Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil

This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease. The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis...

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Veröffentlicht in:Journal of the American College of Cardiology 2006-09, Vol.48 (6), p.1234-1241
Hauptverfasser: RITCHIE, Rebecca H, ZEITZ, Christopher J, WUTTKE, Ronald D, HII, John T. Y, HOROWITZ, John D
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container_end_page 1241
container_issue 6
container_start_page 1234
container_title Journal of the American College of Cardiology
container_volume 48
creator RITCHIE, Rebecca H
ZEITZ, Christopher J
WUTTKE, Ronald D
HII, John T. Y
HOROWITZ, John D
description This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease. The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis of acute hemodynamic actions at rest, but may be unmasked during tachycardia. However, this has not been studied extensively in vivo. The force-interval relationship of the intact human left ventricle was examined before and 10 min after intravenous bolus administration of the negatively inotropic agents metoprolol, sotalol, or verapamil in patients undergoing diagnostic cardiac catheterization. All three drugs similarly reduced maximal rate of increase of left ventricular pressures (LV+dP/dt(max)) by approximately 10%, but diversely modified the force-interval relationship. The parameter c (the reduction in LV+dP/dt(max) of a fixed premature stimulus on mechanical restitution) was significantly reduced by metoprolol (by 9+/- 4%, p < 0.05), was increased by verapamil (by 6 +/- 2%, p < 0.05), and was not significantly changed by sotalol. Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively). These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. These properties may contribute to the relative safety of these agents in patients prone to hemodynamic deterioration during sustained tachycardia.
doi_str_mv 10.1016/j.jacc.2006.04.092
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Y</creatorcontrib><creatorcontrib>HOROWITZ, John D</creatorcontrib><title>Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease. The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis of acute hemodynamic actions at rest, but may be unmasked during tachycardia. However, this has not been studied extensively in vivo. 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Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively). These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. 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Vascular system</subject><subject>Cardiovascular disease</subject><subject>Catheters</subject><subject>Female</subject><subject>Heart</subject><subject>Heart attacks</subject><subject>Heart rate</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Intubation</subject><subject>Ischemia</subject><subject>Male</subject><subject>Mathematical models</subject><subject>Medical sciences</subject><subject>Metoprolol - therapeutic use</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Myocardial Contraction - drug effects</subject><subject>Myocardial Ischemia - drug therapy</subject><subject>Myocardial Ischemia - physiopathology</subject><subject>Pressure</subject><subject>Pulmonary arteries</subject><subject>Restitution</subject><subject>Rodents</subject><subject>Sotalol - therapeutic use</subject><subject>Studies</subject><subject>Systole - drug effects</subject><subject>Time Factors</subject><subject>Veins &amp; arteries</subject><subject>Ventricular Function, Left - drug effects</subject><subject>Verapamil - therapeutic use</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0M-L1TAQB_Agivtc_Qc8SED01jppm6Txtjz8BQte9FymabLNo01qku6yd_9ws_pE8DQMfObLzBDykkHNgIl3p_qEWtcNgKihq0E1j8iBcd5XLVfyMTmAbHnFQMkL8iylExTYM_WUXDChpALWHMjPq5yN3zG74GmwNM-GenNT-ltDnQ85hs1paqw1OqcHsZocthiWsFDMNM0hZqrv9WLoYvxNnlMZo_O-ok_0PT2GdcPoUkm_c3mmKWT8Peonemsibri65Tl5YnFJ5sW5XpLvHz98O36urr9--nK8uq7mFppcSdSI0DUWWmknbrtR9cCZUuUwOXbKCN52XFohRC_HBsau6XAql9qp7VrU7SV5-ye37P9jNykPq0vaLAt6E_Y0iL4XD3EFvv4PnsIefdltYBwEkwJ4U9Srs9rH1UzDFt2K8X74-90C3pwBJo2Ljei1S_9cX0wP0P4CStyK_g</recordid><startdate>20060919</startdate><enddate>20060919</enddate><creator>RITCHIE, Rebecca H</creator><creator>ZEITZ, Christopher J</creator><creator>WUTTKE, Ronald D</creator><creator>HII, John T. 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Vascular system</topic><topic>Cardiovascular disease</topic><topic>Catheters</topic><topic>Female</topic><topic>Heart</topic><topic>Heart attacks</topic><topic>Heart rate</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Intubation</topic><topic>Ischemia</topic><topic>Male</topic><topic>Mathematical models</topic><topic>Medical sciences</topic><topic>Metoprolol - therapeutic use</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Myocardial Contraction - drug effects</topic><topic>Myocardial Ischemia - drug therapy</topic><topic>Myocardial Ischemia - physiopathology</topic><topic>Pressure</topic><topic>Pulmonary arteries</topic><topic>Restitution</topic><topic>Rodents</topic><topic>Sotalol - therapeutic use</topic><topic>Studies</topic><topic>Systole - drug effects</topic><topic>Time Factors</topic><topic>Veins &amp; arteries</topic><topic>Ventricular Function, Left - drug effects</topic><topic>Verapamil - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RITCHIE, Rebecca H</creatorcontrib><creatorcontrib>ZEITZ, Christopher J</creatorcontrib><creatorcontrib>WUTTKE, Ronald D</creatorcontrib><creatorcontrib>HII, John T. 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However, this has not been studied extensively in vivo. The force-interval relationship of the intact human left ventricle was examined before and 10 min after intravenous bolus administration of the negatively inotropic agents metoprolol, sotalol, or verapamil in patients undergoing diagnostic cardiac catheterization. All three drugs similarly reduced maximal rate of increase of left ventricular pressures (LV+dP/dt(max)) by approximately 10%, but diversely modified the force-interval relationship. The parameter c (the reduction in LV+dP/dt(max) of a fixed premature stimulus on mechanical restitution) was significantly reduced by metoprolol (by 9+/- 4%, p &lt; 0.05), was increased by verapamil (by 6 +/- 2%, p &lt; 0.05), and was not significantly changed by sotalol. Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively). These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. These properties may contribute to the relative safety of these agents in patients prone to hemodynamic deterioration during sustained tachycardia.</abstract><cop>New York, NY</cop><pub>Elsevier Science</pub><pmid>16979012</pmid><doi>10.1016/j.jacc.2006.04.092</doi><tpages>8</tpages></addata></record>
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subjects Aged
Angina pectoris
Anti-Arrhythmia Agents - therapeutic use
Biological and medical sciences
Cardiac arrhythmia
Cardiac Catheterization
Cardiac Pacing, Artificial
Cardiology
Cardiology. Vascular system
Cardiovascular disease
Catheters
Female
Heart
Heart attacks
Heart rate
Hemodynamics
Humans
Intubation
Ischemia
Male
Mathematical models
Medical sciences
Metoprolol - therapeutic use
Middle Aged
Mortality
Myocardial Contraction - drug effects
Myocardial Ischemia - drug therapy
Myocardial Ischemia - physiopathology
Pressure
Pulmonary arteries
Restitution
Rodents
Sotalol - therapeutic use
Studies
Systole - drug effects
Time Factors
Veins & arteries
Ventricular Function, Left - drug effects
Verapamil - therapeutic use
title Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil
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