Cardiovascular parameters in anaesthetized guinea pigs: A safety pharmacology screening model

Assessment of cardiovascular functions in vivo is part of the core battery of guideline ICH S7A and is thereby required by regulatory authorities. The haemodynamic effects of repeated intravenous administrations of reference compounds were analyzed in order to validate the guinea pig model for safet...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of pharmacological and toxicological methods 2005-07, Vol.52 (1), p.106-114
Hauptverfasser: Hauser, Daniela S., Stade, Matthias, Schmidt, Angela, Hanauer, Guido
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 114
container_issue 1
container_start_page 106
container_title Journal of pharmacological and toxicological methods
container_volume 52
creator Hauser, Daniela S.
Stade, Matthias
Schmidt, Angela
Hanauer, Guido
description Assessment of cardiovascular functions in vivo is part of the core battery of guideline ICH S7A and is thereby required by regulatory authorities. The haemodynamic effects of repeated intravenous administrations of reference compounds were analyzed in order to validate the guinea pig model for safety pharmacology studies under GLP conditions. Male guinea pigs ( n = 54, weighing 565–762 g) were anaesthetized using 1.5 g/kg, i.p., urethane. Systolic arterial blood pressure (SAP), diastolic arterial blood pressure (DAP), heart rate (HR), left ventricular pressure (LVP), cardiac contractility (d p/d t max), and ECG (RR, QT, and QTc intervals) were recorded continuously. Animals received vehicle i.v. followed by cumulative doses of reference compounds. Vehicle did not produce any relevant changes, either in cardiovascular or ECG parameters. Isoproterenol caused a rapid and significant increase in HR, LVP, and d p/d t max, in contrast to a dose-dependent decrease in SAP and DAP. Epinephrine led to a potent increase in all cardiovascular parameters. Nifedipine produced a slight decrease in HR and LVP, and a potent decrease in blood pressure and d p/d t max. Verapamil caused a dose-dependent decrease in all cardiovascular parameters. Ouabain resulted in a significant increase in SAP, DAP, LVP, and d p/d t max; ECG showed an atrioventricular block and arrhythmia. Terfenadine, cisapride, and sotalol prolonged QT and QTc intervals, whereas vehicle and the other tested compounds did not produce any prolongation of the QTc interval. Our results on HR, blood pressure, and ECG obtained after i.v. administration of reference compounds show the usefulness of the guinea pig in assessing cardiovascular safety. The anaesthetized guinea pig allows the measurement of cardiac contractility and the use of doses higher than in conscious animals. Using this animal model, several cardiovascular parameters can be recorded simultaneously at a modest cost in terms of test compound and the number of animals required.
doi_str_mv 10.1016/j.vascn.2005.03.003
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_17458778</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1056871905000432</els_id><sourcerecordid>17458778</sourcerecordid><originalsourceid>FETCH-LOGICAL-c303t-926cfd8290f9feda4d36b22b192f4b5ff2eca65185eb07104e10c6a40ae494ed3</originalsourceid><addsrcrecordid>eNp9kElrHDEQRoWJ8TLxLzAEnXLrTqml3gI5mMFLwOBLArkEUS2VZjT0FqnbMP716fEM5JZT1eHVV1WPsVsBqQBRfNmlrxhNn2YAeQoyBZBn7EpUpUxUVf36sPSQF0lVivqSXce4g4WohbpglyKvCyGz_Ir9XmOwfjgkzS0GPmLAjiYKkfueY48Upy1N_o0s38y-J-Sj38Sv_I5HdDTt-bjF0KEZ2mGz59EEot73G94NltqP7NxhG-nmVFfs58P9j_VT8vzy-H1995wYCXJK6qwwzlZZDa52ZFFZWTRZ1og6c6rJncvIYJGLKqcGSgGKBJgCFSCpWpGVK_b5mDuG4c-8nKw7Hw21LfY0zFGLUuVVWVYLKI-gCUOMgZweg-8w7LUAfbCqd_rdqj5Y1SD14myZ-nSKn5uO7L-Zk8YF-HYEaHny1VPQ0XjqDVkfyEzaDv6_C_4CN-eLxg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17458778</pqid></control><display><type>article</type><title>Cardiovascular parameters in anaesthetized guinea pigs: A safety pharmacology screening model</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Hauser, Daniela S. ; Stade, Matthias ; Schmidt, Angela ; Hanauer, Guido</creator><creatorcontrib>Hauser, Daniela S. ; Stade, Matthias ; Schmidt, Angela ; Hanauer, Guido</creatorcontrib><description>Assessment of cardiovascular functions in vivo is part of the core battery of guideline ICH S7A and is thereby required by regulatory authorities. The haemodynamic effects of repeated intravenous administrations of reference compounds were analyzed in order to validate the guinea pig model for safety pharmacology studies under GLP conditions. Male guinea pigs ( n = 54, weighing 565–762 g) were anaesthetized using 