Papers

Peer-reviewed International journal
Aug, 2018

Rutaecarpine attenuates osteoclastogenesis by impairing macrophage colony stimulating factor and receptor activator of nuclear factor κ-B ligand-stimulated signalling pathways.

Clinical and experimental pharmacology & physiology
  • Yutaka Fukuma
  • ,
  • Eiko Sakai
  • ,
  • Shunsuke Komaki
  • ,
  • Kazuhisa Nishishita
  • ,
  • Kuniaki Okamoto
  • ,
  • Takayuki Tsukuba

Volume
45
Number
8
First page
863
Last page
865
Language
English
Publishing type
DOI
10.1111/1440-1681.12941

Rutaecarpine is a major alkaloid isolated from Evodia rutaecarpa. Here, we investigated the effects of rutaecarpine on osteoclast differentiation induced by macrophage colony stimulating factor (M-CSF) and receptor activator of nuclear factor κ-B ligand (RANKL) in bone marrow-derived macrophages (BMMs). Treatment with rutaecarpine significantly inhibited osteoclastogenesis and prevented bone resorption of BMM-derived osteoclasts. Mechanistically, rutaecarpine decreased the protein level of nuclear factor of activated T cells cytoplasmic-1 (NFATc1) and the phosphorylation of other signalling pathways during the osteoclast differentiation. Thus, rutaecarpine may be useful as a therapeutic agent for the treatment of bone diseases.

Link information
DOI
https://doi.org/10.1111/1440-1681.12941
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/29582460
ID information
  • DOI : 10.1111/1440-1681.12941
  • Pubmed ID : 29582460

Export
BibTeX RIS