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The liver injury following ischemia and reperfusion is worse in experimental knockout heterozygote mouse model for expression of connexin 43()
PURPOSE: To evaluate that Connexin (Cx43) plays a role in lesions after hepatic ischemia/reperfusion (IR) injury. METHODS: We use Cx43 deficient model (heterozygotes mice) and compared to a wild group. The groups underwent 1 hour ischemia and 24 hours reperfusion. The heterozygote genotype was confi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912844/ https://www.ncbi.nlm.nih.gov/pubmed/31851211 http://dx.doi.org/10.1590/s0102-865020190100000003 |
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author | Trevisan, Alexandre Maximiliano Cogliati, Bruno Homem, Adriana Ribeiro Aloiav, Thiago Pinheiro Arrais de Aquino, Nelson Moreira, Jairo Marques Reno, Leonardo da Cruz Naumann, Alexandre Moulin Galvão, Flavio Henrique Ferreira Andraus, Wellington D'Albuquerque, Luiz Augusto Carneiro |
author_facet | Trevisan, Alexandre Maximiliano Cogliati, Bruno Homem, Adriana Ribeiro Aloiav, Thiago Pinheiro Arrais de Aquino, Nelson Moreira, Jairo Marques Reno, Leonardo da Cruz Naumann, Alexandre Moulin Galvão, Flavio Henrique Ferreira Andraus, Wellington D'Albuquerque, Luiz Augusto Carneiro |
author_sort | Trevisan, Alexandre Maximiliano |
collection | PubMed |
description | PURPOSE: To evaluate that Connexin (Cx43) plays a role in lesions after hepatic ischemia/reperfusion (IR) injury. METHODS: We use Cx43 deficient model (heterozygotes mice) and compared to a wild group. The groups underwent 1 hour ischemia and 24 hours reperfusion. The heterozygote genotype was confirmed by PCR. We analyzed the hepatic enzymes (AST, ALT, GGT) and histology. RESULTS: The mice with Cx43 deficiency showed an ALT mean value of 4166 vs. 307 in the control group (p<0.001); AST mean value of 7231 vs. 471 in the control group (p<0.001); GGT mean value of 9.4 vs. 1.7 in the control group (p=0.001); histology showed necrosis and inflammation in the knockout group. CONCLUSIONS: This research demonstrated that the deficiency of Cx43 worses the prognosis for liver injury. The topic is a promising target for therapeutics advancements in liver diseases and procedures. |
format | Online Article Text |
id | pubmed-6912844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia |
record_format | MEDLINE/PubMed |
spelling | pubmed-69128442019-12-18 The liver injury following ischemia and reperfusion is worse in experimental knockout heterozygote mouse model for expression of connexin 43() Trevisan, Alexandre Maximiliano Cogliati, Bruno Homem, Adriana Ribeiro Aloiav, Thiago Pinheiro Arrais de Aquino, Nelson Moreira, Jairo Marques Reno, Leonardo da Cruz Naumann, Alexandre Moulin Galvão, Flavio Henrique Ferreira Andraus, Wellington D'Albuquerque, Luiz Augusto Carneiro Acta Cir Bras Original Article PURPOSE: To evaluate that Connexin (Cx43) plays a role in lesions after hepatic ischemia/reperfusion (IR) injury. METHODS: We use Cx43 deficient model (heterozygotes mice) and compared to a wild group. The groups underwent 1 hour ischemia and 24 hours reperfusion. The heterozygote genotype was confirmed by PCR. We analyzed the hepatic enzymes (AST, ALT, GGT) and histology. RESULTS: The mice with Cx43 deficiency showed an ALT mean value of 4166 vs. 307 in the control group (p<0.001); AST mean value of 7231 vs. 471 in the control group (p<0.001); GGT mean value of 9.4 vs. 1.7 in the control group (p=0.001); histology showed necrosis and inflammation in the knockout group. CONCLUSIONS: This research demonstrated that the deficiency of Cx43 worses the prognosis for liver injury. The topic is a promising target for therapeutics advancements in liver diseases and procedures. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2019-12-13 /pmc/articles/PMC6912844/ /pubmed/31851211 http://dx.doi.org/10.1590/s0102-865020190100000003 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 Trevisan, Alexandre Maximiliano Cogliati, Bruno Homem, Adriana Ribeiro Aloiav, Thiago Pinheiro Arrais de Aquino, Nelson Moreira, Jairo Marques Reno, Leonardo da Cruz Naumann, Alexandre Moulin Galvão, Flavio Henrique Ferreira Andraus, Wellington D'Albuquerque, Luiz Augusto Carneiro The liver injury following ischemia and reperfusion is worse in experimental knockout heterozygote mouse model for expression of connexin 43() |
title | The liver injury following ischemia and reperfusion is worse in
experimental knockout heterozygote mouse model for expression of connexin 43()
|
title_full | The liver injury following ischemia and reperfusion is worse in
experimental knockout heterozygote mouse model for expression of connexin 43()
|
title_fullStr | The liver injury following ischemia and reperfusion is worse in
experimental knockout heterozygote mouse model for expression of connexin 43()
|
title_full_unstemmed | The liver injury following ischemia and reperfusion is worse in
experimental knockout heterozygote mouse model for expression of connexin 43()
|
title_short | The liver injury following ischemia and reperfusion is worse in
experimental knockout heterozygote mouse model for expression of connexin 43()
|
title_sort | liver injury following ischemia and reperfusion is worse in
experimental knockout heterozygote mouse model for expression of connexin 43() |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912844/ https://www.ncbi.nlm.nih.gov/pubmed/31851211 http://dx.doi.org/10.1590/s0102-865020190100000003 |
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