Metabolic preconditioning of donor organs: Defatting fatty livers by normothermic perfusion ex vivo
Fatty liver is a significant risk factor for liver transplantation, and accounts for nearly half of the livers rejected from the donor pool. We hypothesized that metabolic preconditioning via ex vivo perfusion of the liver graft can reduce fat content and increase post-transplant survival to an acce...
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Veröffentlicht in: | Metabolic engineering 2009-07, Vol.11 (4), p.274-283 |
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creator | Nagrath, Deepak Xu, Hongzhi Tanimura, Yoko Zuo, Rongjun Berthiaume, François Avila, Marco Yarmush, Rubin Yarmush, Martin L. |
description | Fatty liver is a significant risk factor for liver transplantation, and accounts for nearly half of the livers rejected from the donor pool. We hypothesized that metabolic preconditioning via ex vivo perfusion of the liver graft can reduce fat content and increase post-transplant survival to an acceptable range. We describe a perfusate medium containing agents that promote the defatting of hepatocytes and explanted livers. Defatting agents were screened on cultured hepatocytes made fatty by pre-incubation with fatty acids. The most effective agents were then used on fatty livers. Fatty livers were isolated from obese Zucker rats and normothermically perfused with medium containing a combination of defatting agents. This combination decreased the intracellular lipid content of cultured hepatocytes by 35% over 24
h, and of perfused livers by 50% over 3
h. Metabolite analysis suggests that the defatting cocktail upregulated both lipid oxidation and export. Furthermore, gene expression analysis for several enzymes and transcription factors involved in fatty acid oxidation and triglyceride clearance were elevated. We conclude that a cocktail of defatting agents can be used to rapidly clear excess lipid storage in fatty livers, thus providing a new means to recondition donor livers deemed unacceptable or marginally acceptable for transplantation. |
doi_str_mv | 10.1016/j.ymben.2009.05.005 |
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h, and of perfused livers by 50% over 3
h. Metabolite analysis suggests that the defatting cocktail upregulated both lipid oxidation and export. Furthermore, gene expression analysis for several enzymes and transcription factors involved in fatty acid oxidation and triglyceride clearance were elevated. We conclude that a cocktail of defatting agents can be used to rapidly clear excess lipid storage in fatty livers, thus providing a new means to recondition donor livers deemed unacceptable or marginally acceptable for transplantation.</description><identifier>ISSN: 1096-7176</identifier><identifier>EISSN: 1096-7184</identifier><identifier>DOI: 10.1016/j.ymben.2009.05.005</identifier><identifier>PMID: 19508897</identifier><language>eng</language><publisher>Belgium: Elsevier Inc</publisher><subject>Animals ; Cell Culture Techniques ; Cell Survival ; Cells, Cultured ; Fatty Liver - metabolism ; Female ; Hepatocytes ; Hepatocytes - cytology ; Heterozygote ; Homozygote ; Humans ; Liver Transplantation ; Normothermic perfusion ; Nuclear receptors ; Perfusion - methods ; Rats ; Rats, Inbred Lew ; Rats, Zucker ; Steatosis ; Survival Analysis ; Time Factors ; Tissue Donors</subject><ispartof>Metabolic engineering, 2009-07, Vol.11 (4), p.274-283</ispartof><rights>2009 Elsevier Inc.</rights><rights>2009 Elsevier Inc. All rights reserved. 