Energy status of pig donor organs after ischemia is independent of donor type
Abstract Background Literature is controversial whether organs from living donors have a better graft function than brain dead (BD) and non–heart-beating donor organs. Success of transplantation has been correlated with high-energy phosphate (HEP) contents of the graft. Methods HEP contents in heart...
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creator | Stadlbauer, Vanessa, MD Stiegler, Philipp, MD Taeubl, Philipp, MD Sereinigg, Michael, MD Puntschart, Andreas, MD Bradatsch, Andrea, MD Curcic, Pero, MD Seifert-Held, Thomas, MD Zmugg, Gerda Stojakovic, Tatjana, MD Leopold, Barbara Blattl, Daniela Horki, Vera, MD Mayrhauser, Ursula, PhD Wiederstein-Grasser, Iris, DVM Leber, Bettina, PhD Jürgens, Günther Tscheliessnigg, Karlheinz Hallström, Seth |
description | Abstract Background Literature is controversial whether organs from living donors have a better graft function than brain dead (BD) and non–heart-beating donor organs. Success of transplantation has been correlated with high-energy phosphate (HEP) contents of the graft. Methods HEP contents in heart, liver, kidney, and pancreas from living, BD, and donation after cardiac death in a pig model ( n = 6 per donor type) were evaluated systematically. BD was induced under general anesthesia by inflating a balloon in the epidural space. Ten hours after confirmation, organs were retrieved. Cardiac arrest was induced by 9 V direct current. After 10 min of ventricular fibrillation without cardiac output, mechanical and medical reanimation was performed for 30 min before organ retrieval. In living donors, organs were explanted immediately. Freeze-clamped biopsies were taken before perfusion with Celsior solution (heart) or University of Wisconsin solution (abdominal organs) in BD and living donors or with Histidine-Tryptophan-Ketoglutaric solution (all organs) in non–heart-beating donors, after perfusion, and after cold ischemia (4 h for heart, 6 h for liver and pancreas, and 12 h for kidney). HEPs (adenosine triphosphate, adenosine diphosphate, adenosine monophosphate, and phosphocreatine), xanthine, and hypoxanthine were measured by high-performance liquid chromatography. Energy charge and adenosine triphosphate-to-adenosine diphosphate ratio were calculated. Results After ischemia, organs from different donor types showed no difference in energy status. In all organs, a decrease of HEP and an increase in hypoxanthine contents were observed during perfusion and ischemia, irrespective of the donor type. Conclusion Organs from BD or non–heart-beating donors do not differ from living donor organs in their energy status after average tolerable ischemia. |
doi_str_mv | 10.1016/j.jss.2012.05.025 |
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Success of transplantation has been correlated with high-energy phosphate (HEP) contents of the graft. Methods HEP contents in heart, liver, kidney, and pancreas from living, BD, and donation after cardiac death in a pig model ( n = 6 per donor type) were evaluated systematically. BD was induced under general anesthesia by inflating a balloon in the epidural space. Ten hours after confirmation, organs were retrieved. Cardiac arrest was induced by 9 V direct current. After 10 min of ventricular fibrillation without cardiac output, mechanical and medical reanimation was performed for 30 min before organ retrieval. In living donors, organs were explanted immediately. Freeze-clamped biopsies were taken before perfusion with Celsior solution (heart) or University of Wisconsin solution (abdominal organs) in BD and living donors or with Histidine-Tryptophan-Ketoglutaric solution (all organs) in non–heart-beating donors, after perfusion, and after cold ischemia (4 h for heart, 6 h for liver and pancreas, and 12 h for kidney). HEPs (adenosine triphosphate, adenosine diphosphate, adenosine monophosphate, and phosphocreatine), xanthine, and hypoxanthine were measured by high-performance liquid chromatography. Energy charge and adenosine triphosphate-to-adenosine diphosphate ratio were calculated. Results After ischemia, organs from different donor types showed no difference in energy status. In all organs, a decrease of HEP and an increase in hypoxanthine contents were observed during perfusion and ischemia, irrespective of the donor type. Conclusion Organs from BD or non–heart-beating donors do not differ from living donor organs in their energy status after average tolerable ischemia.