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Biotransformation of ginsenosides F4 and Rg6 in zebrafish.
- Source :
- Journal of Asian Natural Products Research; Jul2018, Vol. 20 Issue 7, p686-696, 11p
- Publication Year :
- 2018
-
Abstract
- Ginsenosides F<subscript>4</subscript> and Rg<subscript>6</subscript> (GF<subscript>4</subscript> and GRg<subscript>6</subscript>), two main active components of steamed notoginseng or red ginseng, are dehydrated disaccharide saponins. In this work, biotransformation of ginsenosides F<subscript>4</subscript> and Rg<subscript>6</subscript> in zebrafish was investigated by qualitatively identifying their metabolites and then proposing their possible metabolic pathways. The prediction of possible metabolism of ginsenosides F<subscript>4</subscript> and Rg<subscript>6</subscript> using zebrafish model which can effectively simulate existing mammals model was early and quickly performed. Metabolites of ginsenosides F<subscript>4</subscript> and Rg<subscript>6</subscript> after exposing to zebrafish for 24 h were identified by Ultraperformance Liquid Chromatography/Quadrupole-Time-of-Flight Mass Spectrometry. A total of 8 and 6 metabolites of ginsenosides F<subscript>4</subscript> and Rg<subscript>6</subscript> were identified in zebrafish, respectively. Of these, 7 and 5, including M1, M3−M5, M7−M9 and N1 (N5), N2, N4 (N9), N7−N8 were reported for the first time as far as we know. The mechanisms of their biotransformation involved were further deduced to be desugarization, glucuronidation, sulfation, dehydroxylation, loss of C-17 and/or C-23 residue pathways. It was concluded that loss of rhamnose at position C-6 and glucuronidation at position C-3 in zebrafish were considered as the main physiologic and metabolic processes of ginsenosides F<subscript>4</subscript> and ginsenosides Rg<subscript>6</subscript>, respectively. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10286020
- Volume :
- 20
- Issue :
- 7
- Database :
- Complementary Index
- Journal :
- Journal of Asian Natural Products Research
- Publication Type :
- Academic Journal
- Accession number :
- 133104341
- Full Text :
- https://doi.org/10.1080/10286020.2017.1307184