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
Hauptverfasser: ANDERSSON, M, DOMELLOF, L, HAGGMARK, S, JOHANSSON, G, REIZ, S, GUSTAVSSON, B
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container_end_page 255
container_issue 3
container_start_page 251
container_title Cancer chemotherapy and pharmacology
container_volume 22
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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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 &amp; 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. 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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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