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Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4)
The purpose of this study was to investigate the components of renin–angiotensin system (RAS), liver function and histology in liver fibrogenesis in the rats induced by low-dose chronic carbon tetrachloride (CCL(4)) administration and evaluate the relationship between biochemical variables and compo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111816/ https://www.ncbi.nlm.nih.gov/pubmed/23433841 http://dx.doi.org/10.1016/j.rvsc.2013.01.028 |
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author | Zhang, Wei Miao, JinFeng Li, PengFei Wang, YanXia Zhang, YuanShu |
author_facet | Zhang, Wei Miao, JinFeng Li, PengFei Wang, YanXia Zhang, YuanShu |
author_sort | Zhang, Wei |
collection | PubMed |
description | The purpose of this study was to investigate the components of renin–angiotensin system (RAS), liver function and histology in liver fibrogenesis in the rats induced by low-dose chronic carbon tetrachloride (CCL(4)) administration and evaluate the relationship between biochemical variables and components of RAS. Male Sprague–Dawley (SD) rats were randomly divided into the CCL(4) group which received intraperitoneal injection of 40% CCL(4) dissolved in olive oil every three days for four consecutive weeks (Initial dose was 5 mL/kg, other dose: 3 mL/kg) and the control group which received the same dose of olive oil. The micro-structure of the liver was examined by H&E. Hepatic Ang II and Ang(1–7) was detected. Real-time PCR and Western-blot were performed to determine the gene and protein expression of the RAS. The components of RAS were all up-regulated in CCL(4) group, and the increased extent of ACE-Ang II-AT1 axis was higher than the ACE2-Ang(1–7)-Mas axis. There was a significant correlation between ACE and ACE2 gene expression, AT1 and MAS gene expression, Ang II and Ang(1–7) in the liver of rats. ACE (or ACE2) gene expression strongly correlated with the index of liver injury significantly. These results suggest hepatic fibrogenesis induced by chronic CCL(4) administration may be associated with the relationship of ACE-Ang II-AT1 axis and ACE2-Ang(1–7)-MAS axis. |
format | Online Article Text |
id | pubmed-7111816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71118162020-04-02 Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) Zhang, Wei Miao, JinFeng Li, PengFei Wang, YanXia Zhang, YuanShu Res Vet Sci Article The purpose of this study was to investigate the components of renin–angiotensin system (RAS), liver function and histology in liver fibrogenesis in the rats induced by low-dose chronic carbon tetrachloride (CCL(4)) administration and evaluate the relationship between biochemical variables and components of RAS. Male Sprague–Dawley (SD) rats were randomly divided into the CCL(4) group which received intraperitoneal injection of 40% CCL(4) dissolved in olive oil every three days for four consecutive weeks (Initial dose was 5 mL/kg, other dose: 3 mL/kg) and the control group which received the same dose of olive oil. The micro-structure of the liver was examined by H&E. Hepatic Ang II and Ang(1–7) was detected. Real-time PCR and Western-blot were performed to determine the gene and protein expression of the RAS. The components of RAS were all up-regulated in CCL(4) group, and the increased extent of ACE-Ang II-AT1 axis was higher than the ACE2-Ang(1–7)-Mas axis. There was a significant correlation between ACE and ACE2 gene expression, AT1 and MAS gene expression, Ang II and Ang(1–7) in the liver of rats. ACE (or ACE2) gene expression strongly correlated with the index of liver injury significantly. These results suggest hepatic fibrogenesis induced by chronic CCL(4) administration may be associated with the relationship of ACE-Ang II-AT1 axis and ACE2-Ang(1–7)-MAS axis. Elsevier Ltd. 2013-08 2013-02-21 /pmc/articles/PMC7111816/ /pubmed/23433841 http://dx.doi.org/10.1016/j.rvsc.2013.01.028 Text en Copyright © 2013 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zhang, Wei Miao, JinFeng Li, PengFei Wang, YanXia Zhang, YuanShu Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) |
title | Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) |
title_full | Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) |
title_fullStr | Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) |
title_full_unstemmed | Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) |
title_short | Up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by CCL(4) |
title_sort | up-regulation of components of the renin–angiotensin system in liver fibrosis in the rat induced by ccl(4) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111816/ https://www.ncbi.nlm.nih.gov/pubmed/23433841 http://dx.doi.org/10.1016/j.rvsc.2013.01.028 |
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