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Establishment of a reversible model of prehepatic portal hypertension in rats

The aim of the present study was to improve upon the traditional model of pre-hepatic portal hypertension in rats, and simulate the anhepatic phase of orthotopic liver transplantation without veno-venous bypass. A reversible model of portal hypertension was induced by portal vein ligation, with a la...

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Detalles Bibliográficos
Autores principales: Zhao, Xin, Dou, Jian, Gao, Qing-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950261/
https://www.ncbi.nlm.nih.gov/pubmed/27446299
http://dx.doi.org/10.3892/etm.2016.3405
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author Zhao, Xin
Dou, Jian
Gao, Qing-Jun
author_facet Zhao, Xin
Dou, Jian
Gao, Qing-Jun
author_sort Zhao, Xin
collection PubMed
description The aim of the present study was to improve upon the traditional model of pre-hepatic portal hypertension in rats, and simulate the anhepatic phase of orthotopic liver transplantation without veno-venous bypass. A reversible model of portal hypertension was induced by portal vein ligation, with a label ring ligated along the portal vein. A total of 135 male Wistar rats were divided into three groups: i) Normal control (NC) group; ii) portal hypertensive control (PHTC) group; and iii) reperfusion (R) group. In the R group, rats with portal hypertension underwent simultaneous clamping of the portal triad and retrohepatic vena cava for 1 h, followed by removal of the clamps to enable blood reperfusion. Portal venography and portal vein pressure were recorded during the surgery. Arterial oxygen pressure (PaO(2)), and alanine aminotransferase (ALT), aspartate aminotransferase (AST) and total bilirubin (TBil) levels were determined, and pathological changes of the liver were investigated by immunohistochemical staining. The results demonstrated that, 3 weeks after portal vein ligation, the vein area and the free portal pressures in the PHTC group were significantly increased compared with those in the NC group. The serum ALT and AST levels in the R group at different time points were significantly elevated compared with those in the PHTC group, and reached their maximal levels at 24 h after reperfusion. Furthermore, the PaO(2) at 24 h after reperfusion was significantly decreased. In conclusion, the reversible model of pre-hepatic portal hypertension in rats was successfully established using the introduction of a label ring. This model may be useful for basic research focusing on the anhepatic phase of orthotopic liver transplantation without veno-venous bypass.
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spelling pubmed-49502612016-07-21 Establishment of a reversible model of prehepatic portal hypertension in rats Zhao, Xin Dou, Jian Gao, Qing-Jun Exp Ther Med Articles The aim of the present study was to improve upon the traditional model of pre-hepatic portal hypertension in rats, and simulate the anhepatic phase of orthotopic liver transplantation without veno-venous bypass. A reversible model of portal hypertension was induced by portal vein ligation, with a label ring ligated along the portal vein. A total of 135 male Wistar rats were divided into three groups: i) Normal control (NC) group; ii) portal hypertensive control (PHTC) group; and iii) reperfusion (R) group. In the R group, rats with portal hypertension underwent simultaneous clamping of the portal triad and retrohepatic vena cava for 1 h, followed by removal of the clamps to enable blood reperfusion. Portal venography and portal vein pressure were recorded during the surgery. Arterial oxygen pressure (PaO(2)), and alanine aminotransferase (ALT), aspartate aminotransferase (AST) and total bilirubin (TBil) levels were determined, and pathological changes of the liver were investigated by immunohistochemical staining. The results demonstrated that, 3 weeks after portal vein ligation, the vein area and the free portal pressures in the PHTC group were significantly increased compared with those in the NC group. The serum ALT and AST levels in the R group at different time points were significantly elevated compared with those in the PHTC group, and reached their maximal levels at 24 h after reperfusion. Furthermore, the PaO(2) at 24 h after reperfusion was significantly decreased. In conclusion, the reversible model of pre-hepatic portal hypertension in rats was successfully established using the introduction of a label ring. This model may be useful for basic research focusing on the anhepatic phase of orthotopic liver transplantation without veno-venous bypass. D.A. Spandidos 2016-08 2016-05-30 /pmc/articles/PMC4950261/ /pubmed/27446299 http://dx.doi.org/10.3892/etm.2016.3405 Text en Copyright: © Zhao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhao, Xin
Dou, Jian
Gao, Qing-Jun
Establishment of a reversible model of prehepatic portal hypertension in rats
title Establishment of a reversible model of prehepatic portal hypertension in rats
title_full Establishment of a reversible model of prehepatic portal hypertension in rats
title_fullStr Establishment of a reversible model of prehepatic portal hypertension in rats
title_full_unstemmed Establishment of a reversible model of prehepatic portal hypertension in rats
title_short Establishment of a reversible model of prehepatic portal hypertension in rats
title_sort establishment of a reversible model of prehepatic portal hypertension in rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950261/
https://www.ncbi.nlm.nih.gov/pubmed/27446299
http://dx.doi.org/10.3892/etm.2016.3405
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