Department of Functional Pathology, Shimane University School of Medicine, Izumo, Japan.
Hypertens Res. 2012 May;35(5):477-84. doi: 10.1038/hr.2012.30. Epub 2012 Mar 8.
The stroke-prone spontaneously hypertensive rat (SHRSP) is a unique genetic model of severe hypertension and cerebral stroke. SHRSP, as well as the spontaneously hypertensive rat, the parental strain of SHRSP, has made a tremendous contribution to cardiovascular research. However, the genetic mechanisms underlying hypertension and stroke in these rats have not yet been clarified. Recent studies using whole-genome sequencing and comprehensive gene expression analyses combined with classical quantitative trait loci analyses provided several candidate genes, such as Ephx2, Gstm1 and Slc34a1, which still need further evidence to define their pathological roles. Currently, genome-wide association studies can directly identify candidate genes for hypertension in the human genome. Thus, genetic studies in SHRSP and other rat models must be focused on the pathogenetic roles of 'networks of interacting genes' in hypertension, instead of searching for individual candidate genes.
易卒中型自发性高血压大鼠(SHRSP)是一种严重高血压和脑卒中的独特遗传模型。SHRSP 以及其亲本自发性高血压大鼠对心血管研究做出了巨大贡献。然而,这些大鼠中高血压和脑卒中的遗传机制尚未阐明。最近使用全基因组测序和综合基因表达分析结合经典数量性状位点分析的研究提供了几个候选基因,例如 Ephx2、Gstm1 和 Slc34a1,这些基因仍需要进一步的证据来确定其病理作用。目前,全基因组关联研究可以直接在人类基因组中识别高血压的候选基因。因此,SHRSP 和其他大鼠模型的遗传研究必须集中在高血压中“相互作用基因网络”的发病机制上,而不是寻找单个候选基因。