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分析桔梗皂苷 D 的肠道微生物代谢产物及活性验证。

Analysis of gut microbiota metabolites of platycodin D and activity verification.

机构信息

Institute of Pediatrics, Jiangsu Key Laboratory of Pediatric Respiratory Disease, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China; Medical Metabolomics Center, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.

Institute of Pediatrics, Jiangsu Key Laboratory of Pediatric Respiratory Disease, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China; Medical Metabolomics Center, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China; School of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.

出版信息

J Pharm Biomed Anal. 2024 May 15;242:116016. doi: 10.1016/j.jpba.2024.116016. Epub 2024 Feb 7.

Abstract

As the main saponin component of Platycodon grandiflorum A.DC, Platycodin D has been reported to have an anti-obesity effect. Due to poor oral absorption, the intestinal microflora usually transforms saponins into potential bioactive substances. In this study, we profiled the metabolic changes of platycodin D by incubating it with intestinal microflora extracted from mice feces subjected to either a standard control diet or a high-fat diet. A UPLC-LTQ-Orbitrap-MS method was used for rapid analysis of the metabolic profile of platycodin D. A total of 10 compounds were identified 9 of which were assessed to be metabolized by intestinal microflora. Dehydroxylation and deglycosylation were the major metabolic process of platycodin D. The metabolic profile of platycodin D biotransformed by intestinal microflora was elucidated based on the metabolite information. Platycodin D and its metabolites had anti-inflammatory effects in LPS-stimulated RAW 264.7 cells. Only platycodin D could alleviate lipid accumulation in FFA-treated HepG2 cells.

摘要

作为桔梗的主要皂苷成分,远志酸 D 已被报道具有抗肥胖作用。由于口服吸收不良,肠道微生物通常将皂苷转化为潜在的生物活性物质。在这项研究中,我们通过将远志酸 D 与来自接受标准对照饮食或高脂肪饮食的小鼠粪便中提取的肠道微生物一起孵育,来分析远志酸 D 的代谢变化。采用 UPLC-LTQ-Orbitrap-MS 方法快速分析远志酸 D 的代谢谱。总共鉴定出 10 种化合物,其中 9 种被评估为肠道微生物代谢。去羟基化和去糖基化是远志酸 D 的主要代谢过程。基于代谢物信息,阐明了肠道微生物转化的远志酸 D 的代谢谱。远志酸 D 及其代谢物在 LPS 刺激的 RAW 264.7 细胞中具有抗炎作用。只有远志酸 D 能够减轻 FFA 处理的 HepG2 细胞中的脂质积累。

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