» Articles » PMID: 25992583

Technique of Porcine Liver Procurement and Orthotopic Transplantation Using an Active Porto-caval Shunt

Overview
Journal J Vis Exp
Date 2015 May 21
PMID 25992583
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The success of liver transplantation has resulted in a dramatic organ shortage. Each year, a considerable number of patients on the liver transplantation waiting list die without receiving an organ transplant or are delisted due to disease progression. Even after a successful transplantation, rejection and side effects of immunosuppression remain major concerns for graft survival and patient morbidity. Experimental animal research has been essential to the success of liver transplantation and still plays a pivotal role in the development of clinical transplantation practice. In particular, the porcine orthotopic liver transplantation model (OLTx) is optimal for clinically oriented research for its close resemblance to human size, anatomy, and physiology. Decompression of intestinal congestion during the anhepatic phase of porcine OLTx is important to guarantee reliable animal survival. The use of an active porto-caval-jugular shunt achieves excellent intestinal decompression. The system can be used for short-term as well as long-term survival experiments. The following protocol contains all technical information for a stable and reproducible liver transplantation model in pigs including post-operative animal care.

Citing Articles

Biliary Metabolome Profiling for Evaluation of Liver Metabolism and Biliary Tract Function Related to Organ Preservation Method and Degree of Ischemia in a Porcine Model.

Luczykowski K, Warmuzinska N, Kollmann D, Selzner M, Bojko B Int J Mol Sci. 2023; 24(3).

PMID: 36768452 PMC: 9916698. DOI: 10.3390/ijms24032127.


Normothermic ex situ pancreas perfusion for the preservation of porcine pancreas grafts.

Mazilescu L, Parmentier C, Kalimuthu S, Ganesh S, Kawamura M, Goto T Am J Transplant. 2022; 22(5):1339-1349.

PMID: 35258859 PMC: 9314088. DOI: 10.1111/ajt.17019.


Infection Inhibits Histone Crotonylation to Regulate Immune Response of Porcine Alveolar Macrophages.

Yang J, He Z, Chen C, Li S, Qian J, Zhao J Front Immunol. 2021; 12:696061.

PMID: 34322124 PMC: 8312545. DOI: 10.3389/fimmu.2021.696061.


Adenosine A2a Receptor Stimulation Attenuates Ischemia-Reperfusion Injury and Improves Survival in A Porcine Model of DCD Liver Transplantation.

Czigany Z, Craigie E, Lurje G, Song S, Yonezawa K, Yamamoto Y Int J Mol Sci. 2020; 21(18).

PMID: 32938013 PMC: 7555737. DOI: 10.3390/ijms21186747.


Large Animal Models in Regenerative Medicine and Tissue Engineering: To Do or Not to Do.

Ribitsch I, Baptista P, Lange-Consiglio A, Melotti L, Patruno M, Jenner F Front Bioeng Biotechnol. 2020; 8:972.

PMID: 32903631 PMC: 7438731. DOI: 10.3389/fbioe.2020.00972.


References
1.
Gruttadauria S, Marino G, Catalano F, Sgroi A, Di Mauro G, Basile F . Porcine orthotopic liver autotransplantation: facilitated technique. J Invest Surg. 2001; 14(2):79-82. DOI: 10.1080/08941930152024192. View

2.
Net M, Valero R, Almenara R, Barros P, Capdevila L, Lopez-Boado M . The effect of normothermic recirculation is mediated by ischemic preconditioning in NHBD liver transplantation. Am J Transplant. 2005; 5(10):2385-92. DOI: 10.1111/j.1600-6143.2005.01052.x. View

3.
Kelly D, Demetris A, Fung J, Marcos A, Zhu Y, Subbotin V . Porcine partial liver transplantation: a novel model of the "small-for-size" liver graft. Liver Transpl. 2004; 10(2):253-63. DOI: 10.1002/lt.20073. View

4.
Moench C, Moench K, Lohse A, Thies J, Otto G . Prevention of ischemic-type biliary lesions by arterial back-table pressure perfusion. Liver Transpl. 2003; 9(3):285-9. DOI: 10.1053/jlts.2003.50015. View

5.
Memsic L, Quinones-Baldrich W, Kaufman R, Rasool I, Busuttil R . A comparison of porcine orthotopic liver transplantation using a venous-venous bypass with and without a nonpulsatile perfusion pump. J Surg Res. 1986; 41(1):33-40. DOI: 10.1016/0022-4804(86)90005-3. View