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Minimally effective concentration of zoledronic acid to suppress osteoclasts in vitro

机译:微小有效浓度的唑酮酸,以抑制体外骨质体

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Zoledronic acid is regarded as the most potent bisphosphonate and is widely used in patients with osteoporosis; however, its side effects, including acute-phase reactions, gastrointestinal complaints, renal dysfunction and bisphosphonate-associated osteonecrosis impair the safety and quality of life of patients. The present study was designed to determine the minimal effective concentration of zoledronic acid through testing the dose-dependent effects of zoledronic acid on osteoclast suppression. A primary culture of bone marrow mononuclear cells obtained from C57 mice (age, 6 weeks) was established and induced to form osteoclasts. The number of multinuclear cells was determined by tartrate-resistant acid phosphatase staining and compared among cultured marrow cells treated with different concentrations of zoledronic acid. Furthermore, the cellular properties, including adhesion, migration and bone resorption, were compared at the minimal effective concentration. At a concentration of 1x10(-6) mol/l, zoledronic acid significantly inhibited the formation of osteoclasts. This inhibitory effect was further enhanced at the concentration of 1x10(-5) mol/l. However, the inhibitory effect of zoledronic acid tapered at the concentration of 1x10(-4) mol/l and there was no further dose-dependent increase. In addition, the concentration of 1x10(-6) mol/l was sufficient to alter cellular functions, including cell adhesion, migration and bone resorption. In conclusion, zoledronic acid was effective in reducing osteoclast formation and suppressing cellular functions. The minimal effective concentration of zoledronic acid in vitro was 1 mu mol/l. Based on these results, a comparable dosage should be explored in clinical applications.
机译:唑醇酸被认为是最有效的双膦酸盐,广泛用于骨质疏松症的患者;然而,其副作用,包括急性相反应,胃肠投诉,肾功能紊乱和双膦酸盐相关的骨折坏死损害患者的安全和生活质量。本研究旨在通过测试唑醇酸的剂量依赖性对破骨细胞抑制来确定唑代膦酸的最小有效浓度。建立并诱导从C57小鼠(年龄,6周)获得的骨髓单核细胞的原发性培养物,形成疏松骨液。通过抗酒石酸酸磷酸酶染色和用不同浓度的唑膦酸处理的培养的骨髓细胞进行比较来确定多核细胞的数量。此外,在最小的有效浓度下比较细胞性质,包括粘附性,迁移和骨吸收。浓度为1×10(-6)摩尔/升,唑醇显着抑制了骨酸溶胶的形成。该抑制作用在1×10(-5)摩尔/升浓度下进一步增强。然而,唑代膦酸在1×10(-4)摩尔/ L浓度下锥形锥形的抑制作用,并且没有进一步的剂量依赖性增加。另外,1×10(-6)摩尔/升浓度足以改变细胞功能,包括细胞粘附,迁移和骨吸收。总之,唑醇酸可有效地减少破骨细胞形成和抑制细胞功能。体外唑醇酸的最小有效浓度为1μmol/ l。基于这些结果,应在临床应用中探索可比剂量。

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