Adenosine in Myocardial Protection given through Three Windows of Opportunity. An Experimental Study with Pigs
Objective Adenosine (ADO) has been shown to have beneficial effects against tissue injury after myocardial ischemia. However, the timing and dose of ADO administration have not been defined. This study was designed to determine the cardioprotective effect of exogenous ADO in an experimental open he...
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Veröffentlicht in: | Scandinavian cardiovascular journal : SCJ 2001, Vol.35 (6), p.409-414 |
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description | Objective Adenosine (ADO) has been shown to have beneficial effects against tissue injury after myocardial ischemia. However, the timing and dose of ADO administration have not been defined. This study was designed to determine the cardioprotective effect of exogenous ADO in an experimental open heart surgery model in pigs. Design The animals were openly divided into two groups both undergoing 30 min of total cardiac arrest. In the control group animals received cold crystalloid cardioplegic solution. In the ADO group ADO was added to cardioplegic solution and in addition ADO was infused to the superior vena cava for 2 h starting 30 min before cardiac arrest. The pumping function of the heart was measured with echocardiography and myocardial blood flow was measured with microspheres and positron emission tomography (PET). Cardiomyocyte apoptosis was detected and tumor necrosis factor (TNF) levels were measured. Results Better post-ischemic pumping function was found in the ADO group (relative decrease 43.7% vs 55.4%, p = 0.20 between the groups). The cardiac output decreased significantly from the baseline values ( p < 0.05 in both groups). There was a temporary decrease in myocardial blood flow post-ischemically, followed by a compensatory increase during the later reperfusion period. The cardiomyocyte apoptosis was induced significantly in both groups. Conclusions In this experiment two important details were noticed. Firstly, cardiomyocyte apoptosis is involved in ischemia-reperfusion injury associated with open heart surgery. Secondly, PET is a comparable method with the microsphere technique when coronary flow is studied. No significant effects of ADO against ischemia-reperfusion injury could be shown. However, there were some signs of positive outcome, even though statistical significance could not be reached. |
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An Experimental Study with Pigs</title><source>MEDLINE</source><source>Access via Taylor & Francis</source><creator>Vähäsilta, Tommi ; Virtanen, Jyrki ; Saraste, Antti ; Luotolahti, Matti ; Pulkki, Kari ; Valtonen, Mika ; Voipio-Pulkki, Liisa-Maria ; Savunen, Timo</creator><creatorcontrib>Vähäsilta, Tommi ; Virtanen, Jyrki ; Saraste, Antti ; Luotolahti, Matti ; Pulkki, Kari ; Valtonen, Mika ; Voipio-Pulkki, Liisa-Maria ; Savunen, Timo</creatorcontrib><description>Objective Adenosine (ADO) has been shown to have beneficial effects against tissue injury after myocardial ischemia. However, the timing and dose of ADO administration have not been defined. This study was designed to determine the cardioprotective effect of exogenous ADO in an experimental open heart surgery model in pigs. Design The animals were openly divided into two groups both undergoing 30 min of total cardiac arrest. In the control group animals received cold crystalloid cardioplegic solution. In the ADO group ADO was added to cardioplegic solution and in addition ADO was infused to the superior vena cava for 2 h starting 30 min before cardiac arrest. The pumping function of the heart was measured with echocardiography and myocardial blood flow was measured with microspheres and positron emission tomography (PET). Cardiomyocyte apoptosis was detected and tumor necrosis factor (TNF) levels were measured. Results Better post-ischemic pumping function was found in the ADO group (relative decrease 43.7% vs 55.4%, p = 0.20 between the groups). The cardiac output decreased significantly from the baseline values ( p < 0.05 in both groups). There was a temporary decrease in myocardial blood flow post-ischemically, followed by a compensatory increase during the later reperfusion period. The cardiomyocyte apoptosis was induced significantly in both groups. Conclusions In this experiment two important details were noticed. Firstly, cardiomyocyte apoptosis is involved in ischemia-reperfusion injury associated with open heart surgery. Secondly, PET is a comparable method with the microsphere technique when coronary flow is studied. No significant effects of ADO against ischemia-reperfusion injury could be shown. However, there were some signs of positive outcome, even though statistical significance could not be reached.