Comparison of Etomidate, Ketamine, Midazolam, Propofol, and Thiopental on Function and Metabolism of Isolated Hearts
The authors examined direct myocardial and coronary vascular responses to the anesthetic induction agents etomidate, ketamine, midazolam, propofol, and thiopental and compared their effects on attenuating autoregulation of coronary flow as assessed by changes in oxygen supply/demand relationships. S...
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description | The authors examined direct myocardial and coronary vascular responses to the anesthetic induction agents etomidate, ketamine, midazolam, propofol, and thiopental and compared their effects on attenuating autoregulation of coronary flow as assessed by changes in oxygen supply/demand relationships. Spontaneous heart rate, atrioventricular conduction time during a trial pacing, left ventricular pressure (LVP), coronary flow (CF), percent oxygen extraction, oxygen delivery, and myocardial oxygen consumption (MVo2) were examined in 55 isolated guinea pig hearts divided into five groups of 11 each. Hearts were perfused at constant pressure with one of the drugs administered at steady-state concentrations increasing from 0.5 μM to 1 mM. Adenosine was given to test maximal CF. At concentrations below 10 μM no significant changes were observed; beyond 50 μM for midazolam, etomidate, and propofol, and 100 μM for thiopental and ketamine, each agent caused progressive but differential decreases in heart rate, atrioventricular conduction time (leading to atrioventricular dissociation), LVP, +dLVP/dtrnax, percent oxygen extraction, and MVo2. The concentrations (μM) at which +dLVP/dtmax was reduced by 50% were as followsetomidate, 82 ± 2 (mean ± SEM); propofol, 91 ± 4; midazolam, 105 ± 8; thiopental, 156 ± 11; and ketamine, 323 ± 7; the rank order of potency was etomidate = propofol = midazolam > thiopental > ketamine; results were similar for LVP. At the 100 μM concentration, CF was decreased 11% ± 2% by ketamine and 5% ± 3% by thiopental but was increased 17% ± 6% by etomidate, 21% ± 5% by midazolam, and near maximally to 57% ± 10% by propofol; MVo2 was decreased 8% ± 4% by thiopental, 10% ± 5% by ketamine, 19% ± 5% by midazolam, 29% ± 7% by etomidate, and 37% ± 5% by propofol; oxygen delivery/MVo2 was unchanged by thiopental and ketamine but was increased 62% ± 7% by midazolam, 71% ± 9% by etomidate, and 150% ± 15% by propofol. Between 100 μM and 1 mM, thiopental and ketamine did not increase CF but decreased MVo2 and percent oxygen extraction, whereas propofol maximally increased CF and decreased MVo2 and midazolam and etomidate had intermediate effects. These results indicate that on a molar basis, propofol, and less so midazolam and etomidate, depress cardiac function moderately more than thiopental and ketamine, and that propofol markedly attenuates autoregulation by causing coronary vasodilation. With doses used to induce anesthesia, propofol and thiopental appe |
doi_str_mv | 10.1213/00000539-199204000-00015 |
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Spontaneous heart rate, atrioventricular conduction time during a trial pacing, left ventricular pressure (LVP), coronary flow (CF), percent oxygen extraction, oxygen delivery, and myocardial oxygen consumption (MVo2) were examined in 55 isolated guinea pig hearts divided into five groups of 11 each. Hearts were perfused at constant pressure with one of the drugs administered at steady-state concentrations increasing from 0.5 μM to 1 mM. Adenosine was given to test maximal CF. At concentrations below 10 μM no significant changes were observed; beyond 50 μM for midazolam, etomidate, and propofol, and 100 μM for thiopental and ketamine, each agent caused progressive but differential decreases in heart rate, atrioventricular conduction time (leading to atrioventricular dissociation), LVP, +dLVP/dtrnax, percent oxygen extraction, and MVo2. The concentrations (μM) at which +dLVP/dtmax was reduced by 50% were as followsetomidate, 82 ± 2 (mean ± SEM); propofol, 91 ± 4; midazolam, 105 ± 8; thiopental, 156 ± 11; and ketamine, 323 ± 7; the rank order of potency was etomidate = propofol = midazolam > thiopental > ketamine; results were similar for LVP. At the 100 μM concentration, CF was decreased 11% ± 2% by ketamine and 5% ± 3% by thiopental but was increased 17% ± 6% by etomidate, 