» Articles » PMID: 12201359

Optimisation of Bile Production During Normothermic Preservation of Porcine Livers

Overview
Journal Am J Transplant
Publisher Elsevier
Specialty General Surgery
Date 2002 Aug 31
PMID 12201359
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Machine perfusion of livers may provide a mechanism for extended preservation of marginal donor organs before transplantation, as well as a method for viability assessment. It has proved possible in a series of experimental porcine liver perfusions to maintain liver viability for up to 72 h. However, a reduction in bile production with associated histological evidence of cholestasis was seen after 10 h of perfusion, damaging the biliary canaliculi during the preservation period and leaving these organs in an unacceptable condition for transplantation. It was proposed that reduction in bile production was the result of a relentless depletion of available bile salts, gut recirculation not being possible and de-novo synthesis being unable to keep up with loss. This was proved by measuring porcine native bile acids within serial perfusate and bile samples using gas chromatography mass spectrophotometry. It was shown that all three native pig bile acids were decreased to 30% of their original value by 20 h of unsupplemented perfusion. An infusion of taurocholate managed to maintain bile production at physiological levels throughout the 20-h period (8 mL/h +/- 0.75). It was successfully incorporated by the porcine livers into bile. We propose to use this circuit as a novel means of preserving donor livers for transplantation in which the organ is maintained at normal body temperature and perfused with blood. This will reduce ischaemia reperfusion injury and may enable prolonged preservation. The modification described ensures optimal bile production over the entire perfusion period, preventing inspissation and subsequent damage to the canaliculus.

Citing Articles

Optimization of an in situ liver perfusion method to evaluate hepatic function of juvenile American alligators (Alligator mississippiensis).

Umeki Y, Hala D, Petersen L Biol Open. 2024; 13(8).

PMID: 39189399 PMC: 11381930. DOI: 10.1242/bio.060532.


Current Techniques and Indications for Machine Perfusion and Regional Perfusion in Deceased Donor Liver Transplantation.

Watson C, Gaurav R, Butler A J Clin Exp Hepatol. 2024; 14(2):101309.

PMID: 38274508 PMC: 10806097. DOI: 10.1016/j.jceh.2023.101309.


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

Kruger M, Ruppelt A, Kappler B, Van Soest E, Samsom R, Grinwis G Bioengineering (Basel). 2022; 9(9).

PMID: 36135018 PMC: 9495507. DOI: 10.3390/bioengineering9090471.


The ultrastructural characteristics of bile canaliculus in porcine liver donated after cardiac death and machine perfusion preservation.

Ishihara Y, Bochimoto H, Kondoh D, Obara H, Matsuno N PLoS One. 2020; 15(5):e0233917.

PMID: 32470051 PMC: 7259665. DOI: 10.1371/journal.pone.0233917.


Ischemia-Reperfusion Injury in Marginal Liver Grafts and the Role of Hypothermic Machine Perfusion: Molecular Mechanisms and Clinical Implications.

Czigany Z, Lurje I, Schmelzle M, Schoning W, Ollinger R, Raschzok N J Clin Med. 2020; 9(3).

PMID: 32244972 PMC: 7141496. DOI: 10.3390/jcm9030846.