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管腔内血管紧张素II的浓度与作用

Concentrations and actions of intraluminal angiotensin II.

作者信息

Navar L G, Harrison-Bernard L M, Wang C T, Cervenka L, Mitchell K D

机构信息

Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.

出版信息

J Am Soc Nephrol. 1999 Jan;10 Suppl 11:S189-95.

PMID:9892162
Abstract

Although the presence of angiotensin II (AngII) receptors on the luminal membranes of proximal tubule cells has been recognized for many years, recent immunohistochemical studies using polyclonal and monoclonal antibodies to the AngII type 1 (AT1) receptor have demonstrated an abundance of the AT1 receptor not only on the luminal surface of proximal tubule cells but also on the luminal surfaces of distal nephron segments. An important role for these receptors in the regulation of tubular transport mechanisms was indicated by the recent findings of remarkably high proximal intratubular concentrations of AngII (in the range of 10(-9) to 10(-8) M). The high intratubular concentrations of AngII, as well as angiotensin I and angiotensinogen, are much greater than can be explained on the basis of delivery via glomerular filtration. When coupled with the findings demonstrating the presence of angiotensinogen and angiotensinogen mRNA in proximal tubule cells, the data indicate that AngII or precursors of AngII are secreted directly into the proximal tubule lumen by the epithelial cells. Although the mechanisms responsible for the regulation of intratubular AngII concentrations remain to be determined, micropuncture studies have provided direct evidence that activation of intraluminal AT1 receptors by AngII exerts a substantial stimulatory influence on sodium and bicarbonate transport by both proximal and distal tubules. Collectively, these data provide support for the hypothesis that activation of luminal AT1 receptors by AngII present in the tubular fluid contributes importantly to regulation of the tubular reabsorption rate.

摘要

尽管多年来人们已经认识到近端小管细胞腔面膜上存在血管紧张素II(AngII)受体,但最近使用针对血管紧张素II 1型(AT1)受体的多克隆和单克隆抗体进行的免疫组织化学研究表明,AT1受体不仅大量存在于近端小管细胞的腔表面,也存在于远端肾单位节段的腔表面。最近的研究发现近端小管内AngII浓度极高(在10^(-9)至10^(-8) M范围内),这表明这些受体在调节肾小管转运机制中起着重要作用。肾小管内AngII以及血管紧张素I和血管紧张素原的高浓度,远远超过基于肾小球滤过输送所能解释的范围。当与证明近端小管细胞中存在血管紧张素原和血管紧张素原mRNA的研究结果相结合时,数据表明AngII或AngII的前体由上皮细胞直接分泌到近端小管腔中。尽管负责调节肾小管内AngII浓度的机制仍有待确定,但微穿刺研究提供了直接证据,即AngII激活管腔内AT1受体对近端和远端小管的钠和碳酸氢盐转运具有显著的刺激作用。总体而言,这些数据支持以下假设:管腔液中存在的AngII激活管腔AT1受体对肾小管重吸收率的调节起着重要作用。

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