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Genetic analysis of genes causing hypertension and stroke in spontaneously hypertensive rats: Gene expression profiles in the kidneys

机译:自发性高血压大鼠引起高血压和中风的基因的遗传分析:肾脏中的基因表达谱

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摘要

Spontaneously hypertensive rats (SHRs) and stroke-prone SHRs (SHRSP) are frequently used as models not only of essential hypertension and stroke, but also of attention-deficit hyperactivity disorder (ADHD). Normotensive Wistar-Kyoto (WKY) rats are normally used as controls in these studies. In the present study, we aimed to identify the genes causing hypertension and stroke, as well as the genes involved in ADHD using these rats. We previously analyzed gene expression profiles in the adrenal glands and brain. Since the kidneys can directly influence the functions of the cardiovascular, endocrine and sympathetic nervous systems, gene expression profiles in the kidneys of the 3 rat strains were examined using genome-wide microarray technology when the rats were 3 and 6 weeks old, a period in which rats are considered to be in a pre-hypertensive state. Gene expression profiles were compared between the SHRs and WKY rats and also between the SHRSP and SHRs. A total of 232 unique genes showing more than a 4-fold increase or less than a 4-fold decrease in expression were isolated as SHR- and SHRSP-specific genes. Candidate genes were then selected using two different web tools: the 1st tool was the Database for Annotation, Visualization and Integrated Discovery (DAVID), which was used to search for significantly enriched genes and categorized them using Gene Ontology (GO) terms, and the 2nd was Ingenuity Pathway Analysis (IPA), which was used to search for interactions among SHR- and also SHRSP-specific genes. The analyses of SHR-specific genes using IPA revealed that B-cell CLL/lymphoma 6 (Bcl6) and SRY (sex determining region Y)-box 2 (Sox2) were possible candidate genes responsible for causing hypertension in SHRs. Similar analyses of SHRSP-specific genes revealed that angiotensinogen (Agt), angiotensin II receptor-associated protein (Agtrap) and apolipoprotein H (Apoh) were possible candidate genes responsible for triggering strokes. Since our results revealed that SHRSP-specific genes isolated from the kidneys of rats at 6 weeks of age, included 6 genes related to Huntington's disease, we discussed the genetic association between ADHD and Huntington's disease.
机译:自发性高血压大鼠(SHRs)和中风倾向性SHRs(SHRSP)不仅被用作原发性高血压和中风的模型,而且还被用作注意力不足过动症(ADHD)的模型。在这些研究中,通常将血压正常的Wistar-Kyoto(WKY)大鼠用作对照。在本研究中,我们旨在鉴定导致高血压和中风的基因,以及使用这些大鼠的多动症相关基因。我们先前分析了肾上腺和大脑中的基因表达谱。由于肾脏可以直接影响心血管,内分泌和交感神经系统的功能,因此当大鼠分别在3周和6周龄时,使用全基因组微阵列技术检查了3种大鼠品系的肾脏中的基因表达谱。哪些大鼠被认为处于高血压前状态。比较了SHRs和WKY大鼠之间以及SHRSP和SHRs之间的基因表达谱。共有232个独特的基因被分离为SHR和SHRSP特异性基因,它们的表达量增加了4倍以上或不到4倍。然后使用两个不同的网络工具选择候选基因:第一个工具是注释,可视化和综合发现数据库(DAVID),该数据库用于搜索显着富集的基因,并使用基因本体论(GO)术语对其进行分类,第二个是“创造力途径分析”(IPA),用于搜索SHR特异性基因以及SHRSP特异性基因之间的相互作用。使用IPA对SHR特定基因进行的分析表明,B细胞CLL /淋巴瘤6(Bcl6)和SRY(性别决定区域Y)-框2(Sox2)可能是引起SHR高血压的候选基因。对SHRSP特定基因的类似分析显示,血管紧张素原(Agt),血管紧张素II受体相关蛋白(Agtrap)和载脂蛋白H(Apoh)可能是引发中风的候选基因。由于我们的研究结果表明,从6周龄大鼠的肾脏中分离出的SHRSP特异性基因包括与亨廷顿氏病相关的6个基因,因此我们讨论了多动症与亨廷顿氏病之间的遗传关联。

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