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塞皮诺酸通过抑制非经典 NF-κB 通路抑制破骨细胞分化,延缓衰老性骨质疏松症小鼠模型的骨丢失。

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

机构信息

Graduate Program in Biotechnology, Faculty of Science, Chulalongkorn University, Phayathai Road, Pathumwan, Bangkok, 10330, Thailand.

Department of Chemistry, School of Science, University of Phayao, Muang, Phayao, 56000, Thailand.

出版信息

Sci Rep. 2018 Apr 4;8(1):5625. doi: 10.1038/s41598-018-23912-3.

Abstract

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 (IC) 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.

摘要

顺式-胡椒烯酸是一种萜类化合物,从药用植物巴豆的根部分离得到,具有广泛的生物活性。在本研究中,通过核因子-κB 受体激活剂(RANKL)诱导的骨髓源性破骨细胞和加速老化小鼠 6 号(SAMP6),在体外和体内研究了顺式-胡椒烯酸对破骨细胞分化的影响。顺式-胡椒烯酸在无明显细胞毒性的浓度下显著抑制 RANKL 诱导的破骨细胞分化。对破骨细胞分化的半最大抑制浓度(IC)为 36.69 μM ± 1.02。顺式-胡椒烯酸处理明显降低了两个关键的破骨细胞分化转录因子 NFATc1 和 c-Fos 的表达。详细的信号分析表明,顺式-胡椒烯酸不影响 MAPK 途径和经典的 NF-κB 途径,但在 RANKL 刺激时破坏了非经典 NF-κB 途径中 p100/p52 的激活。此外,顺式-胡椒烯酸处理还破坏了破骨细胞相关基因 nfatc1、ctsk、irf8、acp5 和 cfos 的表达。经顺式-胡椒烯酸处理的破骨细胞的骨吸收活性受损。在衰老性骨质疏松症小鼠模型 SAMP6 中,与对照组相比,饮食中补充顺式-胡椒烯酸的小鼠骨丢失延迟。总之,植物来源的顺式-胡椒烯酸具有作为骨质疏松症治疗剂的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/306d/5884777/d1185d05a3a9/41598_2018_23912_Fig1_HTML.jpg

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