EFFECTS OF CARDIOTROPHIN-1 ON HAEMODYNAMICS AND CARDIAC FUNCTION IN CONSCIOUS RATS
Cardiotrophin-1 (CT-1), a newly discovered cytokine, has been shown to induce cardiac hypertrophy in vitro and in vivo. The present study examined the effects of CT-1 on haemodynamics and cardiac function. The measurements of haemodynamic parameters were made using in-dwelling catheters and flow pro...
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Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 1998-01, Vol.10 (1), p.19-25 |
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description | Cardiotrophin-1 (CT-1), a newly discovered cytokine, has been shown to induce cardiac hypertrophy in vitro and in vivo. The present study examined the effects of CT-1 on haemodynamics and cardiac function. The measurements of haemodynamic parameters were made using in-dwelling catheters and flow probes in conscious, unrestrained rats. Intravenous administration of CT-1 caused a dose-dependent decrease in mean arterial pressure (MAP), and an increase in heart rate (HR). CT-1 (100 μg/kg) significantly elevated cardiac output and HR, and decreased MAP and systemic vascular resistance. Stroke volume was unaltered, suggesting that the CT-1 induced increase in cardiac output was secondary to increased HR. There was no significant difference in left ventricular maximal dP/dtbetween the CT-1-treated and vehicle-treated groups, suggesting that CT-1 might not induce a meaningful change in ventricular contractility. Pretreatment with intravenous Nω-nitro-l-arginine methyl ester, a specific inhibitor of nitric oxide synthase, significantly attenuated the depressor and tachycardic responses to CT-1. These results indicate that nitric oxide plays an important role in mediating the haemodynamic effects of CT-1. |
doi_str_mv | 10.1006/cyto.1997.0241 |
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The present study examined the effects of CT-1 on haemodynamics and cardiac function. The measurements of haemodynamic parameters were made using in-dwelling catheters and flow probes in conscious, unrestrained rats. Intravenous administration of CT-1 caused a dose-dependent decrease in mean arterial pressure (MAP), and an increase in heart rate (HR). CT-1 (100 μg/kg) significantly elevated cardiac output and HR, and decreased MAP and systemic vascular resistance. Stroke volume was unaltered, suggesting that the CT-1 induced increase in cardiac output was secondary to increased HR. There was no significant difference in left ventricular maximal dP/dtbetween the CT-1-treated and vehicle-treated groups, suggesting that CT-1 might not induce a meaningful change in ventricular contractility. Pretreatment with intravenous Nω-nitro-l-arginine methyl ester, a specific inhibitor of nitric oxide synthase, significantly attenuated the depressor and tachycardic responses to CT-1. These results indicate that nitric oxide plays an important role in mediating the haemodynamic effects of CT-1.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1006/cyto.1997.0241</identifier><identifier>PMID: 9505141</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Cardiac Output - drug effects ; cardiotrophin-1 , cytokine , haemodynamics , cardiac function , nitric oxide ; Cytokines - pharmacology ; Heart - drug effects ; Heart - physiology ; Hemodynamics - drug effects ; Hypotension - chemically induced ; Injections, Intravenous ; Male ; Nitric Oxide - metabolism ; Rats ; Rats, Sprague-Dawley ; Tachycardia ; Ventricular Function, Left - drug effects</subject><ispartof>Cytokine (Philadelphia, Pa.), 1998-01, Vol.10 (1), p.19-25</ispartof><rights>1998 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-37a1038044c50a398b2933f6df39940b67579f2d7beb593d2d3283fa7964c763</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/cyto.1997.0241$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9505141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jin, Hongkui</creatorcontrib><creatorcontrib>Yang, Renhui</creatorcontrib><creatorcontrib>Ko, Annie</creatorcontrib><creatorcontrib>Pennica, Diane</creatorcontrib><creatorcontrib>Wood, William I.</creatorcontrib><creatorcontrib>Paoni, Nicholas F.</creatorcontrib><title>EFFECTS OF CARDIOTROPHIN-1 ON HAEMODYNAMICS AND CARDIAC FUNCTION IN CONSCIOUS RATS</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>Cardiotrophin-1 (CT-1), a newly discovered cytokine, has been shown to induce cardiac hypertrophy in vitro and in vivo. The present study examined the effects of CT-1 on haemodynamics and cardiac function. The measurements of haemodynamic parameters were made using in-dwelling catheters and flow probes in conscious, unrestrained rats. Intravenous administration of CT-1 caused a dose-dependent decrease in mean arterial pressure (MAP), and an increase in heart rate (HR). CT-1 (100 μg/kg) significantly elevated cardiac output and HR, and decreased MAP and systemic vascular resistance. Stroke volume was unaltered, suggesting that the CT-1 induced increase in cardiac output was secondary to increased HR. There was no significant difference in left ventricular maximal dP/dtbetween the CT-1-treated and vehicle-treated groups, suggesting that CT-1 might not induce a meaningful change in ventricular contractility. Pretreatment with intravenous Nω-nitro-l-arginine methyl ester, a specific inhibitor of nitric oxide synthase, significantly attenuated the depressor and tachycardic responses to CT-1. These results indicate that nitric oxide plays an important role in mediating the haemodynamic effects of CT-1.