Effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat

The effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output, blood pressure, mean circulatory filling pressure ( P mcf ), arterial and venous resistances, heart rate and left ventricular end‐diastolic pressure were assessed in rats with acute heart failure by means of co...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:British journal of pharmacology 2009-02, Vol.123 (8), p.1666-1672
Hauptverfasser: Nekooeian, Ali A., Tabrizchi, Reza
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1672
container_issue 8
container_start_page 1666
container_title British journal of pharmacology
container_volume 123
creator Nekooeian, Ali A.
Tabrizchi, Reza
description The effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output, blood pressure, mean circulatory filling pressure ( P mcf ), arterial and venous resistances, heart rate and left ventricular end‐diastolic pressure were assessed in rats with acute heart failure by means of coronary artery occlusion. Animals ( n =6 in each group) were divided into five groups: group I, sham‐operated vehicle‐treated (0.9% saline; 0.018 mL min −1 ); groups II‐V, subject to coronary artery occlusion and treated with vehicle (0.9% saline; 0.018 ml min −1 ) and CGS 21680 (0.1, 0.3 and 1.0 μg kg −1  min −1 ), respectively. Haemodynamic measurements were taken one hour after completion of surgery, ninety minutes after coronary artery occlusion (except in group I), and fifteen minutes after infusion of saline or CGS 21680. Baseline haemodynamic measurements before occlusion were found not to differ significantly between the different groups of animals. However, after occlusion, cardiac output, rate of rise in left ventricular pressure (+d P /dt) and blood pressure were significantly reduced when compared to corresponding values in sham‐operated animals. In addition, occlusion of the coronary artery resulted in a significant elevation in venous resistance, P mcf and left ventricular end‐diastolic pressure as compared to corresponding values in sham‐operated animals. Infusion with CGS 21680 at the highest dose significantly reduced blood pressure, arterial resistance and left ventricular end‐diastolic pressure when compared to occluded vehicle‐treated animals (group II). Administration of CGS 21680 at the highest dose also significantly increased cardiac output (28%) and heart rate (10%) in comparison to occluded vehicle‐treated animals. In addition, the highest dose of CGS 21680 significantly reduced P mcf (9%) and venous resistance (62%) in comparison to occluded vehicle‐treated animals. Administration of CGS 21680 did not significantly affect +d P /dt when compared to occluded vehicle‐treated animals. The results from the present investigation indicate that occlusion of the coronary artery in rats results in a state of heart failure characterized by reduced arterial pressure and cardiac output, and increased venous resistance, P mcf and left ventricular end‐diastolic pressure. Administration of CGS 21680 to animals with acute heart failure resulted in increased cardiac output which was due to reduced venous resistance, as well as increased heart rate. Briti
doi_str_mv 10.1038/sj.bjp.0701764
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1038_sj_bjp_0701764</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1038_sj_bjp_0701764</sourcerecordid><originalsourceid>FETCH-LOGICAL-c844-a7a8dbb876850d9ebe1d986d52fe239f7d7062eee240bc16c17da9a76ac316183</originalsourceid><addsrcrecordid>eNotkMtOwzAQRS0EEqWwZT0f0AQ7D9tdVlV5SJVY0H00sSfUUUgi26kE38LHEqCrubqPWRzG7gVPBc_1Q2jTuh1TrrhQsrhgC1EomZS5FpdswTlXiRBaX7ObEFrO51CVC_a9axoyMcDQwPbpDTIhNV8BQqBu9t2JYAPZBtBSPwTXE3gyNMbBA74PvQtxBUMPBr11aGCY4jhFwN7CCYOZOvTzIMw17A2B6wHNFAmOhD5Cg66b_J8djzSvkMIsovsiCx7jLbtqsAt0d75LdnjcHbbPyf716WW72SdGF0WCCrWta62kLrldU03CrrW0ZdZQlq8bZRWXGRFlBa-NkEYoi2tUEk0upND5kqX_b40fQvDUVKN3H-g_K8GrX7RVaKsZbXVGm_8AaYpvGg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat</title><source>Wiley Online Library Free Content</source><source>Access via Wiley Online Library</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><creator>Nekooeian, Ali A. ; Tabrizchi, Reza</creator><creatorcontrib>Nekooeian, Ali A. ; Tabrizchi, Reza</creatorcontrib><description>The effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output, blood pressure, mean circulatory filling pressure ( P mcf ), arterial and venous resistances, heart rate and left ventricular end‐diastolic pressure were assessed in rats with acute heart failure by means of coronary artery occlusion. Animals ( n =6 in each group) were divided into five groups: group I, sham‐operated vehicle‐treated (0.9% saline; 0.018 mL min −1 ); groups II‐V, subject to coronary artery occlusion and treated with vehicle (0.9% saline; 0.018 ml min −1 ) and CGS 21680 (0.1, 0.3 and 1.0 μg kg −1  min −1 ), respectively. Haemodynamic measurements were taken one hour after completion of surgery, ninety minutes after coronary artery occlusion (except in group I), and fifteen minutes after infusion of saline or CGS 21680. Baseline