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首页> 外文期刊>Archives of pharmacal research >Salvia plebeia R.Br. inhibits signal transduction of IL-6 and prevents ovariectomy-induced bone loss by suppressing osteoclastogenesis
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Salvia plebeia R.Br. inhibits signal transduction of IL-6 and prevents ovariectomy-induced bone loss by suppressing osteoclastogenesis

机译:丹参通过抑制破骨细胞生成抑制IL-6的信号转导并防止卵巢切除术引起的骨丢失

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The interleukin-6 (IL-6) family of cytokines plays a key role in the pathogenesis of rheumatoid arthritis and osteoporosis through the regulation of bone formation and resorption. In this study, it was observed that ethanol extract of Salvia plebeia R.Br. (S.P-EE) inhibited IL-6-induced signaling cascade including phosphorylation of JAK2/STAT3 and ERK. Subsequently, it was examined whether S.P-EE treatment could recover bone loss in ovariectomized (OVX) mice. Indeed, S.P-EE exhibited both preventive and therapeutic effect on OVX-induced bone loss in trabecular microarchitecture along with significant increase in bone mineral density and content. To understand the mechanism of action of S.P-EE in bone metabolism, the effect of S.P-EE on osteoclast differentiation and activity was investigated. S.P-EE significantly inhibited RANKL-induced osteoclast differentiation by suppressing phosphorylation of MAPK and Akt, and expression of NFATc1 and osteoclast marker genes. S.P-EE also inhibited bone-resorbing activity of osteoclasts. Furthermore, isolation and identification of the active compounds which are responsible for the inhibitory effect of S.P-EE on osteoclast differentiation was carried out. Six major flavonoids and plebeiolide A-C were isolated and examined their effects on osteoclast differentiation. Luteolin and hispidulin, and plebeiolide A and C, not B exhibited potent inhibitory activity on RANKL-induced osteoclast formation.
机译:白细胞介素6(IL-6)家族的细胞因子通过调节骨形成和吸收,在类风湿性关节炎和骨质疏松的发病机理中起关键作用。在该研究中,观察到丹参的乙醇提取物R.Br。 (S.P-EE)抑制IL-6诱导的信号传导级联反应,包括JAK2 / STAT3和ERK的磷酸化。随后,检查了S.P-EE处理是否可以恢复卵巢切除(OVX)小鼠的骨质流失。实际上,S.P-EE对小梁微结构中OVX引起的骨质流失具有预防和治疗作用,并且骨矿物质密度和含量显着增加。为了了解S.P-EE在骨代谢中的作用机理,研究了S.P-EE对破骨细胞分化和活性的影响。 S.P-EE通过抑制MAPK和Akt的磷酸化以及NFATc1和破骨细胞标记基因的表达来显着抑制RANKL诱导的破骨细胞分化。 S.P-EE也抑制破骨细胞的骨吸收活性。此外,进行了分离和鉴定负责S.P-EE对破骨细胞分化的抑制作用的活性化合物。分离出六个主要类黄酮和plebeiolide A-C,并检查它们对破骨细胞分化的影响。木犀草素和组织蛋白,以及plebeiolide A和C,而不是B对RANKL诱导的破骨细胞形成表现出有效的抑制活性。

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