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A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis
Associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) in a rat model of liver cirrhosis has not, to the best of our knowledge, been previously investigated. The present study therefore aimed to establish a model of ALPPS in cirrhotic rats and to assess liver regeneratio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601136/ https://www.ncbi.nlm.nih.gov/pubmed/31316615 http://dx.doi.org/10.3892/etm.2019.7688 |
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author | Yang, Xianwei Yang, Chuang Qiu, Yiwen Shen, Shu Kong, Junjie Wang, Wentao |
author_facet | Yang, Xianwei Yang, Chuang Qiu, Yiwen Shen, Shu Kong, Junjie Wang, Wentao |
author_sort | Yang, Xianwei |
collection | PubMed |
description | Associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) in a rat model of liver cirrhosis has not, to the best of our knowledge, been previously investigated. The present study therefore aimed to establish a model of ALPPS in cirrhotic rats and to assess liver regeneration. Rats were randomly divided into an ALPPS group with carbon tetrachloride-induced cirrhosis (group A) and a normal liver (group B). Rat weight, cytokine levels, biochemical parameters and histopathology were assessed 1, 2, 3, 7 and 14 days after ALPPS. Higher aspartate aminotransferase and alanine aminotransferase levels were detected in group A on the first postoperative day. On the first, second and third days, hepatocyte proliferation rate was higher in group B than in group A. After 3 days, hepatocyte proliferation rate in group B began to decrease, but the rate in group A continued to increase until the 14th day. Higher levels of hepatocyte growth factor, interleukin-6 and tumor necrosis factor-α were detected in group A compared with group B, but the differences were not significant. The present study demonstrated that ALPPS promoted liver regeneration in a rat model of cirrhosis, but significantly impaired liver function. Compared with the ALPPS model, group B exhibited a delayed peak of proliferation. The mechanism of liver regeneration induced by ALPPS in cirrhotic rats may be associated with increased cytokine levels. |
format | Online Article Text |
id | pubmed-6601136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-66011362019-07-17 A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis Yang, Xianwei Yang, Chuang Qiu, Yiwen Shen, Shu Kong, Junjie Wang, Wentao Exp Ther Med Articles Associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) in a rat model of liver cirrhosis has not, to the best of our knowledge, been previously investigated. The present study therefore aimed to establish a model of ALPPS in cirrhotic rats and to assess liver regeneration. Rats were randomly divided into an ALPPS group with carbon tetrachloride-induced cirrhosis (group A) and a normal liver (group B). Rat weight, cytokine levels, biochemical parameters and histopathology were assessed 1, 2, 3, 7 and 14 days after ALPPS. Higher aspartate aminotransferase and alanine aminotransferase levels were detected in group A on the first postoperative day. On the first, second and third days, hepatocyte proliferation rate was higher in group B than in group A. After 3 days, hepatocyte proliferation rate in group B began to decrease, but the rate in group A continued to increase until the 14th day. Higher levels of hepatocyte growth factor, interleukin-6 and tumor necrosis factor-α were detected in group A compared with group B, but the differences were not significant. The present study demonstrated that ALPPS promoted liver regeneration in a rat model of cirrhosis, but significantly impaired liver function. Compared with the ALPPS model, group B exhibited a delayed peak of proliferation. The mechanism of liver regeneration induced by ALPPS in cirrhotic rats may be associated with increased cytokine levels. D.A. Spandidos 2019-08 2019-06-18 /pmc/articles/PMC6601136/ /pubmed/31316615 http://dx.doi.org/10.3892/etm.2019.7688 Text en Copyright: © Yang 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 Yang, Xianwei Yang, Chuang Qiu, Yiwen Shen, Shu Kong, Junjie Wang, Wentao A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
title | A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
title_full | A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
title_fullStr | A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
title_full_unstemmed | A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
title_short | A preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
title_sort | preliminary study of associating liver partition and portal vein ligation for staged hepatectomy in a rat model of liver cirrhosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601136/ https://www.ncbi.nlm.nih.gov/pubmed/31316615 http://dx.doi.org/10.3892/etm.2019.7688 |
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