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Lycorine suppresses RANKL-induced osteoclastogenesis in vitro and prevents ovariectomy-induced osteoporosis and titanium particle-induced osteolysis in vivo

机译:肾上腺素在体外抑制RANKL诱导的破骨细胞生成并在体内预防卵巢切除术引起的骨质疏松和钛颗粒引起的骨溶解

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摘要

Osteoclasts play an important role in diseases involving bone loss. In this study, we assessed the effect of a plant-derived natural alkaloid (lycorine, or LY) on osteoclastogenesis in vitro and in vivo. Our in vitro study showed that receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclastogenesis could be inhibited by LY; this effect was due to inhibition of mitogen-activated protein kinase (MAPK) signalling via MAP kinase kinases (MKKs). The MAPK agonist anisomycin could partially rescue the inhibitory effect of LY. Furthermore, LY also played a protective role in both a murine ovariectomy (OVX)-induced osteoporosis model and a titanium particle-induced osteolysis model. These results confirmed that LY was effective in preventing osteoclast-related diseases in vivo. In conclusion, our results show that LY is effective in suppressing osteoclastogenesis and therefore could be used to treat OVX-induced osteoporosis and wear particle-induced osteolysis.
机译:破骨细胞在涉及骨丢失的疾病中起重要作用。在这项研究中,我们评估了植物来源的天然生物碱(lycorine或LY)对体外和体内破骨细胞形成的影响。我们的体外研究表明,LY可以抑制核因子-κB配体(RANKL)诱导的破骨细胞生成的受体激活剂。这种作用是由于通过MAP激酶激酶(MKK)抑制了促分裂原活化蛋白激酶(MAPK)信号传导。 MAPK激动剂茴香霉素可以部分地挽救LY的抑制作用。此外,LY在小鼠卵巢切除术(OVX)诱导的骨质疏松模型和钛颗粒诱导的骨溶解模型中也起着保护作用。这些结果证实了LY在体内预防破骨细胞相关疾病方面是有效的。总之,我们的结果表明LY可有效抑制破骨细胞生成,因此可用于治疗OVX引起的骨质疏松症和磨损颗粒引起的骨溶解。

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