Normothermic extracorporeal membrane oxygenation support: Improving the function of intestinal grafts obtained from cardiac death donors
Extracorporeal membrane oxygenation (ECMO) could ameliorate the energy status and viability of bowel grafts from cardiac death donors. However, the function of these grafts after transplantation is not clear. The purpose of the study was to evaluate the early function of intestinal grafts after tran...
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description | Extracorporeal membrane oxygenation (ECMO) could ameliorate the energy status and viability of bowel grafts from cardiac death donors. However, the function of these grafts after transplantation is not clear. The purpose of the study was to evaluate the early function of intestinal grafts after transplantation from expected cardiac death donors supported with normothermic extracorporeal support using a porcine allogeneic orthotopic segmental small bowel transplantation model. Eighteen domestic crossbred donor pigs were assigned to living donation (LD), donation after cardiac death (DCD), and ECMO groups. In the LD group, small bowels were harvested and preserved immediately in cold storage. In the other two groups, the donor pigs received conventional rapid recovery treatment or 1‐hour normothermic extracorporeal support after 10‐minutes expected cardiac arrest. Subsequently, the small bowels were removed and preserved in cold storage. After 5‐6 hours of preservation, small bowel grafts were transplanted into the recipient pigs that underwent enterectomy. The pathology and electron microscopy results, cell apoptosis rate, tight junction protein expression level in the intestinal mucosa, and plasma endotoxin level were evaluated after transplantation. All grafts functioned on the basis of the maltose absorption test results at day 7 after transplantation. There were no significant differences in the morphological changes in the intestinal mucosa among the three groups at day 7 after transplantation. The cell apoptosis rate and plasma endotoxin level in the ECMO group did not differ significantly than those in the LD group, but were evidently lower than those in the DCD group (P |
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However, the function of these grafts after transplantation is not clear. The purpose of the study was to evaluate the early function of intestinal grafts after transplantation from expected cardiac death donors supported with normothermic extracorporeal support using a porcine allogeneic orthotopic segmental small bowel transplantation model. Eighteen domestic crossbred donor pigs were assigned to living donation (LD), donation after cardiac death (DCD), and ECMO groups. In the LD group, small bowels were harvested and preserved immediately in cold storage. In the other two groups, the donor pigs received conventional rapid recovery treatment or 1‐hour normothermic extracorporeal support after 10‐minutes expected cardiac arrest. Subsequently, the small bowels were removed and preserved in cold storage. After 5‐6 hours of preservation, small bowel grafts were transplanted into the recipient pigs that underwent enterectomy. The pathology and electron microscopy results, cell apoptosis rate, tight junction protein expression level in the intestinal mucosa, and plasma endotoxin level were evaluated after transplantation. All grafts functioned on the basis of the maltose absorption test results at day 7 after transplantation. There were no significant differences in the morphological changes in the intestinal mucosa among the three groups at day 7 after transplantation. The cell apoptosis rate and plasma endotoxin level in the ECMO group did not differ significantly than those in the LD group, but were evidently lower than those in the DCD group (P < .001). The intestinal absorptive function improved significantly in the ECMO group in contrast with that in the DCD group (P < .001). Short‐term ECMO intervention can alleviate ischemia–reperfusion injuries in intestinal grafts and improve intestinal absorptive function in the early stage after transplantation. Reducing caspase‐3 protein expression and cell apoptosis in the intestinal mucosa may be one of the protective mechanisms of ECMO intervention.</description><identifier>ISSN: 0160-564X</identifier><identifier>EISSN: 1525-1594</identifier><identifier>DOI: 10.1111/aor.13697</identifier><identifier>PMID: 32279328</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Absorptivity ; Apoptosis ; cardiac death donors ; Caspase ; Cerebral blood flow ; Cold storage ; Cryopreservation ; Death ; Donors ; early graft function ; Electron microscopy ; Endotoxins ; Energy balance ; Extracorporeal membrane oxygenation ; Grafting ; intestinal graft function ; Ischemia ; large animal model ; Maltose ; Membranes ; Mortality ; Mucosa ; normothermic ; Oxygenation ; Protein expression ; Proteins ; Reperfusion ; small bowel transplantation ; Small intestine transplantation ; Swine ; Transplantation</subject><ispartof>Artificial organs, 2020-10, Vol.44 (10), p.1098-1106</ispartof><rights>2020 International Center for Artificial Organ and Transplantation and Wiley Periodicals LLC.