2010
DOI: 10.1016/j.cryobiol.2010.03.005
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The influence of storage temperature during machine perfusion on preservation quality of marginal donor livers

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Cited by 80 publications
(48 citation statements)
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“…In accordance with these considerations, no signs of anaerobiosis (HIF-1α) or liver injury were observed during oxygenated perfusion at 10 or 20 °C in contrast to perfusion at 30 or 37 °C [60]. Other rodent models demonstrated superior results at 21 °C compared to lower temperatures in DBD [61,62] and DCD [63] models. This indicates an important shift in hepatic metabolism between 20 and 30 °C, explaining the favorable ATP concentrations after subnormothermic machine perfusion (SNTM).…”
Section: Subnormothermic Machine Perfusionmentioning
confidence: 52%
“…In accordance with these considerations, no signs of anaerobiosis (HIF-1α) or liver injury were observed during oxygenated perfusion at 10 or 20 °C in contrast to perfusion at 30 or 37 °C [60]. Other rodent models demonstrated superior results at 21 °C compared to lower temperatures in DBD [61,62] and DCD [63] models. This indicates an important shift in hepatic metabolism between 20 and 30 °C, explaining the favorable ATP concentrations after subnormothermic machine perfusion (SNTM).…”
Section: Subnormothermic Machine Perfusionmentioning
confidence: 52%
“…Three new solutions that are being tested are Vasosol [16], Polysol (Doorzand Medical Innovations, Amsterdam, The Netherlands) and Lifor an acellular oxygen carrying solution being developed by Life Blood Medical, Inc., which they claim has provided good in vitro function data employing a working heart model for 10 hour slow perfusion preservation of guinea pig hearts at room temperature without added oxygen [30]. More recently, a rat liver study with oxygenation was reported comparing several temperatures with the best results at room temprature [31]. We employed KPS-1 (Kidney Perfusion Solution One), a variant of University of Wisconsin solution commonly known as Belzer's Machine Perfusion Solution, oxygenated and supplemented as described in the materials and methods section.…”
Section: Discussionmentioning
confidence: 99%
“…Given that the liver is fully metabolically active, NMP also offers the best opportunity to assess and even improve graft viability prior to reperfusion in vivo (52,57). NMP may lead to sustained viability, improved hemodynamics and attenuate ischemic injury in marginal livers (58). Nevertheless, the high concentration of pro-inflammatory cytokines in the perfusate during NMP after a prolonged period of CS promote concerns on the capacity of NMP to generate effective graft reconditioning and excellent cell metabolism (59) Friend et al were amongst the first to describe NMP and its benefits over standard CS as measured by preservation of alanine-aminotransferase (ALT) and enhanced Factor V production (60).…”
Section: Nmpmentioning
confidence: 99%