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从自发性高血压大鼠(SHR)转移大鼠19号染色体可改善盐敏感型 Dahl 大鼠的高血压、盐敏感性、心血管和肾脏器官损伤。

Rat chromosome 19 transfer from SHR ameliorates hypertension, salt-sensitivity, cardiovascular and renal organ damage in salt-sensitive Dahl rats.

作者信息

Wendt Norbert, Schulz Angela, Siegel Anja-Kristin, Weiss Judith, Wehland Markus, Sietmann Anika, Kossmehl Peter, Grimm Daniela, Stoll Monika, Kreutz Reinhold

机构信息

Institut für Klinische Pharmakologie und Toxikologie, Charité - Universitätsmedizin Berlin, Berlin, Germany.

出版信息

J Hypertens. 2007 Jan;25(1):95-102. doi: 10.1097/HJH.0b013e328010688f.

Abstract

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.

摘要

目的

与 Dahl 盐敏感(SS)大鼠不同,一些自发性高血压(SHR)大鼠品系即使暴露于高盐饮食,也仅出现轻微的器官损伤。在之前的连锁研究中,我们在大鼠 19 号染色体(RNO19)上鉴定出与 SHR 等位基因相关的数量性状位点,提示其对 SS 中盐诱导的高血压性器官损伤具有保护作用。

方法

为了验证这一发现的相关性,我们构建并鉴定了一个代换系 SS-19SHR,其中来自 SHR 的 RNO19 被导入到 SS 的易感背景中。我们比较了低盐(0.2% NaCl)和高盐(4% NaCl)饮食暴露 8 周对雄性代换系动物和 SS 动物(每组 n = 14 - 20)高血压和靶器官损伤发展的影响。

结果

在低盐和高盐饮食条件下,SS-19SHR 的收缩压、相对左心室重量和尿蛋白排泄量均显著低于 SS(P 分别 < 0.05)。高盐饮食后,SS 中左心室心钠素 mRNA 表达相比 SS-19(两倍)有更明显的 4.5 倍增加(P < 0.05)。与低饮食相比,高盐暴露使 SS 的血管主动脉肥厚指数、左心室间质纤维化(增加 210%)和血管周围纤维化(增加 195%)显著增加,但在代换系 SS-19SHR 中未出现(P 分别 < 0.05)。

结论

这些结果表明,来自 SHR 的 RNO19 对 SS 中高血压、盐敏感性、心血管和肾脏器官损伤的发展具有强大的保护作用。特别是,我们证明了一种遗传效应可预防盐敏感性高血压中心脏纤维化的发展。

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