haemodynamic measurements before occlusion were found not to differ significantly between the different groups of animals. However, after occlusion, cardiac output, rate of rise in left ventricular pressure (+d P /dt) and blood pressure were significantly reduced when compared to corresponding values in sham‐operated animals. In addition, occlusion of the coronary artery resulted in a significant elevation in venous resistance, P mcf and left ventricular end‐diastolic pressure as compared to corresponding values in sham‐operated animals. Infusion with CGS 21680 at the highest dose significantly reduced blood pressure, arterial resistance and left ventricular end‐diastolic pressure when compared to occluded vehicle‐treated animals (group II). Administration of CGS 21680 at the highest dose also significantly increased cardiac output (28%) and heart rate (10%) in comparison to occluded vehicle‐treated animals. In addition, the highest dose of CGS 21680 significantly reduced P mcf (9%) and venous resistance (62%) in comparison to occluded vehicle‐treated animals. Administration of CGS 21680 did not significantly affect +d P /dt when compared to occluded vehicle‐treated animals. The results from the present investigation indicate that occlusion of the coronary artery in rats results in a state of heart failure characterized by reduced arterial pressure and cardiac output, and increased venous resistance, P mcf and left ventricular end‐diastolic pressure. Administration of CGS 21680 to animals with acute heart failure resulted in increased cardiac output which was due to reduced venous resistance, as well as increased heart rate. British Journal of Pharmacology (1998) 123 , 1666–1672; doi: 10.1038/sj.bjp.0701764</description><identifier>ISSN: 0007-1188</identifier><identifier>EISSN: 1476-5381</identifier><identifier>DOI: 10.1038/sj.bjp.0701764</identifier><language>eng</language><ispartof>British journal of pharmacology, 2009-02, Vol.123 (8), p.1666-1672</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c844-a7a8dbb876850d9ebe1d986d52fe239f7d7062eee240bc16c17da9a76ac316183</citedby><cites>FETCH-LOGICAL-c844-a7a8dbb876850d9ebe1d986d52fe239f7d7062eee240bc16c17da9a76ac316183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Nekooeian, Ali A.</creatorcontrib><creatorcontrib>Tabrizchi, Reza</creatorcontrib><title>Effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat</title><title>British journal of pharmacology</title><description>The effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output, blood pressure, mean circulatory filling pressure ( P mcf ), arterial and venous resistances, heart rate and left ventricular end‐diastolic pressure were assessed in rats with acute heart failure by means of coronary artery occlusion. Animals ( n =6 in each group) were divided into five groups: group I, sham‐operated vehicle‐treated (0.9% saline; 0.018 mL min −1 ); groups II‐V, subject to coronary artery occlusion and treated with vehicle (0.9% saline; 0.018 ml min −1 ) and CGS 21680 (0.1, 0.3 and 1.0 μg kg −1  min −1 ), respectively. Haemodynamic measurements were taken one hour after completion of surgery, ninety minutes after coronary artery occlusion (except in group I), and fifteen minutes after infusion of saline or CGS 21680. Baseline haemodynamic measurements before occlusion were found not to differ significantly between the different groups of animals. However, after occlusion, cardiac output, rate of rise in left ventricular pressure (+d P /dt) and blood pressure were significantly reduced when compared to corresponding values in sham‐operated animals. In addition, occlusion of the coronary artery resulted in a significant elevation in venous resistance, P mcf and left ventricular end‐diastolic pressure as compared to corresponding values in sham‐operated animals. Infusion with CGS 21680 at the highest dose significantly reduced blood pressure, arterial resistance and left ventricular end‐diastolic pressure when compared to occluded vehicle‐treated animals (group II). Administration of CGS 21680 at the highest dose also significantly increased cardiac output (28%) and heart rate (10%) in comparison to occluded vehicle‐treated animals. In addition, the highest dose of CGS 21680 significantly reduced P mcf (9%) and venous resistance (62%) in comparison to occluded vehicle‐treated animals. Administration of CGS 21680 did not significantly affect +d P /dt when compared to occluded vehicle‐treated animals. The results from the present investigation indicate that occlusion of the coronary artery in rats results in a state of heart failure characterized by reduced arterial pressure and cardiac output, and increased venous resistance, P mcf and left ventricular end‐diastolic pressure. Administration of CGS 21680 to animals with acute heart failure resulted in increased cardiac output which was due to reduced venous resistance, as well as increased heart rate. British Journal of Pharmacology (1998) 123 , 1666–1672; doi: 10.1038/sj.bjp.0701764</description><issn>0007-1188</issn><issn>1476-5381</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNotkMtOwzAQRS0EEqWwZT0f0AQ7D9tdVlV5SJVY0H00sSfUUUgi26kE38LHEqCrubqPWRzG7gVPBc_1Q2jTuh1TrrhQsrhgC1EomZS5FpdswTlXiRBaX7ObEFrO51CVC_a9axoyMcDQwPbpDTIhNV8BQqBu9t2JYAPZBtBSPwTXE3gyNMbBA74PvQtxBUMPBr11aGCY4jhFwN7CCYOZOvTzIMw17A2B6wHNFAmOhD5Cg66b_J8djzSvkMIsovsiCx7jLbtqsAt0d75LdnjcHbbPyf716WW72SdGF0WCCrWta62kLrldU03CrrW0ZdZQlq8bZRWXGRFlBa-NkEYoi2tUEk0upND5kqX_b40fQvDUVKN3H-g_K8GrX7RVaKsZbXVGm_8AaYpvGg</recordid><startdate>20090210</startdate><enddate>20090210</enddate><creator>Nekooeian, Ali A.