Effects of Intracoronary Gallopamil on Coronary Hemodynamics and Myocardial Oxygen Consumption in Humans

The response of coronary hemodynamics to the intracoronary (i.c.) bolus administration of gallopamil, 1.5 and 3.0 μg/kg, was evaluated in 14 patients with normal coronary arteries. Gallopamil, 3.0 μg/kg, induced a small and transient decrease in systolic and mean arterial pressure and a small increa...

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Veröffentlicht in:Journal of cardiovascular pharmacology 1991-05, Vol.17 (5), p.822-829
Hauptverfasser: Vigorito, Carlo, Giordano, Arturo, Caprio, Lorenzo De, Vitale, Dino F, Ferraro, Paolo, Libutti, Nicola, Vastano, Luisa, Naddeo, Corrado, Rengo, Franco
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container_end_page 829
container_issue 5
container_start_page 822
container_title Journal of cardiovascular pharmacology
container_volume 17
creator Vigorito, Carlo
Giordano, Arturo
Caprio, Lorenzo De
Vitale, Dino F
Ferraro, Paolo
Libutti, Nicola
Vastano, Luisa
Naddeo, Corrado
Rengo, Franco
description The response of coronary hemodynamics to the intracoronary (i.c.) bolus administration of gallopamil, 1.5 and 3.0 μg/kg, was evaluated in 14 patients with normal coronary arteries. Gallopamil, 3.0 μg/kg, induced a small and transient decrease in systolic and mean arterial pressure and a small increase in the preejection period. Coronary sinus blood flow increased significantly at 30 s (p < 0.01) and returned to baseline 10 min after gallopamil administration. Coronary vascular resistance was still reduced at 10 min and returned to baseline at 15 min. Myocardial O2 consumption and extraction decreased significantly (p < 0.01) at 30 s. While myocardial O2 consumption returned to baseline 15 min after gallopamil administration, myocardial O2 extraction was still significantly reduced at this time. Milder and more transient changes were observed after i.c. administration of the lower dose (1.5 μg/kg), and no significant changes were found after i.c. administration of saline. These data show that i.e. gallopamil, in patients with normal coronary arteries, induces direct, transient, and dose-related peripheral coronary vasodilation. The reduction of myocardial O2 consumption and extraction suggests a direct negative inotropic and metabolic effect of gallopamil.
doi_str_mv 10.1097/00005344-199105000-00019
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Gallopamil, 3.0 μg/kg, induced a small and transient decrease in systolic and mean arterial pressure and a small increase in the preejection period. Coronary sinus blood flow increased significantly at 30 s (p &lt; 0.01) and returned to baseline 10 min after gallopamil administration. Coronary vascular resistance was still reduced at 10 min and returned to baseline at 15 min. Myocardial O2 consumption and extraction decreased significantly (p &lt; 0.01) at 30 s. While myocardial O2 consumption returned to baseline 15 min after gallopamil administration, myocardial O2 extraction was still significantly reduced at this time. Milder and more transient changes were observed after i.c. administration of the lower dose (1.5 μg/kg), and no significant changes were found after i.c. administration of saline. These data show that i.e. gallopamil, in patients with normal coronary arteries, induces direct, transient, and dose-related peripheral coronary vasodilation. 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Gallopamil, 3.0 μg/kg, induced a small and transient decrease in systolic and mean arterial pressure and a small increase in the preejection period. Coronary sinus blood flow increased significantly at 30 s (p &lt; 0.01) and returned to baseline 10 min after gallopamil administration. Coronary vascular resistance was still reduced at 10 min and returned to baseline at 15 min. Myocardial O2 consumption and extraction decreased significantly (p &lt; 0.01) at 30 s. While myocardial O2 consumption returned to baseline 15 min after gallopamil administration, myocardial O2 extraction was still significantly reduced at this time. Milder and more transient changes were observed after i.c. administration of the lower dose (1.5 μg/kg), and no significant changes were found after i.c. administration of saline. These data show that i.e. gallopamil, in patients with normal coronary arteries, induces direct, transient, and dose-related peripheral coronary vasodilation. The reduction of myocardial O2 consumption and extraction suggests a direct negative inotropic and metabolic effect of gallopamil.