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Whole rat DNA array survey for candidate genes related to hypertension in kidneys from three spontaneously hypertensive rat substrains at two stages of age and with hypotensive induction caused by hydralazine hydrochloride.对来自三个自发性高血压大鼠亚系、处于两个年龄阶段且经盐酸肼屈嗪诱导产生低血压的大鼠肾脏中与高血压相关的候选基因进行全大鼠DNA阵列检测。
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2
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本文引用的文献

1
Gene expression in the adrenal glands of three spontaneously hypertensive rat substrains.三种自发性高血压大鼠亚系肾上腺的基因表达。
Mol Med Rep. 2010 Mar-Apr;3(2):213-22. doi: 10.3892/mmr_00000242.
2
Role of 20-hydroxyeicosatetraenoic and epoxyeicosatrienoic acids in the regulation of vascular function in a model of hypertension and endothelial dysfunction.20-羟二十碳四烯酸和环氧二十碳三烯酸在高血压和血管内皮功能障碍模型中对血管功能调节的作用。
Pharmacology. 2010;86(3):149-56. doi: 10.1159/000317521. Epub 2010 Aug 10.
3
Recent advances in genetics of the spontaneously hypertensive rat.自发性高血压大鼠遗传学研究的新进展。
Curr Hypertens Rep. 2010 Feb;12(1):5-9. doi: 10.1007/s11906-009-0083-9.
4
Whole genome survey of copy number variation in the spontaneously hypertensive rat: relationship to quantitative trait loci, gene expression, and blood pressure.自发性高血压大鼠基因组拷贝数变异的全基因组研究:与数量性状位点、基因表达和血压的关系。
Hypertension. 2010 May;55(5):1231-8. doi: 10.1161/HYPERTENSIONAHA.109.141663. Epub 2010 Mar 15.
5
Hypertension in the elderly.老年人高血压。
Clin Geriatr Med. 2009 Aug;25(3):391-412. doi: 10.1016/j.cger.2009.06.001.
6
Delivery of sry1, but not sry2, to the kidney increases blood pressure and sns indices in normotensive wky rats.将sry1而非sry2输送至肾脏会升高正常血压的WKY大鼠的血压并增加交感神经系统指标。
BMC Physiol. 2009 Jun 5;9:10. doi: 10.1186/1472-6793-9-10.
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Analysis of gene expression data using BRB-ArrayTools.使用BRB-ArrayTools分析基因表达数据。
Cancer Inform. 2007 Feb 4;3:11-7.
8
Central blood pressure, arterial stiffness, and wave reflection: new targets of treatment in essential hypertension.中心血压、动脉僵硬度与波反射:原发性高血压治疗的新靶点
Curr Hypertens Rep. 2009 Jun;11(3):190-6. doi: 10.1007/s11906-009-0034-5.
9
Hypertension: reflections on risks and prognostication.高血压:关于风险与预后的思考
Med Clin North Am. 2009 May;93(3):541-58, Table of Contents. doi: 10.1016/j.mcna.2009.02.006.
10
Soluble epoxide hydrolase inhibitor, AUDA, prevents early salt-sensitive hypertension.可溶性环氧化物水解酶抑制剂AUDA可预防早期盐敏感性高血压。
Front Biosci. 2008 May 1;13:3480-7. doi: 10.2741/2942.

对来自三个自发性高血压大鼠亚系、处于两个年龄阶段且经盐酸肼屈嗪诱导产生低血压的大鼠肾脏中与高血压相关的候选基因进行全大鼠DNA阵列检测。

Whole rat DNA array survey for candidate genes related to hypertension in kidneys from three spontaneously hypertensive rat substrains at two stages of age and with hypotensive induction caused by hydralazine hydrochloride.

作者信息

Kinoshita Kosho, Ashenagar Mohammad Said, Tabuchi Masaki, Higashino Hideaki

机构信息

Department of Pharmacology, Kinki University School of Medicine, Osaka 589-8511, Japan.

出版信息

Exp Ther Med. 2011 Mar;2(2):201-212. doi: 10.3892/etm.2011.193. Epub 2011 Jan 14.

DOI:10.3892/etm.2011.193
PMID:22977489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3440673/
Abstract

Clarification of the genetic nature and more effective care for hypertension are required, given the high incidences of cardiovascular and cerebrovascular mortality. Thus, we surveyed candidate genes for hypertension with rat whole gene DNA microarrays using three novel methods. Gene expression analyses were conducted as follows: Method 1, three types of spontaneously hypertensive rat (SHR) substrains, SHR, stroke-prone SHR (SHRSP) and malignant type of SHRSP (M-SHRSP) were used and compared to normotensive Wistar Kyoto rats; Method 2, the expressed genes between rats of different ages were compared for different blood pressures; and Method 3, genes that were expressed in rats treated with or without an acute hypotensive stimulus, the antihypertensive hydralazine hydrochloride, were compared. This approach identified dozens of genes, including Dusp15, Cyp8b1, Armc 3, Gtpbp4, Mettl2, Mapk14, Prkar2b, frame 12, Anxa13, Ephx2, Myr8 and Pcdh9 by Method 1; Cyp2C and Atp12a by Method 2; and Kcnc3, Vnn1, TC560558 and Gabrq and a number of unknown genes by Methods 2 and 3, as probable candidate genes for hypertension in SHR substrains. Ephx2 was previously reported as a candidate gene in SHRs; however other genes were identified for the first time in this study. Since it was not always possible to completely demonstrate that these genes are responsible for hypertension in SHRs, further research into true candidate genes that participate in the genesis of hypertension in SHR substrains is warranted.

摘要

鉴于心血管和脑血管疾病的高死亡率,有必要明确高血压的遗传本质并提供更有效的治疗。因此,我们使用三种新方法,通过大鼠全基因DNA微阵列对高血压候选基因进行了研究。基因表达分析如下:方法1,使用三种自发性高血压大鼠(SHR)亚系,即SHR、易中风SHR(SHRSP)和恶性型SHRSP(M-SHRSP),并与血压正常的Wistar Kyoto大鼠进行比较;方法2,比较不同年龄、不同血压大鼠之间的表达基因;方法3,比较给予或未给予急性降压刺激(降压药盐酸肼屈嗪)的大鼠中表达的基因。该方法确定了数十个基因,方法1确定的有Dusp15、Cyp8b1、Armc 3、Gtpbp4、Mettl2、Mapk14、Prkar2b、框架12、Anxa13、Ephx2、Myr8和Pcdh9;方法2确定的有Cyp2C和Atp12a;方法2和3确定的有Kcnc3、Vnn1、TC560558和Gabrq以及一些未知基因,这些基因可能是SHR亚系高血压的候选基因。Ephx2此前已被报道为SHR中的候选基因;然而,其他基因是本研究首次鉴定出来的。由于并非总能完全证明这些基因与SHR的高血压有关,因此有必要进一步研究参与SHR亚系高血压发生的真正候选基因。