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c554t-d7da41cdff7122d9bdc42cc366ed04ccea800485901a02ccdf0feb11c8a22de33</citedby><cites>FETCH-LOGICAL-c554t-d7da41cdff7122d9bdc42cc366ed04ccea800485901a02ccdf0feb11c8a22de33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S109671760900041X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19508897$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagrath, Deepak</creatorcontrib><creatorcontrib>Xu, Hongzhi</creatorcontrib><creatorcontrib>Tanimura, Yoko</creatorcontrib><creatorcontrib>Zuo, Rongjun</creatorcontrib><creatorcontrib>Berthiaume, François</creatorcontrib><creatorcontrib>Avila, Marco</creatorcontrib><creatorcontrib>Yarmush, Rubin</creatorcontrib><creatorcontrib>Yarmush, Martin L.</creatorcontrib><title>Metabolic preconditioning of donor organs: Defatting fatty livers by normothermic perfusion ex vivo</title><title>Metabolic engineering</title><addtitle>Metab Eng</addtitle><description>Fatty liver is a significant risk factor for liver transplantation, and accounts for nearly half of the livers rejected from the donor pool. We hypothesized that metabolic preconditioning via ex vivo perfusion of the liver graft can reduce fat content and increase post-transplant survival to an acceptable range. We describe a perfusate medium containing agents that promote the defatting of hepatocytes and explanted livers. Defatting agents were screened on cultured hepatocytes made fatty by pre-incubation with fatty acids. The most effective agents were then used on fatty livers. Fatty livers were isolated from obese Zucker rats and normothermically perfused with medium containing a combination of defatting agents. This combination decreased the intracellular lipid content of cultured hepatocytes by 35% over 24
h, and of perfused livers by 50% over 3
h. Metabolite analysis suggests that the defatting cocktail upregulated both lipid oxidation and export. Furthermore, gene expression analysis for several enzymes and transcription factors involved in fatty acid oxidation and triglyceride clearance were elevated. We conclude that a cocktail of defatting agents can be used to rapidly clear excess lipid storage in fatty livers, thus providing a new means to recondition donor livers deemed unacceptable or marginally acceptable for transplantation.</description><subject>Animals</subject><subject>Cell Culture Techniques</subject><subject>Cell Survival</subject><subject>Cells, Cultured</subject><subject>Fatty Liver - metabolism</subject><subject>Female</subject><subject>Hepatocytes</subject><subject>Hepatocytes - cytology</subject><subject>Heterozygote</subject><subject>Homozygote</subject><subject>Humans</subject><subject>Liver Transplantation</subject><subject>Normothermic perfusion</subject><subject>Nuclear receptors</subject><subject>Perfusion - methods</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Rats, Zucker</subject><subject>Steatosis</subject><subject>Survival Analysis</subject><subject>Time Factors</subject><subject>Tissue Donors</subject><issn>1096-7176</issn><issn>1096-7184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2PFCEQhjtG466rv8DEcPI2bdHdQGOiiVk_kzVe9ExoqJ5l0g0jMB3n30s7k1UveiqSeuql4KmqpxRqCpS_2NXHeUBfNwCyBlYDsHvVJQXJN4L23f27s-AX1aOUdgCUMkkfVhdUMuh7KS4r8xmzHsLkDNlHNMFbl13wzm9JGIkNPkQS4lb79JK8xVHnvLbWeiSTWzAmMhxJoeaQbzHOaw7G8ZBKCMEfZHFLeFw9GPWU8Mm5XlXf3r_7ev1xc_Plw6frNzcbw1iXN1ZY3VFjx1HQprFysKZrjGk5RwudMah7gK5nEqiG0rAjjDhQanpdcGzbq-r1KXd_GGa0Bn2OelL76GYdjypop_7ueHertmFRTU87ELwEPD8HxPD9gCmr2SWD06Q9hkNSXDDBQcr_gg0I4K1gBWxPoIkhpYjj3TYU1GpR7dQvi2q1qICpYrFMPfvzIb9nztoK8OoEYPnOxWFUyTj0Bq0rErOywf3zgp_53LOH</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Nagrath, Deepak</creator><creator>Xu, Hongzhi</creator><creator>Tanimura, Yoko</creator><creator>Zuo, Rongjun</creator><creator>Berthiaume, François</creator><creator>Avila, Marco</creator><creator>Yarmush, Rubin</creator><creator>Yarmush, Martin L.