Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis

Wear particle-stimulated inflammatory bone destruction and the consequent aseptic loosening remain major postoperative problems for artificial joints. Studies have indicated that puerarin promotes osteogenesis and alleviates lipopolysaccharide-induced osteoclastogenesis in vitro. However, the underl...

Full description

Bibliographic Details
Main Authors: Chao Yang, Juehong Li, Kechao Zhu, Xiangwei Yuan, Tao Cheng, Yebin Qian, Xianlong Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-10-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphar.2019.01113/full
_version_ 1818429825332805632
author Chao Yang
Juehong Li
Kechao Zhu
Xiangwei Yuan
Tao Cheng
Yebin Qian
Xianlong Zhang
author_facet Chao Yang
Juehong Li
Kechao Zhu
Xiangwei Yuan
Tao Cheng
Yebin Qian
Xianlong Zhang
author_sort Chao Yang
collection DOAJ
description Wear particle-stimulated inflammatory bone destruction and the consequent aseptic loosening remain major postoperative problems for artificial joints. Studies have indicated that puerarin promotes osteogenesis and alleviates lipopolysaccharide-induced osteoclastogenesis in vitro. However, the underlying molecular mechanism by which puerarin interacts with receptor activator of nuclear factor kappa-B ligand (RANKL)-mediated osteoclast formation in vitro and wear particle-stimulated osteolysis in vivo has not been reported. In this work, the protective effects exerted by puerarin on titanium particle-stimulated bone destruction in vivo and on RANKL-induced osteoclast activation in osteoclastic precursor cells in vitro were investigated. As expected, puerarin significantly inhibited wear particle-mediated bone resorption and proinflammatory cytokine productions in a calvarial resorption model. Additionally, puerarin inhibited RANKL-induced osteoclast activation, bone resorption ability, and F-actin ring formation in vitro as puerarin concentration increased. Furthermore, mechanistic investigation indicated that reduced RANKL-stimulated MEK/ERK/NFATc1 signaling cascades might regulate the protective effect of puerarin. Conclusively, these results indicate that puerarin, a type of polyphenol, might serve as a protective agent to prevent osteoclast-related osteolytic diseases.
first_indexed 2024-12-14T15:23:40Z
format Article
id doaj.art-e0f09bff7e6a4f7c953e06b6beefd181
institution Directory Open Access Journal
issn 1663-9812
language English
last_indexed 2024-12-14T15:23:40Z
publishDate 2019-10-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Pharmacology
spelling doaj.art-e0f09bff7e6a4f7c953e06b6beefd1812022-12-21T22:56:05ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122019-10-011010.3389/fphar.2019.01113465918Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory OsteolysisChao YangJuehong LiKechao ZhuXiangwei YuanTao ChengYebin QianXianlong ZhangWear particle-stimulated inflammatory bone destruction and the consequent aseptic loosening remain major postoperative problems for artificial joints. Studies have indicated that puerarin promotes osteogenesis and alleviates lipopolysaccharide-induced osteoclastogenesis in vitro. However, the underlying molecular mechanism by which puerarin interacts with receptor activator of nuclear factor kappa-B ligand (RANKL)-mediated osteoclast formation in vitro and wear particle-stimulated osteolysis in vivo has not been reported. In this work, the protective effects exerted by puerarin on titanium particle-stimulated bone destruction in vivo and on RANKL-induced osteoclast activation in osteoclastic precursor cells in vitro were investigated. As expected, puerarin significantly inhibited wear particle-mediated bone resorption and proinflammatory cytokine productions in a calvarial resorption model. Additionally, puerarin inhibited RANKL-induced osteoclast activation, bone resorption ability, and F-actin ring formation in vitro as puerarin concentration increased. Furthermore, mechanistic investigation indicated that reduced RANKL-stimulated MEK/ERK/NFATc1 signaling cascades might regulate the protective effect of puerarin. Conclusively, these results indicate that puerarin, a type of polyphenol, might serve as a protective agent to prevent osteoclast-related osteolytic diseases.https://www.frontiersin.org/article/10.3389/fphar.2019.01113/fulltitanium particlesosteolysispuerarinosteoclastogenesisERK pathway
spellingShingle Chao Yang
Juehong Li
Kechao Zhu
Xiangwei Yuan
Tao Cheng
Yebin Qian
Xianlong Zhang
Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis
Frontiers in Pharmacology
titanium particles
osteolysis
puerarin
osteoclastogenesis
ERK pathway
title Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis
title_full Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis
title_fullStr Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis
title_full_unstemmed Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis
title_short Puerarin Exerts Protective Effects on Wear Particle-Induced Inflammatory Osteolysis
title_sort puerarin exerts protective effects on wear particle induced inflammatory osteolysis
topic titanium particles
osteolysis
puerarin
osteoclastogenesis
ERK pathway
url https://www.frontiersin.org/article/10.3389/fphar.2019.01113/full
work_keys_str_mv AT chaoyang puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis
AT juehongli puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis
AT kechaozhu puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis
AT xiangweiyuan puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis
AT taocheng puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis
AT yebinqian puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis
AT xianlongzhang puerarinexertsprotectiveeffectsonwearparticleinducedinflammatoryosteolysis