Title :
Reconditioning of fatty livers for transplantation increased survival of recipients in a rat model
Author :
Mokuno, Y. ; Berthiaume, F. ; Yarmush, Martin L.
Author_Institution :
Center for Eng. in Medicine, Massachusetts Gen. Hosp., Boston, MA, USA
Abstract :
Fatty livers are very sensitive to ischemia-reperfusion and cold preservation-related injuries, which makes them unacceptable for liver transplantation. We hypothesized that removal of the excess fat storage from fatty livers can restore their ability to undergo liver transplantation. We obtained fatty livers from rats fed a choline and methionine-deficient diet (CMDD) for 6 wk, stored them in cold hetastarch-free University of Wisconsin solution for 6 h, and transplanted them into normal recipient rats. While recipient rats had a 90% rate of survival after transplantation of control normal "lean" livers, they all died when receiving CMDD rat livers. If CMDD rats were returned to a normal diet for 3 or 7 days prior to donating livers, effectively reducing the fat content of the livers by 33% and 85%, respectively, the recipients survived at rates similar to the controls. Furthermore, we found that it is possible to eliminate excess fat storage from fatty livers by short-term perfusion of fatty livers ex vivo. These results support the notion that liver perfusion could be used to recondition fatty livers and make them suitable for transplantation.
Keywords :
biochemistry; biorheology; cellular biophysics; liver; organic compounds; patient treatment; proteins; 6 h; 6 wk; CMDD rat livers; apolipoproteins; catabolic hormones; cholesterol; choline-deficient diet; cold hetastarch-free solution; cold preservation-related injuries; control normal lean livers; excess fat storage removal; fat content; fatty acids; fatty liver reconditioning; glucagon; hydrocortisone; ischemia-reperfusion injuries; lipoproteins; liver perfusion; liver transplantation; methionine-deficient diet; normal diet; normal recipient rats; rat model; recipient survival; short-term perfusion; Amino acids; Biomedical engineering; Ducts; Hospitals; Lipidomics; Liver; Polyethylene; Portals; Rats; Veins;
Conference_Titel :
Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint
Print_ISBN :
0-7803-7612-9
DOI :
10.1109/IEMBS.2002.1137076