Biochemical changes induced in the myocardial cell during cardioplegic arrest supplemented with creatine phosphate
The purpose of this work was to evaluate the biochemical changes in the myocardial cell using cardioplegia supplemented with creatine phosphate (CP). Many previous studies have demonstrated the beneficial effect of CP on the ischemic myocardium and its mechanism of action has been assumed to be main...
Gespeichert in:
Veröffentlicht in: | Journal of cardiothoracic and vascular anesthesia 1991-10, Vol.5 (5), p.475-480 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 480 |
---|---|
container_issue | 5 |
container_start_page | 475 |
container_title | Journal of cardiothoracic and vascular anesthesia |
container_volume | 5 |
creator | Pastoris, O. Dossena, M. Vercesi, L. Bruseghini, M. Pagnin, A. Ceriana, P. |
description | The purpose of this work was to evaluate the biochemical changes in the myocardial cell using cardioplegia supplemented with creatine phosphate (CP). Many previous studies have demonstrated the beneficial effect of CP on the ischemic myocardium and its mechanism of action has been assumed to be mainly extracellular. Based on the assumption that CP could also exert some influence on myocardial cellular metabolism, this investigation was carried out. Forty patients undergoing mitral valve replacement were divided into two groups: group 1 was treated with standard cardioplegic solution, and group 2 was treated with cardioplegic solution enriched with CP at a concentration of 10 mmol/L. Samples of papillary muscle, obtained from the removed valve, were studied by means of biochemical methods in order to assess the enzyme activities and the metabolites of the different biochemical pathways related to energy metabolism in the myocardial cell. One papillary muscle sample was used to determine enzyme activities spectrophotometrically; another was used to evaluate metabolite concentrations by spectrophotometric or spectrophotofluorimetric methods. The rate of spontaneous functional recovery after rewarming and weaning from cardiopulmonary bypass (CPB) also was evaluated. In group 2, the Vmax of enzymatic activities was significantly greater (hexokinase, malate dehydrogenase, glutamate dehydrogenase, total NADH cytochrome c reductase) and a better functional state of the heart was observed after CPB. On the basis of the clinical and biochemical data, it is concluded that the myocardium was better preserved when CP was added to the cardioplegic solution. Therefore, the results suggest a possible interaction of exogenous CP with cellular metabolism. |
doi_str_mv | 10.1016/1053-0770(91)90122-A |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72169113</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>105307709190122A</els_id><sourcerecordid>72169113</sourcerecordid><originalsourceid>FETCH-LOGICAL-c301t-e072ab3dbc8abc85bca541f78b2d55279f9ae5e1a25e365adf72980847f71c203</originalsourceid><addsrcrecordid>eNp9kE1P3DAQQC3UisKWf9BKPlQVHAIeZ71OLpW2CFokJC70bE3sycZVvmonVPx7HHbb3nqwxpp5M5p5jH0AcQkCNlcgVJ4JrcV5CRelACmz7RE7AZXLrFhL-Sb9_yDv2GmMP4UAUEofs2Moc7lR8oSFr36wDXXeYsttg_2OIve9my25FPnUEO-eB4vB-YWgtuVuDr7f8dfcMLa085ZjCBQnHucxJTrqp9T-208Nt4Fw8j3xsRni2OBE79nbGttIZ4e4Yj9ubx6vv2f3D9_urrf3mc0FTBkJLbHKXWULTE9VFtUaal1U0ikldVmXSIoApaJ8o9DVWpaFKNa61mClyFfs837uGIZfc9rOdD4uB2BPwxyNlrApAfIErvegDUOMgWozBt9heDYgzKLaLB7N4tGUYF5Vm21q-3iYP1cduX9Ne7ep_ulQx5js1gF76-NfLBEFJHbFvuwxSi6ePAUTrac--feB7GTc4P-_xwsCypxm</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72169113</pqid></control><display><type>article</type><title>Biochemical changes induced in the myocardial cell during cardioplegic arrest supplemented with creatine phosphate</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Pastoris, O. ; Dossena, M. ; Vercesi, L. ; Bruseghini, M. ; Pagnin, A. ; Ceriana, P.</creator><creatorcontrib>Pastoris, O. ; Dossena, M. ; Vercesi, L. ; Bruseghini, M. ; Pagnin, A. ; Ceriana, P.