Evidence map›Paper›PMID 42045036›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2026

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Zihao Deng, Zhuan Wang, Senxiong Meng, Yusheng Yang, Yunping Yang, Liuyi Fan, Lei Wang

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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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.

Zihao DengDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zhuan WangDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Senxiong MengDepartment of Cardiovascular Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Yusheng YangDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Yunping YangDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Liuyi FanDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Lei WangDepartment of Orthopaedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Funding

National Natural Science Foundation of China 82002352
6 · The paper itself

Abstract

objectivesTo investigate the role of cellular senescence in glucocorticoid-induced osteoporosis and explore the therapeutic mechanism of

methodsCultured human umbilical vein endothelial cells (HUVECs) and mouse pre-osteoblasts (MC3T3) were treated with methylprednisolone (MPS) or MPS combined with JTG Capsule dissolved in saline. HUVEC senescence pathways and repair capacity were analyzed using Western blotting, SA-β-Gal staining, DCFH-DA assay, scratch wound healing, and RT-PCR. The osteogenic potential of MC3T3 cells was assessed using immunofluorescence staining, ALP staining, Alizarin Red S staining, and RT-PCR. Osteoclast differentiation was evaluated by TRAP staining. Thirty 3-week-old female SD rats were randomized into control, MPS, and MPS+JTG groups, and the rats in the latter two groups received daily intraperitoneal MPS injections and treated with gavage of saline or JTG Capsule suspension for 3 months. Femurs and venous blood were collected from the rats for micro-CT analysis of femoral bone volume fraction and detection of serum bone metabolism markers.

resultsNetwork pharmacology revealed that the active components of tiger bone had numerous intersection targets with glucocorticoid-induced osteoporosis with a strong binding affinity to cellular senescence-related targets such as P53. In MPS-treated HUVEC-derived osteoclasts, treatment with JTG Capsule significantly inhibited the expressions of P53 and P21, attenuated oxidative stress, and enhanced cell migration and angiogenic capacity. Similarly, JTG Capsule significantly enhanced osteogenic and mineralization capacities of MC3T3 cells and suppressed osteoclast differentiation. In the rat models, intraperitoneal MPS injection for 14 days resulted in significant bone loss in the femur, and JTG Capsule treatment obviously alleviated bone loss and ameliorated the disorder in serum bone metabolic markers.

conclusionsJTG Capsule alleviates MPS-induced HUVEC senescence, enhances osteogenic capacity and suppresses osteoclastogenesis in MC3T3 cells, and promotes intraosseous angiogenesis to improve glucocorticoid-induced osteogenesis inrats.

Indexed as

Cellular SenescenceDrugs, Chinese HerbalOsteogenesisOsteoporosisAnimalsCell DifferentiationCells, CulturedFemaleGlucocorticoidsHumansHuman Umbilical Vein Endothelial CellsMiceOsteoblastsRatsRats, Sprague-DawleyDrugs, Chinese HerbalGlucocorticoidsangiogenesiscell senescenceglucocorticoid-induced osteoporosisJintiange Capsuleosteogenic differentiation

Identifiers

PMID42045036
PMCPMC13120961

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