Ginsenoside-Rg1, one of the major active molecules from Panax ginseng, is a functional ligand of glucocorticoid receptor

Youngjoo Lee, Eunah Chung, Kwang Youl Lee, Yong Hee Lee, Bin Huh, Seung Ki Lee*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

174 Scopus citations

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 languageEnglish (US)
Pages (from-to)135-140
Number of pages6
JournalMolecular and Cellular Endocrinology
Volume133
Issue number2
DOIs
StatePublished - Oct 20 1997

Keywords

  • Dexamethasone
  • Ginseng
  • Ginsenoside-Rg1
  • Glucocorticoid receptor

ASJC Scopus subject areas

  • Endocrinology
  • Molecular Biology
  • Biochemistry

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