Angiotensin II-receptor subtypes in human atria and evidence for alterations in patients with cardiac dysfunction
Angiotensin II (All) has been implicated as an important factor in the pathophysiology of heart diseases. Following the recent identification of two subtypes of the All receptor in cardiac tissue of animals, we investigated the possible occurrence of these, or similar, subtypes in human atrial tissu...
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Veröffentlicht in: | European heart journal 1996-07, Vol.17 (7), p.1112-1120 |
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description | Angiotensin II (All) has been implicated as an important factor in the pathophysiology of heart diseases. Following the recent identification of two subtypes of the All receptor in cardiac tissue of animals, we investigated the possible occurrence of these, or similar, subtypes in human atrial tissue. In right-atrial tissue from patients undergoing heart surgery, we determined the All-receptor profile in receptor binding studies, using [125I]-angiotensin as radioligand and All as well as two compounds selective for the receptor subtypes to identify and quantify All-receptor subpopulations. In 35 patients (23 requiring coronary bypasses, 10 vaivular surgery and two combined coronary and valvular surgery), the left-ventricular ejection fraction was determined in the preoperative phase, and right- and left-atrial pressure during surgery. In membranes of human right atria, All receptors are present in high density (median: Bmax= 294 fmol. mg−1 protein, range: 111-2073) and two different subtypes can be distinguished. Type-1 receptors (AT1) accounted for 33 ± l0% of the population whereas type-2 receptors (AT2) made up 67 ± 10% of the population. There was no correlation between any of the measured cardiac functions and total All-receptor density or receptor affinity. However, the percentage of AT1 receptors was higher in the atria of patients with normal right-atrial pressure; left-ventricular ejection fraction was positively and right-atrial pressure inversely correlated with the percentage of AT1 receptors (r=0·740 and -0·901, respectively; P |
doi_str_mv | 10.1093/oxfordjournals.eurheartj.a015008 |
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Following the recent identification of two subtypes of the All receptor in cardiac tissue of animals, we investigated the possible occurrence of these, or similar, subtypes in human atrial tissue. In right-atrial tissue from patients undergoing heart surgery, we determined the All-receptor profile in receptor binding studies, using [125I]-angiotensin as radioligand and All as well as two compounds selective for the receptor subtypes to identify and quantify All-receptor subpopulations. In 35 patients (23 requiring coronary bypasses, 10 vaivular surgery and two combined coronary and valvular surgery), the left-ventricular ejection fraction was determined in the preoperative phase, and right- and left-atrial pressure during surgery. In membranes of human right atria, All receptors are present in high density (median: Bmax= 294 fmol. mg−1 protein, range: 111-2073) and two different subtypes can be distinguished. Type-1 receptors (AT1) accounted for 33 ± l0% of the population whereas type-2 receptors (AT2) made up 67 ± 10% of the population. There was no correlation between any of the measured cardiac functions and total All-receptor density or receptor affinity. However, the percentage of AT1 receptors was higher in the atria of patients with normal right-atrial pressure; left-ventricular ejection fraction was positively and right-atrial pressure inversely correlated with the percentage of AT1 receptors (r=0·740 and -0·901, respectively; P<0·001, for both). Moreover, the percentage of AT receptors was directly correlated with the levels of left-atrial pressure (r=0·853; P<0·001). It is concluded that the ratio of AT1 to AT2 receptors correlates well with right-atrial pressure and left-ventricular function. This is a first indication of a possible involvement of All-receptor subtypes in the pathophysiology of cardiac dysfunctions.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/oxfordjournals.eurheartj.a015008</identifier><identifier>PMID: 8809530</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Aged ; angiotensin II ; Angiotensin II - analysis ; AT1 ; AT2 ; atrium ; Biological and medical sciences ; cardiac ; Cardiology. Vascular system ; CGP 42 112 A ; Coronary Artery Bypass ; Coronary Disease - physiopathology ; Coronary heart disease ; Culture Techniques ; Female ; Heart ; Heart Atria - metabolism ; Human ; Humans ; Linear Models ; Losartan ; Male ; Medical sciences ; Middle Aged ; receptor ; Receptors, Angiotensin - analysis ; subtype</subject><ispartof>European heart journal, 1996-07, Vol.17 (7), p.1112-1120</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-a4a60eac4a009d3df7f559e00099e350aebb637686e8c90406a93710d92c851a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3138771$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8809530$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rogg, H.