Affiliation:
1. Département de Pharmacologie, Institut National de la Santé et de la Recherche Médicale E00.01, Facultéde Médecine Paris Sud, 94276 Le Kremlin-Bicêtre Cedex;
2. Fédération de Cardiologie, Hôpital Henri Mondor, 94000 Créteil; and
3. Hôpital Antoine Béclère, 92140 Clamart, France
Abstract
Left ventricular (LV) relaxation is crucial for LV function, especially during exercise. We compared the effects of increasing doses of ivabradine, a selective inward hyperpolarization-activated current inhibitor, and atenolol on the rate and extent of LV relaxation (best fit method: time constant τBF, pressure asymptote PBF) at rest and during exercise. Eight dogs were chronically instrumented to measure LV pressure and LV wall stresses. During exercise under saline, heart rate increased from 108 ± 5 to 220 ± 6 beats/min and τBF was significantly reduced from 22 ± 1 to 14 ± 2 ms. At rest, atenolol but not ivabradine increased τBF. For similar heart rate reductions during exercise, atenolol impeded the shortening of τBF (23 ± 2 ms) whereas ivabradine had no effect (15 ± 2 ms). The extent of the relaxation process (PBF) at peak exercise was increased by ivabradine, and to a greater extent by atenolol, compared with saline. Thus, for a similar reduction in heart rate at rest and during exercise, ivabradine, in contrast with atenolol, does not exert any negative lusitropic effect.
Publisher
American Physiological Society
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology
Cited by
87 articles.
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