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Biotransformation of ginsenoside Rb1 via the gypenoside pathway by human gut bacteria
Shen H.; Leung W.-I.; Ruan J.-Q.; Li S.-L.; Lei J.P.C.; Wang Y.-T.; Yan R.
2013
Source PublicationChinese Medicine (United Kingdom)
Volume8Issue:1
Abstract

Background: Bacterial conversion of ginsenosides is crucial for the health-promoting effects of ginsenosides. Previous studies on the biotransformation of ginsenoside Rb1 (Rb1) by gut bacteria have focused on the ginsenoside Rd (Rd) pathway (Rb1 → Rd → ginsenoside F2 (F2) → compound K (Cpd K)). This study aims to examine the gypenoside pathway in human gut bacteria in vitro.Methods: The metabolic pathways of ginsenoside Rb1 and its metabolites ginsenoside Rd and gypenoside XVII in human gut bacteria were investigated by incubating the compounds anaerobically with pooled or individual gut bacteria samples from healthy volunteers. Ginsenoside Rb1, the metabolites generated by human gut bacteria, and degraded products in simulated gastric fluid (SGF) were qualitatively analyzed using an LC/MSD Trap system in the negative ion mode and quantitatively determined by HPLC-UV analysis.Results: When incubated anaerobically with pooled gut bacteria, Rb1 generated five metabolites, namely Rd, F2, Cpd K, and the rare gypenosides XVII (G-XVII) and LXXV (G-LXXV). The gypenoside pathway (Rb1 → G-XVII → G-LXXV → Cpd K) was rapid, intermediate, and minor, and finally converted Rb1 to Cpd K via G-XVII → F2 (major)/G-LXXV (minor). Both the Rd and gypenoside pathways exhibited great inter-individual variations in age-and sex-independent manners (P > 0.05). Rb1 was highly acid-labile and degraded rapidly to form F2, ginsenoside Rg3, ginsenoside Rh2, and Cpd K, but did not generate the gypenosides in SGF. The formation of the gypenosides might be explained by the involvement of a gut bacteria-mediated enzymatic process.Conclusions: Rb1 was metabolized to G-XVII, F2 (major) or G-LXXL (minor), and finally Cpd K by human gut bacteria in vitro. © 2013 Shen et al.; licensee BioMed Central Ltd.

DOI10.1186/1749-8546-8-22
URLView the original
Indexed BySCI
Language英语
WOS Research AreaIntegrative & Complementary Medicine ; Pharmacology & Pharmacy
WOS SubjectIntegrative & Complementary Medicine ; Pharmacology & Pharmacy
WOS IDWOS:000328957900001
The Source to ArticleScopus
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Cited Times [WOS]:18   [WOS Record]     [Related Records in WOS]
Document TypeJournal article
CollectionInstitute of Chinese Medical Sciences
Affiliation1.State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao, China
2.Department of Pharmaceutical Analysis and Metabolomics, Jiangsu Provincial Academy of Traditional Chinese Medicine, Nanjing, Jiangsu, China
3.Clinical Laboratory, Kiang Wu Hospital, Estrada do Repouso, Macao, China
Recommended Citation
GB/T 7714
Shen H.,Leung W.-I.,Ruan J.-Q.,et al. Biotransformation of ginsenoside Rb1 via the gypenoside pathway by human gut bacteria[J]. Chinese Medicine (United Kingdom),2013,8(1).
APA Shen H..,Leung W.-I..,Ruan J.-Q..,Li S.-L..,Lei J.P.C..,...&Yan R..(2013).Biotransformation of ginsenoside Rb1 via the gypenoside pathway by human gut bacteria.Chinese Medicine (United Kingdom),8(1).
MLA Shen H.,et al."Biotransformation of ginsenoside Rb1 via the gypenoside pathway by human gut bacteria".Chinese Medicine (United Kingdom) 8.1(2013).
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