</creatorcontrib><description>The purpose of this work was to evaluate the biochemical changes in the myocardial cell using cardioplegia supplemented with creatine phosphate (CP). Many previous studies have demonstrated the beneficial effect of CP on the ischemic myocardium and its mechanism of action has been assumed to be mainly extracellular. Based on the assumption that CP could also exert some influence on myocardial cellular metabolism, this investigation was carried out. Forty patients undergoing mitral valve replacement were divided into two groups: group 1 was treated with standard cardioplegic solution, and group 2 was treated with cardioplegic solution enriched with CP at a concentration of 10 mmol/L. Samples of papillary muscle, obtained from the removed valve, were studied by means of biochemical methods in order to assess the enzyme activities and the metabolites of the different biochemical pathways related to energy metabolism in the myocardial cell. One papillary muscle sample was used to determine enzyme activities spectrophotometrically; another was used to evaluate metabolite concentrations by spectrophotometric or spectrophotofluorimetric methods. The rate of spontaneous functional recovery after rewarming and weaning from cardiopulmonary bypass (CPB) also was evaluated. In group 2, the Vmax of enzymatic activities was significantly greater (hexokinase, malate dehydrogenase, glutamate dehydrogenase, total NADH cytochrome c reductase) and a better functional state of the heart was observed after CPB. On the basis of the clinical and biochemical data, it is concluded that the myocardium was better preserved when CP was added to the cardioplegic solution. Therefore, the results suggest a possible interaction of exogenous CP with cellular metabolism.</description><identifier>ISSN: 1053-0770</identifier><identifier>EISSN: 1532-8422</identifier><identifier>DOI: 10.1016/1053-0770(91)90122-A</identifier><identifier>PMID: 1932652</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Anesthesia ; Anesthesia depending on type of surgery ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Cardioplegic Solutions - pharmacology ; Energy Metabolism - drug effects ; Female ; Heart - drug effects ; Heart Arrest, Induced ; Heart Valve Prosthesis ; Humans ; Male ; Medical sciences ; Middle Aged ; Mitral Valve ; Myocardium - enzymology ; Myocardium - metabolism ; Phosphocreatine - pharmacology ; Thoracic and cardiovascular surgery. Cardiopulmonary bypass</subject><ispartof>Journal of cardiothoracic and vascular anesthesia, 1991-10, Vol.5 (5), p.475-480</ispartof><rights>1991</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c301t-e072ab3dbc8abc85bca541f78b2d55279f9ae5e1a25e365adf72980847f71c203</citedby><cites>FETCH-LOGICAL-c301t-e072ab3dbc8abc85bca541f78b2d55279f9ae5e1a25e365adf72980847f71c203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/1053-0770(91)90122-A$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5238119$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1932652$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pastoris, O.</creatorcontrib><creatorcontrib>Dossena, M.</creatorcontrib><creatorcontrib>Vercesi, L.</creatorcontrib><creatorcontrib>Bruseghini, M.</creatorcontrib><creatorcontrib>Pagnin, A.</creatorcontrib><creatorcontrib>Ceriana, P.</creatorcontrib><title>Biochemical changes induced in the myocardial cell during cardioplegic arrest supplemented with creatine phosphate</title><title>Journal of cardiothoracic and vascular anesthesia</title><addtitle>J Cardiothorac Vasc Anesth</addtitle><description>The purpose of this work was to evaluate the biochemical changes in the myocardial cell using cardioplegia supplemented with creatine phosphate (CP). Many previous studies have demonstrated the beneficial effect of CP on the ischemic myocardium and its mechanism of action has been assumed to be mainly extracellular. Based on the assumption that CP could also exert some influence on myocardial cellular metabolism, this investigation was carried out. Forty patients undergoing mitral valve replacement were divided into two groups: group 1 was treated with standard cardioplegic solution, and group 2 was treated with cardioplegic