Effect of Savinin to Inhibit RANKL-induced Osteoclast Differentiation

H. Shin, Yongjin Lee, Minam Lee, Young-Jin Son
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Abstract

Osteoporosis is a disease in which bone density is decreased and fractures occur easily due to external environment. The treatment of osteoporosis is important to prevent bone loss and to suppress the formation of osteoclasts involved in bone resorption. Osteoclasts, which are multinucleated cells, are greatly increased and overactivated in bone diseases including osteoporosis and rheumatoid arthritis. In this study, the effect of savinin on osteoclast differentiation by RANKL was investigated. Savinin significantly inhibited RANKL-induced osteoclast differentiation by inhibiting the transcriptional and translational expression of NFATc1, an essential component of RANKL-mediated osteoclast formation. In addition, mRNA expressions of OSCAR, DC-STAMP, and CTSK related to osteoclast differentiation and function were suppressed. Inhibition of osteoclast activity was verified through bone resorptive assay. Therefore, it is confirmed that savinin inhibits osteoclast differentiation, so it has the potential to be used as a therapeutic agent for the treatment of osteoporosis.
沙维素对rankl诱导的破骨细胞分化的抑制作用
骨质疏松症是指受外界环境影响,骨密度降低,易发生骨折的疾病。骨质疏松症的治疗对于防止骨质流失和抑制参与骨吸收的破骨细胞的形成非常重要。破骨细胞是一种多核细胞,在骨质疏松症和类风湿性关节炎等骨病中,破骨细胞数量大幅增加和过度活化。本研究探讨了沙维素对RANKL破骨细胞分化的影响。Savinin通过抑制NFATc1的转录和翻译表达显著抑制rankl诱导的破骨细胞分化,NFATc1是rankl介导的破骨细胞形成的重要组成部分。此外,与破骨细胞分化和功能相关的OSCAR、DC-STAMP和CTSK mRNA表达被抑制。通过骨吸收试验证实了破骨细胞活性的抑制。因此,证实萨维宁具有抑制破骨细胞分化的作用,具有作为治疗骨质疏松症的治疗剂的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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