1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Pharmacologic TWIK‐Related Acid‐Sensitive K+ Channel (TASK‐1) Potassium Channel Inhibitor A293 Facilitates Acute Cardioversion of Paroxysmal Atrial Fibrillation in a Porcine Large Animal Model

      research-article
      , MD 1 , 2 , 3 , , BSc 1 , 3 , , MD 2 , 4 , , MD 1 , 3 , , MSc 1 , 2 , 3 , , BSc 1 , 3 , , MSc 5 , 6 , , MSc 7 , , PhD 7 , , MD 8 , , MD 9 , , MD 8 , , MD 1 , 2 , 3 , , MD 2 , 4 , , PhD 5 , 6 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 ,
      Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
      John Wiley and Sons Inc.
      A293, antiarrhythmic pharmacotherapy, atrial fibrillation, cardioversion, K2P3.1, TASK‐1, Atrial Fibrillation, Electrophysiology, Animal Models of Human Disease, Ion Channels/Membrane Transport

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          The tandem of P domains in a weak inward rectifying K+ channel (TWIK)‐related acid‐sensitive K + channel (TASK‐1; hK 2P3.1) two‐pore–domain potassium channel was recently shown to regulate the atrial action potential duration. In the human heart, TASK‐1 channels are specifically expressed in the atria. Furthermore, upregulation of atrial TASK‐1 currents was described in patients suffering from atrial fibrillation ( AF). We therefore hypothesized that TASK‐1 channels represent an ideal target for antiarrhythmic therapy of AF. In the present study, we tested the antiarrhythmic effects of the high‐affinity TASK‐1 inhibitor A293 on cardioversion in a porcine model of paroxysmal AF.

          Methods and Results

          Heterologously expressed human and porcine TASK‐1 channels are blocked by A293 to a similar extent. Patch clamp measurements from isolated human and porcine atrial cardiomyocytes showed comparable TASK‐1 currents. Computational modeling was used to investigate the conditions under which A293 would be antiarrhythmic. German landrace pigs underwent electrophysiological studies under general anesthesia. Paroxysmal AF was induced by right atrial burst stimulation. After induction of AF episodes, intravenous administration of A293 restored sinus rhythm within cardioversion times of 177±63 seconds. Intravenous administration of A293 resulted in significant prolongation of the atrial effective refractory period, measured at cycle lengths of 300, 400 and 500 ms, whereas the surface ECG parameters and the ventricular effective refractory period lengths remained unchanged.

          Conclusions

          Pharmacological inhibition of atrial TASK‐1 currents exerts antiarrhythmic effects in vivo as well as in silico , resulting in acute cardioversion of paroxysmal AF. Taken together, these experiments indicate the therapeutic potential of A293 for AF treatment.

          Related collections

          Most cited references44

          • Record: found
          • Abstract: found
          • Article: not found

          AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading.

          AutoDock Vina, a new program for molecular docking and virtual screening, is presented. AutoDock Vina achieves an approximately two orders of magnitude speed-up compared with the molecular docking software previously developed in our lab (AutoDock 4), while also significantly improving the accuracy of the binding mode predictions, judging by our tests on the training set used in AutoDock 4 development. Further speed-up is achieved from parallelism, by using multithreading on multicore machines. AutoDock Vina automatically calculates the grid maps and clusters the results in a way transparent to the user. Copyright 2009 Wiley Periodicals, Inc.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility.

