Optimization of liver graft function using a poly-pharmacological drug cocktail CEPT in a simulated transplant model

Kharga, A.; Mojoudi, M.; Chen, H.; Taggart, M. S.; Dinicu, A. T.; Ozgur, O. S.; Uygun, B.; Toner, M.; Tessier, S.; Yeh, H.; Markmann, J. F.; Longchamp, A.; Uygun, K.

doi:10.1101/2024.02.02.578568

bioRxiv · 10.1101/2024.02.02.578568

Optimization of liver graft function using a poly-pharmacological drug cocktail CEPT in a simulated transplant model

Kharga, A.·Mojoudi, M.·Chen, H.·Taggart, M. S.·Dinicu, A. T.·Ozgur, O. S.·Uygun, B.·Toner, M.·Tessier, S.·Yeh, H.·Markmann, J. F.·Longchamp, A.·Uygun, K.

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Abstract

BackgroundThe number of patients in need of a liver transplant far exceeds the supply of available organs. This imbalance could be dramatically reduced should the donor organ pool be expanded by rendering marginal cases transplantable rather than discarded. The poly-pharmacological drug cocktail CEPT (Chroman-1, Emricasan, Polyamine, and Trans-ISRIB (integrated stress inhibitor)) has been found to improve the in-vitro viability of human pluripotent stem cells (hPSCs) following cryopreservation. It is worth exploring CEPTs ability to inhibit various apoptotic pathways and preserve cellular function for potentially mitigating warm ischemic stress of the anhepatic phase of graft implantation and promoting more rapid graft recovery following reperfusion with continuous treatment. MethodsRat livers without warm ischemia and CEPT supplementation are the healthy control: fresh (n=3) group. Room-temperature warm ischemia was used to replicate the anhepatic phase of graft implantation in the control (n=6) group and the experimental CEPT group (n=6) without and with CEPT supplementation, respectively. Transplantation was modeled by ex-vivo reperfusion at 37{degrees}C for six hours with Williams E-based hepatocyte culture media and with CEPT supplementation in the CEPT group. ResultsLivers treated with CEPT during warm ischemia and subsequent reperfusion have improved hepatocellular function as indicated by increased oxygen O2 utilization, stable pH, and improved cholangiocyte function indicated by the increased hourly rate of bile production. Furthermore, resistance, an endothelial injury marker, and caspase 3/7, an apoptotic marker, were lower. ConclusionTo improve the utilization of available donor livers, different stages of the organ transplantation process can be optimized. The anhepatic phase, which includes the period from the removal of the native liver from the recipient to the reperfusion of the donors graft liver through the portal vein during graft implantation, can be targeted using CEPT for mitigating warm ischemia-induced injury that occurs during vascular anastomosis. (S1 Fig: Graphical abstract)

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Kharga, A., Mojoudi, M., Chen, H., Taggart, M. S., Dinicu, A. T., Ozgur, O. S., Uygun, B., Toner, M., Tessier, S., Yeh, H., Markmann, J. F., Longchamp, A., Uygun, K.. 2024-02-07. Optimization of liver graft function using a poly-pharmacological drug cocktail CEPT in a simulated transplant model. https://doi.org/10.1101/2024.02.02.578568

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