</description><identifier>ISSN: 1401-7431</identifier><identifier>EISSN: 1651-2006</identifier><identifier>DOI: 10.1080/14017430152754907</identifier><identifier>PMID: 11837521</identifier><language>eng</language><publisher>Copenhagen: Informa UK Ltd</publisher><subject>Adenosine - administration & dosage ; Adenosine Ischemia-REPERFUSION Apoptosis ; Animals ; Apoptosis ; Biological and medical sciences ; Cardiac Output ; Cardiology. Vascular system ; Cardioplegic Solutions ; Cardiopulmonary Bypass ; Coronary heart disease ; Female ; Heart ; Hypothermia, Induced ; In Situ Nick-End Labeling ; Ischemic Preconditioning, Myocardial - methods ; Male ; Medical sciences ; Microspheres ; Swine ; Tumor Necrosis Factor-alpha - analysis ; Vasodilator Agents - administration & dosage</subject><ispartof>Scandinavian cardiovascular journal : SCJ, 2001, Vol.35 (6), p.409-414</ispartof><rights>2001 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2001</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-c7e1c8823d443fb2d17ccc13f10da7fb264d87ebb6823e81a8255d115240a8f83</citedby><cites>FETCH-LOGICAL-c475t-c7e1c8823d443fb2d17ccc13f10da7fb264d87ebb6823e81a8255d115240a8f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/14017430152754907$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/14017430152754907$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,4024,27923,27924,27925,59647,60436,61221,61402</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13438056$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11837521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vähäsilta, Tommi</creatorcontrib><creatorcontrib>Virtanen, Jyrki</creatorcontrib><creatorcontrib>Saraste, Antti</creatorcontrib><creatorcontrib>Luotolahti, Matti</creatorcontrib><creatorcontrib>Pulkki, Kari</creatorcontrib><creatorcontrib>Valtonen, Mika</creatorcontrib><creatorcontrib>Voipio-Pulkki, Liisa-Maria</creatorcontrib><creatorcontrib>Savunen, Timo</creatorcontrib><title>Adenosine in Myocardial Protection given through Three Windows of Opportunity. An Experimental Study with Pigs</title><title>Scandinavian cardiovascular journal : SCJ</title><addtitle>Scand Cardiovasc J</addtitle><description>Objective Adenosine (ADO) has been shown to have beneficial effects against tissue injury after myocardial ischemia. However, the timing and dose of ADO administration have not been defined. This study was designed to determine the cardioprotective effect of exogenous ADO in an experimental open heart surgery model in pigs. Design The animals were openly divided into two groups both undergoing 30 min of total cardiac arrest. In the control group animals received cold crystalloid cardioplegic solution. In the ADO group ADO was added to cardioplegic solution and in addition ADO was infused to the superior vena cava for 2 h starting 30 min before cardiac arrest. The pumping function of the heart was measured with echocardiography and myocardial blood flow was measured with microspheres and positron emission tomography (PET). Cardiomyocyte apoptosis was detected and tumor necrosis factor (TNF) levels were measured. Results Better post-ischemic pumping function was found in the ADO group (relative decrease 43.7% vs 55.4%, p = 0.20 between the groups). The cardiac output decreased significantly from the baseline values ( p < 0.05 in both groups). There was a temporary decrease in myocardial blood flow post-ischemically, followed by a compensatory increase during the later reperfusion period. The cardiomyocyte apoptosis was induced significantly in both groups. Conclusions In this experiment two important details were noticed. Firstly, cardiomyocyte apoptosis is involved in ischemia-reperfusion injury associated with open heart surgery. Secondly, PET is a comparable method with the microsphere technique when coronary flow is studied. No significant effects of ADO against ischemia-reperfusion injury could be shown. However, there were some signs of positive outcome, even though statistical significance could not be reached.</description><subject>Adenosine - administration & dosage</subject><subject>Adenosine Ischemia-REPERFUSION Apoptosis</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Cardiac Output</subject><subject>Cardiology. Vascular system</subject><subject>Cardioplegic Solutions</subject><subject>Cardiopulmonary Bypass</subject><subject>Coronary heart disease</subject><subject>Female</subject><subject>Heart</subject><subject>Hypothermia, Induced</subject><subject>In Situ Nick-End Labeling</subject><subject>Ischemic Preconditioning, Myocardial - methods</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microspheres</subject><subject>Swine</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><subject>Vasodilator Agents - administration & dosage</subject><issn>1401-7431</issn><issn>1651-2006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFvFCEYhonR2Fr9AV4MF3ubyjcwA0Yvm6ZWk5o2scbjhIVvdmhmYQTGdf69NLumMSY9QeB533w8EPIa2Bkwxd6BYCAFZ9DUshHvmXxCjqFtoKoZa5-WfbmvCgBH5EVKd6yAqoHn5AhAcdnUcEz8yqIPyXmkztOvSzA6WqdHehNDRpNd8HTjfqGneYhh3gz0doiI9IfzNuwSDT29nqYQ8-xdXs7oytOL3xNGt0WfS823PNuF7lwe6I3bpJfkWa_HhK8O6wn5_uni9vxzdXV9-eV8dVUZIZtcGYlglKq5FYL369qCNMYA74FZLctBK6ySuF63hUEFWtVNY6F4EEyrXvETcrrvnWL4OWPK3dYlg-OoPYY5dbIWvJaMFxD2oIkhpYh9N5XZdVw6YN295O4_ySXz5lA-r7doHxIHqwV4ewB0Mnrso_bGpQeOC65Y0xbu455zvg9xq3chjrbLehlD_Bvij83x4Z_4gHrMQ_lA7O7CHH0R_Mgr_gD_lqof</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Vähäsilta, Tommi</creator><creator>Virtanen, Jyrki</creator><creator>Saraste, Antti</creator><creator>Luotolahti, Matti</creator><creator>Pulkki, Kari</creator><creator>Valtonen, Mika</creator><creator>Voipio-Pulkki, Liisa-Maria</creator><creator>Savunen, Timo</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Scandinavian