            We describe the testing and release of AutoDock4 and the accompanying graphical user interface AutoDockTools. AutoDock4 incorporates limited flexibility in the receptor. Several tests are reported here, including a redocking experiment with 188 diverse ligand-protein complexes and a cross-docking experiment using flexible sidechains in 87 HIV protease complexes. We also report its utility in analysis of covalently bound ligands, using both a grid-based docking method and a modification of the flexible sidechain technique. (c) 2009 Wiley Periodicals, Inc.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              The SWISS-MODEL Repository and associated resources

              SWISS-MODEL Repository (http://swissmodel.expasy.org/repository/) is a database of 3D protein structure models generated by the SWISS-MODEL homology-modelling pipeline. The aim of the SWISS-MODEL Repository is to provide access to an up-to-date collection of annotated 3D protein models generated by automated homology modelling for all sequences in Swiss-Prot and for relevant models organisms. Regular updates ensure that target coverage is complete, that models are built using the most recent sequence and template structure databases, and that improvements in the underlying modelling pipeline are fully utilised. As of September 2008, the database contains 3.4 million entries for 2.7 million different protein sequences from the UniProt database. SWISS-MODEL Repository allows the users to assess the quality of the models in the database, search for alternative template structures, and to build models interactively via SWISS-MODEL Workspace (http://swissmodel.expasy.org/workspace/). Annotation of models with functional information and cross-linking with other databases such as the Protein Model Portal (http://www.proteinmodelportal.org) of the PSI Structural Genomics Knowledge Base facilitates the navigation between protein sequence and structure resources.
                Bookmark

                Author and article information

                Contributors
                constanze.schmidt@med.uni-heidelberg.de
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                09 May 2020
                18 May 2020
                : 9
                : 10 ( doiID: 10.1002/jah3.v9.10 )
                : e015751
                Affiliations
                [ 1 ] Department of Cardiology University of Heidelberg Germany
                [ 2 ] DZHK (German Center for Cardiovascular Research) partner site Heidelberg /Mannheim University of Heidelberg Germany
                [ 3 ] HCR Heidelberg Center for Heart Rhythm Disorders University of Heidelberg Germany
                [ 4 ] First Department of Medicine University Medical Center Mannheim Germany
                [ 5 ] Institute for Experimental Cardiovascular Medicine University Heart Center Freiburg Bad Krozingen Germany
                [ 6 ] Medical Center University of Freiburg, and Faculty of Medicine University of Freiburg Germany
                [ 7 ] Institute of Biomedical Engineering Karlsruhe Institute of Technology (KIT) Karlsruhe Germany
                [ 8 ] Department of Cardiac Surgery University Hospital Heidelberg Germany
                [ 9 ] Department of Cardiac Surgery University Hospital Essen Germany
                Author notes
                [*] [* ]Correspondence to: Constanze Schmidt, MD, FESC, SOT, Department of Cardiology, Medical University Hospital Heidelberg, Im Neuenheimer Feld 410, D‐69120 Heidelberg, Germany. E‐mail: constanze.schmidt@ 123456med.uni-heidelberg.de
                Article
                JAH35091
                10.1161/JAHA.119.015751
                7660874
                32390491
                82c5816a-e5b1-490f-905b-692ba33c03d4
                © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 23 December 2019
                : 03 April 2020
                Page count
                Figures: 6, Tables: 0, Pages: 16, Words: 9388
                Funding
                Funded by: University of Heidelberg , open-funder-registry 10.13039/501100001661;
                Funded by: Faculty of Medicine , open-funder-registry 10.13039/501100010794;
                Funded by: German Center for Cardiovascular Research
                Funded by: German Cardiac Society , open-funder-registry 10.13039/501100010578;
                Funded by: German Heart Foundation/German Foundation of Heart Research
                Funded by: Ministry of Science, Research
                Funded by: Arts Baden‐Wuerttemberg
                Funded by: Joachim‐Herz Foundation
                Funded by: German Research Foundation , open-funder-registry 10.13039/501100001659;
                Categories
                Original Research
                Original Research
                Arrhythmia and Electrophysiology
                Custom metadata
                2.0
                18 May 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.2 mode:remove_FC converted:06.10.2020

                Cardiovascular Medicine
                a293,antiarrhythmic pharmacotherapy,atrial fibrillation,cardioversion,k2p3.1,task‐1,electrophysiology,animal models of human disease,ion channels/membrane transport

                Comments

                Comment on this article