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Normothermic Ex Vivo Liver Platform Using Porcine Slaughterhouse Livers for Disease Modeling

  • Melanie Krüger
  • , Alicia Ruppelt (Corresponding author)
  • , Benjamin Kappler
  • , Elke Van Soest
  • , Roos Anne Samsom
  • , Guy C.M. Grinwis
  • , Niels Geijsen
  • , J. Bernd Helms
  • , Marco Stijnen
  • , Linda M. Kock
  • , Marco Rasponi
  • , Hans S. Kooistra
  • , Bart Spee

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

Metabolic and toxic liver disorders, such as fatty liver disease (steatosis) and drug-induced liver injury, are highly prevalent and potentially life-threatening. To allow for the study of these disorders from the early stages onward, without using experimental animals, we collected porcine livers in a slaughterhouse and perfused these livers normothermically. With our simplified protocol, the perfused slaughterhouse livers remained viable and functional over five hours of perfusion, as shown by hemodynamics, bile production, indocyanine green clearance, ammonia metabolism, gene expression and histology. As a proof-of-concept to study liver disorders, we show that an infusion of free fatty acids and acetaminophen results in early biochemical signs of liver damage, including reduced functionality. In conclusion, the present platform offers an accessible system to perform research in a functional, relevant large animal model while avoiding using experimental animals. With further improvements to the model, prolonged exposure could make this model a versatile tool for studying liver diseases and potential treatments.

Original languageEnglish
Article number471
Number of pages19
JournalBioengineering
Volume9
Issue number9
DOIs
Publication statusPublished - 14 Sept 2022

Funding

This research was funded by the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 64268 and No 860715 and was supported by a grant from the Dutch Research Council NWO TTW (15498) to B.S.

Keywords

  • acetaminophen
  • hepatic diseases
  • machine perfusion
  • steatosis

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