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2012.05.025</identifier><identifier>PMID: 22682714</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenosine Triphosphate - metabolism ; Animals ; Brain dead donor ; Brain Death ; Energy Metabolism ; Heart ; High-energy phosphates ; Ischemia - metabolism ; Kidney ; Kidney - metabolism ; Liver ; Liver - metabolism ; Living donor ; Living Donors ; Myocardium - metabolism ; Non–heart-beating donor ; Organ Transplantation ; Pancreas ; Pancreas - metabolism ; Surgery ; Swine ; Tissue Donors</subject><ispartof>The Journal of surgical research, 2013-04, Vol.180 (2), p.356-367</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-ea1246e2893e9597b6b55e416de4404a14714d14ec515678af46260b4583e0403</citedby><cites>FETCH-LOGICAL-c408t-ea1246e2893e9597b6b55e416de4404a14714d14ec515678af46260b4583e0403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022480412004593$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22682714$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stadlbauer, Vanessa, MD</creatorcontrib><creatorcontrib>Stiegler, Philipp, MD</creatorcontrib><creatorcontrib>Taeubl, Philipp, MD</creatorcontrib><creatorcontrib>Sereinigg, Michael, MD</creatorcontrib><creatorcontrib>Puntschart, Andreas, MD</creatorcontrib><creatorcontrib>Bradatsch, Andrea, MD</creatorcontrib><creatorcontrib>Curcic, Pero, MD</creatorcontrib><creatorcontrib>Seifert-Held, Thomas, MD</creatorcontrib><creatorcontrib>Zmugg, Gerda</creatorcontrib><creatorcontrib>Stojakovic, Tatjana, MD</creatorcontrib><creatorcontrib>Leopold, Barbara</creatorcontrib><creatorcontrib>Blattl, Daniela</creatorcontrib><creatorcontrib>Horki, Vera, MD</creatorcontrib><creatorcontrib>Mayrhauser, Ursula, PhD</creatorcontrib><creatorcontrib>Wiederstein-Grasser, Iris, DVM</creatorcontrib><creatorcontrib>Leber, Bettina, PhD</creatorcontrib><creatorcontrib>Jürgens, Günther</creatorcontrib><creatorcontrib>Tscheliessnigg, Karlheinz</creatorcontrib><creatorcontrib>Hallström, Seth</creatorcontrib><title>Energy status of pig donor organs after ischemia is independent of donor type</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Abstract Background Literature is controversial whether organs from living donors have a better graft function than brain dead (BD) and non–heart-beating donor organs. Success of transplantation has been correlated with high-energy phosphate (HEP) contents of the graft. Methods HEP contents in heart, liver, kidney, and pancreas from living, BD, and donation after cardiac death in a pig model ( n = 6 per donor type) were evaluated systematically. BD was induced under general anesthesia by inflating a balloon in the epidural space. Ten hours after confirmation, organs were retrieved. Cardiac arrest was induced by 9 V direct current. After 10 min of ventricular fibrillation without cardiac output, mechanical and medical reanimation was performed for 30 min before organ retrieval. In living donors, organs were explanted immediately. Freeze-clamped biopsies were taken before perfusion with Celsior solution (heart) or University of Wisconsin solution (abdominal organs) in BD and living donors or with Histidine-Tryptophan-Ketoglutaric solution (all organs) in non–heart-beating donors, after perfusion, and after cold ischemia (4 h for heart, 6 h for liver and pancreas, and 12 h for kidney). HEPs (adenosine triphosphate, adenosine diphosphate, adenosine monophosphate, and phosphocreatine), xanthine, and hypoxanthine were measured by high-performance liquid chromatography. Energy charge and adenosine triphosphate-to-adenosine diphosphate ratio were calculated. Results After ischemia, organs from different donor types showed no difference in energy status. In all organs, a decrease of HEP and an increase in hypoxanthine contents were observed during perfusion and ischemia, irrespective of the donor type. Conclusion Organs from BD or non–heart-beating donors do not differ from living donor organs in their energy status after average tolerable ischemia.