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靶向发现肠道微生物组重塑化合物,用于治疗全身炎症反应综合征。

Targeted discovery of gut microbiome-remodeling compounds for the treatment of systemic inflammatory response syndrome.

机构信息

College of Food Science and Engineering, Northwest A&F University, Shaanxi, China.

State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.

出版信息

mSystems. 2024 Oct 22;9(10):e0078824. doi: 10.1128/msystems.00788-24. Epub 2024 Sep 5.

Abstract

Systemic inflammatory response syndrome (SIRS) is a severe inflammatory response that can lead to organ dysfunction and death. Modulating the gut microbiome is a promising therapeutic approach for managing SIRS. This study assesses the therapeutic potential of the Xuanfei Baidu (XFBD) formula in treating SIRS. The results showed that XFBD administration effectively reduced mortality rates and inflammation in SIRS mice. Using 16S rRNA sequencing and fecal microbiota transplantation (FMT), we substantiated that the therapeutic effects of XFBD are partly attributed to gut microbiota modulation. We conducted experiments to accurately assess the gut microbiome remodeling effects of 51 compounds isolated from XFBD. These compounds exhibited varying abilities to induce a microbial structure that closely resembles that of the healthy control group. By quantifying their impact on microbial structure and clustering their regulatory patterns, we devised multiple gut microbiome remodeling compound (GMRC) cocktails. GMRC cocktail C, comprising aucubin, gentiopicroside, syringic acid, gallic acid, p-hydroxybenzaldehyde, para-hydroxybenzoic acid, and isoimperatorin, demonstrated superior efficacy in treating SIRS compared to a single compound or to other cocktails. Finally, experiments showcased that GMRC cocktail C effectively rebalanced bacteria composition in SIRS patients. This study underscores XFBD's therapeutic potential in SIRS and highlights the importance of innovative treatment approaches for this disease by targeting the gut microbiota.IMPORTANCEDeveloping effective treatment strategies for systemic inflammatory response syndrome (SIRS) is crucial due to its severe and often life-threatening nature. While traditional treatments like dexamethasone have shown efficacy, they also come with significant side effects and limitations. This study makes significant strides by demonstrating that the Xuanfei Baidu (XFBD) formula can substantially reduce mortality rates and inflammation in SIRS mice through effective modulation of the gut microbiota. By quantitatively assessing the impact of 51 compounds derived from XFBD on the gut microbiome, we developed a potent gut microbiome remodeling compound cocktail. This cocktail outperformed individual compounds and other mixtures in efficacy against SIRS. These findings highlight the potential of XFBD as a therapeutic solution for SIRS and underscore the critical role of innovative strategies targeting the gut microbiota in addressing this severe inflammatory condition.

摘要

全身炎症反应综合征(SIRS)是一种严重的炎症反应,可导致器官功能障碍和死亡。调节肠道微生物组是治疗 SIRS 的一种有前途的治疗方法。本研究评估了宣肺败毒(XFBD)配方治疗 SIRS 的治疗潜力。结果表明,XFBD 给药可有效降低 SIRS 小鼠的死亡率和炎症。通过 16S rRNA 测序和粪便微生物群移植(FMT),我们证实 XFBD 的治疗效果部分归因于肠道微生物群的调节。我们进行了实验,以准确评估从 XFBD 中分离的 51 种化合物对肠道微生物组重塑的影响。这些化合物表现出不同的诱导微生物结构的能力,使其与健康对照组的微生物结构非常相似。通过量化它们对微生物结构的影响并对其调节模式进行聚类,我们设计了多种肠道微生物组重塑化合物(GMRC)鸡尾酒。GMRC 鸡尾酒 C,由梓醇、龙胆苦苷、丁香酸、没食子酸、对羟基苯甲醛、对羟基苯甲酸和异欧前胡素组成,在治疗 SIRS 方面比单一化合物或其他鸡尾酒更有效。最后,实验表明 GMRC 鸡尾酒 C 可有效重新平衡 SIRS 患者的细菌组成。这项研究强调了 XFBD 在 SIRS 中的治疗潜力,并强调了通过靶向肠道微生物群为这种疾病开发创新治疗方法的重要性。

重要性

开发有效的全身炎症反应综合征(SIRS)治疗策略至关重要,因为它具有严重且经常危及生命的性质。虽然传统治疗方法,如地塞米松,已显示出疗效,但它们也存在显著的副作用和局限性。本研究通过证明 XFBD 配方通过有效调节肠道微生物群,可显著降低 SIRS 小鼠的死亡率和炎症,取得了重大进展。通过定量评估从 XFBD 中提取的 51 种化合物对肠道微生物组的影响,我们开发了一种有效的肠道微生物组重塑化合物鸡尾酒。该鸡尾酒在治疗 SIRS 方面的疗效优于单个化合物和其他混合物。这些发现强调了 XFBD 作为 SIRS 治疗方法的潜力,并强调了靶向肠道微生物群的创新策略在解决这种严重炎症状况方面的关键作用。

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