Pectolinarigenin prevents bone loss in ovariectomized mice and inhibits RANKL‐induced osteoclastogenesis via blocking activation of MAPK and NFATc1 signaling. Issue 8 (11th January 2019)
- Record Type:
- Journal Article
- Title:
- Pectolinarigenin prevents bone loss in ovariectomized mice and inhibits RANKL‐induced osteoclastogenesis via blocking activation of MAPK and NFATc1 signaling. Issue 8 (11th January 2019)
- Main Title:
- Pectolinarigenin prevents bone loss in ovariectomized mice and inhibits RANKL‐induced osteoclastogenesis via blocking activation of MAPK and NFATc1 signaling
- Authors:
- Xiao, Yu
Li, Kai
Wang, Ziyi
Fu, Fangsheng
Shao, Siyuan
Song, Fangming
Zhao, Jinmin
Chen, Weiwei
Liu, Qian
Xu, Jiake - Abstract:
- Abstract: Osteoporosis (OP) is a metabolic disease caused by multiple factors, which is characterized by a reduction of bone mass per unit volume and destruction of bone microstructure. Aberrant osteoclast function is the main cause of OP, therefore, regulating the differentiation and function of osteoclast is one of the treatment strategies for OP. Pectolinarigenin (PEC) is a medicinal implant isolated from Fragrant Eupatorium . Our experimental data showed that PEC was able to inhibit receptor activator of nuclear factor‐κB ligand (RANKL)‐induced osteoclastogenesis in vitro, by tartrate‐resistant acid phosphatase (TRAcP) staining, Fibrous actin ring formation, and hydroxyapatite resorption assays. In terms of mechanism, PEC inhibited the expression of the osteoclastogenesis‐related gene, including cathepsin K ( Ctsk ), matrix metalloproteinase 9 ( Mmp9), and TRAcP ( Acp5 ). Western blot analysis demonstrated that PEC could significantly block the activation of RANKL‐induced mitogen‐activated protein kinase signaling cascades and was able to suppress the protein expression of nuclear factor of activated T‐cells and c‐Fos. Meanwhile, the intracellular reactive oxygen species levels were also reduced by PEC in a concentration‐dependent manner. Further, PEC could prevent the ovariectomy‐induced bone loss in vivo. Summarizing all, our data suggested that PEC inhibits osteoclast formation and function and RANKL signaling pathways, and thus could potentially be used in theAbstract: Osteoporosis (OP) is a metabolic disease caused by multiple factors, which is characterized by a reduction of bone mass per unit volume and destruction of bone microstructure. Aberrant osteoclast function is the main cause of OP, therefore, regulating the differentiation and function of osteoclast is one of the treatment strategies for OP. Pectolinarigenin (PEC) is a medicinal implant isolated from Fragrant Eupatorium . Our experimental data showed that PEC was able to inhibit receptor activator of nuclear factor‐κB ligand (RANKL)‐induced osteoclastogenesis in vitro, by tartrate‐resistant acid phosphatase (TRAcP) staining, Fibrous actin ring formation, and hydroxyapatite resorption assays. In terms of mechanism, PEC inhibited the expression of the osteoclastogenesis‐related gene, including cathepsin K ( Ctsk ), matrix metalloproteinase 9 ( Mmp9), and TRAcP ( Acp5 ). Western blot analysis demonstrated that PEC could significantly block the activation of RANKL‐induced mitogen‐activated protein kinase signaling cascades and was able to suppress the protein expression of nuclear factor of activated T‐cells and c‐Fos. Meanwhile, the intracellular reactive oxygen species levels were also reduced by PEC in a concentration‐dependent manner. Further, PEC could prevent the ovariectomy‐induced bone loss in vivo. Summarizing all, our data suggested that PEC inhibits osteoclast formation and function and RANKL signaling pathways, and thus could potentially be used in the treatment the osteoclast‐related bone loss diseases. Abstract : Pectolinarigenin (PEC) is a medicinal implant isolated from the Fragrant Eupatorium herb. It was demonstrated that PEC significantly inhibited receptor activator of nuclear factor‐κB ligand‐induced osteoclast differentiation and function in vitro and also could prevent the ovariectomy‐induced bone loss in vivo. Taken together, PEC can be potentially used in the development of a novel drug for osteoclast‐related bone diseases. … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 234:Issue 8(2019:Aug.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 234:Issue 8(2019:Aug.)
- Issue Display:
- Volume 234, Issue 8 (2019)
- Year:
- 2019
- Volume:
- 234
- Issue:
- 8
- Issue Sort Value:
- 2019-0234-0008-0000
- Page Start:
- 13959
- Page End:
- 13968
- Publication Date:
- 2019-01-11
- Subjects:
- MAPK -- osteoclast -- osteoporosis -- pectolinarigenin
Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.28079 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26755.xml