Journal of Bacteriology and Virology · 2018 · 15 citations · 20 references
Life SciencesPharmacologyInflammationInnate ImmunityRedox BiochemistryAnti-inflammatory PharmacologyAntioxidant DefenseInflammatory SignalingOxidative Stress In InflammationOxidative Stress MechanismsReactive Oxygen SpeciesAntioxidant Activity AssaysAntioxidant InhibitionCellular Antioxidant ResponseGlutathione Peroxidase ActivityGlutathione Peroxidase InhibitionInflammatory Stress ResponsesOxidative Stress InjuryPromoter Activity Assays
Minor ginsenosides Rh1 and Rg2 were isolated from Korean red ginseng and reported to have various biological effects on anti-inflammatory and anti-stress activities. However, the effects of Rh1 and Rg2 on antioxidant activity and their regulatory effects on the antioxidant enzymes have not been studied. Since oxidative stress is one of the major toxic inflammatory responses stimulated by lipopolysaccharides (LPS), the present study investigated the role of minor ginsenosides Rh1 and Rg2 on antioxidant effects in LPS-treated RAW 264.7 cells. In this study, we found that treatment with ginsenosides Rh1 and Rg2 strongly inhibited LPS-stimulated intracellular ROS production in cells. Luciferase assay showed that treatment with LPS reduced antioxidant response element (ARE) encoding the pARE-luc promoter activity, while ginsenosides inhibited the pARE-luc promoter activity. Moreover, ginsenosides Rh1 and Rg2 exhibited anti-oxidative activity in LPS-induced cells by upregulating antioxidant enzymes including superoxide dismutase, catalase, and glutathione peroxidase. Our results suggest that minor ginsenosides Rh1 and Rg2 may be potential bio-active compounds for antioxidative effects by inhibiting the generation of ROS in RAW 264.7 cells.
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Two Ginseng UDP-Glycosyltransferases Synthesize Ginsenoside Rg3 and Rd
Suk‐Chae Jung, Woohyun Kim, Sung Chul Park et al. · Plant and Cell Physiology · 2014 · 201 citations
Aileen M. Erickson, Zulimar Nevarea, Jerry J. Gipp et al. · Journal of Biological Chemistry · 2002 · 128 citations · Full text