• 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

高血压和代谢紊乱期间血管平滑肌中电压门控钾通道的调节

Regulation of voltage-gated potassium channels in vascular smooth muscle during hypertension and metabolic disorders.

作者信息

Nieves-Cintrón Madeline, Syed Arsalan U, Nystoriak Matthew A, Navedo Manuel F

机构信息

Department of Pharmacology, University of California, Davis, CA, USA.

Diabetes and Obesity Center, Department of Medicine, University of Louisville, Louisville, KY, USA.

出版信息

Microcirculation. 2018 Jan;25(1). doi: 10.1111/micc.12423.

DOI:10.1111/micc.12423
PMID:29044853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5760350/
Abstract

Voltage-gated potassium (K ) channels are key regulators of vascular smooth muscle contractility and vascular tone, and thus have major influence on the microcirculation. K channels are important determinants of vascular smooth muscle membrane potential (E ). A number of K subunits are expressed in the plasma membrane of smooth muscle cells. Each subunit confers distinct kinetics and regulatory properties that allow for fine control of E to orchestrate vascular tone. Modifications in K subunit expression and/or channel activity can contribute to changes in vascular smooth muscle contractility in response to different stimuli and in diverse pathological conditions. Consistent with this, a number of studies suggest alterations in K subunit expression and/or function as underlying contributing mechanisms for small resistance artery dysfunction in pathologies such as hypertension and metabolic disorders, including diabetes. Here, we review our current knowledge on the effects of these pathologies on K channel expression and function in vascular smooth muscle cells, and the repercussions on (micro)vascular function.

摘要

电压门控钾(K⁺)通道是血管平滑肌收缩性和血管张力的关键调节因子,因此对微循环有重大影响。钾通道是血管平滑肌膜电位(Em)的重要决定因素。多种钾亚基在平滑肌细胞的质膜中表达。每个亚基都具有独特的动力学和调节特性,能够精细控制Em以协调血管张力。钾亚基表达和/或通道活性的改变可导致血管平滑肌收缩性在响应不同刺激和各种病理状况时发生变化。与此一致的是,多项研究表明,在诸如高血压和包括糖尿病在内的代谢紊乱等病理状况下,钾亚基表达和/或功能的改变是小阻力动脉功能障碍的潜在促成机制。在此,我们综述了目前关于这些病理状况对血管平滑肌细胞中钾通道表达和功能的影响以及对(微)血管功能的影响的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/cbe2427743d5/nihms913358f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/c13098606e0e/nihms913358f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/27de9a94fea3/nihms913358f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/cbe2427743d5/nihms913358f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/c13098606e0e/nihms913358f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/27de9a94fea3/nihms913358f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d95/5760350/cbe2427743d5/nihms913358f3.jpg

相似文献

1
Regulation of voltage-gated potassium channels in vascular smooth muscle during hypertension and metabolic disorders.高血压和代谢紊乱期间血管平滑肌中电压门控钾通道的调节
Microcirculation. 2018 Jan;25(1). doi: 10.1111/micc.12423.
2
K channels and the regulation of vascular smooth muscle tone.钾通道与血管平滑肌张力的调节
Microcirculation. 2018 Jan;25(1). doi: 10.1111/micc.12421.
3
Regulation of microvascular function by voltage-gated potassium channels: New tricks for an "ancient" dog.电压门控钾通道对微血管功能的调节:“老狗”的新把戏。
Microcirculation. 2018 Jan;25(1). doi: 10.1111/micc.12435.
4
Detection and implications of potassium channel alterations.钾通道改变的检测及其影响
Vascul Pharmacol. 2002 Jan;38(1):3-12. doi: 10.1016/s1537-1891(02)00121-0.
5
Molecular diversity of vascular potassium channel isoforms.血管钾通道亚型的分子多样性
Clin Exp Pharmacol Physiol. 2002 Apr;29(4):317-23. doi: 10.1046/j.1440-1681.2002.03651.x.
6
Molecular determinants of voltage-gated potassium currents in vascular smooth muscle.血管平滑肌中电压门控钾电流的分子决定因素
Cell Biochem Biophys. 2005;42(2):167-95. doi: 10.1385/CBB:42:2:167.
7
Molecular basis and function of voltage-gated K+ channels in pulmonary arterial smooth muscle cells.肺动脉平滑肌细胞中电压门控钾通道的分子基础与功能
Am J Physiol. 1998 Apr;274(4):L621-35. doi: 10.1152/ajplung.1998.274.4.L621.
8
Preferential expression and function of voltage-gated, O2-sensitive K+ channels in resistance pulmonary arteries explains regional heterogeneity in hypoxic pulmonary vasoconstriction: ionic diversity in smooth muscle cells.电压门控、氧敏感钾通道在肺阻力动脉中的优先表达及功能解释了缺氧性肺血管收缩中的区域异质性:平滑肌细胞中的离子多样性。
Circ Res. 2004 Aug 6;95(3):308-18. doi: 10.1161/01.RES.0000137173.42723.fb. Epub 2004 Jun 24.
9
Different Effects of Hypertension and Age on the Function of Large Conductance Calcium- and Voltage-Activated Potassium Channels in Human Mesentery Artery Smooth Muscle Cells.高血压和年龄对人肠系膜动脉平滑肌细胞中大电导钙激活钾通道和电压门控钾通道功能的不同影响。
J Am Heart Assoc. 2016 Sep 14;5(9):e003913. doi: 10.1161/JAHA.116.003913.
10
Blockade of voltage-gated K⁺ currents in rat mesenteric arterial smooth muscle cells by MK801.MK801对大鼠肠系膜动脉平滑肌细胞电压门控性钾离子电流的阻断作用
J Pharmacol Sci. 2015 Jan;127(1):92-102. doi: 10.1016/j.jphs.2014.11.005. Epub 2014 Nov 17.

