耦合肾元计算模型中反馈介导信号的传导

Ioannis Sgouralis;Anita T. Layton
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引用次数: 8

摘要

肾脏中的肾元通过几种自我调节机制来调节其液体流动。两种主要机制是肌源性反应和小管肾小球反馈(TGF)。肌源性反应是肾小球前血管系统的一种特性,其中血管内压力升高引起血管收缩,从而产生代偿性血管阻力增加。TGF是平衡肾小球滤过和小管重吸收能力的负反馈反应。虽然每个肾单位都有自己的自我调节反应,但肾脏的许多肾单位的反应并不是自主的,而是通过肾小球前血管系统相互作用。为了更好地理解这些信号沿肾小球前小动脉的传导以及肾素偶联对肾素血流动力学的影响,我们建立了两个相邻肾素肾血流动力学的数学模型,这两个相邻肾素的传入小动脉来自一个共同的皮质桡动脉。研究人员进行了模拟,以估计干扰素耦合强度,确定其对血管特性的依赖,并研究耦合对tgf介导的血流振荡的影响。模拟结果表明,减少的间隙连接电导可能会产生更强的肾细胞间TGF耦合和高度不规则的TGF介导的肾细胞动力学振荡,这两种情况在实验中与高血压大鼠有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Conduction of feedback-mediated signal in a computational model of coupled nephrons

Conduction of feedback-mediated signal in a computational model of coupled nephrons

Conduction of feedback-mediated signal in a computational model of coupled nephrons

Conduction of feedback-mediated signal in a computational model of coupled nephrons
The nephron in the kidney regulates its fluid flow by several autoregulatory mechanisms. Two primary mechanisms are the myogenic response and the tubuloglomerular feedback (TGF). The myogenic response is a property of the pre-glomerular vasculature in which a rise in intravascular pressure elicits vasoconstriction that generates a compensatory increase in vascular resistance. TGF is a negative feedback response that balances glomerular filtration with tubular reabsorptive capacity. While each nephron has its own autoregulatory response, the responses of the kidney's many nephrons do not act autonomously but are instead coupled through the pre-glomerular vasculature. To better understand the conduction of these signals along the pre-glomerular arterioles and the impacts of internephron coupling on nephron flow dynamics, we developed a mathematical model of renal haemodynamics of two neighbouring nephrons that are coupled in that their afferent arterioles arise from a common cortical radial artery. Simulations were conducted to estimate internephron coupling strength, determine its dependence on vascular properties and to investigate the effect of coupling on TGF-mediated flow oscillations. Simulation results suggest that reduced gap-junctional conductances may yield stronger internephron TGF coupling and highly irregular TGF-mediated oscillations in nephron dynamics, both of which experimentally have been associated with hypertensive rats.
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