Evidence map›Paper›PMID 40358879›Full record

ArticleChinese journal of integrative medicine2025

Plastrum Testudinis Stimulates Bone Formation through Wnt/β-catenin Signaling Pathway Regulated by miR-214.

Qing Lin, Bi-Yi Zhao, Xiao-Yun Li, Wei-Peng Sun, Hong-Hao Huang, Yu-Mei Yang, Hao-Yu Wang, Xiao-Feng Zhu, Li Yang, Rong-Hua Zhang

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Article in Chinese journal of integrative medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Qing LinCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Bi-Yi ZhaoCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Xiao-Yun LiCollege of Pharmacy, Jinan University, Guangzhou, 510632, China.
Wei-Peng SunCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Hong-Hao HuangCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Yu-Mei YangCollege of Pharmacy, Jinan University, Guangzhou, 510632, China.
Hao-Yu WangCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Xiao-Feng ZhuCollege of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Li YangCollege of Pharmacy, Jinan University, Guangzhou, 510632, China.
Rong-Hua ZhangCollege of Pharmacy, Jinan University, Guangzhou, 510632, China. tzrh@jnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the Wnt signaling pathway and miRNAs mechanism of extracts of Plastrum Testudinis (PT) in the treatment of osteoporosis (OP).

methodsThirty female Sprague Dawley rats were randomly divided into 5 groups by random number table method, including sham group, ovariectomized group (OVX), ovariectomized groups treated with high-, medium-, and low-dose PT (160, 80, 40 mg/kg per day, respectively), with 6 rats in each group. Except for the sham group, the other rats underwent bilateral ovariectomy to simulate OP and received PT by oral gavage for 10 consecutive weeks. After treatment, bone mineral density was measured by dual-energy X-ray absorptiometry; bone microstructure was analyzed by micro-computed tomography and hematoxylin and eosin staining; and the expressions of osteogenic differentiation-related factors were detected by immunochemistry, Western blot, and quantitative polymerase chain reaction. In addition, Dickkopf-1 (Dkk-1) was used to inhibit the Wnt signaling pathway in bone marrow mesenchymal stem cells (BMSCs) and miRNA overexpression was used to evaluate the effect of miR-214 on the osteogenic differentiation of BMSCs. Subsequently, PT extract was used to rescue the effects of Dkk-1 and miR-214, and its impacts on the osteogenic differentiation-related factors of BMSCs were evaluated.

resultsPT-M and PT-L significantly reduced the weight gain in OVX rats (P<0.05). PT also regulated the bone mass and bone microarchitecture of the femur in OVX rats, and increased the expressions of bone formation-related factors including alkaline phosphatase, bone morphogenetic protein type 2, collagen type I alpha 1, and runt-related transcription factor 2 when compared with the OVX group (P<0.05 or P<0.01). Meanwhile, different doses of PT significantly rescued the inhibition of Wnt signaling pathway-related factors in OVX rats, and increased the mRNA or protein expressions of Wnt3a, β-catenin, glycogen synthase kinase-3β, and low-density lipoprotein receptor-related protein 5 (P<0.05 or P<0.01). PT stimulated the osteogenic differentiation of BMSCs inhibited by Dkk-1 and activated the Wnt signaling pathway. In addition, the expression of miR-214 was decreased in OVX rats (P<0.01), and it was negatively correlated with the osteogenic differentiation of BMSCs (P<0.01). MiR-214 mimic inhibited Wnt signaling pathway in BMSCs (P<0.05 or P<0.01). Conversely, PT effectively counteracted the effect of miR-214 mimic, thereby activating the Wnt signaling pathway and stimulating osteogenic differentiation in BMSCs (P<0.05 or P<0.01).

conclusionPT stimulates bone formation in OVX rats through β-catenin-mediated Wnt signaling pathway, which may be related to inhibiting miR-214 in BMSCs.

Indexed as

beta CateninDrugs, Chinese HerbalMicroRNAsOsteogenesisWnt Signaling PathwayAnimalsBone DensityCell DifferentiationFemaleIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsOsteoporosisOvariectomyRatsRats, Sprague-Dawleybeta CateninDkk1 protein, ratDrugs, Chinese HerbalIntercellular Signaling Peptides and ProteinsMicroRNAsMirn214 microRNA, ratbone formationbone mesenchymal stem cellmiR-214osteoporosisPlastrum Testudinis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.