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The effects of curdione on osteoarthritis in mice based on Wnt/β-catenin signaling pathway
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DOI   10.11656/j.issn.1673-9043.2025.09.05
Key Words   curdione;osteoarthritis;mice;Wnt/β-catenin signaling pathway
Author NameAffiliationE-mail
HUANG Chenshuo School of Chinese Medicine, Macau University of Science and Technology, Macau 999078, China  
CHEN Ju Department of Pharmacy, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China  
LIN Hao Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China  
LIANG Zhen Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China  
ZHENG Jinchang Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China  
GUO Weixiong Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China  
ZENG Li School of Chinese Medicine, Macau University of Science and Technology, Macau 999078, China Lzeng@must.edu.mo 
Abstract
    Objective To investigate the effects of curdione on osteoarthritis in mice by regulating Wnt/β-catenin signaling pathway. Methods Thirty SPF grade male C57BL/6 mice were randomly divided into Sham operation group(Sham), model group(OA) and curdione group(ESET, 60 mg/kg), with 10 mice in each group. The osteoarthritis model was constructed by medial meniscus instability. The drug was given by continuous gavage for 4 weeks. The morphological changes of knee joint were observed by saffrine O and HE staining, and serum inflammatory factors(TNF-α, IL-1β, IL-6, IL-10) were detected by ELISA and oxidative stress indexes(GSH-PX, SOD, MDA) were detected by chemiluminescence. The expression levels of key proteins in Wnt/β-catenin pathway were detected by immunohistochemistry and Western Blot. Results Compared with Sham group, a large number of inflammatory cells infiltrated the knee joint of mice in OA group, cartilage tissue was seriously damaged, serum levels of TNF-α, IL-1β, IL-6, IL-10 and MDA were significantly increased(P < 0.01), while the activities of SOD and GSH-PX were significantly decreased(P < 0.01). The relative expression levels of wnt3a and β-catenin in knee joint were significantly increased(P < 0.01). The above indexes can be improved obviously after curdione intervention. Conclusion Curdione may ameliorate osteoarthritis by regulating the Wnt/β-catenin signaling pathway to reduce inflammation and oxidative stress damage.

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