1.5 g/kg, i.p., urethane. Systolic arterial blood pressure (SAP), diastolic arterial blood pressure (DAP), heart rate (HR), left ventricular pressure (LVP), cardiac contractility (d p/d t max), and ECG (RR, QT, and QTc intervals) were recorded continuously. Animals received vehicle i.v. followed by cumulative doses of reference compounds. Vehicle did not produce any relevant changes, either in cardiovascular or ECG parameters. Isoproterenol caused a rapid and significant increase in HR, LVP, and d p/d t max, in contrast to a dose-dependent decrease in SAP and DAP. Epinephrine led to a potent increase in all cardiovascular parameters. Nifedipine produced a slight decrease in HR and LVP, and a potent decrease in blood pressure and d p/d t max. Verapamil caused a dose-dependent decrease in all cardiovascular parameters. Ouabain resulted in a significant increase in SAP, DAP, LVP, and d p/d t max; ECG showed an atrioventricular block and arrhythmia. Terfenadine, cisapride, and sotalol prolonged QT and QTc intervals, whereas vehicle and the other tested compounds did not produce any prolongation of the QTc interval. Our results on HR, blood pressure, and ECG obtained after i.v. administration of reference compounds show the usefulness of the guinea pig in assessing cardiovascular safety. The anaesthetized guinea pig allows the measurement of cardiac contractility and the use of doses higher than in conscious animals. Using this animal model, several cardiovascular parameters can be recorded simultaneously at a modest cost in terms of test compound and the number of animals required.</description><identifier>ISSN: 1056-8719</identifier><identifier>EISSN: 1873-488X</identifier><identifier>DOI: 10.1016/j.vascn.2005.03.003</identifier><identifier>PMID: 15961325</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anaesthetized guinea pigs ; Anesthesia ; Animals ; Blood pressure ; Cardiovascular Agents - adverse effects ; Cardiovascular Agents - classification ; Cardiovascular Physiological Phenomena - drug effects ; Cardiovascular System - drug effects ; Dose-Response Relationship, Drug ; Drug Evaluation, Preclinical - methods ; Drug-Related Side Effects and Adverse Reactions ; ECG ; Electrocardiography ; Epinephrine - adverse effects ; Guinea Pigs ; Hemodynamics - drug effects ; Interval ; Intravenous drug infusion ; Isoproterenol - adverse effects ; Left ventricular pressure ; Male ; Methods ; Models, Animal ; Nifedipine - adverse effects ; Ouabain - adverse effects ; Pharmaceutical Preparations - classification ; Safety pharmacology ; Verapamil - adverse effects</subject><ispartof>Journal of pharmacological and toxicological methods, 2005-07, Vol.52 (1), p.106-114</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c303t-926cfd8290f9feda4d36b22b192f4b5ff2eca65185eb07104e10c6a40ae494ed3</citedby><cites>FETCH-LOGICAL-c303t-926cfd8290f9feda4d36b22b192f4b5ff2eca65185eb07104e10c6a40ae494ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.vascn.2005.03.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15961325$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hauser, Daniela S.</creatorcontrib><creatorcontrib>Stade, Matthias</creatorcontrib><creatorcontrib>Schmidt, Angela</creatorcontrib><creatorcontrib>Hanauer, Guido</creatorcontrib><title>Cardiovascular parameters in anaesthetized guinea pigs: A safety pharmacology screening model</title><title>Journal of pharmacological and toxicological methods</title><addtitle>J Pharmacol Toxicol Methods</addtitle><description>Assessment of cardiovascular functions in vivo is part of the core battery of guideline ICH S7A and is thereby required by regulatory authorities. The haemodynamic effects of repeated intravenous administrations of reference compounds were analyzed in order to validate the guinea pig model for safety pharmacology studies under GLP conditions. Male guinea pigs ( n = 54, weighing 565–762 g) were anaesthetized using 1.5 g/kg, i.p., urethane. Systolic arterial blood pressure (SAP), diastolic arterial blood pressure (DAP), heart rate (HR), left ventricular pressure (LVP), cardiac contractility (d p/d t max), and ECG (RR, QT, and QTc intervals) were recorded continuously. Animals received vehicle i.v. followed by cumulative doses of reference compounds. Vehicle did not produce any relevant changes, either in cardiovascular or ECG parameters. Isoproterenol caused a rapid and significant increase in HR, LVP, and d p/d t max, in contrast to a dose-dependent decrease in SAP and DAP. Epinephrine led to a potent increase in all cardiovascular parameters. Nifedipine produced