• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

上皮钠通道及其调节因子在高血压中的作用。

Role of epithelial sodium channels and their regulators in hypertension.

机构信息

Division of Nephrology, Department of Medicine, University of California, San Francisco, California 94143, USA.

出版信息

J Biol Chem. 2010 Oct 1;285(40):30363-9. doi: 10.1074/jbc.R110.155341. Epub 2010 Jul 12.

DOI:10.1074/jbc.R110.155341
PMID:20624922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2945528/
Abstract

The kidney has a central role in the regulation of blood pressure, in large part through its role in the regulated reabsorption of filtered Na(+). Epithelial Na(+) channels (ENaCs) are expressed in the most distal segments of the nephron and are a target of volume regulatory hormones. A variety of factors regulate ENaC activity, including several aldosterone-induced proteins that are present within an ENaC regulatory complex. Proteases also regulate ENaC by cleaving the channel and releasing intrinsic inhibitory tracts. Polymorphisms or mutations within channel subunits or regulatory pathways that enhance channel activity may contribute to an increase in blood pressure in individuals with essential hypertension.

摘要

肾脏在调节血压方面起着核心作用,这在很大程度上是通过其在过滤的 Na(+)的调节重吸收中的作用来实现的。上皮钠通道 (ENaC) 在肾单位的最远端部分表达,是容量调节激素的靶标。多种因素调节 ENaC 的活性,包括存在于 ENaC 调节复合物中的几种醛固酮诱导蛋白。蛋白酶也通过切割通道和释放内在抑制片段来调节 ENaC。通道亚基或调节途径中的突变或多态性,如果增强了通道的活性,可能会导致原发性高血压患者的血压升高。

相似文献

1
Role of epithelial sodium channels and their regulators in hypertension.上皮钠通道及其调节因子在高血压中的作用。
J Biol Chem. 2010 Oct 1;285(40):30363-9. doi: 10.1074/jbc.R110.155341. Epub 2010 Jul 12.
2
The epithelial sodium channel and the control of sodium balance.上皮钠通道与钠平衡的调控
Biochim Biophys Acta. 2010 Dec;1802(12):1159-65. doi: 10.1016/j.bbadis.2010.06.014. Epub 2010 Jun 27.
3
In Liddle Syndrome, Epithelial Sodium Channel Is Hyperactive Mainly in the Early Part of the Aldosterone-Sensitive Distal Nephron.在利德尔综合征中,上皮钠通道主要在醛固酮敏感的远端肾单位早期过度活跃。
Hypertension. 2016 Jun;67(6):1256-62. doi: 10.1161/HYPERTENSIONAHA.115.07061.
4
Control of ENaC-mediated sodium reabsorption in the distal nephron by Bradykinin.缓激肽对远端肾单位中由ENaC介导的钠重吸收的调控
Vitam Horm. 2015;98:137-54. doi: 10.1016/bs.vh.2014.12.005. Epub 2015 Feb 14.
5
Direct regulation of ENaC by bradykinin in the distal nephron. Implications for renal sodium handling.远端肾单位中缓激肽对 ENaC 的直接调节。对肾脏钠处理的影响。
Curr Opin Nephrol Hypertens. 2014 Mar;23(2):122-9. doi: 10.1097/01.mnh.0000441053.81339.61.
6
Salt-dependent inhibition of epithelial Na+ channel-mediated sodium reabsorption in the aldosterone-sensitive distal nephron by bradykinin.血管紧张素通过抑制醛固酮敏感的远端肾单位上皮钠通道介导的钠重吸收。
Hypertension. 2012 Nov;60(5):1234-41. doi: 10.1161/HYPERTENSIONAHA.112.200469. Epub 2012 Oct 1.
7
[Regulation of kidney on potassium balance and its clinical significance].[肾脏对钾平衡的调节及其临床意义]
Sheng Li Xue Bao. 2023 Apr 25;75(2):216-230.
8
Epithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseases.上皮钠通道(ENaC)家族:系统发育、结构功能、组织分布及相关遗传性疾病
Gene. 2016 Apr 1;579(2):95-132. doi: 10.1016/j.gene.2015.12.061. Epub 2016 Jan 7.
9
Salt, sodium channels, and SGK1.盐、钠通道和血清糖皮质激素调节激酶1
J Clin Invest. 2007 Mar;117(3):592-5. doi: 10.1172/JCI31538.
10
Behavior of the renal kallikrein in spontaneously hypertensive rats: Influence of sexual hormones and aldosterone-sensitive distal nephron ion channels.自发性高血压大鼠中肾激肽释放酶的行为:性激素和醛固酮敏感性远端肾单位离子通道的影响。
Peptides. 2023 Feb;160:170925. doi: 10.1016/j.peptides.2022.170925. Epub 2022 Dec 19.