21% ± 5% by midazolam, and near maximally to 57% ± 10% by propofol; MVo2 was decreased 8% ± 4% by thiopental, 10% ± 5% by ketamine, 19% ± 5% by midazolam, 29% ± 7% by etomidate, and 37% ± 5% by propofol; oxygen delivery/MVo2 was unchanged by thiopental and ketamine but was increased 62% ± 7% by midazolam, 71% ± 9% by etomidate, and 150% ± 15% by propofol. Between 100 μM and 1 mM, thiopental and ketamine did not increase CF but decreased MVo2 and percent oxygen extraction, whereas propofol maximally increased CF and decreased MVo2 and midazolam and etomidate had intermediate effects. These results indicate that on a molar basis, propofol, and less so midazolam and etomidate, depress cardiac function moderately more than thiopental and ketamine, and that propofol markedly attenuates autoregulation by causing coronary vasodilation. With doses used to induce anesthesia, propofol and thiopental appear to depress cardiac function more than ketamine or etomidate.</description><identifier>ISSN: 0003-2999</identifier><identifier>EISSN: 1526-7598</identifier><identifier>DOI: 10.1213/00000539-199204000-00015</identifier><identifier>PMID: 1554122</identifier><identifier>CODEN: AACRAT</identifier><language>eng</language><publisher>Hagerstown, MD: International Anesthesia Research Society</publisher><subject>Adenosine - pharmacology ; Anesthetics - pharmacology ; Anesthetics. Neuromuscular blocking agents ; Animals ; Atrioventricular Node - drug effects ; Atrioventricular Node - physiology ; Biological and medical sciences ; Coronary Circulation - drug effects ; Etomidate - pharmacology ; Guinea Pigs ; Heart - drug effects ; Heart - physiology ; In Vitro Techniques ; Ketamine - pharmacology ; Medical sciences ; Midazolam - pharmacology ; Myocardial Contraction - drug effects ; Myocardium - metabolism ; Neuropharmacology ; Oxygen Consumption - drug effects ; Perfusion ; Pharmacology. Drug treatments ; Propofol - pharmacology ; Thiopental - pharmacology</subject><ispartof>Anesthesia and analgesia, 1992-04, Vol.74 (4), p.547-558</ispartof><rights>1992 International Anesthesia Research Society</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4505-d0b43fa0cba0cb5fbac24f80ec9d6f09e18c6d938c275a9f09205bcb1ea703d83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00000539-199204000-00015$$EHTML$$P50$$Gwolterskluwer$$H</linktohtml><link.rule.ids>314,776,780,4595,27901,27902,65434</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5169222$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1554122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stowe, David F.</creatorcontrib><creatorcontrib>Bosnjak, Zeljko J.</creatorcontrib><creatorcontrib>Kampine, John P.</creatorcontrib><title>Comparison of Etomidate, Ketamine, Midazolam, Propofol, and Thiopental on Function and Metabolism of Isolated Hearts</title><title>Anesthesia and analgesia</title><addtitle>Anesth Analg</addtitle><description>The authors examined direct myocardial and coronary vascular responses to the anesthetic induction agents etomidate, ketamine, midazolam, propofol, and thiopental and compared their effects on attenuating autoregulation of coronary flow as assessed by changes in oxygen supply/demand relationships. Spontaneous heart rate, atrioventricular conduction time during a trial pacing, left ventricular pressure (LVP), coronary flow (CF), percent oxygen extraction, oxygen delivery, and myocardial oxygen consumption (MVo2) were examined in 55 isolated guinea pig hearts divided into five groups of 11 each. Hearts were perfused at constant pressure with one of the drugs administered at steady-state concentrations increasing from 0.5 μM to 1 mM. Adenosine was given to test maximal CF. At concentrations below 10 μM no significant changes were observed; beyond 50 μM for midazolam, etomidate, and propofol, and 100 μM for thiopental and ketamine, each agent caused progressive but differential decreases in heart rate, atrioventricular conduction time (leading to atrioventricular dissociation), LVP, +dLVP/dtrnax, percent oxygen extraction, and MVo2. The concentrations (μM) at which +dLVP/dtmax was reduced by 50% were as followsetomidate, 82 ± 2 (mean ± SEM); propofol, 91 ± 4; midazolam, 105 ± 8; thiopental, 156 ± 11; and ketamine, 323 ± 7; the rank order of potency was etomidate = propofol = midazolam > thiopental > ketamine; results were