Biotransformation of ginsenosides F₄ and Rg₆ in zebrafish

Abstract

Ginsenosides F₄ and Rg₆ (GF₄ and GRg₆), two main active components of steamed notoginseng or red ginseng, are dehydrated disaccharide saponins. In this work, biotransformation of ginsenosides F₄ and Rg₆ in zebrafish was investigated by qualitatively identifying their metabolites and then proposing their possible metabolic pathways. The prediction of possible metabolism of ginsenosides F₄ and Rg₆ using zebrafish model which can effectively simulate existing mammals model was early and quickly performed. Metabolites of ginsenosides F₄ and Rg₆ 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 F₄ and Rg₆ 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 F₄ and ginsenosides Rg₆, respectively.

Keywords:

• Ginsenosides F₄ and Rg₆
• UPLC-Q-TOF/MS
• zebrafish
• biotransformation