Biological heart rate reduction through genetic suppression of gαs protein in the sinoatrial node

• Verfasst von: Lugenbiel, Patrick [VerfasserIn]
• Verfasst von: Bauer, Alexander [VerfasserIn]
• Verfasst von: Kelemen, Kamilla [VerfasserIn]
• Verfasst von: Schweizer, Patrick Alexander [VerfasserIn]
• Verfasst von: Becker, Rüdiger [VerfasserIn]
• Verfasst von: Katus, Hugo [VerfasserIn]
• Verfasst von: Thomas, Dierk [VerfasserIn]
• Titel: Biological heart rate reduction through genetic suppression of gαs protein in the sinoatrial node
• Verf.angabe: Patrick Lugenbiel, Alexander Bauer, Kamilla Kelemen, Patrick A. Schweizer, Rüdiger Becker, Hugo A. Katus, Dierk Thomas
• Jahr: 2012
• Umfang: 10 S.
• Teil: volume:1
• Teil: year:2012
• Teil: number:2
• Teil: extent:10
• Fussnoten: Gesehen am 11.06.2018 ; Der Buchstabe s ist im Titel tiefergestellt
• Titel Quelle: Enthalten in: American Heart AssociationJournal of the American Heart Association
• Ort Quelle: New York, NY : Association, 2012
• Jahr Quelle: 2012
• Band/Heft Quelle: 1(2012,2) Artikel-Nummer e000372, 10 Seiten
• ISSN Quelle: 2047-9980
• DOI: doi:10.1161/JAHA.111.000372
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: electrophysiology
• Sach-SW: gene therapy
• Sach-SW: heart failure
• Sach-SW: heart rate
• Sach-SW: sinoatrial node
• K10plus-PPN: 1576233642

Abstract

Background Elevated heart rate represents an independent risk factor for cardiovascular outcome in patients with heart disease. In the sinoatrial node, rate increase is mediated by β1 adrenoceptor mediated activation of the Gαs pathway. We hypothesized that genetic inactivation of the stimulatory Gαs protein in the sinoatrial node would provide sinus rate control and would prevent inappropriate heart rate acceleration during β-adrenergic activation. Methods and Results Domestic pigs (n=10) were evenly assigned to receive either Ad-small interfering RNA (siRNA)-Gαs gene therapy to inactivate Gαs or adenovirus encoding for green fluorescent protein (Ad-GFP) as control. Adenoviruses were applied through virus injection into the sinoatrial node followed by epicardial electroporation, and heart rates were evaluated for 7 days. Genetic inhibition of Gαs protein significantly reduced mean heart rates on day 7 by 16.5% compared with control animals (110±8.8 vs 131±9.4 beats per minute; P<0.01). On β-adrenergic stimulation with isoproterenol, we observed a tendency toward diminished rate response in the Ad-siRNA-Gαs group (Ad-siRNA-Gαs, +79.3%; Ad-GFP, +61.7%; n=3 animals per group; P= 0.294). Adverse effects of gene transfer on left ventricular ejection fraction (LVEF) were not detected following treatment (LVEFAd-siRNA-Gαs, 66%; LVEFAd-GFP, 60%). Conclusions In this preclinical proof-of-concept study targeted Ad-siRNA-Gαs gene therapy reduced heart rates during normal sinus rhythm compared with Ad-GFP treatment and prevented inappropriate rate increase after β-adrenergic stimulation. Gene therapy may provide an additional therapeutic option for heart rate reduction in cardiac disease. (J Am Heart Assoc. 2012;1:e000372 doi: 10.1161/JAHA.111.000372)