similar for LVP. At the 100 μM concentration, CF was decreased 11% ± 2% by ketamine and 5% ± 3% by thiopental but was increased 17% ± 6% by etomidate, 21% ± 5% by midazolam, and near maximally to 57% ± 10% by propofol; MVo2 was decreased 8% ± 4% by thiopental, 10% ± 5% by ketamine, 19% ± 5% by midazolam, 29% ± 7% by etomidate, and 37% ± 5% by propofol; oxygen delivery/MVo2 was unchanged by thiopental and ketamine but was increased 62% ± 7% by midazolam, 71% ± 9% by etomidate, and 150% ± 15% by propofol. Between 100 μM and 1 mM, thiopental and ketamine did not increase CF but decreased MVo2 and percent oxygen extraction, whereas propofol maximally increased CF and decreased MVo2 and midazolam and etomidate had intermediate effects. These results indicate that on a molar basis, propofol, and less so midazolam and etomidate, depress cardiac function moderately more than thiopental and ketamine, and that propofol markedly attenuates autoregulation by causing coronary vasodilation. With doses used to induce anesthesia, propofol and thiopental appear to depress cardiac function more than ketamine or etomidate.</description><subject>Adenosine - pharmacology</subject><subject>Anesthetics - pharmacology</subject><subject>Anesthetics. Neuromuscular blocking agents</subject><subject>Animals</subject><subject>Atrioventricular Node - drug effects</subject><subject>Atrioventricular Node - physiology</subject><subject>Biological and medical sciences</subject><subject>Coronary Circulation - drug effects</subject><subject>Etomidate - pharmacology</subject><subject>Guinea Pigs</subject><subject>Heart - drug effects</subject><subject>Heart - physiology</subject><subject>In Vitro Techniques</subject><subject>Ketamine - pharmacology</subject><subject>Medical sciences</subject><subject>Midazolam - pharmacology</subject><subject>Myocardial Contraction - drug effects</subject><subject>Myocardium - metabolism</subject><subject>Neuropharmacology</subject><subject>Oxygen Consumption - drug effects</subject><subject>Perfusion</subject><subject>Pharmacology. Drug treatments</subject><subject>Propofol - pharmacology</subject><subject>Thiopental - pharmacology</subject><issn>0003-2999</issn><issn>1526-7598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1UU1v3CAQRVGrdJvmJ1TiUPW0bgEbG47VKmmiJkoO6RmNMWhpsXEBK0p_fXF2m56KNGJ4HzPSAyFMySfKaP2ZrIfXsqJSMtKUR1WK8hO0oZy1VceleIU2BasrJqV8g96m9GOVENGeolPKeUMZ26C8C-MM0aUw4WDxRQ6jGyCbLf5mMoxuKt1tQX4HD-MW38cwBxv8FsM04Ie9C7OZMnhc7JfLpLMrzUrdFncfvEvjOvY6FXs2A74yEHN6h15b8MmcH-8z9P3y4mF3Vd3cfb3efbmpdMMJrwbSN7UFovu1uO1Bs8YKYrQcWkukoUK3g6yFZh0HWRBGeK97aqAj9SDqM_TxMHeO4ddiUlajS9p4D5MJS1IdE60UTVeE4iDUMaQUjVVzdCPEJ0WJWgNXfwNXL4Gr58CL9f1xx9KPZvhnPCRc-A9HHpIGbyNM2qUXGaetZM-y5iB7DD6bmH765dFEtTfg817977vrP3SFmKM</recordid><startdate>199204</startdate><enddate>199204</enddate><creator>Stowe, David F.</creator><creator>Bosnjak, Zeljko J.</creator><creator>Kampine, John P.</creator><general>International Anesthesia Research Society</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199204</creationdate><title>Comparison of Etomidate, Ketamine, Midazolam, Propofol, and Thiopental on Function and Metabolism of Isolated Hearts</title><author>Stowe, David F. ; Bosnjak, Zeljko J. ; Kampine, John P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4505-d0b43fa0cba0cb5fbac24f80ec9d6f09e18c6d938c275a9f09205bcb1ea703d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Adenosine - pharmacology</topic><topic>Anesthetics - pharmacology</topic><topic>Anesthetics. Neuromuscular blocking agents</topic><topic>Animals</topic><topic>Atrioventricular Node - drug effects</topic><topic>Atrioventricular Node - physiology</topic><topic>Biological and medical sciences</topic><topic>Coronary Circulation - drug effects</topic><topic>Etomidate - pharmacology</topic><topic>Guinea Pigs</topic><topic>Heart - drug effects</topic><topic>Heart - physiology</topic><topic>In Vitro Techniques</topic><topic>Ketamine - pharmacology</topic><topic>Medical sciences</topic><topic>Midazolam - pharmacology</topic><topic>Myocardial Contraction - drug effects</topic><topic>Myocardium - metabolism</topic><topic>Neuropharmacology</topic><topic>Oxygen Consumption - drug effects</topic><topic>Perfusion</topic><topic>Pharmacology. Drug treatments</topic><topic>Propofol - pharmacology</topic><topic>Thiopental - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stowe, David F.