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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
Main Authors: Tønnessen, Theis, Christensen, Geir, Øie, Erik, Holt, Even, Kjekshus, Harald, Smiseth, Otto A., Sejersted, Ole M., Attramadal, Håvard
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container_end_page 610
container_issue 3
container_start_page 601
container_title Cardiovascular research
container_volume 33
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 &gt; 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 &lt; 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. 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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 &gt; 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 &lt; 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. 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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. 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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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ispartof Cardiovascular research, 1997-03, Vol.33 (3), p.601-610
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1755-3245
language eng
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source Oxford Journals Online
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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