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...
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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 |
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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> |
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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 |
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