</rights><rights>2020 International Center for Artificial Organs and Transplantation and Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3537-6e45c3792289244d3001ca43e625a22e593caf4299639eff5eb6bd3ae03951aa3</citedby><cites>FETCH-LOGICAL-c3537-6e45c3792289244d3001ca43e625a22e593caf4299639eff5eb6bd3ae03951aa3</cites><orcidid>0000-0002-4453-1749</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Faor.13697$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Faor.13697$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32279328$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Mingxiao</creatorcontrib><creatorcontrib>Lu, Chunlei</creatorcontrib><creatorcontrib>Li, Linlin</creatorcontrib><creatorcontrib>Yao, Danhua</creatorcontrib><creatorcontrib>Li, Yousheng</creatorcontrib><title>Normothermic extracorporeal membrane oxygenation support: Improving the function of intestinal grafts obtained from cardiac death donors</title><title>Artificial organs</title><addtitle>Artif Organs</addtitle><description>Extracorporeal membrane oxygenation (ECMO) could ameliorate the energy status and viability of bowel grafts from cardiac death donors. However, the function of these grafts after transplantation is not clear. The purpose of the study was to evaluate the early function of intestinal grafts after transplantation from expected cardiac death donors supported with normothermic extracorporeal support using a porcine allogeneic orthotopic segmental small bowel transplantation model. Eighteen domestic crossbred donor pigs were assigned to living donation (LD), donation after cardiac death (DCD), and ECMO groups. In the LD group, small bowels were harvested and preserved immediately in cold storage. In the other two groups, the donor pigs received conventional rapid recovery treatment or 1‐hour normothermic extracorporeal support after 10‐minutes expected cardiac arrest. Subsequently, the small bowels were removed and preserved in cold storage. After 5‐6 hours of preservation, small bowel grafts were transplanted into the recipient pigs that underwent enterectomy. The pathology and electron microscopy results, cell apoptosis rate, tight junction protein expression level in the intestinal mucosa, and plasma endotoxin level were evaluated after transplantation. All grafts functioned on the basis of the maltose absorption test results at day 7 after transplantation. There were no significant differences in the morphological changes in the intestinal mucosa among the three groups at day 7 after transplantation. The cell apoptosis rate and plasma endotoxin level in the ECMO group did not differ significantly than those in the LD group, but were evidently lower than those in the DCD group (P < .001). The intestinal absorptive function improved significantly in the ECMO group in contrast with that in the DCD group (P < .001). Short‐term ECMO intervention can alleviate ischemia–reperfusion injuries in intestinal grafts and improve intestinal absorptive function in the early stage after transplantation. Reducing caspase‐3 protein expression and cell apoptosis in the intestinal mucosa may be one of the protective mechanisms of ECMO intervention.</description><subject>Absorptivity</subject><subject>Apoptosis</subject><subject>cardiac death donors</subject><subject>Caspase</subject><subject>Cerebral blood flow</subject><subject>Cold storage</subject><subject>Cryopreservation</subject><subject>Death</subject><subject>Donors</subject><subject>early graft function</subject><subject>Electron microscopy</subject><subject>Endotoxins</subject><subject>Energy balance</subject><subject>Extracorporeal membrane oxygenation</subject><subject>Grafting</subject><subject>intestinal graft function</subject><subject>Ischemia</subject><subject>large animal model</subject><subject>Maltose</subject><subject>Membranes</subject><subject>Mortality</subject><subject>Mucosa</subject><subject>normothermic</subject><subject>Oxygenation</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Reperfusion</subject><subject>small bowel transplantation</subject><subject>Small intestine transplantation</subject><subject>Swine</subject><subject>Transplantation</subject><issn>0160-564X</issn><issn>1525-1594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kctu1TAQhi0EoofCghdAltjAIq2vScyuqrhUqqiEQGIXTZzxqavEPtgO9LwBj43pKSyQmM0s5ptPM_oJec7ZCa91CjGdcNma7gHZcC10w7VRD8mG8ZY1ulVfj8iTnG8YY51i7WNyJIXojBT9hvz8GNMSyzWmxVuKtyWBjWkXE8JMF1zGBAFpvN1vMUDxMdC87uq4vKEXyy7F7z5saV2nbg32bh4d9aFgLj5UxTaBK5nGsYAPOFGX4kItpMmDpRNCuaZTDDHlp-SRgznjs_t-TL68e_v5_ENzefX-4vzssrFSy65pUWkrOyNEb4RSk2SMW1ASW6FBCNRGWnBKGNNKg85pHNtxkoBMGs0B5DF5dfDW47-t9cxh8dniPNc_45oHIauYmU72FX35D3oT11S_qpRSSva9YaxSrw-UTTHnhG7YJb9A2g-cDb_jGWo8w108lX1xb1zHBae_5J88KnB6AH74Gff_Nw1nV58Oyl9T75wp</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Guo, Mingxiao</creator><creator>Lu, Chunlei</creator><creator>Li, Linlin</creator><creator>Yao, Danhua</creator><creator>Li, Yousheng</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4453-1749</orcidid></search><sort><creationdate>202010</creationdate><title>Normothermic extracorporeal membrane