</creatorcontrib><creatorcontrib>de Gasparo, M.</creatorcontrib><creatorcontrib>Graedel, E.</creatorcontrib><creatorcontrib>Stulz, P.</creatorcontrib><creatorcontrib>Burkart, F.</creatorcontrib><creatorcontrib>Eberhard, M.</creatorcontrib><creatorcontrib>Erne, P.</creatorcontrib><title>Angiotensin II-receptor subtypes in human atria and evidence for alterations in patients with cardiac dysfunction</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>Angiotensin II (All) has been implicated as an important factor in the pathophysiology of heart diseases. Following the recent identification of two subtypes of the All receptor in cardiac tissue of animals, we investigated the possible occurrence of these, or similar, subtypes in human atrial tissue. In right-atrial tissue from patients undergoing heart surgery, we determined the All-receptor profile in receptor binding studies, using [125I]-angiotensin as radioligand and All as well as two compounds selective for the receptor subtypes to identify and quantify All-receptor subpopulations. In 35 patients (23 requiring coronary bypasses, 10 vaivular surgery and two combined coronary and valvular surgery), the left-ventricular ejection fraction was determined in the preoperative phase, and right- and left-atrial pressure during surgery. In membranes of human right atria, All receptors are present in high density (median: Bmax= 294 fmol. mg−1 protein, range: 111-2073) and two different subtypes can be distinguished. Type-1 receptors (AT1) accounted for 33 ± l0% of the population whereas type-2 receptors (AT2) made up 67 ± 10% of the population. There was no correlation between any of the measured cardiac functions and total All-receptor density or receptor affinity. However, the percentage of AT1 receptors was higher in the atria of patients with normal right-atrial pressure; left-ventricular ejection fraction was positively and right-atrial pressure inversely correlated with the percentage of AT1 receptors (r=0·740 and -0·901, respectively; P<0·001, for both). Moreover, the percentage of AT receptors was directly correlated with the levels of left-atrial pressure (r=0·853; P<0·001). It is concluded that the ratio of AT1 to AT2 receptors correlates well with right-atrial pressure and left-ventricular function. This is a first indication of a possible involvement of All-receptor subtypes in the pathophysiology of cardiac dysfunctions.</description><subject>Adult</subject><subject>Aged</subject><subject>angiotensin II</subject><subject>Angiotensin II - analysis</subject><subject>AT1</subject><subject>AT2</subject><subject>atrium</subject><subject>Biological and medical sciences</subject><subject>cardiac</subject><subject>Cardiology. Vascular system</subject><subject>CGP 42 112 A</subject><subject>Coronary Artery Bypass</subject><subject>Coronary Disease - physiopathology</subject><subject>Coronary heart disease</subject><subject>Culture Techniques</subject><subject>Female</subject><subject>Heart</subject><subject>Heart Atria - metabolism</subject><subject>Human</subject><subject>Humans</subject><subject>Linear Models</subject><subject>Losartan</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>receptor</subject><subject>Receptors, Angiotensin - analysis</subject><subject>subtype</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF2PEyEUhonRrHX1J5hwYYw3U6EMMNy5rh9t0uiNms3ekFPmjKVOmVlgdPvvZW3TxCsI75OXcx5C3nA258yIt8N9N8R2N0wxQJ_mOMUtQsy7OTAuGWsekRmXi0VlVC0fkxnjRlZKNTdPybOUdqwQiqsLctE0zEjBZuTuKvz0Q8aQfKCrVRXR4ZiHSNO0yYcREy3v22kPgUKOHiiEluJv32JwSMswFPqMEbIfwj92LFcMOdE_Pm-pg9h6cLQ9pG4K7oF6Tp50ZXZ8cTovyfdPH79dL6v118-r66t15WrJcwU1KIbgamDMtKLtdCelwbKCMSgkA9xslNCqUdg4w2qmwAjNWWsWrpEcxCV5fewd43A3Ycp275PDvoeAw5SsboTQRuoCvjuCLg4pRezsGP0e4sFyZh-s2_-t27N1e7JeKl6e_po2e2zPBSfNJX91yiE56LsIwfl0xgQXjda8YNUR8ynj_TmG-MsqLbS0y5tbq7-ID-v3tz_sUvwFhKimBw</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>Rogg, H.</creator><creator>de Gasparo, M.</creator><creator>Graedel, E.</creator><creator>Stulz, P.</creator><creator>Burkart, F.</creator><creator>Eberhard, M.</creator><creator>Erne, P.