Literature DB >> 29944638

The naturally derived small compound Osthole inhibits osteoclastogenesis to prevent ovariectomy-induced bone loss in mice.

Dongfeng Zhao1,2,3, Qiang Wang1,2,3, Yongjian Zhao1,2,3, Hao Zhang1,2,3, Nannan Sha1,2,3, Dezhi Tang1,2,3, Shufen Liu1,2,3, Sheng Lu1,2,3, Qi Shi1,2,3, Yan Zhang1,2,3, Yufeng Dong4, Yongjun Wang1,2,3,5, Bing Shu1,2,3.   

Abstract

OBJECTIVE: This study was to determine the bone protective effects and underlying mechanisms of Osthole (OT) in ovariectomized (OVX) mice. We found that the inhibitory effects of OT on receptor activator of nuclear factor kappa-B ligand (RANKL)-activated osteoclastogenesis are responsible for its bone protective effects in OVX mice.
METHODS: Eight-week-old mice were ovariectomized and OT (10 mg/kg/d) was intraperitoneally administrated to OVX mice 7 days after the surgery and were sacrificed at the end of the 3 months. Osteoclasts were generated from primary bone marrow macrophages (BMMs) to investigate the inhibitory effects of OT. The activity of RANKL-activated signaling was simultaneously analyzed in vitro and in vivo using immunohistochemistry, Western blot, and PCR assays.
RESULTS: OT dose dependently inhibited RANKL-mediated osteoclastogenesis in BMM cultures. OT administration attenuated bone loss (mg Ha/cm: 894.68 ± 33.56 vs 748.08 ± 19.51, P < 0.05) in OVX mice. OT inhibits osteoclastogenesis (Oc.N/per view area: 72 ± 4.3 vs 0.8 ± 0.4, P < 0.05) and bone resorption activity (bone resorbed percentages %, 48.56 ± 7.25 vs 3.25 ± 1.37, P < 0.05) from BMMs. Mechanistically, OT inhibited the expressions of nuclear factor of activated T-cells c1 (NFATc1) and c-Fos. Moreover, OT suppressed the expression of RANKL-induced osteoclast marker genes, including matrix metalloproteinase 9 (MMP9), Cathepsin K (Ctsk), tartrate-resistant acid phosphatase (TRAP), and carbonic anhydrase II (Car2).
CONCLUSIONS: OT inhibits RANKL-mediated osteoclastogenesis and prevents bone loss in OVX mice. Our findings revealed that OT is a potential new drug for treating postmenopausal osteoporosis.

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Year:  2018        PMID: 29944638     DOI: 10.1097/GME.0000000000001150

Source DB:  PubMed          Journal:  Menopause        ISSN: 1072-3714            Impact factor:   2.953


  4 in total

1.  Cnidium lactone stimulates osteogenic differentiation of bone marrow mesenchymal stem cells via BMP-2/smad-signaling cascades mediated by estrogen receptor.

Authors:  Zhao Wang; Hong-Wei Bao
Journal:  Am J Transl Res       Date:  2019-08-15       Impact factor: 4.060

2.  Osthole-loaded N-octyl-O-sulfonyl chitosan micelles (NSC-OST) inhibits RANKL-induced osteoclastogenesis and prevents ovariectomy-induced bone loss in rats.

Authors:  Lining Wang; Suyang Zheng; Guicheng Huang; Jie Sun; Yalan Pan; Yuhao Si; Pengcheng Tu; Guihua Xu; Yong Ma; Yang Guo
Journal:  J Cell Mol Med       Date:  2020-03-03       Impact factor: 5.310

3.  Effects of osthole on osteoporotic rats: a systematic review and meta-analysis.

Authors:  Bin Wu; Xiu-Fang Zhu; Xiao-Qiang Yang; Wei-Yi Wang; Jian-Hua Lu
Journal:  Pharm Biol       Date:  2022-12       Impact factor: 3.889

4.  The Coumarin Derivative 5'-Hydroxy Auraptene Suppresses Osteoclast Differentiation via Inhibiting MAPK and c-Fos/NFATc1 Pathways.

Authors:  Basem M Abdallah; Enas M Ali; Hany Elsawy; Gehan M Badr; Ashraf M Abdel-Moneim; Abdullah M Alzahrani
Journal:  Biomed Res Int       Date:  2019-12-28       Impact factor: 3.411

  4 in total

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