Abstract
We have examined the possibility that a component of Panax ginseng, ginsenoside-Rg1 (G-Rg1), acts by binding to the glucocorticoid receptor (GR). G-Rg1 competed for [3H]dexamethasone (Dex) binding to GR with a specific affinity of 1-10 μM and activated a glucocorticoid responsive element-containing luciferase reporter gene. The dose-dependence patterns of G-Rg1 and Dex for these two effects were nearly identical, although two to three orders of magnitude higher concentration of G-Rg1 than that of Dex was required for the same magnitude of response. At the cellular level, the growth of FT02B cells was suppressed by G-Rg1 as well as by Dex, each of whose effects were abolished by RU486. These results demonstrate that G-Rg1 is a functional ligand of GR.
Original language | English (US) |
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Pages (from-to) | 135-140 |
Number of pages | 6 |
Journal | Molecular and Cellular Endocrinology |
Volume | 133 |
Issue number | 2 |
DOIs | |
State | Published - Oct 20 1997 |
Keywords
- Dexamethasone
- Ginseng
- Ginsenoside-Rg1
- Glucocorticoid receptor
ASJC Scopus subject areas
- Endocrinology
- Molecular Biology
- Biochemistry