Literature DB >> 21835177

Naringin abrogates osteoclastogenesis and bone resorption via the inhibition of RANKL-induced NF-κB and ERK activation.

Estabelle S M Ang1, Xiaohong Yang, Honghui Chen, Qian Liu, Ming H Zheng, Jiake Xu.   

Abstract

Osteolytic bone diseases including osteoporosis are commonly accompanied with enhanced osteoclast formation and bone resorption. Naringin, a natural occurring flavonoid has been found to protect against retinoic acid-induced osteoporosis and improve bone quality in rats. Here, we showed that naringin perturbs osteoclast formation and bone resorption by inhibiting RANK-mediated NF-κB and ERK signaling. Naringin suppressed gene expression of key osteoclast marker genes. Naringin was found to inhibit RANKL-induced activation of NF-κB by suppressing RANKL-mediated IκB-α degradation. In addition, naringin inhibited RANKL-induced phosphorylation of ERK. This study identifies naringin as an inhibitor for osteoclast formation and bone resorption, and provides evidence that natural compounds such as naringin might be beneficial as an alternative medicine for the prevention and treatment of osteolysis.
Copyright © 2011. Published by Elsevier B.V.

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Year:  2011        PMID: 21835177     DOI: 10.1016/j.febslet.2011.07.046

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  27 in total

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Journal:  J Mol Signal       Date:  2012-01-04

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Journal:  Sci Rep       Date:  2016-04-25       Impact factor: 4.379

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Authors:  Yonghui Wu; Changhong Cai; Yijia Xiang; Huan Zhao; Lingchun Lv; Chunlai Zeng
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8.  Potential antiosteoporotic agents from plants: a comprehensive review.

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9.  The Effects of Combined Treatment with Naringin and Treadmill Exercise on Osteoporosis in Ovariectomized Rats.

Authors:  Xiaolei Sun; Fengbo Li; Xinlong Ma; Jianxiong Ma; Bin Zhao; Yang Zhang; Yanjun Li; Jianwei Lv; Xinmin Meng
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10.  Therapeutic potentials of naringin on polymethylmethacrylate induced osteoclastogenesis and osteolysis, in vitro and in vivo assessments.

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Journal:  Drug Des Devel Ther       Date:  2013-12-10       Impact factor: 4.162

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