University Press</general><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>2001</creationdate><title>Adenosine in Myocardial Protection given through Three Windows of Opportunity. An Experimental Study with Pigs</title><author>Vähäsilta, Tommi ; Virtanen, Jyrki ; Saraste, Antti ; Luotolahti, Matti ; Pulkki, Kari ; Valtonen, Mika ; Voipio-Pulkki, Liisa-Maria ; Savunen, Timo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-c7e1c8823d443fb2d17ccc13f10da7fb264d87ebb6823e81a8255d115240a8f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adenosine - administration & dosage</topic><topic>Adenosine Ischemia-REPERFUSION Apoptosis</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Cardiac Output</topic><topic>Cardiology. Vascular system</topic><topic>Cardioplegic Solutions</topic><topic>Cardiopulmonary Bypass</topic><topic>Coronary heart disease</topic><topic>Female</topic><topic>Heart</topic><topic>Hypothermia, Induced</topic><topic>In Situ Nick-End Labeling</topic><topic>Ischemic Preconditioning, Myocardial - methods</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microspheres</topic><topic>Swine</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><topic>Vasodilator Agents - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vähäsilta, Tommi</creatorcontrib><creatorcontrib>Virtanen, Jyrki</creatorcontrib><creatorcontrib>Saraste, Antti</creatorcontrib><creatorcontrib>Luotolahti, Matti</creatorcontrib><creatorcontrib>Pulkki, Kari</creatorcontrib><creatorcontrib>Valtonen, Mika</creatorcontrib><creatorcontrib>Voipio-Pulkki, Liisa-Maria</creatorcontrib><creatorcontrib>Savunen, Timo</creatorcontrib><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>Scandinavian cardiovascular journal : SCJ</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vähäsilta, Tommi</au><au>Virtanen, Jyrki</au><au>Saraste, Antti</au><au>Luotolahti, Matti</au><au>Pulkki, Kari</au><au>Valtonen, Mika</au><au>Voipio-Pulkki, Liisa-Maria</au><au>Savunen, Timo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenosine in Myocardial Protection given through Three Windows of Opportunity. An Experimental Study with Pigs</atitle><jtitle>Scandinavian cardiovascular journal : SCJ</jtitle><addtitle>Scand Cardiovasc J</addtitle><date>2001</date><risdate>2001</risdate><volume>35</volume><issue>6</issue><spage>409</spage><epage>414</epage><pages>409-414</pages><issn>1401-7431</issn><eissn>1651-2006</eissn><abstract>Objective Adenosine (ADO) has been shown to have beneficial effects against tissue injury after myocardial ischemia. However, the timing and dose of ADO administration have not been defined. This study was designed to determine the cardioprotective effect of exogenous ADO in an experimental open heart surgery model in pigs. Design The animals were openly divided into two groups both undergoing 30 min of total cardiac arrest. In the control group animals received cold crystalloid cardioplegic solution. In the ADO group ADO was added to cardioplegic solution and in addition ADO was infused to the superior vena cava for 2 h starting 30 min before cardiac arrest. The pumping function of the heart was measured with echocardiography and myocardial blood flow was measured with microspheres and positron emission tomography (PET). Cardiomyocyte apoptosis was detected and tumor necrosis factor (TNF) levels were measured. Results Better post-ischemic pumping function was found in the ADO group (relative decrease 43.7% vs 55.4%, p = 0.20 between the groups). The cardiac output decreased significantly from the baseline values ( p < 0.05 in both groups). There was a temporary decrease in myocardial blood flow post-ischemically, followed by a compensatory increase during the later reperfusion period. The cardiomyocyte apoptosis was induced significantly in both groups. Conclusions In this experiment two important details were noticed. Firstly, cardiomyocyte apoptosis is involved in ischemia-reperfusion injury associated with open heart surgery. Secondly, PET is a comparable method with the microsphere technique when coronary flow is studied. No significant effects of ADO against ischemia-reperfusion injury could be shown. However, there were some signs of positive outcome, even though statistical significance could not be reached.</abstract><cop>Copenhagen</cop><cop>Oslo</cop><cop>Stockholm</cop><pub>Informa UK Ltd</pub><pmid>11837521</pmid><doi>10.1080/14017430152754907</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine - administration & dosage Adenosine Ischemia-REPERFUSION Apoptosis Animals Apoptosis Biological and medical sciences Cardiac Output Cardiology. Vascular system Cardioplegic Solutions Cardiopulmonary Bypass Coronary heart disease Female Heart Hypothermia, Induced In Situ Nick-End Labeling Ischemic Preconditioning, Myocardial - methods Male Medical sciences Microspheres Swine Tumor Necrosis Factor-alpha - analysis Vasodilator Agents - administration & dosage |
title | Adenosine in Myocardial Protection given through Three Windows of Opportunity. An Experimental Study with Pigs |
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