Literature DB >> 18449536

Two-pore potassium channels in the cardiovascular system.

Alison Gurney1, Boris Manoury.   

Abstract

Two-pore domain (K(2P)) channels emerged about a decade ago and since then have been an expanding area of interest. This is because their biophysical and pharmacological properties make them good candidates to support background potassium currents and membrane potential in many cell types. There is clear evidence for TREK-1 and TASK-1 in the heart and these channels are likely to regulate cardiac action potential duration through their regulation by stretch, polyunsaturated fatty acids, pH, and neurotransmitters. TREK-1 may also have a critical role in mediating the vasodilator response of resistance arteries to polyunsaturated fatty acids, thus contributing to their protective effect on the cardiovascular system. TASK-1, on the other hand, is a strong candidate for a role in hypoxic vasoconstriction of pulmonary arteries. Many other members of the K(2P) channel family have been identified in the cardiovascular system, although their functional roles are still to be demonstrated. This review provides an up to date summary of what is known about the involvement of members of the K(2P) channel family in cells of the heart and arterial circulation. Our knowledge of their roles will improve with the rapidly increasing interest in them and as new selective pharmacological tools emerge. As their physiological roles emerge, the K(2P) family of potassium channels may offer promising therapeutic solutions to target cardiovascular diseases.

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Year:  2008        PMID: 18449536     DOI: 10.1007/s00249-008-0326-8

Source DB:  PubMed          Journal:  Eur Biophys J        ISSN: 0175-7571            Impact factor:   1.733


  124 in total

1.  Mechano- or acid stimulation, two interactive modes of activation of the TREK-1 potassium channel.

Authors:  F Maingret; A J Patel; F Lesage; M Lazdunski; E Honoré
Journal:  J Biol Chem       Date:  1999-09-17       Impact factor: 5.157

2.  The acid-sensitive potassium channel TASK-1 in rat cardiac muscle.

Authors:  Caroline Putzke; Konstantin Wemhöner; Frank B Sachse; Susanne Rinné; Günter Schlichthörl; Xian Tao Li; Lucas Jaé; Ines Eckhardt; Erhard Wischmeyer; Hinnerk Wulf; Regina Preisig-Müller; Jürgen Daut; Niels Decher
Journal:  Cardiovasc Res       Date:  2007-02-28       Impact factor: 10.787

Review 3.  The role of twin pore domain and other K+ channels in hypoxic pulmonary vasoconstriction.

Authors:  Alison M Gurney; Shreena Joshi
Journal:  Novartis Found Symp       Date:  2006

4.  Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel.

Authors:  Y Kubo; E Reuveny; P A Slesinger; Y N Jan; L Y Jan
Journal:  Nature       Date:  1993-08-26       Impact factor: 49.962

5.  An open rectifier potassium channel with two pore domains in tandem cloned from rat cerebellum.

Authors:  D Leonoudakis; A T Gray; B D Winegar; C H Kindler; M Harada; D M Taylor; R A Chavez; J R Forsayeth; C S Yost
Journal:  J Neurosci       Date:  1998-02-01       Impact factor: 6.167

6.  PIP2 hydrolysis underlies agonist-induced inhibition and regulates voltage gating of two-pore domain K+ channels.

Authors:  Coeli M B Lopes; Tibor Rohács; Gábor Czirják; Tamás Balla; Péter Enyedi; Diomedes E Logothetis
Journal:  J Physiol       Date:  2005-01-27       Impact factor: 5.182

7.  Identification of epoxyeicosatrienoic acids as endothelium-derived hyperpolarizing factors.

Authors:  W B Campbell; D Gebremedhin; P F Pratt; D R Harder
Journal:  Circ Res       Date:  1996-03       Impact factor: 17.367

8.  Polyunsaturated fatty acids are cerebral vasodilators via the TREK-1 potassium channel.

Authors:  Nicolas Blondeau; Olivier Pétrault; Stella Manta; Valérie Giordanengo; Pierre Gounon; Régis Bordet; Michel Lazdunski; Catherine Heurteaux
Journal:  Circ Res       Date:  2007-06-07       Impact factor: 17.367

