Cardiopulmonary hemodynamics and pharmacokinetics after hepatic intraarterial infusion of 5-fluorouracil (5-FU): an experimental study in the pig
Reported 5-FU-induced cardiac side effects may be explained by drug-induced hemodynamic changes and/or by direct myocardial toxicity due to regional drug uptake. This question was studied in 11 animals given constant infusions and 6 animals given bolus 5-FU infusions into the hepatic artery. Six ani...
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Veröffentlicht in: | Cancer chemotherapy and pharmacology 1988-01, Vol.22 (3), p.251-255 |
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creator | ANDERSSON, M DOMELLOF, L HAGGMARK, S JOHANSSON, G REIZ, S GUSTAVSSON, B |
description | Reported 5-FU-induced cardiac side effects may be explained by drug-induced hemodynamic changes and/or by direct myocardial toxicity due to regional drug uptake. This question was studied in 11 animals given constant infusions and 6 animals given bolus 5-FU infusions into the hepatic artery. Six animals, which received normal saline infusion, served as controls. A second aim was to study possible pulmonary drug clearance. Aortic, pulmonary arterial, and coronary sinus plasma 5-FU concentrations were determined during constant and after the bolus infusions of 5-FU. The V5 ECG, aortic, pulmonary arterial, and right atrial pressures were recorded continuously, and cardiac output and coronary sinus blood flow were recorded intermittently in all animals. No significant alterations in hemodynamic variables were seen during constant infusion. After the bolus infusion, an increased arterio-mixed venous oxygen content difference was recorded. Pharmacokinetic data after 3-min infusions indicated pulmonary drug uptake and release; during constant infusions, the data indicated myocardial drug uptake. As there were no alterations in myocardial oxygen demand or supply or in systemic hemodynamics during this myocardial drug uptake, it is likely that the cardiotoxicity is related to the direct effects of the drug on cardiac myocytes. |
doi_str_mv | 10.1007/BF00273420 |
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This question was studied in 11 animals given constant infusions and 6 animals given bolus 5-FU infusions into the hepatic artery. Six animals, which received normal saline infusion, served as controls. A second aim was to study possible pulmonary drug clearance. Aortic, pulmonary arterial, and coronary sinus plasma 5-FU concentrations were determined during constant and after the bolus infusions of 5-FU. The V5 ECG, aortic, pulmonary arterial, and right atrial pressures were recorded continuously, and cardiac output and coronary sinus blood flow were recorded intermittently in all animals. No significant alterations in hemodynamic variables were seen during constant infusion. After the bolus infusion, an increased arterio-mixed venous oxygen content difference was recorded. Pharmacokinetic data after 3-min infusions indicated pulmonary drug uptake and release; during constant infusions, the data indicated myocardial drug uptake. As there were no alterations in myocardial oxygen demand or supply or in systemic hemodynamics during this myocardial drug uptake, it is likely that the cardiotoxicity is related to the direct effects of the drug on cardiac myocytes.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/BF00273420</identifier><identifier>PMID: 3409458</identifier><identifier>CODEN: CCPHDZ</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Antineoplastic agents ; Biological and medical sciences ; Female ; Fluorouracil - administration & dosage ; Fluorouracil - pharmacokinetics ; Fluorouracil - pharmacology ; General aspects ; Hemodynamics - drug effects ; Hepatic Artery ; Infusions, Intra-Arterial ; Liver - metabolism ; Lung - metabolism ; Medical sciences ; Myocardium - metabolism ; Oxygen - blood ; Pharmacology. Drug treatments ; Swine</subject><ispartof>Cancer chemotherapy and pharmacology, 1988-01, Vol.22 (3), p.251-255</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c270t-91540299ea2de6b1612fb149882f01287c981567cfee1b54aa7ab51762c786c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6997709$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3409458$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ANDERSSON, M</creatorcontrib><creatorcontrib>DOMELLOF, L</creatorcontrib><creatorcontrib>HAGGMARK, S</creatorcontrib><creatorcontrib>JOHANSSON, G</creatorcontrib><creatorcontrib>REIZ, S</creatorcontrib><creatorcontrib>GUSTAVSSON, B</creatorcontrib><title>Cardiopulmonary hemodynamics and pharmacokinetics after hepatic intraarterial infusion of 5-fluorouracil (5-FU): an experimental study in the pig</title><title>Cancer chemotherapy and pharmacology</title><addtitle>Cancer Chemother Pharmacol</addtitle><description>Reported 5-FU-induced cardiac side effects may be explained by drug-induced hemodynamic changes and/or by direct myocardial toxicity due to regional drug uptake. This question was studied in 11 animals given constant infusions and 6 animals given bolus 5-FU infusions into the hepatic artery. Six animals, which received normal saline infusion, served as controls. A second aim was to study possible pulmonary drug clearance. Aortic, pulmonary arterial, and coronary sinus plasma 5-FU concentrations were determined during constant and after the bolus infusions of 5-FU. The V5 ECG, aortic, pulmonary arterial, and right atrial pressures were recorded continuously, and cardiac output and coronary sinus blood flow were recorded intermittently in all animals. No significant alterations in hemodynamic variables were seen during constant infusion. After the bolus infusion, an increased arterio-mixed venous oxygen content difference was recorded. Pharmacokinetic data after 3-min infusions indicated pulmonary drug uptake and release; during constant infusions, the data indicated myocardial drug uptake. As there were no alterations in myocardial oxygen demand or supply or in systemic hemodynamics during this myocardial drug uptake, it is likely that the cardiotoxicity is related to the direct effects of the drug on cardiac myocytes.