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远志皂苷元对新生大鼠皮质神经元的营养作用
引用本文:皮婷,薛小燕,林炼峰,苏钜年,程欣,罗焕敏.远志皂苷元对新生大鼠皮质神经元的营养作用[J].中国药理学与毒理学杂志,2011,25(1):40-44.
作者姓名:皮婷  薛小燕  林炼峰  苏钜年  程欣  罗焕敏
作者单位:1. 暨南大学,医学院药理学系,广东,广州,510632
2. 暨南大学,医学院组胚教研室,广东,广州,510632
3. 暨南大学,医学院药理学系,广东,广州,510632;暨南大学,药学院神经药理研究室,广东,广州,510632;暨南大学,暨南大学-香港大学脑功能与健康联合实验室,广东,广州,510632
基金项目:中央高校基本科研业务费专项基金资助(21609101)~~
摘    要:目的 研究远志皂苷元(senegenin)对新生大鼠皮质神经元的神经营养作用.方法 原代培养新生24 h内SD大鼠皮质神经元,采用0.4% B27+DMEM/F12培养基制备营养缺乏模型.远志皂苷元0.5,1 和2 μmol·L-1及阳性对照组碱性成纤维细胞生长因子(bFGF)10 μg·L-1.倒置显微镜下观察各组皮...

关 键 词:远志皂苷元  皮质神经元  神经营养  突起生长
收稿时间:2010-9-2

Neurotrophic effects of senegenin on the cultures of newborn rat cortical neurons
PI Ting,XUE Xiao-yan,LIN Lian-feng,SU Ju-nian,CHENG Xin,LUO Huan-min.Neurotrophic effects of senegenin on the cultures of newborn rat cortical neurons[J].Chinese Journal of Pharmacology and Toxicology,2011,25(1):40-44.
Authors:PI Ting  XUE Xiao-yan  LIN Lian-feng  SU Ju-nian  CHENG Xin  LUO Huan-min
Institution:(1. Department of Pharmacology, School of Medicine, 2. Neuroparmachology Laboratory, College of Pharmacy, 3. Department of Histology and Embryology, School of Medicine, 4. Joint Laboratory of Brain Function and Health, Jinan University-Hong Kong University, Jinan University, Guangzhou 510632,China)
Abstract:OBJECTIVCE To explore the neurotrophic effects of different concentration of senegenin on cortical neurons in newborn rat. METHODS Primary cultured cortical neurons from 24 h newly born rat were dissociated and cultured. And the cultured cortical neurons were randomly divided into 7 groups: blank control group(2%B27+DMEM/F12);model group(0.4%+DMEM/F12) , to detection cells survival in the trophic withdrawl culture; solvent control group(0.1% DMSO), senegenin 0.5, 1, 2 μmol·L-1 groups, and basic fibroblast growth factor 10 μg·L-1 control group. Morphology and the average growth projections of each cortical neurons group were observed by inverted microscope. An image analysis software, the Image pro plus 6.0, was adopted to collect data of average neurite outgrowth for analysis of effects of different concentration of senegenin on the neurite growth. Neurite situation were observed using immunofluorescent staining .Additionally, in the trophic with drawal cultured condition, the neurons survival was detected by MTT method. RESULTS After intervention for 3 d, in normal cultured condition, compared to solvent control group, senegenin 0.5, 1 and 2 μmol·L-1 significantly promoted neurite growth, from (152±46)μm to 186±51, 188±34 and (193±43)μm, respectively , and senegenin 2 μmol·L-1 showed the strongest promotion effect (P<0.01), slightly lower than bFGF control group (203±40)μm. Compared to the normal cultured condition, cell survival under the trophic withdrawal condition was decreased from (100.0±5.4)% to (90.8±4.6)%. Senegenin 0.5, 1, 2 μmol·L-1 can obviously improved cells death cased by the trophic withdrawal condition, and survival are (109.7±3.2)%, (111.3±1.6)% and (112.9±4.8)%, respectively. CONCLUSION Senegenin can promote neurons survival, and can enhance cortical neuron neurite growth , has the neurotrophic effects.
Keywords:sesnegenin  cortical neurons  neurotrophic  neurite outgrowth
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