首页 | 本学科首页   官方微博 | 高级检索  
     检索      

三七总皂苷对新生大鼠海马神经干细胞活性影响及促分化作用
引用本文:魏楚蓉,孙弋,张建平.三七总皂苷对新生大鼠海马神经干细胞活性影响及促分化作用[J].井冈山学院学报,2008,29(8):64-68.
作者姓名:魏楚蓉  孙弋  张建平
作者单位:井冈山大学医学院,江西吉安343000
摘    要:目的研究三七总皂苷对海马神经干细胞活性的影响和分化作用。方法体外培养海马神经干细胞,分别接种于96孔板和12孔板,96孔板细胞按三七总皂苷不同浓度梯度和同一浓度的不同时间点进行干预,应用MTT法检测海马神经干细胞的OD值,观察三七总皂苷对海马神经干细胞活性的影响;12细胞孔板分为对照组和给药组,应用免疫荧光染色方法检测神经元新生特异抗原(Tuj-1)和胶质细胞新生抗原(Vimentin)的表达,以观察三七总皂苷对海马神经干细胞分化的影响。结果(1)一定浓度范围内三七总皂苷能增强海马神经干细胞活性;(2)三七总皂苷能促进海马神经干细胞向神经元和胶质细胞方向分化。结论三七总皂苷能增强海马神经干细胞的活性并能促进海马神经干细胞分化。

关 键 词:海马神经干细胞  三七总皂苷  活性  分化  神经元  胶质细胞

Effects of panax notoginseng saponing on activity and differentiation of neonate rat hippocampus neural stem cells in vitro
WEI Chu-rong,SUN Yi,ZHANG Jian-ping.Effects of panax notoginseng saponing on activity and differentiation of neonate rat hippocampus neural stem cells in vitro[J].Journal of Jinggangshan University,2008,29(8):64-68.
Authors:WEI Chu-rong  SUN Yi  ZHANG Jian-ping
Institution:(School of Medicine,Jinggangshan University, Jian 343009, China)
Abstract:Objective: Study the effects of panax notoginseng saponing on activity and differentiation of hippocampus neural stem cells in vitro.Methods: Hippocampus neural stem cells cultured in vitro differently were seeded in 96 plate and 12 plate,and the cells cultured in 96 plate were intervented with diversity concentration panax notoginseng saponing and at different time with same concentration and applying MTT method to detect OD value,and then observing effect of panax notoginseng saponing on activity.Results:(1) Panax notoginseng saponins can enhance activity of hippocampal neural stem cells under a certain concentration extent.(2) Hippocampal neural stem cells can differentiate into neuron and glial with panax notoginseng saponing.Conclusion: Panax notoginseng saponing can enhance the activity of hippocampus and promote hippocampus the differentiation of neural stem cells.
Keywords:hippocampal neural stem cells  panax notoginseng saponins  activity  differentiation  neurons  glia
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号