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Increased cardiac expression of endothelin-1 mRNA in ischemic heart failure in rats
Objectives: Plasma endothelin (ET) concentrations are increased in heart failure. The aims of the present study were to investigate to what extent cardiac ET mRNA expression is induced in ischemic heart failure and whether there may be compensatory downregulation of myocardial mRNA levels for the ET...
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Published in: | Cardiovascular research 1997-03, Vol.33 (3), p.601-610 |
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container_title | Cardiovascular research |
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creator | Tønnessen, Theis Christensen, Geir Øie, Erik Holt, Even Kjekshus, Harald Smiseth, Otto A. Sejersted, Ole M. Attramadal, Håvard |
description | Objectives: Plasma endothelin (ET) concentrations are increased in heart failure. The aims of the present study were to investigate to what extent cardiac ET mRNA expression is induced in ischemic heart failure and whether there may be compensatory downregulation of myocardial mRNA levels for the ETA and ETB receptor subtypes. Methods: In rats with ischemic heart failure (left ventricular end-diastolic pressure > 15 mmHg) due to left coronary artery ligation, Northern blot analyses were performed on mRNA isolated from cardiac tissues. Results: A substantial upregulation was revealed in all chambers of the failing hearts. Up to 27-fold upregulation (mean 10.6 ± 4.0, P = 0.002) of left ventricular ET-1 mRNA levels was measured 1 week after myocardial infarction, whereas only a modest upregulation was detected after 6 weeks (mean 2.7 ± 0.5, P < 0.05). Ribonuclease protection assay revealed 2.8 ± 0.4-fold higher levels of ET-1 mRNA in the left ventricular area subjected to myocardial infarction compared to the non-infarcted tissue after 1 week. Left ventricular ET-1 mRNA correlated significantly with left ventricular end-diastolic pressure after 1 week (r2 = 0.86, P = 0.007). The ETA and ETB receptor mRNA levels tended to increase 1 week after myocardial infarction although these changes were not statistically significant. Conclusions: Cardiac ET-1 mRNA levels are increased in ischemic heart failure and correlate significantly with left ventricular end-diastolic pressure 1 week after myocardial infarction. The increase in cardiac ET-1 mRNA is not accompanied by a decrease in ET receptor mRNA. |
doi_str_mv | 10.1016/S0008-6363(96)00266-0 |
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The aims of the present study were to investigate to what extent cardiac ET mRNA expression is induced in ischemic heart failure and whether there may be compensatory downregulation of myocardial mRNA levels for the ETA and ETB receptor subtypes. Methods: In rats with ischemic heart failure (left ventricular end-diastolic pressure > 15 mmHg) due to left coronary artery ligation, Northern blot analyses were performed on mRNA isolated from cardiac tissues. Results: A substantial upregulation was revealed in all chambers of the failing hearts. Up to 27-fold upregulation (mean 10.6 ± 4.0, P = 0.002) of left ventricular ET-1 mRNA levels was measured 1 week after myocardial infarction, whereas only a modest upregulation was detected after 6 weeks (mean 2.7 ± 0.5, P < 0.05). Ribonuclease protection assay revealed 2.8 ± 0.4-fold higher levels of ET-1 mRNA in the left ventricular area subjected to myocardial infarction compared to the non-infarcted tissue after 1 week. Left ventricular ET-1 mRNA correlated significantly with left ventricular end-diastolic pressure after 1 week (r2 = 0.86, P = 0.007). The ETA and ETB receptor mRNA levels tended to increase 1 week after myocardial infarction although these changes were not statistically significant. Conclusions: Cardiac ET-1 mRNA levels are increased in ischemic heart failure and correlate significantly with left ventricular end-diastolic pressure 1 week after myocardial infarction. The increase in cardiac ET-1 mRNA is not accompanied by a decrease in ET receptor mRNA.