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唑来膦酸通过 SIRT3/SOD2 通路减轻氧化应激加速骨髓间充质干细胞成骨作用,从而缓解骨质疏松症。

Zoledronic acid accelerates osteogenesis of bone marrow mesenchymal stem cells by attenuating oxidative stress via the SIRT3/SOD2 pathway and thus alleviates osteoporosis.

机构信息

Department of Orthopedics, Handan First Hospital, Handan, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Feb;24(4):2095-2101. doi: 10.26355/eurrev_202002_20389.

DOI:10.26355/eurrev_202002_20389
PMID:32141579
Abstract

OBJECTIVE

The aim of this study was to clarify the potential effect of zoledronic acid on alleviating oxidative stress and promoting bone marrow mesenchymal stem cells (BMSCs) osteogenesis through the SIRT3/SOD2 pathway, thus alleviating the progression of osteoporosis.

MATERIALS AND METHODS

Relative expression levels of osteogenesis-related genes (ALP, RUNX2, and Bglap) were determined. Meanwhile, ALP activity and capacity of mineralization in BMSCs treated with different doses of zoledronic acid were measured. Subsequently, viability and ROS level in H2O2-induced BMSCs influenced by zoledronic acid treatment were assessed. The regulatory effect of zoledronic acid on the SIRT3/SOD2 pathway was detected by Western blot. Furthermore, the involvement of the SIRT3/SOD2 pathway in zoledronic acid-mediated BMSCs osteogenesis was evaluated.

RESULTS

Zoledronic acid treatment significantly up-regulated the levels of ALP, RUNX2, and Bglap. Meanwhile, it improved ALP activity and capacity of mineralization in BMSCs dose-dependently. H2O2 induction markedly suppressed viability and enhanced ROS level in BMSCs, which were reversed by zoledronic acid treatment. Besides, zoledronic acid protected H2O2-induced SIRT3 down-regulation and AC-SOD2/SOD2 up-regulation in BMSCs. In addition, silence of SIRT3 reversed the protective effects of zoledronic acid on osteogenesis of BMSCs.

CONCLUSIONS

Zoledronic acid alleviates the progression of osteoporosis. Meanwhile, it accelerates BMSCs osteogenesis by inhibiting oxidative stress via the SIRT3/SOD2 pathway.

摘要

目的

本研究旨在阐明唑来膦酸通过 SIRT3/SOD2 通路缓解氧化应激、促进骨髓间充质干细胞(BMSCs)成骨,从而缓解骨质疏松症进展的潜在作用。

材料和方法

测定成骨相关基因(ALP、RUNX2 和 Bglap)的相对表达水平。同时,测定不同剂量唑来膦酸处理的 BMSCs 的 ALP 活性和矿化能力。随后,评估唑来膦酸处理对 H2O2 诱导的 BMSCs 活力和 ROS 水平的影响。通过 Western blot 检测唑来膦酸对 SIRT3/SOD2 通路的调节作用。此外,评估 SIRT3/SOD2 通路在唑来膦酸介导的 BMSCs 成骨中的作用。

结果

唑来膦酸处理显著上调了 ALP、RUNX2 和 Bglap 的水平。同时,它剂量依赖性地提高了 BMSCs 的 ALP 活性和矿化能力。H2O2 诱导显著抑制了 BMSCs 的活力,并增强了其 ROS 水平,而唑来膦酸处理则逆转了这一作用。此外,唑来膦酸保护了 H2O2 诱导的 SIRT3 下调和 AC-SOD2/SOD2 上调。此外,沉默 SIRT3 逆转了唑来膦酸对 BMSCs 成骨的保护作用。

结论

唑来膦酸可缓解骨质疏松症的进展。同时,它通过 SIRT3/SOD2 通路抑制氧化应激,加速 BMSCs 成骨。

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