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心肾轴在动静脉瘘引起的降压反应中的突出作用:一种计算机分析。

Preeminent role of the cardiorenal axis in the antihypertensive response to an arteriovenous fistula: an in silico analysis.

机构信息

Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.

John D. Bower School of Population Health, University of Mississippi Medical Center, Jackson, Mississippi.

出版信息

Am J Physiol Heart Circ Physiol. 2019 Nov 1;317(5):H1002-H1012. doi: 10.1152/ajpheart.00354.2019. Epub 2019 Aug 30.

Abstract

Percutaneous creation of a small central arteriovenous (AV) fistula is currently being evaluated for the treatment of uncontrolled hypertension (HT). Although the mechanisms that contribute to the antihypertensive effects of the fistula are unclear, investigators have speculated that chronic blood pressure (BP) lowering may be due to ) reduced total peripheral resistance (TPR), ) increased secretion of atrial natriuretic peptide (ANP), and/or ) suppression of renal sympathetic nerve activity (RSNA). We used an established integrative mathematical model of human physiology to investigate these possibilities from baseline conditions that mimic sympathetic overactivity and impaired renal function in patients with resistant HT. After a small fistula was stimulated, there were sustained increases in cardiac output, atrial pressures, and plasma ANP concentration (3-fold), without suppression of RSNA; at 8 wk, BP was reduced 14 mmHg along with a 32% fall in TPR. In contrast, when this simulation was repeated while clamping ANP at baseline BP decreased only 4 mmHg, despite a comparable fall in TPR. Furthermore, when chronic resetting of atrial mechanoreceptors was prevented during the fistula, RSNA decreased 7%, and along with the same threefold increase in ANP, BP fell 19 mmHg. This exaggerated fall in BP occurred with a similar decrease in TPR when compared with the above simulations. These findings suggest that ANP, but not TPR, is a key determinant of long-term BP lowering after the creation of an AV fistula and support a contribution of suppressed RSNA if resetting of the atrial-renal reflex is truly incomplete. The mechanisms that contribute to the antihypertensive effects of a small arteriovenous (AV) fistula comparable to the size used by the ROX coupler currently in clinical trials are unclear and not readily testable in clinical or experimental studies. The integrative mathematical model of human physiology used in the current study provides a tool for understanding key causal relationships that account for blood pressure (BP) lowering and for testing competing hypotheses. The findings from the simulations suggest that after creation of a small AV fistula increased ANP secretion plays a critical role in mediating long-term reductions in BP. Measurement of natriuretic peptide levels in hypertensive patients implanted with the ROX coupler would provide one critical test of this hypothesis.

摘要

经皮创建小型中央动静脉(AV)瘘目前正在评估用于治疗不受控制的高血压(HT)。尽管导致瘘管降压作用的机制尚不清楚,但研究人员推测,慢性血压(BP)降低可能是由于)降低总外周阻力(TPR),)心房利钠肽(ANP)分泌增加,和/或)抑制肾交感神经活动(RSNA)。我们使用已建立的人体生理学综合数学模型,从模仿高血压患者交感神经过度活跃和肾功能受损的基线条件下,研究这些可能性。在刺激小瘘管后,心输出量、心房压力和血浆 ANP 浓度持续增加(增加 3 倍),而 RSNA 未被抑制;在 8 周时,BP 降低 14mmHg,同时 TPR 下降 32%。相比之下,当在基础 BP 下夹闭 ANP 时重复此模拟,尽管 TPR 下降幅度相当,但 BP 仅降低 4mmHg。此外,当在瘘管期间防止心房机械感受器的慢性重置时,RSNA 下降 7%,同时 ANP 增加 3 倍,BP 下降 19mmHg。与上述模拟相比,当心房-肾反射的重置确实不完全时,BP 的这种夸张下降伴随着 TPR 的相似下降。这些发现表明,ANP 而不是 TPR 是 AV 瘘形成后长期降低 BP 的关键决定因素,如果心房-肾反射的重置确实不完全,则支持 RSNA 抑制的贡献。目前正在临床试验中使用的 ROX 耦合器大小相似的小动静脉(AV)瘘的降压作用机制尚不清楚,并且在临床或实验研究中不易测试。当前研究中使用的人体生理学综合数学模型提供了一种工具,用于理解导致血压(BP)降低的关键因果关系,并测试竞争性假设。模拟结果表明,在创建小型 AV 瘘后,增加的 ANP 分泌在介导长期降低 BP 方面起着关键作用。在植入 ROX 耦合器的高血压患者中测量利钠肽水平将是对该假设的一个关键测试。

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