</description><identifier>ISSN: 0008-6363</identifier><identifier>EISSN: 1755-3245</identifier><identifier>DOI: 10.1016/S0008-6363(96)00266-0</identifier><identifier>PMID: 9093530</identifier><identifier>CODEN: CVREAU</identifier><language>eng</language><publisher>Oxford: Elsevier Science</publisher><subject>Animals ; Biological and medical sciences ; Blotting, Northern ; Cardiology. Vascular system ; Coronary heart disease ; Endothelin ; Endothelin-1 - genetics ; Heart ; Heart failure ; Male ; Medical sciences ; mRNA ; Myocardial Infarction - metabolism ; Myocardial Ischemia - metabolism ; Myocardium - metabolism ; Rat ; Rats ; Rats, Wistar ; Receptors, Endothelin - metabolism ; RNA, Messenger - analysis ; RNA, Messenger - metabolism ; Stroke Volume</subject><ispartof>Cardiovascular research, 1997-03, Vol.33 (3), p.601-610</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-ec8c711c1c6316457590fe643b8a0bbaa339dfb25e74f0e22ab684889655d6a23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2600496$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9093530$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tønnessen, Theis</creatorcontrib><creatorcontrib>Christensen, Geir</creatorcontrib><creatorcontrib>Øie, Erik</creatorcontrib><creatorcontrib>Holt, Even</creatorcontrib><creatorcontrib>Kjekshus, Harald</creatorcontrib><creatorcontrib>Smiseth, Otto A.</creatorcontrib><creatorcontrib>Sejersted, Ole M.</creatorcontrib><creatorcontrib>Attramadal, Håvard</creatorcontrib><title>Increased cardiac expression of endothelin-1 mRNA in ischemic heart failure in rats</title><title>Cardiovascular research</title><addtitle>Cardiovasc Res</addtitle><description>Objectives: Plasma endothelin (ET) concentrations are increased in heart failure. The aims of the present study were to investigate to what extent cardiac ET mRNA expression is induced in ischemic heart failure and whether there may be compensatory downregulation of myocardial mRNA levels for the ETA and ETB receptor subtypes. Methods: In rats with ischemic heart failure (left ventricular end-diastolic pressure > 15 mmHg) due to left coronary artery ligation, Northern blot analyses were performed on mRNA isolated from cardiac tissues. Results: A substantial upregulation was revealed in all chambers of the failing hearts. Up to 27-fold upregulation (mean 10.6 ± 4.0, P = 0.002) of left ventricular ET-1 mRNA levels was measured 1 week after myocardial infarction, whereas only a modest upregulation was detected after 6 weeks (mean 2.7 ± 0.5, P < 0.05). Ribonuclease protection assay revealed 2.8 ± 0.4-fold higher levels of ET-1 mRNA in the left ventricular area subjected to myocardial infarction compared to the non-infarcted tissue after 1 week. Left ventricular ET-1 mRNA correlated significantly with left ventricular end-diastolic pressure after 1 week (r2 = 0.86, P = 0.007). The ETA and ETB receptor mRNA levels tended to increase 1 week after myocardial infarction although these changes were not statistically significant. Conclusions: Cardiac ET-1 mRNA levels are increased in ischemic heart failure and correlate significantly with left ventricular end-diastolic pressure 1 week after myocardial infarction. The increase in cardiac ET-1 mRNA is not accompanied by a decrease in ET receptor mRNA.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Cardiology. Vascular system</subject><subject>Coronary heart disease</subject><subject>Endothelin</subject><subject>Endothelin-1 - genetics</subject><subject>Heart</subject><subject>Heart failure</subject><subject>Male</subject><subject>Medical sciences</subject><subject>mRNA</subject><subject>Myocardial Infarction - metabolism</subject><subject>Myocardial Ischemia - metabolism</subject><subject>Myocardium - metabolism</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Endothelin - metabolism</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - metabolism</subject><subject>Stroke Volume</subject><issn>0008-6363</issn><issn>1755-3245</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNo9kFtrFEEQRpugxDXmJwT6QUQfRqunL9P9GDbqRoOCiRDy0tT01LCtc9l0z0L8985ml30qiu_UhcPYhYCPAoT5dAsAtjDSyPfOfAAojSnghC1EpXUhS6VfsMURecVe5_xnbrWu1Ck7deCklrBgt9dDSISZGh4wNREDp6dNopzjOPCx5TQ047SmLg6F4P2vH5c8DjzmsKY-Br4mTBNvMXbbRLsk4ZTfsJctdpnOD_WM_f7y-W65Km5-fr1eXt4UQVk1FRRsqIQIIhgpjNKVdtCSUbK2CHWNKKVr2rrUVKkWqCyxNlZZ64zWjcFSnrF3-72bND5uKU--nx-jrsOBxm32lXXSSmtnUO_BkMacE7V-k2KP6Z8X4Hcy_bNMvzPlnfHPMj3McxeHA9u6p-Y4dbA3528POeaAXZtwCDEfsdIAKGdmrNhjMU_0dIwx_fWmkpX2q_sHL-9W2n4vr_w3-R-O9Yqd</recordid><startdate>19970301</startdate><enddate>19970301</enddate><creator>Tønnessen, Theis</creator><creator>Christensen, Geir</creator><creator>Øie, Erik</creator><creator>Holt, Even</creator><creator>Kjekshus, Harald</creator><creator>Smiseth, Otto A.</creator><creator>Sejersted, Ole M.