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Morroniside Inhibits Inflammatory Bone Loss through the TRAF6-Mediated NF-κB/MAPK Signalling Pathway.

作者信息

Xiao Jirimutu, Han Qiuge, Yu Ziceng, Liu Mengmin, Sun Jie, Wu Mao, Yin Heng, Fu Jingyue, Guo Yang, Wang Lining, Ma Yong

机构信息

Laboratory of New Techniques of Restoration & Reconstruction, Institute of Traumatology & Orthopedics, Nanjing University of Chinese Medicine, Nanjing 210023, China.

School of Mongolia Medicine, Inner Mongolia Medical University, Hohhot 010110, China.

出版信息

Pharmaceuticals (Basel). 2023 Oct 10;16(10):1438. doi: 10.3390/ph16101438.


DOI:10.3390/ph16101438
PMID:37895909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10609728/
Abstract

Osteoporosis is a chronic inflammatory disease that severely affects quality of life. is a Chinese herbal medicine with various bioactive ingredients, among which morroniside is its signature ingredient. Although anti-bone resorption drugs are the main treatment for bone loss, promoting bone anabolism is more suitable for increasing bone mass. Therefore, identifying changes in bone formation induced by morroniside may be conducive to developing effective intervention methods. In this study, morroniside was found to promote the osteogenic differentiation of bone marrow stem cells (BMSCs) and inhibit inflammation-induced bone loss in an in vivo mouse model of inflammatory bone loss. Morroniside enhanced bone density and bone microstructure, and inhibited the expression of IL6, IL1β, and ALP in serum ( < 0.05). Furthermore, in in vitro experiments, BMSCs exposed to 0-256 μM morroniside did not show cytotoxicity. Morroniside inhibited the expression of IL6 and IL1β and promoted the expression of the osteogenic transcription factors Runx2 and OCN. Furthermore, morroniside promoted osteocalcin and Runx2 expression and inhibited TRAF6-mediated NF-κB and MAPK signaling, as well as osteoblast growth and NF-κB nuclear transposition. Thus, morroniside promoted osteogenic differentiation of BMSCs, slowed the occurrence of the inflammatory response, and inhibited bone loss in mice with inflammatory bone loss.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/8a8a07be12ff/pharmaceuticals-16-01438-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/f459c1251fa2/pharmaceuticals-16-01438-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/c1f829b99448/pharmaceuticals-16-01438-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/94c40c4b1d4d/pharmaceuticals-16-01438-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/8a8a07be12ff/pharmaceuticals-16-01438-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/f459c1251fa2/pharmaceuticals-16-01438-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/c1f829b99448/pharmaceuticals-16-01438-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/94c40c4b1d4d/pharmaceuticals-16-01438-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86ac/10609728/8a8a07be12ff/pharmaceuticals-16-01438-g004.jpg

相似文献

[1]
Morroniside Inhibits Inflammatory Bone Loss through the TRAF6-Mediated NF-κB/MAPK Signalling Pathway.

Pharmaceuticals (Basel). 2023-10-10

[2]
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[3]
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[4]
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Arch Biochem Biophys. 2021-7-30

[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[1]
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[2]
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Front Vet Sci. 2025-6-18

[3]
TNF receptor-associated factors: promising targets of natural products for the treatment of osteoporosis.

Front Physiol. 2025-5-27

[4]
Therapeutic potential of total flavonoids of Rhizoma Drynariae: inhibiting adipogenesis and promoting osteogenesis via MAPK/HIF-1α pathway in primary osteoporosis.

J Orthop Surg Res. 2025-3-11

[5]
Zuogui Wan modulates macrophage polarization and promotes osteogenic differentiation through regulation of CD51-positive bone marrow mesenchymal stem cells.

Sci Rep. 2024-10-30

[6]
A review of the sources and pharmacological research of morroniside.

Front Pharmacol. 2024-9-4

[7]
Plant-Derived Senotherapeutics for the Prevention and Treatment of Intervertebral Disc Degeneration and Aging.

Metabolites. 2024-2-28

[8]
The Role of Herbal Medicine in Modulating Bone Homeostasis.

Curr Top Med Chem. 2024

本文引用的文献

[1]
Morroniside ameliorates inflammatory skeletal muscle atrophy inhibiting canonical and non-canonical NF-κB and regulating protein synthesis/degradation.

Front Pharmacol. 2022-12-23

[2]
Denosumab Discontinuation.

Curr Osteoporos Rep. 2023-2

[3]
USP1 Inhibits NF-κB/NLRP3 Induced Pyroptosis through TRAF6 in Osteoblastic MC3T3-E1 Cells.

J Musculoskelet Neuronal Interact. 2022-12-1

[4]
AgeAnno: a knowledgebase of single-cell annotation of aging in human.

Nucleic Acids Res. 2023-1-6

[5]
Morroniside Protects Human Granulosa Cells against HO-Induced Oxidative Damage by Regulating the Nrf2 and MAPK Signaling Pathways.

Evid Based Complement Alternat Med. 2022-9-9

[6]
Hypoxic preconditioned aged BMSCs accelerates MI injury repair by modulating inflammation, oxidative stress and apoptosis.

Biochem Biophys Res Commun. 2022-10-30

[7]
Mogrol Attenuates Osteoclast Formation and Bone Resorption by Inhibiting the TRAF6/MAPK/NF-κB Signaling Pathway and Protects Against Osteoporosis in Postmenopausal Mice.

Front Pharmacol. 2022-3-9

[8]
Anti-Osteoporotic Effect of Morroniside on Osteoblast and Osteoclast Differentiation In Vitro and Ovariectomized Mice In Vivo.

Int J Mol Sci. 2021-9-30

[9]
LINC00899 promotes osteogenic differentiation by targeting miR-374a and RUNX2 expression.

Exp Ther Med. 2021-10

[10]
The regulation of the TLR4/NF-κB and Nrf2/HO-1 signaling pathways is involved in the inhibition of lipopolysaccharide-induced inflammation and oxidative reactions by morroniside in RAW 264.7 macrophages.

Arch Biochem Biophys. 2021-7-30

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