a slight decrease in HR and LVP, and a potent decrease in blood pressure and d p/d t max. Verapamil caused a dose-dependent decrease in all cardiovascular parameters. Ouabain resulted in a significant increase in SAP, DAP, LVP, and d p/d t max; ECG showed an atrioventricular block and arrhythmia. Terfenadine, cisapride, and sotalol prolonged QT and QTc intervals, whereas vehicle and the other tested compounds did not produce any prolongation of the QTc interval. Our results on HR, blood pressure, and ECG obtained after i.v. administration of reference compounds show the usefulness of the guinea pig in assessing cardiovascular safety. The anaesthetized guinea pig allows the measurement of cardiac contractility and the use of doses higher than in conscious animals. Using this animal model, several cardiovascular parameters can be recorded simultaneously at a modest cost in terms of test compound and the number of animals required.</description><subject>Anaesthetized guinea pigs</subject><subject>Anesthesia</subject><subject>Animals</subject><subject>Blood pressure</subject><subject>Cardiovascular Agents - adverse effects</subject><subject>Cardiovascular Agents - classification</subject><subject>Cardiovascular Physiological Phenomena - drug effects</subject><subject>Cardiovascular System - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Evaluation, Preclinical - methods</subject><subject>Drug-Related Side Effects and Adverse Reactions</subject><subject>ECG</subject><subject>Electrocardiography</subject><subject>Epinephrine - adverse effects</subject><subject>Guinea Pigs</subject><subject>Hemodynamics - drug effects</subject><subject>Interval</subject><subject>Intravenous drug infusion</subject><subject>Isoproterenol - adverse effects</subject><subject>Left ventricular pressure</subject><subject>Male</subject><subject>Methods</subject><subject>Models, Animal</subject><subject>Nifedipine - adverse effects</subject><subject>Ouabain - adverse effects</subject><subject>Pharmaceutical Preparations - classification</subject><subject>Safety pharmacology</subject><subject>Verapamil - adverse effects</subject><issn>1056-8719</issn><issn>1873-488X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kElrHDEQRoWJ8TLxLzAEnXLrTqml3gI5mMFLwOBLArkEUS2VZjT0FqnbMP716fEM5JZT1eHVV1WPsVsBqQBRfNmlrxhNn2YAeQoyBZBn7EpUpUxUVf36sPSQF0lVivqSXce4g4WohbpglyKvCyGz_Ir9XmOwfjgkzS0GPmLAjiYKkfueY48Upy1N_o0s38y-J-Sj38Sv_I5HdDTt-bjF0KEZ2mGz59EEot73G94NltqP7NxhG-nmVFfs58P9j_VT8vzy-H1995wYCXJK6qwwzlZZDa52ZFFZWTRZ1og6c6rJncvIYJGLKqcGSgGKBJgCFSCpWpGVK_b5mDuG4c-8nKw7Hw21LfY0zFGLUuVVWVYLKI-gCUOMgZweg-8w7LUAfbCqd_rdqj5Y1SD14myZ-nSKn5uO7L-Zk8YF-HYEaHny1VPQ0XjqDVkfyEzaDv6_C_4CN-eLxg</recordid><startdate>200507</startdate><enddate>200507</enddate><creator>Hauser, Daniela S.</creator><creator>Stade, Matthias</creator><creator>Schmidt, Angela</creator><creator>Hanauer, Guido</creator><general>Elsevier Inc</general><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>200507</creationdate><title>Cardiovascular parameters in anaesthetized guinea pigs: A safety pharmacology screening model</title><author>Hauser, Daniela S. ; Stade, Matthias ; Schmidt, Angela ; Hanauer, Guido</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-926cfd8290f9feda4d36b22b192f4b5ff2eca65185eb07104e10c6a40ae494ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Anaesthetized guinea pigs</topic><topic>Anesthesia</topic><topic>Animals</topic><topic>Blood pressure</topic><topic>Cardiovascular Agents - adverse effects</topic><topic>Cardiovascular Agents - classification</topic><topic>Cardiovascular Physiological Phenomena - drug effects</topic><topic>Cardiovascular System - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Evaluation, Preclinical - methods</topic><topic>Drug-Related Side Effects and Adverse Reactions</topic><topic>ECG</topic><topic>Electrocardiography</topic><topic>Epinephrine - adverse effects</topic><topic>Guinea Pigs</topic><topic>Hemodynamics - drug effects</topic><topic>Interval</topic><topic>Intravenous drug infusion</topic><topic>Isoproterenol - adverse effects</topic><topic>Left ventricular pressure</topic><topic>Male</topic><topic>Methods</topic><topic>Models, Animal</topic><topic>Nifedipine - adverse effects</topic><topic>Ouabain - adverse effects</topic><topic>Pharmaceutical Preparations - classification</topic><topic>Safety pharmacology</topic><topic>Verapamil - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hauser, Daniela S.