</creatorcontrib><creatorcontrib>Bosnjak, Zeljko J.</creatorcontrib><creatorcontrib>Kampine, John P.</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>Anesthesia and analgesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stowe, David F.</au><au>Bosnjak, Zeljko J.</au><au>Kampine, John P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of Etomidate, Ketamine, Midazolam, Propofol, and Thiopental on Function and Metabolism of Isolated Hearts</atitle><jtitle>Anesthesia and analgesia</jtitle><addtitle>Anesth Analg</addtitle><date>1992-04</date><risdate>1992</risdate><volume>74</volume><issue>4</issue><spage>547</spage><epage>558</epage><pages>547-558</pages><issn>0003-2999</issn><eissn>1526-7598</eissn><coden>AACRAT</coden><abstract>The authors examined direct myocardial and coronary vascular responses to the anesthetic induction agents etomidate, ketamine, midazolam, propofol, and thiopental and compared their effects on attenuating autoregulation of coronary flow as assessed by changes in oxygen supply/demand relationships. Spontaneous heart rate, atrioventricular conduction time during a trial pacing, left ventricular pressure (LVP), coronary flow (CF), percent oxygen extraction, oxygen delivery, and myocardial oxygen consumption (MVo2) were examined in 55 isolated guinea pig hearts divided into five groups of 11 each. Hearts were perfused at constant pressure with one of the drugs administered at steady-state concentrations increasing from 0.5 μM to 1 mM. Adenosine was given to test maximal CF. At concentrations below 10 μM no significant changes were observed; beyond 50 μM for midazolam, etomidate, and propofol, and 100 μM for thiopental and ketamine, each agent caused progressive but differential decreases in heart rate, atrioventricular conduction time (leading to atrioventricular dissociation), LVP, +dLVP/dtrnax, percent oxygen extraction, and MVo2. The concentrations (μM) at which +dLVP/dtmax was reduced by 50% were as followsetomidate, 82 ± 2 (mean ± SEM); propofol, 91 ± 4; midazolam, 105 ± 8; thiopental, 156 ± 11; and ketamine, 323 ± 7; the rank order of potency was etomidate = propofol = midazolam > thiopental > ketamine; results were similar for LVP. At the 100 μM concentration, CF was decreased 11% ± 2% by ketamine and 5% ± 3% by thiopental but was increased 17% ± 6% by etomidate, 21% ± 5% by midazolam, and near maximally to 57% ± 10% by propofol; MVo2 was decreased 8% ± 4% by thiopental, 10% ± 5% by ketamine, 19% ± 5% by midazolam, 29% ± 7% by etomidate, and 37% ± 5% by propofol; oxygen delivery/MVo2 was unchanged by thiopental and ketamine but was increased 62% ± 7% by midazolam, 71% ± 9% by etomidate, and 150% ± 15% by propofol. Between 100 μM and 1 mM, thiopental and ketamine did not increase CF but decreased MVo2 and percent oxygen extraction, whereas propofol maximally increased CF and decreased MVo2 and midazolam and etomidate had intermediate effects. These results indicate that on a molar basis, propofol, and less so midazolam and etomidate, depress cardiac function moderately more than thiopental and ketamine, and that propofol markedly attenuates autoregulation by causing coronary vasodilation. With doses used to induce anesthesia, propofol and thiopental appear to depress cardiac function more than ketamine or etomidate.</abstract><cop>Hagerstown, MD</cop><pub>International Anesthesia Research Society</pub><pmid>1554122</pmid><doi>10.1213/00000539-199204000-00015</doi><tpages>12</tpages></addata></record> |
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subjects | Adenosine - pharmacology Anesthetics - pharmacology Anesthetics. Neuromuscular blocking agents Animals Atrioventricular Node - drug effects Atrioventricular Node - physiology Biological and medical sciences Coronary Circulation - drug effects Etomidate - pharmacology Guinea Pigs Heart - drug effects Heart - physiology In Vitro Techniques Ketamine - pharmacology Medical sciences Midazolam - pharmacology Myocardial Contraction - drug effects Myocardium - metabolism Neuropharmacology Oxygen Consumption - drug effects Perfusion Pharmacology. Drug treatments Propofol - pharmacology Thiopental - pharmacology |
title | Comparison of Etomidate, Ketamine, Midazolam, Propofol, and Thiopental on Function and Metabolism of Isolated Hearts |
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