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尿素转运体被鉴定为新型利尿药物靶点。

Urea Transporters Identified as Novel Diuretic Drug Targets.

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, China.

出版信息

Curr Drug Targets. 2020;21(3):279-287. doi: 10.2174/1389450120666191129101915.

Abstract

BACKGROUND

Urea Transporters are a family of membrane channel proteins that facilitate the passive transport of urea across the plasma membrane. UTs are divided into two subgroups, UT-A and UT-B. UT-As are primarily located in renal tubule epithelia and UT-Bs are highly expressed in renal descending vasa recta and extrarenal multiple tissues. Various urea transporter knockout mice exhibit low urine concentrating ability, which suggests that UTs are novel diuretic targets. With highthroughput screening of small molecule drug-like compound libraries, various potent UT inhibitors with IC50 at nanomolar level were identified. Furthermore, selective UT inhibitors exhibit diuretic activity without disturbing electrolyte and metabolism balance, which confirms the potential of UTs as diuretic targets and UT inhibitors as novel diuretics that do not cause electrolyte imbalance.

OBJECTIVE

This review article summarizes the identification and validation of urea transporter as a potential diuretic target and the discovery of small molecule UT inhibitors as a novel type of diuretics.

CONCLUSION

UTs are a potential diuretic target. UT inhibitors play significant diuresis and can be developed to diuretics without disturbing electrolyte balance.

摘要

背景

尿素转运蛋白是一类膜通道蛋白,可促进尿素穿过质膜的被动转运。UT 分为两个亚群,UT-A 和 UT-B。UT-A 主要位于肾小管上皮细胞,UT-B 则在肾降支细段和肾外的多种组织中高度表达。各种尿素转运体敲除小鼠表现出低尿浓缩能力,这表明 UT 是新型利尿靶点。通过高通量筛选小分子类药物化合物库,鉴定出各种具有纳摩尔级 IC50 的强效 UT 抑制剂。此外,选择性 UT 抑制剂具有利尿活性而不干扰电解质和代谢平衡,这证实了 UT 作为利尿靶点和 UT 抑制剂作为新型不引起电解质失衡的利尿剂的潜力。

目的

本文综述了尿素转运蛋白作为潜在利尿靶点的鉴定和验证,以及小分子 UT 抑制剂作为新型利尿剂的发现。

结论

UT 是一个潜在的利尿靶点。UT 抑制剂具有显著的利尿作用,且不会干扰电解质平衡,可开发为新型利尿剂。

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