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Cyperenoic acid suppresses osteoclast differentiation and delays bone loss in a senile osteoporosis mouse model by inhibiting non-canonical NF-κB pathway

机译:环戊烯酸通过抑制非规范性NF-κB途径抑制老年性骨质疏松小鼠模型中的破骨细胞分化并延迟骨丢失

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摘要

Cyperenoic acid is a terpenoid isolated from the root of a medicinal plant Croton crassifolius with a wide range of biological activities. In this study, the effects of cyperenoic acid on osteoclast differentiation were investigated both in vitro and in vivo using receptor activator of nuclear factor-κB ligand (RANKL)-induced bone marrow-derived osteoclasts and senescence-accelerated mouse prone 6 (SAMP6). Cyperenoic acid significantly suppressed RANKL-induced osteoclast differentiation at the concentrations with no apparent cytotoxicity. The half maximum inhibitory concentration (IC50) for osteoclast differentiation was 36.69 μM ± 1.02. Cyperenoic acid treatment evidently reduced the expression of two key transcription factors in osteoclast differentiation, NFATc1 and c-Fos. Detailed signaling analysis revealed that cyperenoic acid did not affect MAPK pathways and canonical NF-κB pathway but impaired activation of p100/p52 in the non-canonical NF-κB pathway upon RANKL stimulation. Moreover, the expression of osteoclast-related genes, nfatc1, ctsk, irf8, acp5 and cfos were disrupted by cyperenoic acid treatment. The bone resorption activity by cyperenoic acid-treated osteoclasts were impaired. In a senile osteoporosis mouse model SAMP6, mice fed on diet supplemented with cyperenoic acid showed delay in bone loss, compared to the control. Taken together, plant-derived cyperenoic acid shows great potential as therapeutic agent for osteoporosis.
机译:环戊烯酸是一种从药用植物巴豆crassifolius的根中分离出来的萜类化合物,具有广泛的生物活性。在这项研究中,使用核因子-κB配体(RANKL)诱导的骨髓来源的破骨细胞和衰老促进的小鼠俯卧6(SAMP6)受体激活剂,研究了环戊烯酸对破骨细胞分化的影响。环戊烯酸在没有明显细胞毒性的浓度下能显着抑制RANKL诱导的破骨细胞分化。破骨细胞分化的半数最大抑制浓度(IC50)为36.69μM±1.02。环戊烯酸处理可明显降低破骨细胞分化过程中两个关键转录因子NFATc1和c-Fos的表达。详细的信号分析表明,环戊烯酸不会影响MAPK途径和经典NF-κB途径,但会损害RANKL刺激后非经典NF-κB途径中p100 / p52的激活。此外,破骨细胞相关基因nfatc1,ctsk,irf8,acp5和cfos的表达被环戊烯酸破坏。环戊烯酸处理的破骨细胞的骨吸收活性受损。与对照相比,在老年骨质疏松症小鼠模型SAMP6中,饲喂补充了环戊烯酸饮食的小鼠表现出骨质流失延迟。两者合计,植物来源的环戊烯酸显示出巨大的潜力作为骨质疏松症的治疗剂。

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