</creator><creator>Attramadal, Håvard</creator><general>Elsevier Science</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>19970301</creationdate><title>Increased cardiac expression of endothelin-1 mRNA in ischemic heart failure in rats</title><author>Tønnessen, Theis ; Christensen, Geir ; Øie, Erik ; Holt, Even ; Kjekshus, Harald ; Smiseth, Otto A. ; Sejersted, Ole M. ; Attramadal, Håvard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-ec8c711c1c6316457590fe643b8a0bbaa339dfb25e74f0e22ab684889655d6a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Cardiology. Vascular system</topic><topic>Coronary heart disease</topic><topic>Endothelin</topic><topic>Endothelin-1 - genetics</topic><topic>Heart</topic><topic>Heart failure</topic><topic>Male</topic><topic>Medical sciences</topic><topic>mRNA</topic><topic>Myocardial Infarction - metabolism</topic><topic>Myocardial Ischemia - metabolism</topic><topic>Myocardium - metabolism</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Endothelin - metabolism</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - metabolism</topic><topic>Stroke Volume</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tønnessen, Theis</creatorcontrib><creatorcontrib>Christensen, Geir</creatorcontrib><creatorcontrib>Øie, Erik</creatorcontrib><creatorcontrib>Holt, Even</creatorcontrib><creatorcontrib>Kjekshus, Harald</creatorcontrib><creatorcontrib>Smiseth, Otto A.</creatorcontrib><creatorcontrib>Sejersted, Ole M.</creatorcontrib><creatorcontrib>Attramadal, Håvard</creatorcontrib><collection>Istex</collection><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><collection>MEDLINE - Academic</collection><jtitle>Cardiovascular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tønnessen, Theis</au><au>Christensen, Geir</au><au>Øie, Erik</au><au>Holt, Even</au><au>Kjekshus, Harald</au><au>Smiseth, Otto A.</au><au>Sejersted, Ole M.</au><au>Attramadal, Håvard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased cardiac expression of endothelin-1 mRNA in ischemic heart failure in rats</atitle><jtitle>Cardiovascular research</jtitle><addtitle>Cardiovasc Res</addtitle><date>1997-03-01</date><risdate>1997</risdate><volume>33</volume><issue>3</issue><spage>601</spage><epage>610</epage><pages>601-610</pages><issn>0008-6363</issn><eissn>1755-3245</eissn><coden>CVREAU</coden><abstract>Objectives: Plasma endothelin (ET) concentrations are increased in heart failure. The aims of the present study were to investigate to what extent cardiac ET mRNA expression is induced in ischemic heart failure and whether there may be compensatory downregulation of myocardial mRNA levels for the ETA and ETB receptor subtypes. Methods: In rats with ischemic heart failure (left ventricular end-diastolic pressure > 15 mmHg) due to left coronary artery ligation, Northern blot analyses were performed on mRNA isolated from cardiac tissues. Results: A substantial upregulation was revealed in all chambers of the failing hearts. Up to 27-fold upregulation (mean 10.6 ± 4.0, P = 0.002) of left ventricular ET-1 mRNA levels was measured 1 week after myocardial infarction, whereas only a modest upregulation was detected after 6 weeks (mean 2.7 ± 0.5, P < 0.05). Ribonuclease protection assay revealed 2.8 ± 0.4-fold higher levels of ET-1 mRNA in the left ventricular area subjected to myocardial infarction compared to the non-infarcted tissue after 1 week. Left ventricular ET-1 mRNA correlated significantly with left ventricular end-diastolic pressure after 1 week (r2 = 0.86, P = 0.007). The ETA and ETB receptor mRNA levels tended to increase 1 week after myocardial infarction although these changes were not statistically significant. Conclusions: Cardiac ET-1 mRNA levels are increased in ischemic heart failure and correlate significantly with left ventricular end-diastolic pressure 1 week after myocardial infarction. The increase in cardiac ET-1 mRNA is not accompanied by a decrease in ET receptor mRNA.</abstract><cop>Oxford</cop><pub>Elsevier Science</pub><pmid>9093530</pmid><doi>10.1016/S0008-6363(96)00266-0</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Blotting, Northern Cardiology. Vascular system Coronary heart disease Endothelin Endothelin-1 - genetics Heart Heart failure Male Medical sciences mRNA Myocardial Infarction - metabolism Myocardial Ischemia - metabolism Myocardium - metabolism Rat Rats Rats, Wistar Receptors, Endothelin - metabolism RNA, Messenger - analysis RNA, Messenger - metabolism Stroke Volume |
title | Increased cardiac expression of endothelin-1 mRNA in ischemic heart failure in rats |
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