Evidence map›Paper›PMID 37831321›Full record

ArticleIn vitro cellular & developmental biology. Animal2023

Drynaria Naringin alleviated mechanical stress deficiency-caused bone loss deterioration via Rspo1/Lgr4-mediated Wnt/β-catenin signalling pathway.

Gui-Xun Shi, Wei-Dong Sun, Zeng-Huan Chen, Chuan-Jun Yang, Wang-Lin Luo, Dan-Feng Wang, Ze-Zhu Zhou

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 70% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 0 citations in OpenAlex.

  1. Pooled it
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Gui-Xun Shi *Department of Orthopedic Surgery, Anting Hospital, Jiading District, Shanghai, 200805, China.
Wei-Dong Sun *Department of Orthopedic Surgery, Anting Hospital, Jiading District, Shanghai, 200805, China.
Zeng-Huan ChenDepartment of Anesthesiology, Putuo Central Hospital, Putuo District, Shanghai, 200333, China.
Chuan-Jun YangDepartment of Orthopedic Surgery, Anting Hospital, Jiading District, Shanghai, 200805, China.
Wang-Lin LuoDepartment of Orthopedic Surgery, Anting Hospital, Jiading District, Shanghai, 200805, China.
Dan-Feng WangDepartment of Orthopedic Surgery, Anting Hospital, Jiading District, Shanghai, 200805, China.
Ze-Zhu ZhouDepartment of Orthopedics, Shanghai Tenth People's Hospital, Tongji University School of Medicine, 301 Yanchang Road, Shanghai, 200072, China. zezhuzhou@sina.com.
Jiading District Central Hospital · CNCentral Hospital of Putuo District · CNShanghai Tenth People's Hospital · CN

Funding

Nature Science Foundation of Jiading district of Shanghai in China JDKW-2020-0030
6 · The paper itself

Abstract

Osteoporosis is a metabolic condition distinguished by the degradation of bone microstructure and mechanical characteristics. Traditional Chinese medicine (TCM) has been employed in China for the treatment of various illnesses. Naringin, an ingredient found in Drynariae TCM, is known to have a significant impact on bone metabolism. For this research, we studied the precise potential effect of Drynaria Naringin on protecting against bone loss caused by stress deficiency. In this study, a tail-suspension (TS) test was performed to establish a mouse model with hind leg bone loss. Some mice received subcutaneous injections of Drynaria Naringin for 30 d. Trabecular bone microarchitecture was evaluated using micro-computed tomography analysis and bone histological analysis. Bone formation and resorption markers were quantified in blood samples from mice or in the supernatant of MC3T3-E1 cells by ELISA analysis, Western blotting, and PCR. Immunofluorescence was utilized to visualize the location of β-catenin. Additionally, siRNA was employed to knockdown-specific genes in the cells. Our findings highlight the efficacy of Drynaria Naringin in protecting against the deterioration of bone loss and promoting bone formation and Rspo1 expression in a mouse model following the TS test. Specifically, in vitro experiments also indicated that Drynaria Naringin may promote osteogenesis through the Wnt/β-catenin signalling pathway. Moreover, our results suggest that Drynaria Naringin upregulates the expression of Rspo1/Lgr4, leading to the promotion of osteogenesis via the Wnt/β-catenin signalling pathway. Therefore, Drynaria Naringin holds potential as a therapeutic medication for osteoporosis. Drynaria Naringin alleviates bone loss deterioration caused by mechanical stress deficiency through the Rspo1/Lgr4-mediated Wnt/β-catenin signalling pathway.

Indexed as

OsteoporosisPolypodiaceaeAnimalsbeta CateninCell DifferentiationFlavanonesMiceOsteogenesisReceptors, G-Protein-CoupledStress, MechanicalThrombospondinsWnt Signaling PathwayX-Ray Microtomographybeta CateninFlavanonesLGR4 protein, mousenaringinReceptors, G-Protein-CoupledRSPO1 protein, mouseThrombospondinsDrynaria NaringinMechanical stressOsteoporosisR-spondin1Wnt/β-catenin signalling pathway

Identifiers

PMID37831321
OpenAlexW4387599334

What OpenQuestion holds

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Registered trials

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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.