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杨戈,林水淼,赵伟康,金红姝,徐品初,周如倩,郁志华,张钦传,王健.调心方有效部位对类AD大鼠脑组织凋亡信号转导分子Caspase-3及凋亡相关基因bcl-2、bax mRNA表达的影响[J].,2006,(2):147-151
调心方有效部位对类AD大鼠脑组织凋亡信号转导分子Caspase-3及凋亡相关基因bcl-2、bax mRNA表达的影响
Effect of TX0201 on Expression of the Apoptosis Signal Transduction Molecule Caspase-3 and Apoptosis Associated Genes bcl-2 and bax mRNA in Brain Tissue of Rat Analogue Model of Alzheimer’s Disease
  
DOI:
中文关键词:  调心方有效部位  β-淀粉样蛋白  细胞凋亡  β-淀粉样蛋白前体蛋白
英文关键词:Alzheimer’s disease  TX0201  neuron apoptosis  β-amyloid precursor protein
基金项目:
Author NameAffiliation
YANG Ge 上海市中医老年医学研究所 上海200032 
LIN Shui-miao 上海市中医老年医学研究所 上海200032 
ZHAO Wei-kang 上海市中医老年医学研究所 上海200032 
金红姝 上海市中医老年医学研究所 上海200032 
徐品初 上海市中医老年医学研究所 上海200032 
周如倩 上海市中医老年医学研究所 上海200032 
郁志华 上海市中医老年医学研究所 上海200032 
张钦传 上海市中医老年医学研究所 上海200032 
王健 上海市中医老年医学研究所 上海200032 
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中文摘要:
      目的研究调心方有效部位(TX0201)对Aβ2535所致类AD模型大鼠脑组织凋亡相关基因调节作用机制的异同。方法采用双侧杏仁核注射Aβ2535造成类AD大鼠模型,观察大鼠Morris水迷宫空间记忆能力,并分别通过RTPCR和免疫组化方法研究类AD大鼠神经元细胞凋亡相关基因bax、bcl2mRNA,特异的凋亡信号转导分子Caspase3和Aβ阳性神经元变化以及TX0201的影响。结果类AD模型大鼠Morris水迷宫测试出现空间记忆能力下降,App695mRNA表达提高,Caspase3和bax/bcl2上升。TX0201能有效控制以上病理变化。结论TX0201提高模型大鼠定向学习记忆能力,可能通过降低bax/bcl2、下调Caspase3而减轻神经细胞凋亡而发挥作用。提示通过有效调节神经元凋亡相关基因是TX0201的重要作用机制之一。
英文摘要:
      Objective To study the mechanism of TX0201, an effective fraction extracted from Tiaoxin recipe in regulating apoptosis associated genes in brain tissue of rat analogue model of Alzheimer’s disease (AD) induced by β-amyloid protein 25-35 (Aβ 25-35). Methods The model of AD was induced by bilateral amygdala injection of Aβ 25-35 to study the spatial memory capacity using Morris water maze test, and by means of RT-PCR and immunohistochemistry assay, the expressions of β-amyloid precursor protein (APP), apoptosis correlative genes (bcl-2, bax), and apoptosis signal transduction molecule (Caspase-3) in the brain, and the effect of TX0201 on expressions of these genes were examined. Results In AD model group, the spatial capacity was damaged significantly. Caspase-3 and the expression of APP mRNA and bax/bcl-2 mRNA were increased in the cortex and hippocampus; TX0201 ameliorated all the pathologic changes mentioned above. Conclusion TX0201 could improve the oriented learning and memory capacity in AD rats by decreasing bax/bcl-2 and down-regulating Caspase-3 to reduce neurocyte apoptosis, suggesting that effective regulation of neuron apoptosis associated genes may be one of the mechanisms of TX0201.
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