引用本文的文献

1
Arterial Myocyte Pannexin 1 Channel Controls Vascular Reactivity in Diabetic Hyperglycemia.动脉心肌细胞泛连接蛋白1通道调控糖尿病高血糖状态下的血管反应性。
Circ Res. 2025 Jul 10. doi: 10.1161/CIRCRESAHA.125.326260.
2
Insulin resistance, Ca signaling alterations and vascular dysfunction in prediabetes and metabolic syndrome.糖尿病前期和代谢综合征中的胰岛素抵抗、钙信号改变与血管功能障碍。
Front Physiol. 2025 Jun 10;16:1535153. doi: 10.3389/fphys.2025.1535153. eCollection 2025.
3
The roles of melatonin and potassium channels in relaxation response to ang 1-7 in diabetic rat isolated aorta.

本文引用的文献

1
Predominant contribution of L-type Cav1.2 channel stimulation to impaired intracellular calcium and cerebral artery vasoconstriction in diabetic hyperglycemia.L 型 Cav1.2 通道刺激在糖尿病高血糖致细胞内钙异常和脑血管收缩中的主要贡献。
Channels (Austin). 2017 Jul 4;11(4):340-346. doi: 10.1080/19336950.2017.1293220. Epub 2017 Feb 10.
2
Role of renal vascular potassium channels in physiology and pathophysiology.肾脏血管钾通道在生理和病理生理学中的作用。
Acta Physiol (Oxf). 2017 Sep;221(1):14-31. doi: 10.1111/apha.12882. Epub 2017 Apr 25.
3
Heteromeric complexes of aldo-keto reductase auxiliary Kβ subunits (AKR6A) regulate sarcolemmal localization of K1.5 in coronary arterial myocytes.
褪黑素和钾通道在糖尿病大鼠离体主动脉对血管紧张素1-7舒张反应中的作用
Cytotechnology. 2025 Apr;77(2):55. doi: 10.1007/s10616-025-00720-y. Epub 2025 Feb 5.
4
Effect of Hydrogen Sulfide on Sympathoinhibition in Obese Pithed Rats and Participation of K Channel.硫化氢对肥胖去大脑大鼠交感神经抑制作用及钾通道的参与
Int J Hypertens. 2024 Nov 4;2024:5848352. doi: 10.1155/2024/5848352. eCollection 2024.
5
Blood pressure variability compromises vascular function in middle-aged mice.血压变异性损害中年小鼠的血管功能。
bioRxiv. 2024 Oct 24:2024.10.21.619509. doi: 10.1101/2024.10.21.619509.
6
Vascular Function and Ion Channels in Alzheimer's Disease.阿尔茨海默病中的血管功能和离子通道。
Microcirculation. 2024 Oct;31(7):e12881. doi: 10.1111/micc.12881. Epub 2024 Aug 27.
7
Effect of Type-2 Diabetes Mellitus on the Expression and Function of Smooth Muscle ATP-Sensitive Potassium Channels in Human Internal Mammary Artery Grafts.2型糖尿病对人乳内动脉移植物中平滑肌ATP敏感性钾通道表达及功能的影响。
Pharmaceuticals (Basel). 2024 Jul 1;17(7):857. doi: 10.3390/ph17070857.
8
Kv beta complex facilitates exercise-induced augmentation of myocardial perfusion and cardiac growth.Kvβ复合体促进运动诱导的心肌灌注增加和心脏生长。
