首页> 外文期刊>Journal of Alzheimer's disease: JAD >Discrepancy in Expression of beta-Secretase and Amyloid-beta Protein Precursor in Alzheimer-Related Genes in the Rat Medial Temporal Lobe Cortex Following Transient Global Brain Ischemia
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Discrepancy in Expression of beta-Secretase and Amyloid-beta Protein Precursor in Alzheimer-Related Genes in the Rat Medial Temporal Lobe Cortex Following Transient Global Brain Ischemia

机译:在短暂性全脑缺血后大鼠内侧颞叶皮质中阿尔茨海默氏症相关基因中β-分泌酶和淀粉样蛋白-β蛋白前体的表达差异。

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摘要

Brain ischemia may be causally related with Alzheimer's disease. Presumably, beta-secretase and amyloid-beta protein precursor gene expression changes may be associated with Alzheimer's disease neuropathology. Consequently, we have examined quantitative changes in both beta-secretase and amyloid-beta protein precursor genes in the medial temporal lobe cortex with the use of quantitative rtPCR analysis following 10-min global brain ischemia in rats with survival of 2, 7, and 30 days. The greatest significant overexpression of beta-secretase gene was noted on the 2nd day, while on days 7-30 the expression of this gene was only modestly downregulated. Amyloid-beta protein precursor gene was downregulated on the 2nd day, but on days 7-30 postischemia, there was a significant reverse tendency. Thus, the demonstrated alterations indicate that the considerable changes of expression of beta-secretase and amyloid-beta protein precursor genes may be connected with a response of neurons in medial temporal lobe cortex to transient global brain ischemia. Finally, the ischemia-induced gene changes may play a key role in a late and slow onset of Alzheimer-type pathology.
机译:脑缺血可能与阿尔茨海默氏病有因果关系。据推测,β-分泌酶和β-淀粉样蛋白前体基因表达的变化可能与阿尔茨海默氏病的神经病理学有关。因此,我们通过定量rtPCR分析,在存活2、7和30岁的大鼠中进行了10分钟的整体性脑缺血后,通过定量rtPCR分析检查了内侧颞叶皮质中β-分泌酶和淀粉样蛋白-β蛋白前体基因的数量变化。天。在第2天注意到最大的β-分泌酶基因过度表达,而在第7-30天,该基因的表达仅适度下调。淀粉样蛋白β蛋白前体基因在第2天被下调,但在缺血后7-30天有明显的逆转趋势。因此,已证明的改变表明,β-分泌酶和淀粉样蛋白-β蛋白前体基因表达的显着变化可能与内侧颞叶皮质神经元对短暂性全脑缺血的反应有关。最后,缺血诱导的基因变化可能在阿尔茨海默氏病类型的迟发和缓慢发作中起关键作用。

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