Evidence map›Paper›PMID 39819480›Full record

ArticleJournal of orthopaedic surgery and research2025

Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair.

Jiangbo Ai, Jingzhou Zheng

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Article in Journal of orthopaedic surgery and research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Jiangbo AiDepartment of Orthopaedics, The Second Affiliated Hospital of Nanchang University, No.1 Minde Road, Nanchang, Jiangxi, 330000, China.
Jingzhou ZhengDepartment of Hand and Foot Microsurgery, Jiangxi Careyou Shuguang Orthopedic Hospital, Jiayou Healthy City, No. 858 Fusheng Road, Xihu District, Nanchang, Jiangxi, 330002, China. zhengjingzhou@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonunion following a long bone fracture has gained a lot of attention due to the dreadful impact on the life quality of tremendous patients. Recent data have demonstrated the important involvement of angiogenesis in improving fracture healing. Tetramethylpyrazine (TMP) is an active component of Chinese herbal medicine with various biological activities including pro-angiogenesis property. However, the activity and mechanism of action of TMP in osteo-angiogenesis during bone fracture repair bone fracture healing remain unknown. In this study, TMP was tested for its specific activities in rat aortic endothelial cells (RAECs) and fractured rat model.

methodsThe effect of TMP on angiogenesis and migration in RAECs was detected by conducting matrigel tubulogenesis assay and transwell assay. Histopathological changes were observed in the rats from each group using H&E staining. The levels of inflammation and coagulation markers in rats were evaluated by ELISA. The expression of osteogenesis-related genes in rats was assessed by RT-qPCR and western blotting.

resultsTMP promoted angiogenesis processes and migratory ability in RAECs. TMP improved histopathological changes in fractured rat model. The concentration of inflammatory markers (IL-2, IL-6, IL-1beta) in the serum of fractured rats were suppressed by TMP treatment. TMP also had the potential to inhibit blood coagulation in rat tibia fracture model. In addition, the expression and protein levels of osteogenesis-related markers (ALP, Runx2, and OPN-1) were elevated by TMP in the tissues from the fractured rats. In mechanism, TMP significantly promoted the activation of VEGF/FLK1 pathway in vitro and in vivo.

conclusionTMP accelerated the repair of bone fracture by promoting angiogenesis and osteogenesis.

Indexed as

Fracture HealingNeovascularization, PhysiologicOsteogenesisPyrazinesAngiogenesisAnimalsCell MovementCells, CulturedDisease Models, AnimalEndothelial CellsMaleRatsRats, Sprague-DawleyPyrazinestetramethylpyrazineAngiogenesisBone fractureEndothelial cellsTetramethylpyrazine

Identifiers

PMID39819480
PMCPMC11740429

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