systematic review was conducted following the PRISMA guideline 2020. Multiple databases, including Web of Science, PubMed, Cochrane Library, EMBASE, and Scopus, were searched thoroughly for existing literature. After considering the inclusion and exclusion criteria for the review, 18 articles were included. Data were collected and registered into an Excel file for further investigations and conclusions.

Results: Polyphenols by reducing Reactive Oxygen Species (ROS) levels, increasing inflammatory factor Interleukin 10 (IL-10), reducing Nuclear Factor kappa B (NF-κB) and Tumour Necrosis Fac-tor-α (TNF-α), IL-6, IL-1α, IL-1β, Granulocyte Colony-stimulating Factor (G-CSF), and Monocyte Chemoattractant Protein-1 (MCP-1) and Macrophage Inflammatory Protein-1 alpha (MIP-1α) lev-els, and regulating the expression of Bcl-2 and Bax, make the growth and replication conditions of C. difficile more difficult and prevent it from producing toxins. Furthermore, polyphenols can ex-hibit prebiotic properties, promoting the growth of beneficial Bifidobacterium and Lactobacillus species and consequently regulating gut microbiota, exerting antimicrobial activities against C. dif-ficile. They also induce their beneficial effects by inhibiting the production of C. difficile TcdA and TcdB.

Conclusion: Polyphenols have been reported to inhibit C. difficile growth and toxin production by several mechanisms in preclinical studies. However, more clinical studies are needed to investigate their safety in humans.

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