oxygenation support: Improving the function of intestinal grafts obtained from cardiac death donors</title><author>Guo, Mingxiao ; Lu, Chunlei ; Li, Linlin ; Yao, Danhua ; Li, Yousheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3537-6e45c3792289244d3001ca43e625a22e593caf4299639eff5eb6bd3ae03951aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Absorptivity</topic><topic>Apoptosis</topic><topic>cardiac death donors</topic><topic>Caspase</topic><topic>Cerebral blood flow</topic><topic>Cold storage</topic><topic>Cryopreservation</topic><topic>Death</topic><topic>Donors</topic><topic>early graft function</topic><topic>Electron microscopy</topic><topic>Endotoxins</topic><topic>Energy balance</topic><topic>Extracorporeal membrane oxygenation</topic><topic>Grafting</topic><topic>intestinal graft function</topic><topic>Ischemia</topic><topic>large animal model</topic><topic>Maltose</topic><topic>Membranes</topic><topic>Mortality</topic><topic>Mucosa</topic><topic>normothermic</topic><topic>Oxygenation</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Reperfusion</topic><topic>small bowel transplantation</topic><topic>Small intestine transplantation</topic><topic>Swine</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Mingxiao</creatorcontrib><creatorcontrib>Lu, Chunlei</creatorcontrib><creatorcontrib>Li, Linlin</creatorcontrib><creatorcontrib>Yao, Danhua</creatorcontrib><creatorcontrib>Li, Yousheng</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Artificial organs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Mingxiao</au><au>Lu, Chunlei</au><au>Li, Linlin</au><au>Yao, Danhua</au><au>Li, Yousheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Normothermic extracorporeal membrane oxygenation support: Improving the function of intestinal grafts obtained from cardiac death donors</atitle><jtitle>Artificial organs</jtitle><addtitle>Artif Organs</addtitle><date>2020-10</date><risdate>2020</risdate><volume>44</volume><issue>10</issue><spage>1098</spage><epage>1106</epage><pages>1098-1106</pages><issn>0160-564X</issn><eissn>1525-1594</eissn><abstract>Extracorporeal membrane oxygenation (ECMO) could ameliorate the energy status and viability of bowel grafts from cardiac death donors. However, the function of these grafts after transplantation is not clear. The purpose of the study was to evaluate the early function of intestinal grafts after transplantation from expected cardiac death donors supported with normothermic extracorporeal support using a porcine allogeneic orthotopic segmental small bowel transplantation model. Eighteen domestic crossbred donor pigs were assigned to living donation (LD), donation after cardiac death (DCD), and ECMO groups. In the LD group, small bowels were harvested and preserved immediately in cold storage. In the other two groups, the donor pigs received conventional rapid recovery treatment or 1‐hour normothermic extracorporeal support after 10‐minutes expected cardiac arrest. Subsequently, the small bowels were removed and preserved in cold storage. After 5‐6 hours of preservation, small bowel grafts were transplanted into the recipient pigs that underwent enterectomy. The pathology and electron microscopy results, cell apoptosis rate, tight junction protein expression level in the intestinal mucosa, and plasma endotoxin level were evaluated after transplantation. All grafts functioned on the basis of the maltose absorption test results at day 7 after transplantation. There were no significant differences in the morphological changes in the intestinal mucosa among the three groups at day 7 after transplantation. The cell apoptosis rate and plasma endotoxin level in the ECMO group did not differ significantly than those in the LD group, but were evidently lower than those in the DCD group (P < .001). The intestinal absorptive function improved significantly in the ECMO group in contrast with that in the DCD group (P < .001). Short‐term ECMO intervention can alleviate ischemia–reperfusion injuries in intestinal grafts and improve intestinal absorptive function in the early stage after transplantation. Reducing caspase‐3 protein expression and cell apoptosis in the intestinal mucosa may be one of the protective mechanisms of ECMO intervention.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32279328</pmid><doi>10.1111/aor.13697</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4453-1749</orcidid></addata></record> |
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subjects | Absorptivity Apoptosis cardiac death donors Caspase Cerebral blood flow Cold storage Cryopreservation Death Donors early graft function Electron microscopy Endotoxins Energy balance Extracorporeal membrane oxygenation Grafting intestinal graft function Ischemia large animal model Maltose Membranes Mortality Mucosa normothermic Oxygenation Protein expression Proteins Reperfusion small bowel transplantation Small intestine transplantation Swine Transplantation |
title | Normothermic extracorporeal membrane oxygenation support: Improving the function of intestinal grafts obtained from cardiac death donors |
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