Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair

Abstract Background Nonunion 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 acti...

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Main Authors: Jiangbo Ai, Jingzhou Zheng
Format: Article
Language:English
Published: BMC 2025-01-01
Series:Journal of Orthopaedic Surgery and Research
Subjects:
Online Access:https://doi.org/10.1186/s13018-024-05371-x
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author Jiangbo Ai
Jingzhou Zheng
author_facet Jiangbo Ai
Jingzhou Zheng
author_sort Jiangbo Ai
collection DOAJ
description Abstract Background Nonunion 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. Methods The 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. Results TMP 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. Conclusion TMP accelerated the repair of bone fracture by promoting angiogenesis and osteogenesis.
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spelling doaj-art-fbd06e24f0b84aef8d929e2d0e6301e32025-01-19T12:32:50ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2025-01-012011910.1186/s13018-024-05371-xTetramethylpyrazine promotes osteo-angiogenesis during bone fracture repairJiangbo Ai0Jingzhou Zheng1Department of Orthopaedics, The Second Affiliated Hospital of Nanchang UniversityDepartment of Hand and Foot Microsurgery, Jiangxi Careyou Shuguang Orthopedic HospitalAbstract Background Nonunion 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. Methods The 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. Results TMP 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. Conclusion TMP accelerated the repair of bone fracture by promoting angiogenesis and osteogenesis.https://doi.org/10.1186/s13018-024-05371-xTetramethylpyrazineBone fractureEndothelial cellsAngiogenesis
spellingShingle Jiangbo Ai
Jingzhou Zheng
Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair
Journal of Orthopaedic Surgery and Research
Tetramethylpyrazine
Bone fracture
Endothelial cells
Angiogenesis
title Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair
title_full Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair
title_fullStr Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair
title_full_unstemmed Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair
title_short Tetramethylpyrazine promotes osteo-angiogenesis during bone fracture repair
title_sort tetramethylpyrazine promotes osteo angiogenesis during bone fracture repair
topic Tetramethylpyrazine
Bone fracture
Endothelial cells
Angiogenesis
url https://doi.org/10.1186/s13018-024-05371-x
work_keys_str_mv AT jiangboai tetramethylpyrazinepromotesosteoangiogenesisduringbonefracturerepair
AT jingzhouzheng tetramethylpyrazinepromotesosteoangiogenesisduringbonefracturerepair