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首页> 外文期刊>American Journal of Physiology >Sex-specific computational models for blood pressure regulation in the rat
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Sex-specific computational models for blood pressure regulation in the rat

机译:老鼠血压调节的性别特定计算模型

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摘要

In the past decades, substantial effort has been devoted to the development of computational models of the cardiovascular system. Some of these models simulate blood pressure regulation in humans and include components of the circulatory, renal, and neurohormonal systems. Although such human models are intended to have clinical value in that they can be used to assess the effects and reveal mechanisms of hypertensive therapeutic treatments, rodent models would be more useful in assisting the interpretation of animal experiments. Also, despite well-known sexual dimorphism in blood pressure regulation, almost all published models are gender neutral. Given these observations, the goal of this project is to develop the first computational models of blood pressure regulation for male and female rats. The resulting sex-specific models represent the interplay among cardiovascular function, renal hemodynamics, and kidney function in the rat; they also include the actions of the renal sympathetic nerve activity and the renin-angiotensin-aldosterone system as well as physiological sex differences. We explore mechanisms responsible for blood pressure and renal autoregulation and notable sexual dimorphism. Model simulations suggest that fluid and sodium handling in the kidney of female rats, which differs significantly from males, may contribute to their observed lower salt sensitivity as compared with males. Additionally, model simulations highlight sodium handling in the kidney and renal sympathetic nerve activity sensitivity as key players in the increased resistance of females to angiotensin II-induced hypertension as compared with males.
机译:在过去的几十年中,大量努力已经致力于开发心血管系统的计算模型。其中一些模型模拟了人类的血压调节,包括循环,肾和神经异常系统的组成部分。虽然这种人类模型旨在具有临床价值,因为它们可用于评估高血压治疗治疗的效果和揭示机制,啮齿动物模型在协助动物实验的解释方面更有用。此外,尽管在血压调节中具有众所周知的性别二态性,但几乎所有公布的模型都是性别中性的。鉴于这些观察结果,该项目的目标是为雄性和女性大鼠制定第一批血压调节的计算模型。由此产生的性别特定模型代表了大鼠心血管功能,肾血流动力学和肾功能之间的相互作用;它们还包括肾交感神经活动和肾素 - 血管紧张素 - 醛固酮系统以及生理性别差异的作用。我们探索负责血压和肾自动调节和显着的性二态性的机制。模型模拟表明,与雄性显着不同的雌性大鼠肾脏的流体和钠处理,与雄性相比,它们观察到的较低盐敏感性。此外,模型仿真突出了肾脏和肾交感神经活动敏感性的钠处理,因为与雄性相比,女性对血管紧张素II诱导的高血压率增加的关键球员。

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