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作 者:裴凌鹏[1]
机构地区:[1]中央民族大学少数民族传统医学研究院,北京100081
出 处:《河南师范大学学报(自然科学版)》2008年第6期114-116,共3页Journal of Henan Normal University(Natural Science Edition)
基 金:国家自然科学基金(30171169)
摘 要:目的:研究反式白藜芦醇对体外破骨细胞分化的影响.方法建立由骨保护素配体(RANKL)和巨噬细胞集落刺激因子(M-CSF)共同细胞因子的小鼠破骨细胞骨髓诱导体系,将不同浓度的反式白藜芦醇作用于破骨细胞.受试细胞分为对照组、反式白藜芦醇低剂量组(10-8mol.L-1)、反式白藜芦醇中剂量组(10-7mol.L-1)和反式白藜芦醇高剂量组(10-6mol.L-1),并设立空白对照组.7 d后取细胞玻片进行抗酒石酸酸性磷酸酶(TRAP)染色,观察破骨细胞并计数;测量抗酒石酸酸性磷酸酶(TRAP)活性以及破骨细胞表面NF-κB活化受体(RANK)mRNA表达量.结果诱导培养的破骨细胞形态特征明显;反式白藜芦醇中、高剂量组在细胞数量、TRAP活性上与对照组相比有明显统计学差异(P<0.05);反式白藜芦醇各剂量组在(RANK)mRNA表达量上与对照组相比有明显统计学差异(P<0.05),且呈量效关系.结论:反式白藜芦醇可以抑制体外培养的破骨细胞分化.Objective:Effect of trans-resveratrol on the differentiation of osteoclast induced from bone marrow in vitro. Methods Mononuclear cells of mice bone marrow are incubated with DMEM containing macrophage colony stimulating factor (M-CSF) and receptor activator of NF-κB ligand (RANKL). The culture is treated with trans-resveratrol of different concentrations (10^-8, 10^-7, 10^- 6 mol · L^-1). On the 7 d, the culture cells are fixed and are stained for tartate-resistant acid phossphatase (TRAP). The formation of osteoclasts is quantified by counting the number of TRAP + multinuclear cells. TRAP activity and the expression of receptor activator of NF-κB (RANK) mRNA are measured. Results: The appearance of reduced mice osteoclasts is typical. Compared with the control group, the number of TRAP+ multinuclear cells and TRAP activity of trans-resveratrol middle-dose group and trans-resveratrol high-dose group have significantly decreased(P〈0.05). But the expression of RANK mRNA has significantly increased(P〈0.05)being treated in different dose trans-resveratrol. Conclusion:Trans-resveratrol can inhibit osteoclasts differentiation in vitro.
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