論文

査読有り
2016年7月

5,6-Dehydrokawain from Alpinia zerumbet promotes osteoblastic MC3T3-E1 cell differentiation

BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
  • Momochika Kumagai
  • ,
  • Takashi Mishima
  • ,
  • Akio Watanabe
  • ,
  • Teppei Harada
  • ,
  • Izumi Yoshida
  • ,
  • Kazuhiro Fujita
  • ,
  • Masatoshi Watai
  • ,
  • Shinkichi Tawata
  • ,
  • Keisuke Nishikawa
  • ,
  • Yoshiki Morimoto

80
7
開始ページ
1425
終了ページ
1432
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1080/09168451.2016.1153959
出版者・発行元
TAYLOR & FRANCIS LTD

Bone homeostasis is maintained by balancing bone formation and bone resorption, but an imbalance between them is associated with various bone-related diseases such as osteoporosis and rheumatoid arthritis. We found that 5,6-dehydrokawain (DK) and dihydro-5,6-dehydrokawain (DDK), which were isolated as promising compounds from Alpinia zerumbet rhizomes, promote differentiation of osteoblastic MC3T3-E1 cells. DK and DDK increased the alkaline phosphatase activity and matrix mineralization of MC3T3-E1 cells. DK exerts larger effects than DDK. The gene expression of runt-related transcription factor 2 and osterix, which are essential transcription factors in the early period of osteoblast differentiation, was significantly increased by DK treatment. The mRNA level of distal-less homeobox 5 was also enhanced by DK treatment, and DK activated the p38 mitogen-activated protein kinase pathway. Therefore, DK may have clinical potential for preventing osteoporosis, and could be considered as a potential anabolic therapeutic agent.

リンク情報
DOI
https://doi.org/10.1080/09168451.2016.1153959
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000379186000025&DestApp=WOS_CPL
ID情報
  • DOI : 10.1080/09168451.2016.1153959
  • ISSN : 0916-8451
  • eISSN : 1347-6947
  • Web of Science ID : WOS:000379186000025

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