</creator><creator>Tabrizchi, Reza</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20090210</creationdate><title>Effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat</title><author>Nekooeian, Ali A. ; Tabrizchi, Reza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c844-a7a8dbb876850d9ebe1d986d52fe239f7d7062eee240bc16c17da9a76ac316183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nekooeian, Ali A.</creatorcontrib><creatorcontrib>Tabrizchi, Reza</creatorcontrib><collection>CrossRef</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nekooeian, Ali A.</au><au>Tabrizchi, Reza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat</atitle><jtitle>British journal of pharmacology</jtitle><date>2009-02-10</date><risdate>2009</risdate><volume>123</volume><issue>8</issue><spage>1666</spage><epage>1672</epage><pages>1666-1672</pages><issn>0007-1188</issn><eissn>1476-5381</eissn><abstract>The effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output, blood pressure, mean circulatory filling pressure ( P mcf ), arterial and venous resistances, heart rate and left ventricular end‐diastolic pressure were assessed in rats with acute heart failure by means of coronary artery occlusion. Animals ( n =6 in each group) were divided into five groups: group I, sham‐operated vehicle‐treated (0.9% saline; 0.018 mL min −1 ); groups II‐V, subject to coronary artery occlusion and treated with vehicle (0.9% saline; 0.018 ml min −1 ) and CGS 21680 (0.1, 0.3 and 1.0 μg kg −1  min −1 ), respectively. Haemodynamic measurements were taken one hour after completion of surgery, ninety minutes after coronary artery occlusion (except in group I), and fifteen minutes after infusion of saline or CGS 21680. Baseline haemodynamic measurements before occlusion were found not to differ significantly between the different groups of animals. However, after occlusion, cardiac output, rate of rise in left ventricular pressure (+d P /dt) and blood pressure were significantly reduced when compared to corresponding values in sham‐operated animals. In addition, occlusion of the coronary artery resulted in a significant elevation in venous resistance, P mcf and left ventricular end‐diastolic pressure as compared to corresponding values in sham‐operated animals. Infusion with CGS 21680 at the highest dose significantly reduced blood pressure, arterial resistance and left ventricular end‐diastolic pressure when compared to occluded vehicle‐treated animals (group II). Administration of CGS 21680 at the highest dose also significantly increased cardiac output (28%) and heart rate (10%) in comparison to occluded vehicle‐treated animals. In addition, the highest dose of CGS 21680 significantly reduced P mcf (9%) and venous resistance (62%) in comparison to occluded vehicle‐treated animals. Administration of CGS 21680 did not significantly affect +d P /dt when compared to occluded vehicle‐treated animals. The results from the present investigation indicate that occlusion of the coronary artery in rats results in a state of heart failure characterized by reduced arterial pressure and cardiac output, and increased venous resistance, P mcf and left ventricular end‐diastolic pressure. Administration of CGS 21680 to animals with acute heart failure resulted in increased cardiac output which was due to reduced venous resistance, as well as increased heart rate. British Journal of Pharmacology (1998) 123 , 1666–1672; doi: 10.1038/sj.bjp.0701764</abstract><doi>10.1038/sj.bjp.0701764</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0007-1188
ispartof British journal of pharmacology, 2009-02, Vol.123 (8), p.1666-1672
issn 0007-1188
1476-5381
language eng
recordid cdi_crossref_primary_10_1038_sj_bjp_0701764
source Wiley Online Library Free Content; Access via Wiley Online Library; PubMed Central; Alma/SFX Local Collection; EZB Electronic Journals Library
title Effects of CGS 21680, a selective A 2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T11%3A41%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20CGS%2021680,%20a%20selective%20A%202A%20adenosine%20receptor%20agonist,%20on%20cardiac%20output%20and%20vascular%20resistance%20in%20acute%20heart%20failure%20in%20the%20anaesthetized%20rat&rft.jtitle=British%20journal%20of%20pharmacology&rft.au=Nekooeian,%20Ali%20A.&rft.date=2009-02-10&rft.volume=123&rft.issue=8&rft.spage=1666&rft.epage=1672&rft.pages=1666-1672&rft.issn=0007-1188&rft.eissn=1476-5381&rft_id=info:doi/10.1038/sj.bjp.0701764&rft_dat=%3Ccrossref%3E10_1038_sj_bjp_0701764%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true