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dc.contributor.authorPeter Olschewskien_US
dc.contributor.authorPaul Gaßen_US
dc.contributor.authorVeeravorn Ariyakhagornen_US
dc.contributor.authorKerstin Jasseen_US
dc.contributor.authorGerhard Hunolden_US
dc.contributor.authorMartin Menzelen_US
dc.contributor.authorWenzel Schöningen_US
dc.contributor.authorVolker Schmitzen_US
dc.contributor.authorPeter Neuhausen_US
dc.contributor.authorGero Puhlen_US
dc.date.accessioned2018-09-04T04:41:16Z-
dc.date.available2018-09-04T04:41:16Z-
dc.date.issued2010-06-01en_US
dc.identifier.issn10902392en_US
dc.identifier.issn00112240en_US
dc.identifier.other2-s2.0-77952671314en_US
dc.identifier.other10.1016/j.cryobiol.2010.03.005en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77952671314&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50460-
dc.description.abstractBackground: Although non-heart-beating donors have the potential to increase the number of available organs, the livers are used very seldom because of the risk of primary non-function. There is evidence that machine perfusion is able to improve the preservation of marginal organs, and therefore we evaluated in our study the influence of the perfusate temperature during oxygenated machine perfusion on the graft quality. Methods: Livers from male Wistar rats were harvested after 60-min warm ischemia induced by cardiac arrest. The portal vein was cannulated and the liver flushed with Lifor® (Lifeblood Medical, Inc.) organ preservation solution for oxygenated machine perfusion (MP) at 4, 12 or 21 °C. Other livers were flushed with HTK and stored at 4 °C by conventional cold storage (4 °C-CS). Furthermore two groups with either warm ischemic damage only or without any ischemic damage serve as control groups. After 6. h of either machine perfusion or cold storage all livers were normothermic reperfused with Krebs-Henseleit buffer, and functional as well as structural data were analyzed. Results: Contrary to livers stored by static cold storage, machine perfused livers showed independently of the perfusate temperature a significantly decreased enzyme release of hepatic transaminases (ALT) during isolated reperfusion. Increasing the machine perfusion temperature to 21°C resulted in a marked reduction of portal venous resistance and an increased bile production. Conclusions: Oxygenated machine perfusion improves viability of livers after prolonged warm ischemic damage. Elevated perfusion temperature of 21°C reconstitutes the hepatic functional capacity better than perfusion at 4 or 12°C. © 2010 Elsevier Inc.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleThe influence of storage temperature during machine perfusion on preservation quality of marginal donor liversen_US
dc.typeJournalen_US
article.title.sourcetitleCryobiologyen_US
article.volume60en_US
article.stream.affiliationsCharité – Universitätsmedizin Berlinen_US
article.stream.affiliationsChiang Mai Universityen_US
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