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毛蕊花苷和异毛蕊花苷对树突状细胞增殖的影响

Effects of verbascoside and isoverbascoside on proliferation of dendritic Cells

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【作者】 唐永富黄丹菲谢明勇谢小梅万茵戴丹丹

【Author】 TANG Yong-fu1,HUANG Dan-fei1,XIE Ming-yong1,XIE Xiao-mei2,WAN Yin1,DAI Dan-dan2(1.State Key Laboratory of Food Science and Technology,Nanchang University,Nanchang 330047,China;2.Key Laboratory of Modern Preparation of TCM of Ministry of Education,Jiangxi Chinese Medical University,Nanchang 330004,China)

【机构】 南昌大学食品科学与技术国家重点实验室江西中医学院现代中药制剂教育部重点实验室

【摘要】 目的观察大粒车前子提取物苯乙醇苷类化合物毛蕊花苷(verbascoside)和异毛蕊花苷(isoverbascoside)对小鼠骨髓来源树突状细胞增殖的影响。方法采用噻唑盐(MTT)法,以细胞因子(rmGM-CSF+rmIL-4)作为阳性对照,观察不同浓度的毛蕊花苷和异毛蕊花苷对小鼠骨髓来源树突状细胞增殖的影响。结果毛蕊花苷和异毛蕊花苷均可促进小鼠树突状细胞的增殖,与阳性对照组比较,毛蕊花苷在1.60×10-7~1.60×10-4mol·L-1内,异毛蕊花苷在所有浓度范围内作用效果均非常显著(P<0.05)。毛蕊花苷和异毛蕊花苷在1.60×10-6和1.60×10-5mol·L-1的浓度与细胞因子联用时,可显著刺激小鼠树突状细胞的增殖(P<0.05)。结论毛蕊花苷和异毛蕊花苷不仅可以直接促进小鼠骨髓来源树突状细胞的增殖,而且与细胞因子有明显的协同作用。

【Abstract】 OBJECTIVE To investigate the effects of verbascoside and isoverbascoside on proliferation of murine bone marrow-devried dendritic cells.METHODS The tetrazolium salt reduction(MTT) assay was used to investigate the effect of verbascoside or isoverbascoside on proliferation of murine bone marrow-devried dendritic cells,and the cytokine(rmGM-CSF+ rmIL-4) was used as positive control.RESULTS Both verbascoside and isoverbascoside stimulated the proliferation of DCs significantly.Verbascoside had promoting effect in the concentration range of 1.60×10-7~1.60×10-4 mol·L-1(P<0.05),while isoverbascoside also showed promoting effect in all test concentrations(P<0.05).Further more,verbascoside and isoverbascoside at the concentrations of 1.60×10-6 and 1.60 10-5 mol/L stimulated the proliferation of murine bone marrow-devried dendritic cells significantly(P<0.05),white being coordinated with cytokine(rmGM-CSF+rmIL-4).CONCLUSIONS Verbascoside and isoverbascoside could induce the proliferation of murine bone marrow-devried dendritic cells,and show synergistic effect with the coordination with cytokine.

【基金】 国家自然科学基金资助项目(30660226);教育部长江学者和创新团队发展计划资助项目(IRT0540)
  • 【文献出处】 中国药学杂志 ,Chinese Pharmaceutical Journal , 编辑部邮箱 ,2008年23期
  • 【分类号】R285.5
  • 【被引频次】40
  • 【下载频次】300
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