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Animals</subject><subject>Brain dead donor</subject><subject>Brain Death</subject><subject>Energy Metabolism</subject><subject>Heart</subject><subject>High-energy phosphates</subject><subject>Ischemia - metabolism</subject><subject>Kidney</subject><subject>Kidney - metabolism</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Living donor</subject><subject>Living Donors</subject><subject>Myocardium - metabolism</subject><subject>Non–heart-beating donor</subject><subject>Organ Transplantation</subject><subject>Pancreas</subject><subject>Pancreas - metabolism</subject><subject>Surgery</subject><subject>Swine</subject><subject>Tissue Donors</subject><issn>0022-4804</issn><issn>1095-8673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFv1DAQhS0EarelP4ALypFLwoxjO4mQkFBVClIRB-BseZ3J4pC1g50g7b_H0RYOHLiMx9J7TzPfMPYCoUJA9XqsxpQqDsgrkBVw-YTtEDpZtqqpn7IdAOelaEFcsquURsj_rqkv2CXnquUNih37dOcpHk5FWsyypiIMxewORR98iEWIB-NTYYaFYuGS_U5HZ3JTON_TTLn4ZXOc1ctppufs2WCmRDeP7zX79v7u6-2H8uHz_cfbdw-lFdAuJRnkQhFvu5o62TV7tZeSBKqehABhUOTZehRkJUrVtGYQiivYC9nWBALqa_bqnDvH8HOltOhjno-myXgKa9JYY9NKhaiyFM9SG0NKkQY9R3c08aQR9EZRjzpT1BtFDVJnitnz8jF-3R-p_-v4gy0L3pwFlJf85SjqZB15S72LZBfdB_ff-Lf_uO3kvLNm-kEnSmNYo8_0NOqUPfrLdsbtisgBhOzq-jdaXJWm</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Stadlbauer, Vanessa, MD</creator><creator>Stiegler, Philipp, MD</creator><creator>Taeubl, Philipp, MD</creator><creator>Sereinigg, Michael, MD</creator><creator>Puntschart, Andreas, MD</creator><creator>Bradatsch, Andrea, MD</creator><creator>Curcic, Pero, MD</creator><creator>Seifert-Held, Thomas, MD</creator><creator>Zmugg, Gerda</creator><creator>Stojakovic, Tatjana, MD</creator><creator>Leopold, Barbara</creator><creator>Blattl, Daniela</creator><creator>Horki, Vera, MD</creator><creator>Mayrhauser, Ursula, PhD</creator><creator>Wiederstein-Grasser, Iris, DVM</creator><creator>Leber, Bettina, PhD</creator><creator>Jürgens, Günther</creator><creator>Tscheliessnigg, Karlheinz</creator><creator>Hallström, Seth</creator><general>Elsevier Inc</general><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>20130401</creationdate><title>Energy status of pig donor organs after ischemia is independent of donor type</title><author>Stadlbauer, Vanessa, MD ; Stiegler, Philipp, MD ; Taeubl, Philipp, MD ; Sereinigg, Michael, MD ; Puntschart, Andreas, MD ; Bradatsch, Andrea, MD ; Curcic, Pero, MD ; Seifert-Held, Thomas, MD ; Zmugg, Gerda ; Stojakovic, Tatjana, MD ; Leopold, Barbara ; Blattl, Daniela ; Horki, Vera, MD ; Mayrhauser, Ursula, PhD ; Wiederstein-Grasser, Iris, DVM ; Leber, Bettina, PhD ; Jürgens, Günther ; Tscheliessnigg, Karlheinz ; Hallström, Seth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-ea1246e2893e9597b6b55e416de4404a14714d14ec515678af46260b4583e0403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Animals</topic><topic>Brain dead donor</topic><topic>Brain Death</topic><topic>Energy Metabolism</topic><topic>Heart</topic><topic>High-energy phosphates</topic><topic>Ischemia - metabolism</topic><topic>Kidney</topic><topic>Kidney - metabolism</topic><topic>Liver</topic><topic>Liver - metabolism</topic><topic>Living donor</topic><topic>Living Donors</topic><topic>Myocardium - metabolism</topic><topic>Non–heart-beating donor</topic><topic>Organ Transplantation</topic><topic>Pancreas</topic><topic>Pancreas - metabolism</topic><topic>Surgery</topic><topic>Swine</topic><topic>Tissue