solution enriched with CP at a concentration of 10 mmol/L. Samples of papillary muscle, obtained from the removed valve, were studied by means of biochemical methods in order to assess the enzyme activities and the metabolites of the different biochemical pathways related to energy metabolism in the myocardial cell. One papillary muscle sample was used to determine enzyme activities spectrophotometrically; another was used to evaluate metabolite concentrations by spectrophotometric or spectrophotofluorimetric methods. The rate of spontaneous functional recovery after rewarming and weaning from cardiopulmonary bypass (CPB) also was evaluated. In group 2, the Vmax of enzymatic activities was significantly greater (hexokinase, malate dehydrogenase, glutamate dehydrogenase, total NADH cytochrome c reductase) and a better functional state of the heart was observed after CPB. On the basis of the clinical and biochemical data, it is concluded that the myocardium was better preserved when CP was added to the cardioplegic solution. Therefore, the results suggest a possible interaction of exogenous CP with cellular metabolism.</description><subject>Anesthesia</subject><subject>Anesthesia depending on type of surgery</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Cardioplegic Solutions - pharmacology</subject><subject>Energy Metabolism - drug effects</subject><subject>Female</subject><subject>Heart - drug effects</subject><subject>Heart Arrest, Induced</subject><subject>Heart Valve Prosthesis</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mitral Valve</subject><subject>Myocardium - enzymology</subject><subject>Myocardium - metabolism</subject><subject>Phosphocreatine - pharmacology</subject><subject>Thoracic and cardiovascular surgery. Cardiopulmonary bypass</subject><issn>1053-0770</issn><issn>1532-8422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P3DAQQC3UisKWf9BKPlQVHAIeZ71OLpW2CFokJC70bE3sycZVvmonVPx7HHbb3nqwxpp5M5p5jH0AcQkCNlcgVJ4JrcV5CRelACmz7RE7AZXLrFhL-Sb9_yDv2GmMP4UAUEofs2Moc7lR8oSFr36wDXXeYsttg_2OIve9my25FPnUEO-eB4vB-YWgtuVuDr7f8dfcMLa085ZjCBQnHucxJTrqp9T-208Nt4Fw8j3xsRni2OBE79nbGttIZ4e4Yj9ubx6vv2f3D9_urrf3mc0FTBkJLbHKXWULTE9VFtUaal1U0ikldVmXSIoApaJ8o9DVWpaFKNa61mClyFfs837uGIZfc9rOdD4uB2BPwxyNlrApAfIErvegDUOMgWozBt9heDYgzKLaLB7N4tGUYF5Vm21q-3iYP1cduX9Ne7ep_ulQx5js1gF76-NfLBEFJHbFvuwxSi6ePAUTrac--feB7GTc4P-_xwsCypxm</recordid><startdate>199110</startdate><enddate>199110</enddate><creator>Pastoris, O.</creator><creator>Dossena, M.</creator><creator>Vercesi, L.</creator><creator>Bruseghini, M.</creator><creator>Pagnin, A.</creator><creator>Ceriana, P.</creator><general>Elsevier Inc</general><general>Elsevier</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>199110</creationdate><title>Biochemical changes induced in the myocardial cell during cardioplegic arrest supplemented with creatine phosphate</title><author>Pastoris, O. ; Dossena, M. ; Vercesi, L. ; Bruseghini, M. ; Pagnin, A. ; Ceriana, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-e072ab3dbc8abc85bca541f78b2d55279f9ae5e1a25e365adf72980847f71c203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Anesthesia</topic><topic>Anesthesia depending on type of surgery</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cardioplegic Solutions - pharmacology</topic><topic>Energy Metabolism - drug effects</topic><topic>Female</topic><topic>Heart - drug effects</topic><topic>Heart Arrest, Induced</topic><topic>Heart Valve Prosthesis</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mitral Valve</topic><topic>Myocardium - enzymology</topic><topic>Myocardium - metabolism</topic><topic>Phosphocreatine - pharmacology</topic><topic>Thoracic and cardiovascular surgery. Cardiopulmonary bypass</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pastoris, O.</creatorcontrib><creatorcontrib>Dossena, M.</creatorcontrib><creatorcontrib>Vercesi, L.</creatorcontrib><creatorcontrib>Bruseghini, M.</creatorcontrib><creatorcontrib>Pagnin, A.</creatorcontrib><creatorcontrib>Ceriana, P.