Comparative Analysis of the Rats’ Gut Microbiota Composition in Animals with Different Ginsenosides Metabolizing Activity

• Published in: Journal of agricultural and food chemistry Vol. 65; no. 2; pp. 327 - 337
• Main Authors: Dong, Wei-Wei, Xuan, Fang-Ling, Zhong, Fei-Liang, Jiang, Jun, Wu, Songquan, Li, Donghao, Quan, Lin-Hu
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 18.01.2017
• Subjects: Administration, Oral; Animals; Colon - drug effects; Colon - metabolism; Gastrointestinal Microbiome - drug effects; Gastrointestinal Microbiome - genetics; Ginsenosides - analysis; Ginsenosides - metabolism; Ginsenosides - pharmacokinetics; Inactivation, Metabolic; Male; Panax; Plant Extracts - administration & dosage; Plant Extracts - pharmacokinetics; Rats, Sprague-Dawley; RNA, Ribosomal, 16S; Tandem Mass Spectrometry; ginsenoside; LC-MS/MS; metabolism; rats gut microbiota; Panax ginseng
• ISSN: 0021-8561; 1520-5118
• DOI: 10.1021/acs.jafc.6b04848

Following oral intake of Panax ginseng, major ginsenosides are metabolized to deglycosylated ginsenosides by gut microbiota before absorption into the blood. As the composition of gut microbiota varies between individuals, metabolic activities are significantly different. We selected 6 rats with low efficiency metabolism (LEM) and 6 rats with high efficiency metabolism (HEM) from 60 rats following oral administration of Panax ginseng extract, and analyzed their gut microbiota composition using Illumina HiSeq sequencing of the 16S rRNA gene. The components of gut microbiota between the LEM and HEM groups were significantly different. Between the 2 groups, S24-7, Alcaligenaceae, and Erysipelotrichaceae occupied most OTUs of the HEM group, which was notably higher than the LEM group. Furthermore, we isolated Bifidobacterium animalis GM1 that could convert the ginsenoside Rb1 to Rd. The result implies that these specific intestinal bacteria may dominate the metabolism of Panax ginseng.