Front Cardiovasc Med. 2024 Jun 24;11:1411354. doi: 10.3389/fcvm.2024.1411354. eCollection 2024.
9
Aberrant splicing of Ca1.2 calcium channel induced by decreased Rbfox1 enhances arterial constriction during diabetic hyperglycemia.在糖尿病高血糖期间,Rbfox1 减少引起的 Ca1.2 钙通道异常剪接增强了动脉收缩。
Cell Mol Life Sci. 2024 Apr 4;81(1):164. doi: 10.1007/s00018-024-05198-z.
10
Hypotensive and Vasorelaxant Effects of Sanguisorbae Radix Ethanol Extract in Spontaneously Hypertensive and Sprague Dawley Rats.地榆根乙醇提取物对自发性高血压和 Sprague Dawley 大鼠的降压和血管舒张作用。
Nutrients. 2023 Oct 24;15(21):4510. doi: 10.3390/nu15214510.
醛糖酮还原酶辅助Kβ亚基(AKR6A)的异源复合物调节冠状动脉心肌细胞中K1.5的肌膜定位。
Chem Biol Interact. 2017 Oct 1;276:210-217. doi: 10.1016/j.cbi.2017.03.011. Epub 2017 Mar 22.
4
Smooth Muscle Ion Channels and Regulation of Vascular Tone in Resistance Arteries and Arterioles.阻力动脉和微动脉中的平滑肌离子通道与血管张力调节
Compr Physiol. 2017 Mar 16;7(2):485-581. doi: 10.1002/cphy.c160011.
5
Ser1928 phosphorylation by PKA stimulates the L-type Ca2+ channel CaV1.2 and vasoconstriction during acute hyperglycemia and diabetes.蛋白激酶A介导的1928位丝氨酸磷酸化在急性高血糖和糖尿病期间可刺激L型钙通道CaV1.2并导致血管收缩。
Sci Signal. 2017 Jan 24;10(463):eaaf9647. doi: 10.1126/scisignal.aaf9647.
6
Synergistic interplay of Gβγ and phosphatidylinositol 4,5-bisphosphate dictates Kv7.4 channel activity.Gβγ与磷脂酰肌醇4,5-二磷酸的协同相互作用决定了Kv7.4通道的活性。
Pflugers Arch. 2017 Feb;469(2):213-223. doi: 10.1007/s00424-016-1916-4. Epub 2016 Dec 15.
7
Contribution of K1.5 Channel to Hydrogen Peroxide-Induced Human Arteriolar Dilation and Its Modulation by Coronary Artery Disease.K1.5通道对过氧化氢诱导的人小动脉舒张的作用及其受冠状动脉疾病的调节
Circ Res. 2017 Feb 17;120(4):658-669. doi: 10.1161/CIRCRESAHA.116.309491. Epub 2016 Nov 21.
8
Potassium channels in the heart: structure, function and regulation.心脏中的钾通道:结构、功能与调节
J Physiol. 2017 Apr 1;595(7):2209-2228. doi: 10.1113/JP272864. Epub 2016 Nov 13.
9
The Action of Smooth Muscle Cell Potassium Channels in the Pathology of Pulmonary Arterial Hypertension.平滑肌细胞钾通道在肺动脉高压病理过程中的作用
Pediatr Cardiol. 2017 Jan;38(1):1-14. doi: 10.1007/s00246-016-1491-7. Epub 2016 Nov 8.
10
Molecular and functional characterization of Kv 7 channels in penile arteries and corpus cavernosum of healthy and metabolic syndrome rats.健康大鼠和代谢综合征大鼠阴茎动脉及海绵体中Kv 7通道的分子与功能特性
Br J Pharmacol. 2016 May;173(9):1478-90. doi: 10.1111/bph.13444. Epub 2016 Feb 26.