Inhibitory effect of Carthamus tinctorius L. seed extracts on bone resorption mediated by tyrosine kinase, COX-2 (cyclooxygenase) and PG (prostaglandin) E2

  • Tae Han Yuk
  • , Joon Hyeog Kang
  • , Sang Ryoung Lee
  • , Sang Won Yuk
  • , Kwang Gyu Lee
  • , Beum Yong Song
  • , Cheorl Ho Kim
  • , Dong Wook Kim
  • , Dong Il Kim
  • , Tae Kyun Lee
  • , Chang Hyun Lee

Research output: Contribution to journalArticlepeer-review

Abstract

Anti-bone resorption properties of the Korean herbal formulation, Honghwain (HHI; Carthamus tinctorius L. seed) was biochemically investigated. On processing bone metabolism, PGE2 accelerated production of IL-1β in fetal mouse osteoblast and stimulated physiological activation substance, IL-1β. The novel class of Src tyrosine kinase inhibitors, Herbimycin A (HERB) and HHI reduced COX-2 mRNA levels as well as PGE2 production induced by IL-1β, TNF-α and IL-6. HHI inhibited in vitro and in vivo bone resorption by inhibition of phosphorylation of peptide substrates. HHI dose-dependently reduced the hypercalcemia induced in mice by IL-1β and partly prevented bone loss and microarchitectural changes in young ovariectomized rats, showing that the protective effect on bone was exerted via the inhibition of bone resorption. These results indicate that the synergy between IL-β, TNF-α, IL-6 on PGE2 production is due to an enhanced gene expression of COX-2 and that tyrosine kinase (s) are involved in the signal transduction of COX-2 in mouse calvarial osteoblasts. Thus, HHI as a possible Src family kinase inhibitor may be useful for the treatment of diseases associated with elevated bone loss.

Original languageEnglish
Pages (from-to)95-108
Number of pages14
JournalAmerican Journal of Chinese Medicine
Volume30
Issue number1
DOIs
StatePublished - 2002
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Bone Resorption
  • Carthamus tinctorius
  • Cox-2
  • Prostaglandin E
  • Tyrosine Kinase

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