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本文引用的文献

1
Beneficial Effects of High Potassium: Contribution of Renal Basolateral K Channels.高钾的有益作用:肾基底外侧钾通道的贡献
Hypertension. 2018 Jun;71(6):1015-1022. doi: 10.1161/HYPERTENSIONAHA.118.10267. Epub 2018 Apr 30.
2
Kir4.1-Dependent Astrocyte-Fast Motor Neuron Interactions Are Required for Peak Strength.Kir4.1 依赖性星形胶质细胞-快速运动神经元相互作用是峰值强度所必需的。
Neuron. 2018 Apr 18;98(2):306-319.e7. doi: 10.1016/j.neuron.2018.03.010. Epub 2018 Apr 5.
3
Astrocytic Kir4.1 channels and gap junctions account for spontaneous epileptic seizure.星形胶质细胞 Kir4.1 通道和缝隙连接导致自发性癫痫发作。
PLoS Comput Biol. 2018 Mar 28;14(3):e1005877. doi: 10.1371/journal.pcbi.1005877. eCollection 2018 Mar.
4
Role of ATR (Angiotensin Type 2 Receptor) in Maintaining Sodium-Potassium Balance.血管紧张素2型受体(ATR)在维持钠钾平衡中的作用。
Hypertension. 2018 Apr;71(4):563-565. doi: 10.1161/HYPERTENSIONAHA.117.10552. Epub 2018 Feb 26.
5
AT2R (Angiotensin II Type 2 Receptor)-Mediated Regulation of NCC (Na-Cl Cotransporter) and Renal K Excretion Depends on the K Channel, Kir4.1.血管紧张素 II 型受体(AT2R)通过调节 NCC(钠-氯共转运体)和肾脏钾排泄,这一过程依赖于钾通道 Kir4.1。
Hypertension. 2018 Apr;71(4):622-630. doi: 10.1161/HYPERTENSIONAHA.117.10471. Epub 2018 Feb 26.
6
Astroglial Kir4.1 in the lateral habenula drives neuronal bursts in depression.外侧缰核星形胶质细胞 Kir4.1 驱动抑郁中的神经元爆发。
Nature. 2018 Feb 14;554(7692):323-327. doi: 10.1038/nature25752.
7
Inhibition of Inwardly Rectifying Potassium (Kir) 4.1 Channels Facilitates Brain-Derived Neurotrophic Factor (BDNF) Expression in Astrocytes.内向整流钾通道(Kir)4.1的抑制促进星形胶质细胞中脑源性神经营养因子(BDNF)的表达。
Front Mol Neurosci. 2017 Dec 7;10:408. doi: 10.3389/fnmol.2017.00408. eCollection 2017.
8
Potassium intake modulates the thiazide-sensitive sodium-chloride cotransporter (NCC) activity via the Kir4.1 potassium channel.钾的摄入通过 Kir4.1 钾通道调节噻嗪类敏感的钠-氯共转运体(NCC)活性。
Kidney Int. 2018 Apr;93(4):893-902. doi: 10.1016/j.kint.2017.10.023. Epub 2018 Jan 6.
9
Dietary K and Cl independently regulate basolateral conductance in principal and intercalated cells of the collecting duct.膳食 K 和 Cl 分别独立调节集合管主细胞和闰细胞的基底外侧电导。
Pflugers Arch. 2018 Feb;470(2):339-353. doi: 10.1007/s00424-017-2084-x. Epub 2017 Nov 13.
10
Transcriptomes of major renal collecting duct cell types in mouse identified by single-cell RNA-seq.单细胞 RNA-seq 鉴定的小鼠主要肾集合管细胞类型的转录组。
Proc Natl Acad Sci U S A. 2017 Nov 14;114(46):E9989-E9998. doi: 10.1073/pnas.1710964114. Epub 2017 Oct 31.

远曲小管基底外侧钾通道:调节的细胞和分子机制。

Distal tubule basolateral potassium channels: cellular and molecular mechanisms of regulation.

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin.

Department of Integrative Biology and Pharmacology, University of Texas Health Science Center, Houston, Texas, USA.

出版信息

Curr Opin Nephrol Hypertens. 2018 Sep;27(5):373-378. doi: 10.1097/MNH.0000000000000437.

DOI:10.1097/MNH.0000000000000437
PMID:29894319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6217967/
Abstract

PURPOSE OF REVIEW

Multiple clinical and translational evidence support benefits of high potassium diet; however, there many uncertainties underlying the molecular and cellular mechanisms determining effects of dietary potassium. Kir4.1 and Kir5.1 proteins form a functional heteromer (Kir4.1/Kir5.1), which is the primary inwardly rectifying potassium channel on the basolateral membrane of both distal convoluted tubule (DCT) and the collecting duct principal cells. The purpose of this mini-review is to summarize latest advances in our understanding of the evolution, physiological relevance and mechanisms controlling these channels.

RECENT FINDINGS

Kir4.1 and Kir5.1 channels play a critical role in determining electrolyte homeostasis in the kidney and blood pressure, respectively. It was reported that Kir4.1/Kir5.1 serves as potassium sensors in the distal nephron responding to variations in dietary intake and hormonal stimuli. Global and kidney specific knockouts of either channel resulted in hypokalemia and severe cardiorenal phenotypes. Furthermore, knock out of Kir5.1 in Dahl salt-sensitive rat background revealed the crucial role of the Kir4.1/Kir5.1 channel in salt-induced hypertension.

SUMMARY

Here, we focus on reviewing novel experimental evidence of the physiological function, expression and hormonal regulation of renal basolateral inwardly rectifying potassium channels. Further investigation of molecular and cellular mechanisms controlling Kir4.1 and Kir4.1/Kir5.1-mediating pathways and development of specific compounds targeting these channels function is essential for proper control of electrolyte homeostasis and blood pressure.

摘要

目的综述

多项临床和转化证据支持高钾饮食的益处,但饮食钾确定作用的分子和细胞机制背后存在许多不确定性。Kir4.1 和 Kir5.1 蛋白形成功能性异聚体(Kir4.1/Kir5.1),这是远曲小管(DCT)和集合管主细胞基底外侧膜上的主要内向整流钾通道。本综述的目的是总结我们对这些通道的进化、生理相关性和调控机制的最新认识。

最新发现

Kir4.1 和 Kir5.1 通道分别在确定肾脏电解质稳态和血压方面起着关键作用。据报道,Kir4.1/Kir5.1 作为远曲小管中的钾传感器,对饮食摄入和激素刺激的变化作出反应。通道的全局和肾脏特异性敲除导致低钾血症和严重的心肾表型。此外,Dahl 盐敏感大鼠背景下的 Kir5.1 敲除揭示了 Kir4.1/Kir5.1 通道在盐诱导高血压中的关键作用。

总结

本文重点综述了肾脏基底外侧内向整流钾通道的生理功能、表达和激素调节的新实验证据。进一步研究调控 Kir4.1 和 Kir4.1/Kir5.1 介导途径的分子和细胞机制以及开发针对这些通道功能的特异性化合物对于电解质稳态和血压的适当控制至关重要。