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Inhibitory effects of a fermented ginseng extract, BST204, on the expression of inducible nitric oxide synthase and nitric oxide production in lipopolysaccharide-activated murine macrophages

  • Jin Young Seo
  • , Jun Ho Lee
  • , Nam Wook Kim
  • , Yong Jun Kim
  • , Sung Ho Chang
  • , Na Young Ko
  • , Erk Her
  • , Young Hyo Yoo
  • , Jie Wan Kim
  • , Beob Yi Lee
  • , Hoi Young Lee
  • , Young Mi Kim
  • , Wahn Soo Choi

Research output: Contribution to journalArticlepeer-review

Abstract

In this study, the effects of BST204, a fermented ginseng extract, on the expression of inducible nitric oxide synthase (iNOS) and nitric oxide (NO) production are looked into. Crude ginseng extract was incubated with ginsenoside-β-glucosidase to prepare BST204. BST204, unlike lipopolysaccharide (LPS) and crude ginseng extract, did not affect the level of iNOS protein and NO production in unstimulated RAW 264.7 cells. However, it suppressed the level of iNOS protein and NO production in LPS-stimulated RAW 264.7 cells but did not manifest the same effect on the iNOS mRNA level. An investigation of the activating phosphorylation of p70 S6 kinase and 4E-BP1, which are important for translation, was conducted to investigate the suppressive mechanism of iNOS protein. LPS increased the phosphorylation of p70 S6 kinase, but not 4E-BP1, in a time-dependent manner, and BST204 inhibited it in a dose-dependent manner. The expression of iNOS protein, however, was partially suppressed by rapamycin, an upstream inhibitor of p70 S6 kinase. Therefore, this paper suggests that the suppression of iNOS protein by BST204 was partially correlated with the inhibition of p70 56 kinase activation.

Original languageEnglish (US)
Pages (from-to)911-918
Number of pages8
JournalJournal of Pharmacy and Pharmacology
Volume57
Issue number7
DOIs
StatePublished - Jul 2005
Externally publishedYes

ASJC Scopus subject areas

  • General Medicine

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