9.  TASK channel deletion in mice causes primary hyperaldosteronism.

Authors:  Lucinda A Davies; Changlong Hu; Nick A Guagliardo; Neil Sen; Xiangdong Chen; Edmund M Talley; Robert M Carey; Douglas A Bayliss; Paula Q Barrett
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-04       Impact factor: 11.205

10.  A mechanosensitive K+ channel in heart cells. Activation by arachidonic acid.

Authors:  D Kim
Journal:  J Gen Physiol       Date:  1992-12       Impact factor: 4.086

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  52 in total

1.  TASK1 (K(2P)3.1) K(+) channel inhibition by endothelin-1 is mediated through Rho kinase-dependent phosphorylation.

Authors:  C Seyler; E Duthil-Straub; E Zitron; J Gierten; E P Scholz; R H A Fink; C A Karle; R Becker; H A Katus; D Thomas
Journal:  Br J Pharmacol       Date:  2012-03       Impact factor: 8.739

Review 2.  Gating the pore of potassium leak channels.

Authors:  Asi Cohen; Yuval Ben-Abu; Noam Zilberberg
Journal:  Eur Biophys J       Date:  2009-04-29       Impact factor: 1.733

3.  Discrete change in volatile anesthetic sensitivity in mice with inactivated tandem pore potassium ion channel TRESK.

Authors:  Yun Jeong Chae; Jianan Zhang; Paul Au; Marta Sabbadini; Guo-Xi Xie; C Spencer Yost
Journal:  Anesthesiology       Date:  2010-12       Impact factor: 7.892

Review 4.  Altered and dynamic ion selectivity of K+ channels in cell development and excitability.

Authors:  Haijun Chen; Franck C Chatelain; Florian Lesage
Journal:  Trends Pharmacol Sci       Date:  2014-07-09       Impact factor: 14.819

5.  Reduced sialylation impacts ventricular repolarization by modulating specific K+ channel isoforms distinctly.

Authors:  Andrew R Ednie; Eric S Bennett
Journal:  J Biol Chem       Date:  2014-12-18       Impact factor: 5.157

Review 6.  Ion Channels in the Heart.

Authors:  Daniel C Bartos; Eleonora Grandi; Crystal M Ripplinger
Journal:  Compr Physiol       Date:  2015-07-01       Impact factor: 9.090

Review 7.  Much more than a leak: structure and function of K₂p-channels.

Authors:  Vijay Renigunta; Günter Schlichthörl; Jürgen Daut
Journal:  Pflugers Arch       Date:  2015-03-21       Impact factor: 3.657

8.  K2P channel gating mechanisms revealed by structures of TREK-2 and a complex with Prozac.

Authors:  Yin Yao Dong; Ashley C W Pike; Alexandra Mackenzie; Conor McClenaghan; Prafulla Aryal; Liang Dong; Andrew Quigley; Mariana Grieben; Solenne Goubin; Shubhashish Mukhopadhyay; Gian Filippo Ruda; Michael V Clausen; Lishuang Cao; Paul E Brennan; Nicola A Burgess-Brown; Mark S P Sansom; Stephen J Tucker; Elisabeth P Carpenter
Journal:  Science       Date:  2015-03-13       Impact factor: 47.728

9.  Ability to induce atrial fibrillation in the peri-operative period is associated with phosphorylation-dependent inhibition of TWIK protein-related acid-sensitive potassium channel 1 (TASK-1).

Authors:  Erin Harleton; Alessandra Besana; George M Comas; Peter Danilo; Tove S Rosen; Michael Argenziano; Michael R Rosen; Richard B Robinson; Steven J Feinmark
Journal:  J Biol Chem       Date:  2012-12-10       Impact factor: 5.157

Review 10.  Emerging roles for two-pore-domain potassium channels and their potential therapeutic impact.

Authors:  Douglas A Bayliss; Paula Q Barrett
Journal:  Trends Pharmacol Sci       Date:  2008-09-25       Impact factor: 14.819

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