Donors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stadlbauer, Vanessa, MD</creatorcontrib><creatorcontrib>Stiegler, Philipp, MD</creatorcontrib><creatorcontrib>Taeubl, Philipp, MD</creatorcontrib><creatorcontrib>Sereinigg, Michael, MD</creatorcontrib><creatorcontrib>Puntschart, Andreas, MD</creatorcontrib><creatorcontrib>Bradatsch, Andrea, MD</creatorcontrib><creatorcontrib>Curcic, Pero, MD</creatorcontrib><creatorcontrib>Seifert-Held, Thomas, MD</creatorcontrib><creatorcontrib>Zmugg, Gerda</creatorcontrib><creatorcontrib>Stojakovic, Tatjana, MD</creatorcontrib><creatorcontrib>Leopold, Barbara</creatorcontrib><creatorcontrib>Blattl, Daniela</creatorcontrib><creatorcontrib>Horki, Vera, MD</creatorcontrib><creatorcontrib>Mayrhauser, Ursula, PhD</creatorcontrib><creatorcontrib>Wiederstein-Grasser, Iris, DVM</creatorcontrib><creatorcontrib>Leber, Bettina, PhD</creatorcontrib><creatorcontrib>Jürgens, Günther</creatorcontrib><creatorcontrib>Tscheliessnigg, Karlheinz</creatorcontrib><creatorcontrib>Hallström, Seth</creatorcontrib><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>The Journal of surgical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stadlbauer, Vanessa, MD</au><au>Stiegler, Philipp, MD</au><au>Taeubl, Philipp, MD</au><au>Sereinigg, Michael, MD</au><au>Puntschart, Andreas, MD</au><au>Bradatsch, Andrea, MD</au><au>Curcic, Pero, MD</au><au>Seifert-Held, Thomas, MD</au><au>Zmugg, Gerda</au><au>Stojakovic, Tatjana, MD</au><au>Leopold, Barbara</au><au>Blattl, Daniela</au><au>Horki, Vera, MD</au><au>Mayrhauser, Ursula, PhD</au><au>Wiederstein-Grasser, Iris, DVM</au><au>Leber, Bettina, PhD</au><au>Jürgens, Günther</au><au>Tscheliessnigg, Karlheinz</au><au>Hallström, Seth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Energy status of pig donor organs after ischemia is independent of donor type</atitle><jtitle>The Journal of surgical research</jtitle><addtitle>J Surg Res</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>180</volume><issue>2</issue><spage>356</spage><epage>367</epage><pages>356-367</pages><issn>0022-4804</issn><eissn>1095-8673</eissn><abstract>Abstract Background Literature is controversial whether organs from living donors have a better graft function than brain dead (BD) and non–heart-beating donor organs. Success of transplantation has been correlated with high-energy phosphate (HEP) contents of the graft. Methods HEP contents in heart, liver, kidney, and pancreas from living, BD, and donation after cardiac death in a pig model ( n = 6 per donor type) were evaluated systematically. BD was induced under general anesthesia by inflating a balloon in the epidural space. Ten hours after confirmation, organs were retrieved. Cardiac arrest was induced by 9 V direct current. After 10 min of ventricular fibrillation without cardiac output, mechanical and medical reanimation was performed for 30 min before organ retrieval. In living donors, organs were explanted immediately. Freeze-clamped biopsies were taken before perfusion with Celsior solution (heart) or University of Wisconsin solution (abdominal organs) in BD and living donors or with Histidine-Tryptophan-Ketoglutaric solution (all organs) in non–heart-beating donors, after perfusion, and after cold ischemia (4 h for heart, 6 h for liver and pancreas, and 12 h for kidney). HEPs (adenosine triphosphate, adenosine diphosphate, adenosine monophosphate, and phosphocreatine), xanthine, and hypoxanthine were measured by high-performance liquid chromatography. Energy charge and adenosine triphosphate-to-adenosine diphosphate ratio were calculated. Results After ischemia, organs from different donor types showed no difference in energy status. In all organs, a decrease of HEP and an increase in hypoxanthine contents were observed during perfusion and ischemia, irrespective of the donor type. Conclusion Organs from BD or non–heart-beating donors do not differ from living donor organs in their energy status after average tolerable ischemia.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22682714</pmid><doi>10.1016/j.jss.2012.05.025</doi><tpages>12</tpages></addata></record> |
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subjects | Adenosine Triphosphate - metabolism Animals Brain dead donor Brain Death Energy Metabolism Heart High-energy phosphates Ischemia - metabolism Kidney Kidney - metabolism Liver Liver - metabolism Living donor Living Donors Myocardium - metabolism Non–heart-beating donor Organ Transplantation Pancreas Pancreas - metabolism Surgery Swine Tissue Donors |
title | Energy status of pig donor organs after ischemia is independent of donor type |
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