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利用 - 发酵人参对高脂血症进行肠道微生物群靶向干预。 (注:原文中“-Fermented Ginseng”这里的“-”不太明确其具体含义,可能是有缺失或错误表述,暂且按此翻译)

Gut Microbiota-Targeted Intervention of Hyperlipidemia Using -Fermented Ginseng.

作者信息

Zhou Qing, Yang Cuiting, Jia Mingyue, Qu Qingsong, Peng Xinhui, Ren Weishuo, Li Guoqing, Xie Yueyang, Li Bingxuan, Shi Xinyuan

机构信息

School of Chinese Materia Medica, Beijing University of Chinese Medicine, Yangguang South Street, Beijing 102488, China.

School of Life Science, Beijing University of Chinese Medicine, Yangguang South Street, Beijing 102488, China.

出版信息

Pharmaceuticals (Basel). 2025 Apr 30;18(5):661. doi: 10.3390/ph18050661.

Abstract

Hyperlipidemia (HLP) encompasses a spectrum of poorly understood lipid metabolism disorders that are frequently overlooked or misdiagnosed, potentially leading to multiple complications. While the gut microbiota has been implicated in HLP pathogenesis, the causal relationships and molecular mechanisms remain elusive. This study aimed to investigate the therapeutic mechanisms of -fermented ginseng (MFG) on HLP through gut microbiota modulation and explore treatment potential via fecal microbiota transplantation (FMT). The MFG-modulated gut microbiota was transplanted into HLP mice. Systemic evaluations, including serum biochemical parameter detection, histopathological section analysis, 16S rRNA sequencing, and fecal metabolomics, were conducted to assess therapeutic efficacy and identify associated metabolic pathways. FMT significantly improved lipid profiles, reduced body weight, and attenuated hepatic lipid accumulation in HLP mice. Mechanistically, it enhanced cholesterol excretion and fatty acid β-oxidation while suppressing lipogenic regulators, concurrently promoting primary-to-secondary bile acid conversion. Gut microbiota analysis revealed that the MFG intervention effectively normalized the Firmicutes/Bacteroidetes ratio and enriched beneficial microbiota. These findings demonstrate FMT's therapeutic value in HLP management and provide new perspectives on utilizing fermented herbal medicines for metabolic disorders via gut microbiota reprogramming.

摘要

高脂血症(HLP)涵盖了一系列脂质代谢紊乱,这些紊乱常常被忽视或误诊,可能导致多种并发症,但其发病机制尚不清楚。虽然肠道微生物群与HLP的发病机制有关,但其因果关系和分子机制仍然难以捉摸。本研究旨在通过调节肠道微生物群来研究人参发酵产物(MFG)对HLP的治疗机制,并通过粪便微生物群移植(FMT)探索其治疗潜力。将MFG调节的肠道微生物群移植到HLP小鼠体内。通过血清生化参数检测、组织病理学切片分析、16S rRNA测序和粪便代谢组学等系统评估,来评估治疗效果并确定相关代谢途径。FMT显著改善了HLP小鼠的血脂水平,降低了体重,并减轻了肝脏脂质积累。从机制上讲,它增强了胆固醇排泄和脂肪酸β-氧化,同时抑制了脂肪生成调节因子,同时促进了初级胆汁酸向次级胆汁酸的转化。肠道微生物群分析表明,MFG干预有效地使厚壁菌门/拟杆菌门比例正常化,并富集了有益微生物群。这些发现证明了FMT在HLP管理中的治疗价值,并为通过肠道微生物群重编程利用发酵草药治疗代谢紊乱提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f00/12114913/7892b2733d83/pharmaceuticals-18-00661-g001.jpg

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