</creatorcontrib><creatorcontrib>Stade, Matthias</creatorcontrib><creatorcontrib>Schmidt, Angela</creatorcontrib><creatorcontrib>Hanauer, Guido</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of pharmacological and toxicological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hauser, Daniela S.</au><au>Stade, Matthias</au><au>Schmidt, Angela</au><au>Hanauer, Guido</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiovascular parameters in anaesthetized guinea pigs: A safety pharmacology screening model</atitle><jtitle>Journal of pharmacological and toxicological methods</jtitle><addtitle>J Pharmacol Toxicol Methods</addtitle><date>2005-07</date><risdate>2005</risdate><volume>52</volume><issue>1</issue><spage>106</spage><epage>114</epage><pages>106-114</pages><issn>1056-8719</issn><eissn>1873-488X</eissn><abstract>Assessment of cardiovascular functions in vivo is part of the core battery of guideline ICH S7A and is thereby required by regulatory authorities. The haemodynamic effects of repeated intravenous administrations of reference compounds were analyzed in order to validate the guinea pig model for safety pharmacology studies under GLP conditions. Male guinea pigs ( n = 54, weighing 565–762 g) were anaesthetized using 1.5 g/kg, i.p., urethane. Systolic arterial blood pressure (SAP), diastolic arterial blood pressure (DAP), heart rate (HR), left ventricular pressure (LVP), cardiac contractility (d p/d t max), and ECG (RR, QT, and QTc intervals) were recorded continuously. Animals received vehicle i.v. followed by cumulative doses of reference compounds. Vehicle did not produce any relevant changes, either in cardiovascular or ECG parameters. Isoproterenol caused a rapid and significant increase in HR, LVP, and d p/d t max, in contrast to a dose-dependent decrease in SAP and DAP. Epinephrine led to a potent increase in all cardiovascular parameters. Nifedipine produced a slight decrease in HR and LVP, and a potent decrease in blood pressure and d p/d t max. Verapamil caused a dose-dependent decrease in all cardiovascular parameters. Ouabain resulted in a significant increase in SAP, DAP, LVP, and d p/d t max; ECG showed an atrioventricular block and arrhythmia. Terfenadine, cisapride, and sotalol prolonged QT and QTc intervals, whereas vehicle and the other tested compounds did not produce any prolongation of the QTc interval. Our results on HR, blood pressure, and ECG obtained after i.v. administration of reference compounds show the usefulness of the guinea pig in assessing cardiovascular safety. The anaesthetized guinea pig allows the measurement of cardiac contractility and the use of doses higher than in conscious animals. Using this animal model, several cardiovascular parameters can be recorded simultaneously at a modest cost in terms of test compound and the number of animals required.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15961325</pmid><doi>10.1016/j.vascn.2005.03.003</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1056-8719
ispartof Journal of pharmacological and toxicological methods, 2005-07, Vol.52 (1), p.106-114
issn 1056-8719
1873-488X
language eng
recordid cdi_proquest_miscellaneous_17458778
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Anaesthetized guinea pigs
Anesthesia
Animals
Blood pressure
Cardiovascular Agents - adverse effects
Cardiovascular Agents - classification
Cardiovascular Physiological Phenomena - drug effects
Cardiovascular System - drug effects
Dose-Response Relationship, Drug
Drug Evaluation, Preclinical - methods
Drug-Related Side Effects and Adverse Reactions
ECG
Electrocardiography
Epinephrine - adverse effects
Guinea Pigs
Hemodynamics - drug effects
Interval
Intravenous drug infusion
Isoproterenol - adverse effects
Left ventricular pressure
Male
Methods
Models, Animal
Nifedipine - adverse effects
Ouabain - adverse effects
Pharmaceutical Preparations - classification
Safety pharmacology
Verapamil - adverse effects
title Cardiovascular parameters in anaesthetized guinea pigs: A safety pharmacology screening model
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T08%3A20%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cardiovascular%20parameters%20in%20anaesthetized%20guinea%20pigs:%20A%20safety%20pharmacology%20screening%20model&rft.jtitle=Journal%20of%20pharmacological%20and%20toxicological%20methods&rft.au=Hauser,%20Daniela%20S.&rft.date=2005-07&rft.volume=52&rft.issue=1&rft.spage=106&rft.epage=114&rft.pages=106-114&rft.issn=1056-8719&rft.eissn=1873-488X&rft_id=info:doi/10.1016/j.vascn.2005.03.003&rft_dat=%3Cproquest_cross%3E17458778%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17458778&rft_id=info:pmid/15961325&rft_els_id=S1056871905000432&rfr_iscdi=true