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黑骨藤抑制破骨细胞分化及骨吸收能力的活性部位研究
引用本文:甄茹,俸婷婷,赵致,陈琳,赵程成,周英. 黑骨藤抑制破骨细胞分化及骨吸收能力的活性部位研究[J]. 中国实验方剂学杂志, 2015, 21(1): 112-116
作者姓名:甄茹  俸婷婷  赵致  陈琳  赵程成  周英
作者单位:1. 贵州大学药学院,贵阳 550025;贵州省中药民族药创制工程中心,贵阳 550025
2. 贵州大学药学院,贵阳 550025;贵州省药用植物繁育与种植重点实验室,贵阳 550025
基金项目:贵州省高校工程技术研究中心建设项目“贵州省中药民族药创制工程中心”(黔教合KY字[2012]018号);贵阳市科技计划 (筑科合社字[2012]2049号);贵州大学研究生创新基金 (研农2013024);贵州省国际科技合作计划项目(黔科合外G字[2013]7009号);贵州大学引进人才科研项目(贵大人基合字(2012)010号);贵州省药用植物繁育与种植人才基地(黔人领发[2013]15号)
摘    要:目的:探究黑骨藤对破骨细胞分化的影响并确定其活性部位。方法:采用维生素D3(VD3)诱导兔骨髓细胞法获得破骨细胞,以形态学观察、苏木素和伊红(HE)染色、抗酒石酸酸性磷酸酶(TRAP)染色鉴定破骨细胞,然后通过测定黑骨藤各极性部位低、中、高剂量组(1,10,100 mg·L-1)对破骨细胞TRAP酶活力,TRAP+细胞计数及骨吸收陷窝面积的影响来确定活性部位。结果:黑骨藤水饱和正丁醇层的高剂量组及乙酸乙酯层的中、高剂量组均对骨髓细胞向破骨细胞分化具有显著的抑制作用(P<0.01),并具有剂量依赖性。在抑制破骨细胞骨吸收能力实验中,黑骨藤乙酸乙酯层各剂量组均有显著抑制骨吸收陷窝面积的作用(P<0.01),而正丁醇层中、高剂量组具有显著抑制作用(P<0.01),均呈剂量依赖性。结论:黑骨藤抑制骨髓细胞向破骨细胞分化及骨吸收能力的主要活性部位是乙酸乙酯部位。

关 键 词:黑骨藤  破骨细胞  活性部位  骨吸收  乙酸乙酯层
收稿时间:2014-06-10

Research on Active Fraction of Periploca forrestii Inhibiting Osteoclast Differentiation and Bone Resorption Ability
ZHEN Ru,FENG Ting-ting,ZHAO Zhi,CHEN Lin,ZHAO Cheng-cheng and ZHOU Ying. Research on Active Fraction of Periploca forrestii Inhibiting Osteoclast Differentiation and Bone Resorption Ability[J]. China Journal of Experimental Traditional Medical Formulae, 2015, 21(1): 112-116
Authors:ZHEN Ru  FENG Ting-ting  ZHAO Zhi  CHEN Lin  ZHAO Cheng-cheng  ZHOU Ying
Affiliation:School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China;Guizhou Engineering Center for Innovative Traditional Chinese Medicine(TCM) and Ethnic Medicine, Guiyang 550025, China;School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China;Guizhou Engineering Center for Innovative Traditional Chinese Medicine(TCM) and Ethnic Medicine, Guiyang 550025, China;School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China;Guizhou Engineering Laboratory of Propagation and Cultivation on TCM Materials, Guiyang 550025, China;School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China;Guizhou Engineering Center for Innovative Traditional Chinese Medicine(TCM) and Ethnic Medicine, Guiyang 550025, China;School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China;Guizhou Engineering Center for Innovative Traditional Chinese Medicine(TCM) and Ethnic Medicine, Guiyang 550025, China;School of Pharmaceutical Sciences, Guizhou University, Guiyang 550025, China;Guizhou Engineering Center for Innovative Traditional Chinese Medicine(TCM) and Ethnic Medicine, Guiyang 550025, China
Abstract:Objective: To investigate the effects of Periploca forrestii against osteoclast differentiation and determine its active fraction. Method: The three indicators-morphological observation, hematoxylin and eosin(HE)staining, tartrate-resisstant acid phosphatase(TRAP) staining were used to identify osteoclasts which was obtained by vitamin D3(VD3) inducing rabbit bone marrow cells. The active fraction was determined, the inhibitory effects of each polarity of P. forrestii with different doses-low, medium and high dose groups (1, 10,100 mg·L-1) on the TRAP enzyme activity of osteoclasts, TRAP+ cells and bone resorption whirlpool area were measured. Result: In addition to the high-dose of water-saturated n-butanol layer, high-dose group as well as middle-dose of ethyl acetate layer also had significant inhibition on marrow cells differentiating into osteoclasts with dose-dependent manner(P<0.01).The measuring result of the bone resorption ability of osteoclast, showed that ethyl acetate layer inhibited bone resorption whirlpool area dose-dependently (P<0.01), while the high-dose group of n-butanol layer also had apparent effects (P<0.01). Conclusion: Ethyl acetate fraction is the most active part of P. forrestii to suppress differentiation of bone marrow cells into osteoclast and bone resorption capacity.
Keywords:Periploca forrestii  osteoclasts  active fraction  bone resorption  ethyl acetate layer
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