</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>Journal of cardiothoracic and vascular anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pastoris, O.</au><au>Dossena, M.</au><au>Vercesi, L.</au><au>Bruseghini, M.</au><au>Pagnin, A.</au><au>Ceriana, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biochemical changes induced in the myocardial cell during cardioplegic arrest supplemented with creatine phosphate</atitle><jtitle>Journal of cardiothoracic and vascular anesthesia</jtitle><addtitle>J Cardiothorac Vasc Anesth</addtitle><date>1991-10</date><risdate>1991</risdate><volume>5</volume><issue>5</issue><spage>475</spage><epage>480</epage><pages>475-480</pages><issn>1053-0770</issn><eissn>1532-8422</eissn><abstract>The purpose of this work was to evaluate the biochemical changes in the myocardial cell using cardioplegia supplemented with creatine phosphate (CP). Many previous studies have demonstrated the beneficial effect of CP on the ischemic myocardium and its mechanism of action has been assumed to be mainly extracellular. Based on the assumption that CP could also exert some influence on myocardial cellular metabolism, this investigation was carried out. Forty patients undergoing mitral valve replacement were divided into two groups: group 1 was treated with standard cardioplegic solution, and group 2 was treated with cardioplegic solution enriched with CP at a concentration of 10 mmol/L. Samples of papillary muscle, obtained from the removed valve, were studied by means of biochemical methods in order to assess the enzyme activities and the metabolites of the different biochemical pathways related to energy metabolism in the myocardial cell. One papillary muscle sample was used to determine enzyme activities spectrophotometrically; another was used to evaluate metabolite concentrations by spectrophotometric or spectrophotofluorimetric methods. The rate of spontaneous functional recovery after rewarming and weaning from cardiopulmonary bypass (CPB) also was evaluated. In group 2, the Vmax of enzymatic activities was significantly greater (hexokinase, malate dehydrogenase, glutamate dehydrogenase, total NADH cytochrome c reductase) and a better functional state of the heart was observed after CPB. On the basis of the clinical and biochemical data, it is concluded that the myocardium was better preserved when CP was added to the cardioplegic solution. Therefore, the results suggest a possible interaction of exogenous CP with cellular metabolism.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>1932652</pmid><doi>10.1016/1053-0770(91)90122-A</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1053-0770 |
ispartof | Journal of cardiothoracic and vascular anesthesia, 1991-10, Vol.5 (5), p.475-480 |
issn | 1053-0770 1532-8422 |
language | eng |
recordid | cdi_proquest_miscellaneous_72169113 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Anesthesia Anesthesia depending on type of surgery Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Cardioplegic Solutions - pharmacology Energy Metabolism - drug effects Female Heart - drug effects Heart Arrest, Induced Heart Valve Prosthesis Humans Male Medical sciences Middle Aged Mitral Valve Myocardium - enzymology Myocardium - metabolism Phosphocreatine - pharmacology Thoracic and cardiovascular surgery. Cardiopulmonary bypass |
title | Biochemical changes induced in the myocardial cell during cardioplegic arrest supplemented with creatine phosphate |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T13%3A42%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biochemical%20changes%20induced%20in%20the%20myocardial%20cell%20during%20cardioplegic%20arrest%20supplemented%20with%20creatine%20phosphate&rft.jtitle=Journal%20of%20cardiothoracic%20and%20vascular%20anesthesia&rft.au=Pastoris,%20O.&rft.date=1991-10&rft.volume=5&rft.issue=5&rft.spage=475&rft.epage=480&rft.pages=475-480&rft.issn=1053-0770&rft.eissn=1532-8422&rft_id=info:doi/10.1016/1053-0770(91)90122-A&rft_dat=%3Cproquest_cross%3E72169113%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=72169113&rft_id=info:pmid/1932652&rft_els_id=105307709190122A&rfr_iscdi=true |