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - pharmacokinetics</subject><subject>Fluorouracil - pharmacology</subject><subject>General aspects</subject><subject>Hemodynamics - drug effects</subject><subject>Hepatic Artery</subject><subject>Infusions, Intra-Arterial</subject><subject>Liver - metabolism</subject><subject>Lung - metabolism</subject><subject>Medical sciences</subject><subject>Myocardium - metabolism</subject><subject>Oxygen - blood</subject><subject>Pharmacology. Drug treatments</subject><subject>Swine</subject><issn>0344-5704</issn><issn>1432-0843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE9r3DAQxUVJ2Wy2veQe0CGHpuB09MeWlVu7dJtCIJf0vIxlKavEtoxkQ_Zj5BtHbZbtaZj3fvMYHiHnDK4ZgPr2YwPAlZAcPpAlk4IXUEtxQpYgpCxKBfKUnKX0BACSCbEgCyFBy7Jektc1xtaHce76MGDc053tQ7sfsPcmURxaOu4w9mjCsx_s9E90k42ZGzGv1A9TRIxZ8tjlzc3Jh4EGR8vCdXOIYY5ofEe_lMXmz9VNzqT2Zcx4b4cpn6Rpbvf5kE47S0f_-Il8dNgl-_kwV-Rh8_NhfVvc3f_6vf5-VxiuYCo0KyVwrS3y1lYNqxh3DZO6rrkDxmtldM3KShlnLWtKiaiwKZmquFF1ZcSKfH2PNTGkFK3bjvml3MCWwfZvq9v_rWb44h0e56a37RE91Jj9y4OPyWDnIg7GpyNWaa0UaPEGgPiAdA</recordid><startdate>19880101</startdate><enddate>19880101</enddate><creator>ANDERSSON, M</creator><creator>DOMELLOF, L</creator><creator>HAGGMARK, S</creator><creator>JOHANSSON, G</creator><creator>REIZ, S</creator><creator>GUSTAVSSON, B</creator><general>Springer</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></search><sort><creationdate>19880101</creationdate><title>Cardiopulmonary hemodynamics and pharmacokinetics after hepatic intraarterial infusion of 5-fluorouracil (5-FU): an experimental study in the pig</title><author>ANDERSSON, M ; DOMELLOF, L ; HAGGMARK, S ; JOHANSSON, G ; REIZ, S ; GUSTAVSSON, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-91540299ea2de6b1612fb149882f01287c981567cfee1b54aa7ab51762c786c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Fluorouracil - administration & dosage</topic><topic>Fluorouracil - pharmacokinetics</topic><topic>Fluorouracil - pharmacology</topic><topic>General aspects</topic><topic>Hemodynamics - drug effects</topic><topic>Hepatic Artery</topic><topic>Infusions, Intra-Arterial</topic><topic>Liver - metabolism</topic><topic>Lung - metabolism</topic><topic>Medical sciences</topic><topic>Myocardium - metabolism</topic><topic>Oxygen - blood</topic><topic>Pharmacology. Drug treatments</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ANDERSSON, M</creatorcontrib><creatorcontrib>DOMELLOF, L</creatorcontrib><creatorcontrib>HAGGMARK, S</creatorcontrib><creatorcontrib>JOHANSSON, G</creatorcontrib><creatorcontrib>REIZ, S</creatorcontrib><creatorcontrib>GUSTAVSSON, B</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><jtitle>Cancer chemotherapy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ANDERSSON, M</au><au>DOMELLOF, L</au><au>HAGGMARK, S</au><au>JOHANSSON, G</au><au>REIZ, S</au><au>GUSTAVSSON, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiopulmonary hemodynamics and pharmacokinetics after hepatic intraarterial infusion of 5-fluorouracil (5-FU): an experimental study in the pig</atitle><jtitle>Cancer chemotherapy and pharmacology</jtitle><addtitle>Cancer Chemother Pharmacol</addtitle><date>1988-01-01</date><risdate>1988</risdate><volume>22</volume><issue>3</issue><spage>251</spage><epage>255</epage><pages>251-255</pages><issn>0344-5704</issn><eissn>1432-0843</eissn><coden>CCPHDZ</coden><abstract>Reported 5-FU-induced cardiac side effects may be explained by drug-induced hemodynamic changes and/or by direct myocardial toxicity due to regional drug uptake. This question was studied in 11 animals given constant infusions and 6 animals given bolus 5-FU infusions into the hepatic artery. Six animals, which received normal saline infusion, served as controls. A second aim was to study possible pulmonary drug clearance. Aortic, pulmonary arterial, and coronary sinus plasma 5-FU concentrations were determined during constant and after the bolus infusions of 5-FU. The V5 ECG, aortic, pulmonary arterial, and right atrial pressures were recorded continuously, and cardiac output and coronary sinus blood flow were recorded intermittently in all animals. No significant alterations in hemodynamic variables were seen during constant infusion. After the bolus infusion, an increased arterio-mixed venous oxygen content difference was recorded. Pharmacokinetic data after 3-min infusions indicated pulmonary drug uptake and release; during constant infusions, the data indicated myocardial drug uptake. As there were no alterations in myocardial oxygen demand or supply or in systemic hemodynamics during this myocardial drug uptake, it is likely that the cardiotoxicity is related to the direct effects of the drug on cardiac myocytes.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>3409458</pmid><doi>10.1007/BF00273420</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Animals Antineoplastic agents Biological and medical sciences Female Fluorouracil - administration & dosage Fluorouracil - pharmacokinetics Fluorouracil - pharmacology General aspects Hemodynamics - drug effects Hepatic Artery Infusions, Intra-Arterial Liver - metabolism Lung - metabolism Medical sciences Myocardium - metabolism Oxygen - blood Pharmacology. Drug treatments Swine |
title | Cardiopulmonary hemodynamics and pharmacokinetics after hepatic intraarterial infusion of 5-fluorouracil (5-FU): an experimental study in the pig |
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