引用本文的文献

1
Multifaceted roles of Epac signaling in renal functions.Epac信号通路在肾功能中的多方面作用。
Biochem J. 2025 May 14;482(10):553-68. doi: 10.1042/BCJ20253103.
2
Structural insights into subunit-dependent functional regulation in epithelial sodium channels.上皮钠通道中依赖亚基的功能调节的结构见解
Structure. 2025 Feb 6;33(2):349-362.e4. doi: 10.1016/j.str.2024.11.013. Epub 2024 Dec 11.
3
Angiotensin II-Type-1a Receptor and Renal K + Wasting during Overnight Low-Na + Intake.过夜低钠摄入期间的血管紧张素II 1a型受体与肾脏钾离子流失
J Am Soc Nephrol. 2024 Nov 1;35(11):1478-1492. doi: 10.1681/ASN.0000000000000429. Epub 2024 Jun 24.
4
Proteolytic Activation of the Epithelial Sodium Channel (ENaC): Its Mechanisms and Implications.蛋白水解激活上皮钠离子通道(ENaC):其机制和意义。
Int J Mol Sci. 2023 Dec 16;24(24):17563. doi: 10.3390/ijms242417563.
5
Epithelial Transport in Disease: An Overview of Pathophysiology and Treatment.疾病中的上皮转运:病理生理学和治疗概述。
Cells. 2023 Oct 15;12(20):2455. doi: 10.3390/cells12202455.
6
Effects of a high-salt diet on MAP and expression levels of renal ENaCs and aquaporins in SHR.高盐饮食对 SHR 血压和肾脏 ENaC 和水通道蛋白表达水平的影响。
Exp Biol Med (Maywood). 2023 Oct;248(20):1768-1779. doi: 10.1177/15353702231198085. Epub 2023 Oct 12.
7
The epithelial sodium channel in inflammation and blood pressure modulation.炎症与血压调节中的上皮钠通道
Front Cardiovasc Med. 2023 Apr 12;10:1130148. doi: 10.3389/fcvm.2023.1130148. eCollection 2023.
8
Aldosterone: Renal Action and Physiological Effects.醛固酮:肾脏作用和生理效应。
Compr Physiol. 2023 Mar 30;13(2):4409-4491. doi: 10.1002/cphy.c190043.
9
Ubiquitination of NKCC2 by the cullin-RING E3 ubiquitin ligase family in the thick ascending limb of the loop of Henle.在 Henle 袢的升支粗段中,cullin-RING E3 泛素连接酶家族对 NKCC2 进行泛素化修饰。
Am J Physiol Renal Physiol. 2023 Mar 1;324(3):F315-F328. doi: 10.1152/ajprenal.00079.2022. Epub 2023 Feb 2.
10
Role of ion channels in the mechanism of proteinuria (Review).离子通道在蛋白尿机制中的作用(综述)
Exp Ther Med. 2022 Nov 24;25(1):27. doi: 10.3892/etm.2022.11726. eCollection 2023 Jan.

本文引用的文献

1
Regulation of the epithelial sodium channel (ENaC) by membrane trafficking.通过膜转运对上皮钠通道(ENaC)进行调控。
Biochim Biophys Acta. 2010 Dec;1802(12):1166-77. doi: 10.1016/j.bbadis.2010.03.010. Epub 2010 Mar 27.
2
mTOR complex-2 activates ENaC by phosphorylating SGK1.mTOR 复合物-2 通过磷酸化 SGK1 激活 ENaC。
J Am Soc Nephrol. 2010 May;21(5):811-8. doi: 10.1681/ASN.2009111168. Epub 2010 Mar 25.
3
A mutation of the epithelial sodium channel associated with atypical cystic fibrosis increases channel open probability and reduces Na+ self inhibition.与非典型囊性纤维化相关的上皮钠通道突变增加了通道的开放概率,并降低了 Na+ 的自我抑制。
J Physiol. 2010 Apr 15;588(Pt 8):1211-25. doi: 10.1113/jphysiol.2009.180224. Epub 2010 Mar 1.
4
Extracellular chloride regulates the epithelial sodium channel.细胞外氯离子调节上皮钠通道。
J Biol Chem. 2009 Oct 23;284(43):29320-5. doi: 10.1074/jbc.M109.046771. Epub 2009 Aug 27.
5
Aldosterone mediates activation of the thiazide-sensitive Na-Cl cotransporter through an SGK1 and WNK4 signaling pathway.醛固酮通过SGK1和WNK4信号通路介导噻嗪类敏感型钠氯共转运体的激活。
J Clin Invest. 2009 Sep;119(9):2601-12. doi: 10.1172/JCI38323. Epub 2009 Aug 17.
6
The physiological impact of the serum and glucocorticoid-inducible kinase SGK1.血清与糖皮质激素诱导激酶SGK1的生理影响。
Curr Opin Nephrol Hypertens. 2009 Sep;18(5):439-48. doi: 10.1097/MNH.0b013e32832f125e.
7
Expression and phosphorylation of the Na+-Cl- cotransporter NCC in vivo is regulated by dietary salt, potassium, and SGK1.体内钠氯共转运体NCC的表达和磷酸化受膳食盐、钾和血清糖皮质激素调节激酶1(SGK1)的调控。
Am J Physiol Renal Physiol. 2009 Sep;297(3):F704-12. doi: 10.1152/ajprenal.00030.2009. Epub 2009 Jul 1.
8
Cnksr3 is a direct mineralocorticoid receptor target gene and plays a key role in the regulation of the epithelial sodium channel.Cnksr3是盐皮质激素受体的直接靶基因,在上皮钠通道的调节中起关键作用。
FASEB J. 2009 Nov;23(11):3936-46. doi: 10.1096/fj.09-134759. Epub 2009 Jun 30.
9
Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease.囊性纤维化样疾病患者中阿米洛利敏感性上皮钠通道的突变
Hum Mutat. 2009 Jul;30(7):1093-103. doi: 10.1002/humu.21011.
10
ENaC at the cutting edge: regulation of epithelial sodium channels by proteases.处于前沿的上皮钠通道:蛋白酶对上皮钠通道的调控
J Biol Chem. 2009 Jul 31;284(31):20447-51. doi: 10.1074/jbc.R800083200. Epub 2009 Apr 28.