</creator><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>19960701</creationdate><title>Angiotensin II-receptor subtypes in human atria and evidence for alterations in patients with cardiac dysfunction</title><author>Rogg, H. ; de Gasparo, M. ; Graedel, E. ; Stulz, P. ; Burkart, F. ; Eberhard, M. ; Erne, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-a4a60eac4a009d3df7f559e00099e350aebb637686e8c90406a93710d92c851a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Aged</topic><topic>angiotensin II</topic><topic>Angiotensin II - analysis</topic><topic>AT1</topic><topic>AT2</topic><topic>atrium</topic><topic>Biological and medical sciences</topic><topic>cardiac</topic><topic>Cardiology. Vascular system</topic><topic>CGP 42 112 A</topic><topic>Coronary Artery Bypass</topic><topic>Coronary Disease - physiopathology</topic><topic>Coronary heart disease</topic><topic>Culture Techniques</topic><topic>Female</topic><topic>Heart</topic><topic>Heart Atria - metabolism</topic><topic>Human</topic><topic>Humans</topic><topic>Linear Models</topic><topic>Losartan</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>receptor</topic><topic>Receptors, Angiotensin - analysis</topic><topic>subtype</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rogg, H.</creatorcontrib><creatorcontrib>de Gasparo, M.</creatorcontrib><creatorcontrib>Graedel, E.</creatorcontrib><creatorcontrib>Stulz, P.</creatorcontrib><creatorcontrib>Burkart, F.</creatorcontrib><creatorcontrib>Eberhard, M.</creatorcontrib><creatorcontrib>Erne, P.</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>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rogg, H.</au><au>de Gasparo, M.</au><au>Graedel, E.</au><au>Stulz, P.</au><au>Burkart, F.</au><au>Eberhard, M.</au><au>Erne, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Angiotensin II-receptor subtypes in human atria and evidence for alterations in patients with cardiac dysfunction</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>17</volume><issue>7</issue><spage>1112</spage><epage>1120</epage><pages>1112-1120</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>Angiotensin II (All) has been implicated as an important factor in the pathophysiology of heart diseases. Following the recent identification of two subtypes of the All receptor in cardiac tissue of animals, we investigated the possible occurrence of these, or similar, subtypes in human atrial tissue. In right-atrial tissue from patients undergoing heart surgery, we determined the All-receptor profile in receptor binding studies, using [125I]-angiotensin as radioligand and All as well as two compounds selective for the receptor subtypes to identify and quantify All-receptor subpopulations. In 35 patients (23 requiring coronary bypasses, 10 vaivular surgery and two combined coronary and valvular surgery), the left-ventricular ejection fraction was determined in the preoperative phase, and right- and left-atrial pressure during surgery. In membranes of human right atria, All receptors are present in high density (median: Bmax= 294 fmol. mg−1 protein, range: 111-2073) and two different subtypes can be distinguished. Type-1 receptors (AT1) accounted for 33 ± l0% of the population whereas type-2 receptors (AT2) made up 67 ± 10% of the population. There was no correlation between any of the measured cardiac functions and total All-receptor density or receptor affinity. However, the percentage of AT1 receptors was higher in the atria of patients with normal right-atrial pressure; left-ventricular ejection fraction was positively and right-atrial pressure inversely correlated with the percentage of AT1 receptors (r=0·740 and -0·901, respectively; P<0·001, for both). Moreover, the percentage of AT receptors was directly correlated with the levels of left-atrial pressure (r=0·853; P<0·001). It is concluded that the ratio of AT1 to AT2 receptors correlates well with right-atrial pressure and left-ventricular function. This is a first indication of a possible involvement of All-receptor subtypes in the pathophysiology of cardiac dysfunctions.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>8809530</pmid><doi>10.1093/oxfordjournals.eurheartj.a015008</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged angiotensin II Angiotensin II - analysis AT1 AT2 atrium Biological and medical sciences cardiac Cardiology. Vascular system CGP 42 112 A Coronary Artery Bypass Coronary Disease - physiopathology Coronary heart disease Culture Techniques Female Heart Heart Atria - metabolism Human Humans Linear Models Losartan Male Medical sciences Middle Aged receptor Receptors, Angiotensin - analysis subtype |
title | Angiotensin II-receptor subtypes in human atria and evidence for alterations in patients with cardiac dysfunction |
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