</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090701</creationdate><title>Metabolic preconditioning of donor organs: Defatting fatty livers by normothermic perfusion ex vivo</title><author>Nagrath, Deepak ; Xu, Hongzhi ; Tanimura, Yoko ; Zuo, Rongjun ; Berthiaume, François ; Avila, Marco ; Yarmush, Rubin ; Yarmush, Martin L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c554t-d7da41cdff7122d9bdc42cc366ed04ccea800485901a02ccdf0feb11c8a22de33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cell Culture Techniques</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>Fatty Liver - metabolism</topic><topic>Female</topic><topic>Hepatocytes</topic><topic>Hepatocytes - cytology</topic><topic>Heterozygote</topic><topic>Homozygote</topic><topic>Humans</topic><topic>Liver Transplantation</topic><topic>Normothermic perfusion</topic><topic>Nuclear receptors</topic><topic>Perfusion - methods</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Rats, Zucker</topic><topic>Steatosis</topic><topic>Survival Analysis</topic><topic>Time Factors</topic><topic>Tissue Donors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagrath, Deepak</creatorcontrib><creatorcontrib>Xu, Hongzhi</creatorcontrib><creatorcontrib>Tanimura, Yoko</creatorcontrib><creatorcontrib>Zuo, Rongjun</creatorcontrib><creatorcontrib>Berthiaume, François</creatorcontrib><creatorcontrib>Avila, Marco</creatorcontrib><creatorcontrib>Yarmush, Rubin</creatorcontrib><creatorcontrib>Yarmush, Martin L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Metabolic engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagrath, Deepak</au><au>Xu, Hongzhi</au><au>Tanimura, Yoko</au><au>Zuo, Rongjun</au><au>Berthiaume, François</au><au>Avila, Marco</au><au>Yarmush, Rubin</au><au>Yarmush, Martin L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic preconditioning of donor organs: Defatting fatty livers by normothermic perfusion ex vivo</atitle><jtitle>Metabolic engineering</jtitle><addtitle>Metab Eng</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>11</volume><issue>4</issue><spage>274</spage><epage>283</epage><pages>274-283</pages><issn>1096-7176</issn><eissn>1096-7184</eissn><abstract>Fatty liver is a significant risk factor for liver transplantation, and accounts for nearly half of the livers rejected from the donor pool. We hypothesized that metabolic preconditioning via ex vivo perfusion of the liver graft can reduce fat content and increase post-transplant survival to an acceptable range. We describe a perfusate medium containing agents that promote the defatting of hepatocytes and explanted livers. Defatting agents were screened on cultured hepatocytes made fatty by pre-incubation with fatty acids. The most effective agents were then used on fatty livers. Fatty livers were isolated from obese Zucker rats and normothermically perfused with medium containing a combination of defatting agents. This combination decreased the intracellular lipid content of cultured hepatocytes by 35% over 24
h, and of perfused livers by 50% over 3
h. Metabolite analysis suggests that the defatting cocktail upregulated both lipid oxidation and export. Furthermore, gene expression analysis for several enzymes and transcription factors involved in fatty acid oxidation and triglyceride clearance were elevated. We conclude that a cocktail of defatting agents can be used to rapidly clear excess lipid storage in fatty livers, thus providing a new means to recondition donor livers deemed unacceptable or marginally acceptable for transplantation.</abstract><cop>Belgium</cop><pub>Elsevier Inc</pub><pmid>19508897</pmid><doi>10.1016/j.ymben.2009.05.005</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Culture Techniques Cell Survival Cells, Cultured Fatty Liver - metabolism Female Hepatocytes Hepatocytes - cytology Heterozygote Homozygote Humans Liver Transplantation Normothermic perfusion Nuclear receptors Perfusion - methods Rats Rats, Inbred Lew Rats, Zucker Steatosis Survival Analysis Time Factors Tissue Donors |
title | Metabolic preconditioning of donor organs: Defatting fatty livers by normothermic perfusion ex vivo |
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