[1]杨悦 孔祥英 万红叶 苏晓慧 林娜.地乌三萜皂苷W1对破骨细胞分化和骨吸收功能
的影响[J].环球中医药,2014,7(03):191-0.
YANG Yue,KONG Xiang ying,WAN Hong ye,et al.Effect of triterpene saponin W1 from rhizome of Anemone Flaccid on osteoclasts differentiation and bone resoroption[J].,2014,7(03):191-0.
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地乌三萜皂苷W1对破骨细胞分化和骨吸收功能
的影响(
)
《环球中医药》[ISSN:1006-6977/CN:61-1281/TN]
- 卷:
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第7卷
- 期数:
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2014年03期
- 页码:
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191-0
- 栏目:
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论著
- 出版日期:
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2014-03-06
文章信息/Info
- Title:
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Effect of triterpene saponin W1 from rhizome of Anemone Flaccid on osteoclasts differentiation and bone resoroption
- 作者:
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杨悦 孔祥英 万红叶 苏晓慧 林娜
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- Author(s):
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YANG Yue; KONG Xiangying; WAN Hongye; et al.
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Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Beijing 100700,China
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- 关键词:
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地乌三萜皂苷W1; 小鼠单核/巨噬细胞RAW2647; 肿瘤坏死因子α; 骨吸收
- Keywords:
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Triterpene saponin W1 from rhizome of Anemone Flaccid ; RAW2647; Tumor necrosis factorα; Bone resoroption
- 分类号:
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R2855
- DOI:
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- 文献标志码:
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A
- 摘要:
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目的探讨地乌三萜皂苷类成分W1对体外破骨细胞分化及骨吸收功能的影响。方法3个不同浓度(00625,0125,025 μg/ml)的W1与核因子κB受体活化因子配体(receptor activator of nuclear factor kB ligand,RANKL)诱导的小鼠单核/巨噬细胞RAW 2647共孵育7天,抗酒石酸酸性磷酸酶(tartrate resistant acid phosphatase,TRAP)染色观察TRAP阳性多核细胞的形成,甲苯胺蓝染色及扫描电镜观察骨吸收陷窝的形成,图像分析计算骨吸收陷窝面积百分比;同3个浓度的W1与RANKL诱导的RAW2647细胞共孵育24小时后收集细胞上清液,放射免疫法检测肿瘤坏死因子α(tumor necrosis factorα,TNFα)的含量;甲基噻唑基四唑(methyl thiazolyl tetrazolium,MTT)法检测W1对RAW2647细胞毒性影响。结果RANKL组诱导RAW 2647细胞形成多量TRAP阳性多核细胞,形成明显的骨吸收陷窝,并诱导TNFα在RAW2647细胞上清中异常高表达;与RANKL组相比,3个浓度的W1均能显著减少TRAP阳性细胞数(P<001),显著减少骨吸收陷窝面积(P<001,P<0001,P<0001),明显降低TNFα的表达量(P<005,P<001,P<001),且未观察到对RAW2647的细胞毒性。结论W1对由RANKL诱导的体外破骨细胞分化和骨吸收功能有一定的负调节作用。
- Abstract:
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ObjectiveTo observe the effect of W1 from rhizome of Anemone Flaccid on osteoclasts formation and bone resoroption in vitro. MethodsRAW2647 cells induced by RANKL were cultured with three variable concentration(00625,0125,0.25 μg·ml-1 )of W1 in vitro for 7 days. The influence of W1 on osteoclasts differentiation was assessed by osteoclastlike number and tartrate resistant acid phosphatase (TRAP) activity; resorption lacunae were stained by toluidine blue and were visualized by Philips XL30 scanning electron microscope. The number of TRAP+ cells and the percentage of resorption pits were counted. RAW2647 cells induced by RANKL were incubated with three variable concentration of W1 in vitro for 24 hours, the level of TNFα in cell culture supernatant was examined by Iodine\
[125I\] Tunmor Necrosis Factor Radioimmunoassay kit; RAW2647 cell viability was assayed by MTT. ResultsRANKL could induce RAW2647 cells to form TRAP positive multinucleated cells and form bone resorption pits on bone. RANKL could induce abnormally high expression of TNFα in RAW2647 cells. W1 (00625,0125,025 μg· ml-1 )could decrease the number of TRAP+ cells (P<001) as well as the area of bone resorption pits(P<001,P<0001,P<0001),and showed no cytotoxicity to RAW2647; W1 (00625025 μg· ml-1 )could suppresse the expression of TNFa(P<005,P<001,P<001). ConclusionRANKL induced osteoclastogenesis in these monocytic cells,and W1 inhibited RANKLinduced tumor necrosis factorα production and osteoclast differentiation and bone resorption pit formation.
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备注/Memo
- 备注/Memo:
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基金项目:国家科技重大专项(2011ZX0910100603);北京市自然科学基金(7112096);中国中医科学院基本科研业务费自主选题(ZZ070836)
作者单位:100700 北京,中国中医科学院中药研究所中药理论与本草文献研究中心作者简介:杨悦(1989- ),女, 2011级硕士研究生。研究方向:中药药理研究。Email: yangyue8675658@163.com通讯作者:林娜(1963- ),女,博士,研究员,博士生导师。研究方向:中药药性理论与中药药理。Email:linna888@163.com
更新日期/Last Update:
1900-01-01