Literature DB >> 28959005

Machine Perfusion at 20°C Prevents Ischemic Injury and Reduces Hypoxia-Inducible Factor-1α Expression During Rat Liver Preservation.

Clarissa Berardo1, Laura Giuseppina Di Pasqua1, Veronica Siciliano1, Vittoria Rizzo2, Plinio Richelmi1, Andrea Ferrigno1, Mariapia Vairetti1.   

Abstract

BACKGROUND Ischemic cholangitis is the main cause of liver failure after transplantation and subnormothermic machine perfusion may represent a better strategy than conventional cold storage, minimizing preservation injury. We compared livers preserved by machine perfusion at 20°C (MP20) or by cold storage at 4°C (CS4) with regard to hypoxia-inducible factor (HIF)-1α mRNA expression and protein stabilization in hypoxic conditions. MATERIAL AND METHODS Livers from male Wistar rats were stored on ice at 4°C in UW solution (CS4) or perfused with oxygenated Krebs-Henseleit buffer at 20°C (MP20) for six hours. After preservation, the livers were reperfused for two hours with oxygenated Krebs-Henseleit buffer at 37°C to simulate reimplantation. We collected bile, perfusate, and tissue samples. Transaminases, lactate dehydrogenase, bilirubin, and lactic acid were assayed in the perfusate and bile. ATP/ADP, glycogen, HIF-1α mRNA, and protein expression were measured in the tissue homogenates. RESULTS At the end of preservation, as well as after reperfusion, HIF-1α mRNA expression was significantly higher in the ischemic CS4 livers. Although the hypoxic conditions found in CS4 preservation stabilized HIF-1α protein was significantly higher in the CS4 livers at the end of preservation, no difference was observed after reperfusion, likely because of the oxygen in the reperfusion medium. After reperfusion, the MP20 livers released less transaminases and LDH. The MP20 livers had higher ATP/ADP, glycogen, and biliary bilirubin after both preservation and reperfusion when compared with the CS4 livers. CONCLUSIONS The data demonstrated that MP20 was associated with a lower HIF-1α expression and organ injury with respect to CS4, suggesting that oxygen provided by this preservation setting might approximate the organ request, thus avoiding the ischemic injury usually observed during organ preservation by cold storage.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28959005     DOI: 10.12659/aot.904631

Source DB:  PubMed          Journal:  Ann Transplant        ISSN: 1425-9524            Impact factor:   1.530


  5 in total

Review 1.  Optimizing organs for transplantation; advancements in perfusion and preservation methods.

Authors:  Elizabeth Soo; Christopher Marsh; Robert Steiner; Lisa Stocks; Dianne B McKay
Journal:  Transplant Rev (Orlando)       Date:  2019-10-17       Impact factor: 3.943

2.  Liver Graft Susceptibility during Static Cold Storage and Dynamic Machine Perfusion: DCD versus Fatty Livers.

Authors:  Andrea Ferrigno; Laura G Di Pasqua; Clarissa Berardo; Veronica Siciliano; Vittoria Rizzo; Barbara Mannucci; Plinio Richelmi; Anna Cleta Croce; Mariapia Vairetti
Journal:  Int J Mol Sci       Date:  2017-12-31       Impact factor: 5.923

3.  Damage-Associated Molecular Patterns Induce Inflammatory Injury During Machine Preservation of the Liver: Potential Targets to Enhance a Promising Technology.

Authors:  Uwe Scheuermann; Minghua Zhu; Mingqing Song; John Yerxa; Qimeng Gao; Robert P Davis; Min Zhang; William Parker; Matthew G Hartwig; Jean Kwun; Todd V Brennan; Jaewoo Lee; Andrew S Barbas
Journal:  Liver Transpl       Date:  2019-03-15       Impact factor: 5.799

4.  Two Compartment Evaluation of Liver Grafts During Acellular Room Temperature Machine Perfusion (acRTMP) in a Rat Liver Transplant Model.

Authors:  Nader Abraham; Min Zhang; Paul Cray; Qimeng Gao; Kannan P Samy; Ryan Neill; Greta Cywinska; JonCarlo Migaly; Riley Kahan; Arya Pontula; Samantha E Halpern; Caroline Rush; Jude Penaflor; Samuel J Kesseli; Madison Krischak; Mingqing Song; Matthew G Hartwig; Justin J Pollara; Andrew S Barbas
Journal:  Front Med (Lausanne)       Date:  2022-02-24

Review 5.  The Effect of Preservation Temperature on Liver, Kidney, and Pancreas Tissue ATP in Animal and Preclinical Human Models.

Authors:  Maria Irene Bellini; Janice Yiu; Mikhail Nozdrin; Vassilios Papalois
Journal:  J Clin Med       Date:  2019-09-09       Impact factor: 4.241

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.