Hemodynamic effects of Corwin (ICI 118,587), a new cardioselective beta-adenoceptor partial agonist

To describe the mechanisms of action of Corwin (ICI 118, 587), a new cardioselective beta-adrenoceptor partial agonist, ten cardiac patients with mild to moderate functional cardiac impairment were studied. Hemodynamic measurements were made at rest and during three consecutive levels of sub maximal...

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Veröffentlicht in:European heart journal 1983-08, Vol.4 (8), p.584-591
Hauptverfasser: DETRY, J.-M. R., DECOSTER, P. M., BRASSEUR, L. A.
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DECOSTER, P. M.
BRASSEUR, L. A.
description To describe the mechanisms of action of Corwin (ICI 118, 587), a new cardioselective beta-adrenoceptor partial agonist, ten cardiac patients with mild to moderate functional cardiac impairment were studied. Hemodynamic measurements were made at rest and during three consecutive levels of sub maximal exercise, before and 10 min after intravenous administration of 0.2 mg/kg of the drug. At rest, Corwin increased heart rate (HR) from 75 to 88 bpm and mean systemic blood pressure (BP) and decreased mean pulmonary capillary wedge pressure (PCWP); the resting cardiac output (CO) tended to increase in patients with a slow control HR. During exercise of low intensity (control HR: 103 bpm), the drug had no significant effect, except for a slight decrease in BP. During exercise of moderate and heavy intensity (control HR: 121 and 149 bpm), Corwin decreased HR (−10 and −24 bpm), BP and PCWP; at the heaviest exercise level, CO also decreased after Corwin. Thus, at rest, when the sympathetic tone is low, Corwin acts mainly as a beta-adrenoceptor agonist. As the sympathetic tone progressively increases with the intensity of the exercise, the beta-adrenoceptor antagonist action of Corwin becomes apparent and is most evident at the highest exercise level. In contrast to a full antagonist, these effects of Corwin appear to be less marked and they are accompanied by an unchanged or decreased PCWP. Corwin has thus interesting hemodynamic properties which deserve further investigation.
doi_str_mv 10.1093/oxfordjournals.eurheartj.a061524
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During exercise of moderate and heavy intensity (control HR: 121 and 149 bpm), Corwin decreased HR (−10 and −24 bpm), BP and PCWP; at the heaviest exercise level, CO also decreased after Corwin. Thus, at rest, when the sympathetic tone is low, Corwin acts mainly as a beta-adrenoceptor agonist. As the sympathetic tone progressively increases with the intensity of the exercise, the beta-adrenoceptor antagonist action of Corwin becomes apparent and is most evident at the highest exercise level. In contrast to a full antagonist, these effects of Corwin appear to be less marked and they are accompanied by an unchanged or decreased PCWP. 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During exercise of low intensity (control HR: 103 bpm), the drug had no significant effect, except for a slight decrease in BP. During exercise of moderate and heavy intensity (control HR: 121 and 149 bpm), Corwin decreased HR (−10 and −24 bpm), BP and PCWP; at the heaviest exercise level, CO also decreased after Corwin. Thus, at rest, when the sympathetic tone is low, Corwin acts mainly as a beta-adrenoceptor agonist. As the sympathetic tone progressively increases with the intensity of the exercise, the beta-adrenoceptor antagonist action of Corwin becomes apparent and is most evident at the highest exercise level. In contrast to a full antagonist, these effects of Corwin appear to be less marked and they are accompanied by an unchanged or decreased PCWP. 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A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hemodynamic effects of Corwin (ICI 118,587), a new cardioselective beta-adenoceptor partial agonist</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>1983-08</date><risdate>1983</risdate><volume>4</volume><issue>8</issue><spage>584</spage><epage>591</epage><pages>584-591</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>To describe the mechanisms of action of Corwin (ICI 118, 587), a new cardioselective beta-adrenoceptor partial agonist, ten cardiac patients with mild to moderate functional cardiac impairment were studied. Hemodynamic measurements were made at rest and during three consecutive levels of sub maximal exercise, before and 10 min after intravenous administration of 0.2 mg/kg of the drug. At rest, Corwin increased heart rate (HR) from 75 to 88 bpm and mean systemic blood pressure (BP) and decreased mean pulmonary capillary wedge pressure (PCWP); the resting cardiac output (CO) tended to increase in patients with a slow control HR. During exercise of low intensity (control HR: 103 bpm), the drug had no significant effect, except for a slight decrease in BP. During exercise of moderate and heavy intensity (control HR: 121 and 149 bpm), Corwin decreased HR (−10 and −24 bpm), BP and PCWP; at the heaviest exercise level, CO also decreased after Corwin. Thus, at rest, when the sympathetic tone is low, Corwin acts mainly as a beta-adrenoceptor agonist. As the sympathetic tone progressively increases with the intensity of the exercise, the beta-adrenoceptor antagonist action of Corwin becomes apparent and is most evident at the highest exercise level. In contrast to a full antagonist, these effects of Corwin appear to be less marked and they are accompanied by an unchanged or decreased PCWP. Corwin has thus interesting hemodynamic properties which deserve further investigation.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>6139282</pmid><doi>10.1093/oxfordjournals.eurheartj.a061524</doi><tpages>8</tpages></addata></record>
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subjects Adrenergic beta-Agonists - pharmacology
Adult
beta adrenoceptor partial agonist
beta-adrenoceptor blockade
Blood Pressure - drug effects
Cardiac Output - drug effects
Corwin
Exercise Test
Female
Heart Diseases - drug therapy
Heart Rate - drug effects
hemodynamics
Hemodynamics - drug effects
Humans
Male
Middle Aged
Propanolamines - pharmacology
Pulmonary Wedge Pressure - drug effects
Xamoterol
title Hemodynamic effects of Corwin (ICI 118,587), a new cardioselective beta-adenoceptor partial agonist
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