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Cathepsin A Mediates Ventricular Remote Remodeling and Atrial Cardiomyopathy in Rats With Ventricular Ischemia/Reperfusion.
Hohl, Mathias; Erb, Katharina; Lang, Lisa; Ruf, Sven; Hübschle, Thomas; Dhein, Stefan; Linz, Wolfgang; Elliott, Adrian D; Sanders, Prashanthan; Zamyatkin, Olesja; Böhm, Michael; Schotten, Ulrich; Sadowski, Thorsten; Linz, Dominik.
Afiliación
  • Hohl M; Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.
  • Erb K; Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.
  • Lang L; Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.
  • Ruf S; Sanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
  • Hübschle T; Sanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
  • Dhein S; Herzzentrum Leipzig Abt. Herzchirurgie, Leipzig, Germany.
  • Linz W; Sanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
  • Elliott AD; Centre for Heart Rhythm Disorders, South Australian Health and Medical Research Institute, Royal Adelaide Hospital, University of Adelaide, Adelaide, Australia.
  • Sanders P; Centre for Heart Rhythm Disorders, South Australian Health and Medical Research Institute, Royal Adelaide Hospital, University of Adelaide, Adelaide, Australia.
  • Zamyatkin O; Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.
  • Böhm M; Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.
  • Schotten U; Department of Physiology, University of Maastricht, Maastricht, the Netherlands.
  • Sadowski T; Sanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
  • Linz D; Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.
JACC Basic Transl Sci ; 4(3): 332-344, 2019 Jun.
Article en En | MEDLINE | ID: mdl-31312757
ABSTRACT
After myocardial infarction, remote ventricular remodeling and atrial cardiomyopathy progress despite successful revascularization. In a rat model of ventricular ischemia/reperfusion, pharmacological inhibition of the protease activity of cathepsin A initiated at the time point of reperfusion prevented extracellular matrix remodeling in the atrium and the ventricle remote from the infarcted area. This scenario was associated with preservation of more viable ventricular myocardium and the prevention of an arrhythmogenic and functional substrate for atrial fibrillation. Remote ventricular extracellular matrix remodeling and atrial cardiomyopathy may represent a promising target for pharmacological atrial fibrillation upstream therapy following myocardial infarction.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: JACC Basic Transl Sci Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: JACC Basic Transl Sci Año: 2019 Tipo del documento: Article País de afiliación: Alemania