局部使用唑来膦酸钠可抑制早期骨吸收,促进骨形成。

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM JBMR Plus Pub Date : 2024-03-09 eCollection Date: 2024-05-01 DOI:10.1093/jbmrpl/ziae031
Ming-Kai Hsieh, Chi-Yun Wang, Fu-Cheng Kao, Hui-Ting Su, Mei-Feng Chen, Tsung-Ting Tsai, Po-Liang Lai
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引用次数: 0

摘要

骨移植手术后,因早期骨吸收而导致的不愈合很常见。在这些患者中,不稳定性或骨质疏松症会导致相对于合成代谢的过度分解代谢,从而导致移植物吸收而非融合。全身应用唑来膦酸盐可抑制破骨细胞生成,被广泛用于预防骨质疏松症;然而,由于成骨细胞细胞毒性、不可控的剂量方案和局部释放方法,有关局部应用唑来膦酸盐的证据还存在争议。我们研究了唑伦膦酸钠对破骨细胞生成和成骨细胞生成的影响,并探索了相应的信号通路。我们用不同浓度的唑伦膦酸评估了MC3T3E1细胞、大鼠骨髓基质细胞(BMSCs)和破骨细胞前期(RAW264.7细胞)的体外细胞毒性和分化。将不同浓度的唑仑膦酸盐与β-磷酸三钙(TCP)骨替代物一起移植到大鼠股骨临界大小骨缺损处,测试体内骨再生能力。在体外,低于 2.5 × 10-7 M 的唑伦膦酸浓度不会影响三种细胞系的活力,也不会促进 MC3T3E1 细胞和 BMSCs 的成骨分化。在 RAW264.7 细胞中,唑来膦酸盐抑制了细胞外调节蛋白激酶和 c-Jun n 端激酶的信号转导,下调了 c-Fos 和 NFATc1 的表达,降低了融合相关树突状细胞特异性跨膜蛋白和破骨细胞特异性 Ctsk 和酒石酸抗性酸性磷酸酶()的表达。 在体内,组织学染色显示,使用 500 μM 和 2000 μM 的唑来膦酸盐后,骨形成和新生血管增加,纤维化组织减少。6 周后,在正常生理盐水组中发现了更多的破骨细胞,唑来膦酸盐处理后出现了连续的破骨细胞形成,这表明在早期胼胝体形成期间抑制了骨吸收,但没有抑制后期的骨重塑。在体内,用500 μM或2000 μM唑来膦酸盐浸泡β-TCP人工骨是一种很有前景的骨再生方法,有望应用于骨移植。
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Local application of zoledronate inhibits early bone resorption and promotes bone formation.

Nonunion resulting from early bone resorption is common after bone transplantation surgery. In these patients, instability or osteoporosis causes hyperactive catabolism relative to anabolism, leading to graft resorption instead of fusion. Systemic zoledronate administration inhibits osteoclastogenesis and is widely used to prevent osteoporosis; however, evidence on local zoledronate application is controversial due to osteoblast cytotoxicity, uncontrolled dosing regimens, and local release methods. We investigated the effects of zolendronate on osteoclastogenesis and osteogenesis and explored the corresponding signaling pathways. In vitro cytotoxicity and differentiation of MC3T3E1 cells, rat bone marrow stromal cells (BMSCs) and preosteoclasts (RAW264.7 cells) were evaluated with different zolendronate concentrations. In vivo bone regeneration ability was tested by transplanting different concentrations of zolendronate with β-tricalcium phosphate (TCP) bone substitute into rat femoral critical-sized bone defects. In vitro, zolendronate concentrations below 2.5 × 10-7 M did not compromise viability in the three cell lines and did not promote osteogenic differentiation in MC3T3E1 cells and BMSCs. In RAW264.7 cells, zoledronate inhibited extracellular regulated protein kinases and c-Jun n-terminal kinase signaling, downregulating c-Fos and NFATc1 expression, with reduced expression of fusion-related dendritic cell‑specific transmembrane protein and osteoclast-specific Ctsk and tartrate-resistant acid phosphatase (. In vivo, histological staining revealed increased osteoid formation and neovascularization and reduced fibrotic tissue with 500 μM and 2000 μM zolendronate. More osteoclasts were found in the normal saline group after 6 weeks, and sequential osteoclast formation occurred after zoledronate treatment, indicating inhibition of bone resorption during early callus formation without inhibition of late-stage bone remodeling. In vivo, soaking β-TCP artificial bone with 500 μM or 2000 μM zoledronate is a promising approach for bone regeneration, with potential applications in bone transplantation.

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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
期刊最新文献
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