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肾素-血管紧张素系统在控制钠排泄和动脉血压中的作用。

Role of the renin-angiotensin system in control of sodium excretion and arterial pressure.

作者信息

Hall J E, Guyton A C, Mizelle H L

机构信息

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

出版信息

Acta Physiol Scand Suppl. 1990;591:48-62.

PMID:2220409
Abstract

The RAS is part of an extremely powerful feedback system for long-term control of arterial pressure and volume homeostasis as illustrated in Figure 4. Disturbances that tend to lower blood pressure such as heart failure, cirrhosis, and peripheral vasodilation, cause sodium and water retention until blood pressure returns to normal due in large part to the combined actions of ANGII and reduced renal perfusion pressure. In response to disturbances such as high sodium intake, suppression of ANGII greatly amplifies the effectiveness of the basic pressure natriuresis and diuresis mechanism, thereby preventing large increases in body fluid volumes and blood pressure. In circumstances in which the RAS is inappropriately activated, the sodium-water retaining effects of ANGII necessitate increased blood pressure to maintain sodium and water balance via pressure natriuresis. The sodium retaining actions of the RAS are mediated by intrarenal as well as extrarenal mechanisms. The intrarenal actions of ANGII include a direct effect on tubular sodium transport as well as a potent constrictor action on efferent arterioles which increases tubular reabsorption by altering peritubular capillary physical forces. The constrictor action of ANGII on efferent arterioles also plays an important role in stabilizing GFR and therefore in preventing fluctuations in excretion of metabolic waste products that depend upon a high GFR for excretion. ANGII is known to stimulate proximal reabsorption, but the effects on more distal tubular segments have not been completely elucidated. The primary extra-known to stimulate proximal reabsorption, but the effects on more distal tubular segments have not been completely elucidated. The primary extra-renal effect of ANGII which influences sodium excretion is stimulation of aldosterone secretion. Current evidence, however, suggests that the various intrarenal actions of ANGII are quantitatively more important in causing sodium retention than those mediated by changes in aldosterone secretion. However, the combined intrarenal and extrarenal actions of ANGII on sodium reabsorption provide the body with one of its most potent feedback systems for long-term regulation of body fluid volumes and arterial pressure.

摘要

如图4所示,肾素-血管紧张素系统(RAS)是动脉血压和容量稳态长期控制的一个极其强大的反馈系统的一部分。诸如心力衰竭、肝硬化和外周血管舒张等倾向于降低血压的干扰,会导致钠和水潴留,直到血压恢复正常,这在很大程度上归因于血管紧张素II(ANGII)和肾灌注压降低的联合作用。响应于高钠摄入等干扰,ANGII的抑制极大地增强了基本压力利钠和利尿机制的有效性,从而防止体液量和血压大幅升高。在RAS被不适当激活的情况下,ANGII的保钠保水作用需要升高血压,以通过压力利钠作用维持钠和水平衡。RAS的保钠作用由肾内和肾外机制介导。ANGII的肾内作用包括对肾小管钠转运的直接作用以及对出球小动脉的强力收缩作用,后者通过改变肾小管周围毛细血管的物理力来增加肾小管重吸收。ANGII对出球小动脉的收缩作用在稳定肾小球滤过率(GFR)方面也起重要作用,因此在防止依赖高GFR排泄的代谢废物排泄波动方面也起重要作用。已知ANGII刺激近端重吸收,但对更远端肾小管节段的影响尚未完全阐明。ANGII影响钠排泄的主要肾外作用是刺激醛固酮分泌。然而,目前的证据表明,ANGII的各种肾内作用在导致钠潴留方面在数量上比由醛固酮分泌变化介导的作用更重要。然而,ANGII对钠重吸收的肾内和肾外联合作用为身体提供了其用于长期调节体液量和动脉血压的最强大反馈系统之一。

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