Morusin Inhibits RANKL-induced Osteoclastogenesis and Ovariectomized Osteoporosis
- Authors: Jin C.1, Zheng J.2, Yang Q.3, Jia Y.2, Li H.1, Liu X.3, Xu Y.2, Chen Z.2, He L.4
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Affiliations:
- Department of Orthopaedics, Shaoxing People's Hospital
- Department of Orthopaedics, Shaoxing Peoples Hospital,
- Department of Orthopaedics, Shaoxing Peoples Hospital
- Department of Orthopaedics,, , Shaoxing Peoples Hospital,
- Issue: Vol 27, No 9 (2024)
- Pages: 1358-1370
- Section: Chemistry
- URL: https://vietnamjournal.ru/1386-2073/article/view/645001
- DOI: https://doi.org/10.2174/0113862073252310230925062415
- ID: 645001
Cite item
Full Text
Abstract
Background::Postmenopausal osteoporosis (PMOP) is a classic type of osteoporosis that has gradually become a significant health problem worldwide. There is an urgent need for a safe alternative therapeutic agent considering the poor therapeutic strategies currently available for this disease. The roots and bark of the Morus australis tree (Moraceae) are used to make a traditional Chinese medicine known as \"Morusin\", and accumulating evidence has demonstrated its multiple activities, such as anti-inflammatory and anti-tumor effects.
Objective::In this study, we aim to explore the effect of Morusin on mouse osteoclasts and its mechanism.
Methods::In this study, we explored the inhibitory effects of Morusin on murine osteoclasts in vitro and its mechanism, and the protective effect of Morusin on an ovariectomy (OVX)-induced osteoporosis model in vivo.
Results::The results showed that Morusin prevented OVX-induced bone loss and dramatically decreased RANKL-induced osteoclastogenesis. Morusin interfered with RANKL-activated NF- κB, MAPK, and PI3K/AKT signaling pathways. The expression of three master factors that control osteoclast differentiation, c-Fos, NFATc1, and c-Jun, was reduced by Morusin treatment. Collectively, in vitro results indicated that Morusin has a protective effect on OVX-induced bone loss in a mouse model.
Conclusion::Our data provide encouraging evidence that Morusin may be an effective treatment for PMOP.
About the authors
Cong Jin
Department of Orthopaedics, Shaoxing People's Hospital
Email: info@benthamscience.net
Jiewen Zheng
Department of Orthopaedics, Shaoxing Peoples Hospital,
Email: info@benthamscience.net
Qichang Yang
Department of Orthopaedics, Shaoxing Peoples Hospital
Email: info@benthamscience.net
Yewei Jia
Department of Orthopaedics, Shaoxing Peoples Hospital,
Email: info@benthamscience.net
Haibo Li
Department of Orthopaedics, Shaoxing People's Hospital
Email: info@benthamscience.net
Xuewen Liu
Department of Orthopaedics, Shaoxing Peoples Hospital
Email: info@benthamscience.net
Yangjun Xu
Department of Orthopaedics, Shaoxing Peoples Hospital,
Email: info@benthamscience.net
Zhuolin Chen
Department of Orthopaedics, Shaoxing Peoples Hospital,
Email: info@benthamscience.net
Lei He
Department of Orthopaedics,, , Shaoxing Peoples Hospital,
Author for correspondence.
Email: info@benthamscience.net
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