A New Animal Model to Study Endogenous Cardiotonic Steroids and the Progression of Cardiovascular Events in Salt-Sensitive Hypertension.

Estela S Estape, Ivette Torres-Negron, Lorena Gonzalez, Manuel Martinez-Maldonado
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Abstract

The Dahl salt-sensitive rat is a well-established model to study essential hypertension. We first described a subgroup of these rats based on the unique response pattern in systolic blood pressure during the first weeks of exposure to a high salt diet that included cataract formation. We classified this group as cataract-prone Dahl salt-sensitive rat. We also were able to predict and prevent cataract formation in these rats. Further studies showed an inhibition of lens Na, K-ATPase activity which may be in part responsible for the cataract formation. Other studies in Dahl salt-sensitive rats maintained on a high salt diet have also shown decreased Na, K-ATPase activity in several tissues and increased levels of endogenous circulating Na, K pump inhibitors. For over 20 years, endogenous cardiotonic steroids have been postulated to inhibit Na, K-ATPase in both humans as well as in experimental animal models of hypertension. Recent findings have shown results suggesting that there are several forms of cardiotonic steroids with minor differences in structural functionalities, site of production, and specific pump selectivity. We present original data that supports a role for cardiotonic steroids in disease progression related to increased salt-sensitivity. We found increased levels of free endogenous cardiotonic steroids in those rats that were classified as cataract-prone according to their initial systolic blood pressure response to a high salt intake when compared to non-cataract prone Dahl salt-sensitive rats and their control Dahl salt-resistant rats. The cataract-prone Dahl salt-sensitive rat is an animal model that can help and contribute to open a new door to possibly elucidate the role of endogenous cardiotonic steroids in the pathogenesis and progression of diseases related to salt-sensitive hypertension.

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研究盐敏感性高血压患者内源性强心类固醇和心血管事件进展的新动物模型
达尔盐敏感大鼠是研究原发性高血压的成熟模型。我们首先根据大鼠在接触高盐饮食的最初几周内收缩压的独特反应模式(包括白内障的形成)描述了这些大鼠中的一个亚群。我们将这一群体归类为易患白内障的达尔盐敏感大鼠。我们还能预测和预防这些大鼠白内障的形成。进一步的研究表明,晶状体 Na、K-ATP 酶的活性受到抑制,这可能是白内障形成的部分原因。对以高盐饮食饲养的达尔盐敏感大鼠进行的其他研究也显示,多种组织中的 Na、K-ATPase 活性降低,内源性循环 Na、K 泵抑制剂水平升高。20 多年来,人们一直推测内源性强心类固醇会抑制人类和高血压实验动物模型中的 Na、K-ATP 酶。最近的研究结果表明,有几种形式的强心类固醇在结构功能、产生部位和特异性泵选择性方面存在细微差别。我们提供的原始数据支持强心类固醇在与盐敏感性增加有关的疾病进展中发挥作用。我们发现,与非白内障易发达氏盐敏感大鼠及其对照组达氏耐盐大鼠相比,根据大鼠对高盐摄入的初始收缩压反应而被归类为白内障易发大鼠的大鼠体内游离的内源性强心类固醇水平升高。易患白内障的达尔耐盐大鼠是一种动物模型,它有助于为阐明内源性强心类固醇在盐敏感性高血压相关疾病的发病和发展过程中的作用打开一扇新的大门。
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