Liver transplantation (LTx) is accepted therapy for various liver diseases. However, there are two problems: primary nonfunction (PNF) and shortage of livers. PNF, caused by preservation or reperfusion injury, necessitates a retransplant. This contributes to the shortage of livers. PNF contributes to the enormous cost of LTx and significant patient discomfort. Improving preservation of the liver would contribute significantly to improved results in LTx. Our goals in this project are to improve liver preservation to reduce PNF, decrease cost, decrease shortage of livers and deaths on the waiting list, provide a method to judge viability of the liver, and increase utilization of marginal livers (ischemic). We hypothesize that significant improvements in liver preservation will require continuous hypothermic machine perfusion (HMP). We shall demonstrate the feasibility of excellent quality, long-term liver preservation by HMP accomplishing these five specific aims: 1) optimize the method of liver perfusion, 2) optimize the perfusate specifically for the liver, 3) enhance preservation with cytoprotective agents previously shown to decrease liver injury, 4) develop a viability assay based on liver hypothermic metabolism, and 5) optimize HMP of the liver to salvage marginal (ischemically injured) livers. How these research strategies affect the quality and longevity of liver preservation will be judged by survival in the orthotopic rat liver transplant model (OLTx) and the degree of metabolic injury.using the isolated perfused liver (IPL). Integrity of the microvascular system and sinusoids will be assessed by electron microscopy. Strategies that show significant enhancement of rat liver preservation will be confirmed in the dog liver Tx model. The new information generated will lead to a more comprehensive understanding of liver preservation/reperfusion injury, develop a new state-of-the-art for liver preservation, provide measures of liver viability during HMP, and increase the donor pool by salvaging marginal livers. Successful HMP could have a dramatic effect on the outcome of clinical LTx and become the technique of choice in large transplant centers such as ours.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK035143-12
Application #
2838080
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Program Officer
Serrano, Jose
Project Start
1986-08-01
Project End
2000-11-30
Budget Start
1998-12-22
Budget End
1999-11-30
Support Year
12
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Surgery
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Mangino, Martin J; Tian, Tao; Ametani, Mary et al. (2008) Cytoskeletal involvement in hypothermic renal preservation injury. Transplantation 85:427-36
Knes, Jane M; Hansen, Thomas N; Gilligan, Barbara et al. (2005) Loss of endothelium-dependent relaxation in abdominal aorta preserved in a co-storage system. Transpl Int 17:699-706
Lindell, Susanne L; Compagnon, Philippe; Mangino, Martin J et al. (2005) UW solution for hypothermic machine perfusion of warm ischemic kidneys. Transplantation 79:1358-61
Mangino, Martin J; Ametani, Mary S; Gilligan, Barbara J et al. (2005) Role of peroxynitrite anion in renal hypothermic preservation injury. Transplantation 80:1455-60
Compagnon, Philippe; Lindell, Susanne; Ametani, Mary S et al. (2005) Ischemic preconditioning and liver tolerance to warm or cold ischemia: experimental studies in large animals. Transplantation 79:1393-400
Mangino, Martin J; Kosieradzki, Maciej; Gilligan, Barbara et al. (2003) The effects of donor brain death on renal function and arachidonic acid metabolism in a large animal model of hypothermic preservation injury. Transplantation 75:1640-7
Compagnon, Philippe; Wang, Hongbing; Lindell, Susanne L et al. (2002) Brain death does not affect hepatic allograft function and survival after orthotopic transplantation in a canine model. Transplantation 73:1218-27
Van der Hoeven, J A; Lindell, S; van Schilfgaarde, R et al. (2001) Donor brain death reduces survival after transplantation in rat livers preserved for 20 hr. Transplantation 72:1632-6
Kim, J S; Southard, J H (2000) Effect of phospholipase A2 inhibitors on the release of arachidonic acid and cell viability in cold-stored hepatocytes. Cryobiology 40:27-35
Southard, J H; Lindell, S; Ametani, M et al. (2000) Kupffer cell activation in liver preservation: cold storage vs machine perfusion. Transplant Proc 32:27-8

Showing the most recent 10 out of 48 publications