</description><subject>Adult</subject><subject>Aged</subject><subject>Antianginal agents. Coronary vasodilator agents</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Coronary Circulation - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Gallopamil - administration &amp; dosage</subject><subject>Gallopamil - pharmacology</subject><subject>Heart - drug effects</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myocardium - metabolism</subject><subject>Oxygen Consumption - drug effects</subject><subject>Pharmacology. 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Coronary vasodilator agents</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular system</topic><topic>Coronary Circulation - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Gallopamil - administration &amp; dosage</topic><topic>Gallopamil - pharmacology</topic><topic>Heart - drug effects</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myocardium - metabolism</topic><topic>Oxygen Consumption - drug effects</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vigorito, Carlo</creatorcontrib><creatorcontrib>Giordano, Arturo</creatorcontrib><creatorcontrib>Caprio, Lorenzo De</creatorcontrib><creatorcontrib>Vitale, Dino F</creatorcontrib><creatorcontrib>Ferraro, Paolo</creatorcontrib><creatorcontrib>Libutti, Nicola</creatorcontrib><creatorcontrib>Vastano, Luisa</creatorcontrib><creatorcontrib>Naddeo, Corrado</creatorcontrib><creatorcontrib>Rengo, Franco</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cardiovascular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vigorito, Carlo</au><au>Giordano, Arturo</au><au>Caprio, Lorenzo De</au><au>Vitale, Dino F</au><au>Ferraro, Paolo</au><au>Libutti, Nicola</au><au>Vastano, Luisa</au><au>Naddeo, Corrado</au><au>Rengo, Franco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Intracoronary Gallopamil on Coronary Hemodynamics and Myocardial Oxygen Consumption in Humans</atitle><jtitle>Journal of cardiovascular pharmacology</jtitle><addtitle>J Cardiovasc Pharmacol</addtitle><date>1991-05</date><risdate>1991</risdate><volume>17</volume><issue>5</issue><spage>822</spage><epage>829</epage><pages>822-829</pages><issn>0160-2446</issn><eissn>1533-4023</eissn><coden>JCPCDT</coden><abstract>The response of coronary hemodynamics to the intracoronary (i.c.) bolus administration of gallopamil, 1.5 and 3.0 μg/kg, was evaluated in 14 patients with normal coronary arteries. Gallopamil, 3.0 μg/kg, induced a small and transient decrease in systolic and mean arterial pressure and a small increase in the preejection period. Coronary sinus blood flow increased significantly at 30 s (p &lt; 0.01) and returned to baseline 10 min after gallopamil administration. Coronary vascular resistance was still reduced at 10 min and returned to baseline at 15 min. Myocardial O2 consumption and extraction decreased significantly (p &lt; 0.01) at 30 s. While myocardial O2 consumption returned to baseline 15 min after gallopamil administration, myocardial O2 extraction was still significantly reduced at this time. Milder and more transient changes were observed after i.c. administration of the lower dose (1.5 μg/kg), and no significant changes were found after i.c. administration of saline. These data show that i.e. gallopamil, in patients with normal coronary arteries, induces direct, transient, and dose-related peripheral coronary vasodilation. 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subjects Adult
Aged
Antianginal agents. Coronary vasodilator agents
Biological and medical sciences
Cardiovascular system
Coronary Circulation - drug effects
Dose-Response Relationship, Drug
Female
Gallopamil - administration & dosage
Gallopamil - pharmacology
Heart - drug effects
Hemodynamics - drug effects
Humans
Male
Medical sciences
Middle Aged
Myocardium - metabolism
Oxygen Consumption - drug effects
Pharmacology. Drug treatments
title Effects of Intracoronary Gallopamil on Coronary Hemodynamics and Myocardial Oxygen Consumption in Humans
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