</description><subject>Animals</subject><subject>Cardiac Output - drug effects</subject><subject>cardiotrophin-1 , cytokine , haemodynamics , cardiac function , nitric oxide</subject><subject>Cytokines - pharmacology</subject><subject>Heart - drug effects</subject><subject>Heart - physiology</subject><subject>Hemodynamics - drug effects</subject><subject>Hypotension - chemically induced</subject><subject>Injections, Intravenous</subject><subject>Male</subject><subject>Nitric Oxide - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Tachycardia</subject><subject>Ventricular Function, Left - drug effects</subject><issn>1043-4666</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE9PgzAYxhujmTq9ejPhC4BvaWnpkXTgSDZqgB08NVBKgnFugWmyby-ExZun90meP3nzQ-gJg4cB2Is5nw4eFoJ74FN8he4wCOYC-OR60pS4lDF2i-6H4QMABOF8gRYigABTfIfyOEliWRaOShwZ5atUlbl6W6eZix2VOeso3qrVexZtU1k4UbaaQ5F0kl0my3SMpJkjVVbIVO0KJ4_K4gHdtNXnYB8vd4nKJC7l2t2o11RGG9cQIk4u4RUGEgKlJoCKiLD2BSEta1oiBIWa8YCL1m94betAkMZviB-StuKCUcMZWSJvnjX9YRh62-pj3-2r_qwx6AmNntDoCY2e0IyF57lw_K73tvmLX1iMfjj7dnz6p7O9Hkxnv4xtut6ak24O3X_Tv6L1agk</recordid><startdate>199801</startdate><enddate>199801</enddate><creator>Jin, Hongkui</creator><creator>Yang, Renhui</creator><creator>Ko, Annie</creator><creator>Pennica, Diane</creator><creator>Wood, William I.</creator><creator>Paoni, Nicholas F.</creator><general>Elsevier Ltd</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></search><sort><creationdate>199801</creationdate><title>EFFECTS OF CARDIOTROPHIN-1 ON HAEMODYNAMICS AND CARDIAC FUNCTION IN CONSCIOUS RATS</title><author>Jin, Hongkui ; Yang, Renhui ; Ko, Annie ; Pennica, Diane ; Wood, William I. ; Paoni, Nicholas F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-37a1038044c50a398b2933f6df39940b67579f2d7beb593d2d3283fa7964c763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Cardiac Output - drug effects</topic><topic>cardiotrophin-1 , cytokine , haemodynamics , cardiac function , nitric oxide</topic><topic>Cytokines - pharmacology</topic><topic>Heart - drug effects</topic><topic>Heart - physiology</topic><topic>Hemodynamics - drug effects</topic><topic>Hypotension - chemically induced</topic><topic>Injections, Intravenous</topic><topic>Male</topic><topic>Nitric Oxide - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Tachycardia</topic><topic>Ventricular Function, Left - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jin, Hongkui</creatorcontrib><creatorcontrib>Yang, Renhui</creatorcontrib><creatorcontrib>Ko, Annie</creatorcontrib><creatorcontrib>Pennica, Diane</creatorcontrib><creatorcontrib>Wood, William I.</creatorcontrib><creatorcontrib>Paoni, Nicholas F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jin, Hongkui</au><au>Yang, Renhui</au><au>Ko, Annie</au><au>Pennica, Diane</au><au>Wood, William I.</au><au>Paoni, Nicholas F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EFFECTS OF CARDIOTROPHIN-1 ON HAEMODYNAMICS AND CARDIAC FUNCTION IN CONSCIOUS RATS</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>1998-01</date><risdate>1998</risdate><volume>10</volume><issue>1</issue><spage>19</spage><epage>25</epage><pages>19-25</pages><issn>1043-4666</issn><eissn>1096-0023</eissn><abstract>Cardiotrophin-1 (CT-1), a newly discovered cytokine, has been shown to induce cardiac hypertrophy in vitro and in vivo. The present study examined the effects of CT-1 on haemodynamics and cardiac function. The measurements of haemodynamic parameters were made using in-dwelling catheters and flow probes in conscious, unrestrained rats. Intravenous administration of CT-1 caused a dose-dependent decrease in mean arterial pressure (MAP), and an increase in heart rate (HR). CT-1 (100 μg/kg) significantly elevated cardiac output and HR, and decreased MAP and systemic vascular resistance. Stroke volume was unaltered, suggesting that the CT-1 induced increase in cardiac output was secondary to increased HR. There was no significant difference in left ventricular maximal dP/dtbetween the CT-1-treated and vehicle-treated groups, suggesting that CT-1 might not induce a meaningful change in ventricular contractility. Pretreatment with intravenous Nω-nitro-l-arginine methyl ester, a specific inhibitor of nitric oxide synthase, significantly attenuated the depressor and tachycardic responses to CT-1. These results indicate that nitric oxide plays an important role in mediating the haemodynamic effects of CT-1.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>9505141</pmid><doi>10.1006/cyto.1997.0241</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Cardiac Output - drug effects cardiotrophin-1 , cytokine , haemodynamics , cardiac function , nitric oxide Cytokines - pharmacology Heart - drug effects Heart - physiology Hemodynamics - drug effects Hypotension - chemically induced Injections, Intravenous Male Nitric Oxide - metabolism Rats Rats, Sprague-Dawley Tachycardia Ventricular Function, Left - drug effects |
title | EFFECTS OF CARDIOTROPHIN-1 ON HAEMODYNAMICS AND CARDIAC FUNCTION IN CONSCIOUS RATS |
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