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Cardiac and renal effects of liver cirrhosis in a growing animal model
PURPOSE: To assess the biochemical, histological, histomorphometric and molecular effects of biliary duct ligation (BDL) induced liver cirrhosis in the heart and kidneys. METHODS: Thirty-two weaning rats (21 days old, 50-70 g) underwent BDL and were divided in four groups (euthanasia after two, four...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516424/ https://www.ncbi.nlm.nih.gov/pubmed/34644774 http://dx.doi.org/10.1590/ACB360806 |
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author | Tannuri, Ana Cristina Aoun Chavez, Leiliane Somoggi Guimarães, Juliana Xavier Gonçalves, Josiane de Oliveira Serafini, Suellen de Souza, Gabriela Carvalho Malheiros, Denise Maria Avancini Costa Paes, Vitor Ribeiro Tannuri, Uenis |
author_facet | Tannuri, Ana Cristina Aoun Chavez, Leiliane Somoggi Guimarães, Juliana Xavier Gonçalves, Josiane de Oliveira Serafini, Suellen de Souza, Gabriela Carvalho Malheiros, Denise Maria Avancini Costa Paes, Vitor Ribeiro Tannuri, Uenis |
author_sort | Tannuri, Ana Cristina Aoun |
collection | PubMed |
description | PURPOSE: To assess the biochemical, histological, histomorphometric and molecular effects of biliary duct ligation (BDL) induced liver cirrhosis in the heart and kidneys. METHODS: Thirty-two weaning rats (21 days old, 50-70 g) underwent BDL and were divided in four groups (euthanasia after two, four, six, and eight weeks, respectively) and compared to control groups. RESULTS: The animals’ hearts of group 3 were bigger than those of the control group (p=0.042), including thinner right ventricle wall, decreased internal diameter of ventricles, and increased perivascular collagen deposition in left ventricle, as well as increased interstitial collagen in right ventricle after six weeks. In the kidneys of groups 3 and 4, bilirubin impregnation in the tubules, hydropic degeneration, loss of nuclei and lack of plasmatic membrane limits were noted. Nitric oxide synthase (NOS) gene expressions were higher in group 1 (p=0.008), and endothelial nitric oxide synthase (eNOS) gene expressions were elevated in all experimental groups (p=0.008, p=0.001, p=0.022, and p=0.013, respectively). In the heart, a decreased expression of eNOS in group 1 (p=0.04) was observed. CONCLUSIONS: Liver cirrhosis leads to histological and histomorphometric alterations in the heart and kidneys, with changes in the NOS and eNOS gene expressions, that may suggest a role in the associated myocardial and renal manifestations. |
format | Online Article Text |
id | pubmed-8516424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia |
record_format | MEDLINE/PubMed |
spelling | pubmed-85164242021-10-26 Cardiac and renal effects of liver cirrhosis in a growing animal model Tannuri, Ana Cristina Aoun Chavez, Leiliane Somoggi Guimarães, Juliana Xavier Gonçalves, Josiane de Oliveira Serafini, Suellen de Souza, Gabriela Carvalho Malheiros, Denise Maria Avancini Costa Paes, Vitor Ribeiro Tannuri, Uenis Acta Cir Bras Original Article PURPOSE: To assess the biochemical, histological, histomorphometric and molecular effects of biliary duct ligation (BDL) induced liver cirrhosis in the heart and kidneys. METHODS: Thirty-two weaning rats (21 days old, 50-70 g) underwent BDL and were divided in four groups (euthanasia after two, four, six, and eight weeks, respectively) and compared to control groups. RESULTS: The animals’ hearts of group 3 were bigger than those of the control group (p=0.042), including thinner right ventricle wall, decreased internal diameter of ventricles, and increased perivascular collagen deposition in left ventricle, as well as increased interstitial collagen in right ventricle after six weeks. In the kidneys of groups 3 and 4, bilirubin impregnation in the tubules, hydropic degeneration, loss of nuclei and lack of plasmatic membrane limits were noted. Nitric oxide synthase (NOS) gene expressions were higher in group 1 (p=0.008), and endothelial nitric oxide synthase (eNOS) gene expressions were elevated in all experimental groups (p=0.008, p=0.001, p=0.022, and p=0.013, respectively). In the heart, a decreased expression of eNOS in group 1 (p=0.04) was observed. CONCLUSIONS: Liver cirrhosis leads to histological and histomorphometric alterations in the heart and kidneys, with changes in the NOS and eNOS gene expressions, that may suggest a role in the associated myocardial and renal manifestations. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2021-10-08 /pmc/articles/PMC8516424/ /pubmed/34644774 http://dx.doi.org/10.1590/ACB360806 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Tannuri, Ana Cristina Aoun Chavez, Leiliane Somoggi Guimarães, Juliana Xavier Gonçalves, Josiane de Oliveira Serafini, Suellen de Souza, Gabriela Carvalho Malheiros, Denise Maria Avancini Costa Paes, Vitor Ribeiro Tannuri, Uenis Cardiac and renal effects of liver cirrhosis in a growing animal model |
title | Cardiac and renal effects of liver cirrhosis in a growing animal
model |
title_full | Cardiac and renal effects of liver cirrhosis in a growing animal
model |
title_fullStr | Cardiac and renal effects of liver cirrhosis in a growing animal
model |
title_full_unstemmed | Cardiac and renal effects of liver cirrhosis in a growing animal
model |
title_short | Cardiac and renal effects of liver cirrhosis in a growing animal
model |
title_sort | cardiac and renal effects of liver cirrhosis in a growing animal
model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516424/ https://www.ncbi.nlm.nih.gov/pubmed/34644774 http://dx.doi.org/10.1590/ACB360806 |
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