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首页> 外文期刊>Journal of hypertension >Rat chromosome 19 transfer from SHR ameliorates hypertension, salt-sensitivity, cardiovascular and renal organ damage in salt-sensitive Dahl rats.
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Rat chromosome 19 transfer from SHR ameliorates hypertension, salt-sensitivity, cardiovascular and renal organ damage in salt-sensitive Dahl rats.

机译:来自SHR的大鼠19号染色体转移改善了盐敏感性Dahl大鼠的高血压,盐敏感性,心血管和肾器官损害。

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OBJECTIVES: Unlike Dahl salt-sensitive (SS) rats, some strains of spontaneously hypertensive (SHR) rats develop only minor organ damage even when exposed to high-salt diet. In previous linkage studies, we identified quantitative trait loci on rat chromosome 19 (RNO19) linked to the SHR allele suggesting a protective effect against salt-induced hypertensive organ damage in SS. METHODS: To test the relevance of this finding, we generated and characterized a consomic strain SS-19SHR in which RNO19 from SHR was introgressed into the susceptible background of SS. We compared the effects of low-salt (0.2% NaCl) and high-salt (4% NaCl) diet exposure for 8 weeks on the development of hypertension and target organ damage in male consomic and SS animals (n=14-20, each). RESULTS: Systolic blood pressure, relative left ventricular weight and urinary protein excretion were significantly lower in SS-19SHR compared to SS under both low-salt and high-salt diet (P < 0.05, respectively). Left ventricular atrial natriuretic peptide mRNA expression showed a more pronounced 4.5-fold increase in SS compared to SS-19 (two-fold) after high-salt (P < 0.05). In comparison to low diet, high-salt exposure induced a significant increase in vascular aortic hypertrophy index, left ventricular interstitial fibrosis (+210%) and perivascular fibrosis (+195%) in SS but not in consomic SS-19SHR (P < 0.05, respectively). CONCLUSIONS: These results demonstrate a strong protective effect of RNO19 from SHR on the development of hypertension, salt-sensitivity, cardiovascular and renal organ damage in SS. In particular, we demonstrate a genetic effect protecting against the development of cardiac fibrosis in salt-sensitive hypertension.
机译:目的:与达尔盐敏感性(SS)大鼠不同,某些品系的自发性高血压(SHR)大鼠即使暴露于高盐饮食也只会造成较小的器官损伤。在先前的连锁研究中,我们确定了与SHR等位基因相关的大鼠19号染色体(RNO19)上的定量性状基因座,表明其对盐诱导的SS高血压器官损害具有保护作用。方法:为了检验这一发现的相关性,我们生成并鉴定了一个纯系SS-19SHR,其中来自SHR的RNO19渗入SS的易感背景。我们比较了低盐(0.2%NaCl)和高盐(4%NaCl)饮食暴露8周对雄性清醒和SS动物(n = 14-20,每只)的高血压发展和靶器官损伤的影响)。结果:在低盐和高盐饮食下,SS-19SHR的收缩压,相对左心室重量和尿蛋白排泄均显着低于SS(分别为P <0.05)。高盐后,左心房利钠肽mRNA的表达与SS-19相比,SS升高了4.5倍(2倍)(P <0.05)。与低饮食相比,高盐暴露在SS中引起血管主动脉肥大指数,左心室间质纤维化(+ 210%)和血管周围纤维化(+ 195%)的显着增加,但在纯SS-19SHR中则没有(P <0.05 , 分别)。结论:这些结果表明,SHR的RNO19对SS的高血压,盐敏感性,心血管和肾器官损害有很强的保护作用。特别是,我们证明了在盐敏感型高血压中预防心脏纤维化发展的遗传效应。

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