Cargando…
Changes of renal histopathology and the role of Nrf2/HO-1 in asphyxial cardiac arrest model in rats
PURPOSE: To investigate the role of Nrf2/HO-1 in renal histopathological ailments time-dependently in asphyxial cardiac arrest (CA) rat model. METHODS: Eighty-eight Sprague Dawley male rats were divided into five groups of eight rats each. Asphyxial CA was induced in all the experimental rats except...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291904/ https://www.ncbi.nlm.nih.gov/pubmed/34287609 http://dx.doi.org/10.1590/ACB360607 |
_version_ | 1783724737274314752 |
---|---|
author | Jawad, Ali Yoo, Yeo-Jin Yoon, Jae Chol Tian, Weishun Islam, Md Sadikul Lee, Eui-Yong Shin, Ha-Young Kim, So Eun Ahn, Dongchoon Park, Byung-Yong Tae, Hyun-Jin Kim, In-Shik |
author_facet | Jawad, Ali Yoo, Yeo-Jin Yoon, Jae Chol Tian, Weishun Islam, Md Sadikul Lee, Eui-Yong Shin, Ha-Young Kim, So Eun Ahn, Dongchoon Park, Byung-Yong Tae, Hyun-Jin Kim, In-Shik |
author_sort | Jawad, Ali |
collection | PubMed |
description | PURPOSE: To investigate the role of Nrf2/HO-1 in renal histopathological ailments time-dependently in asphyxial cardiac arrest (CA) rat model. METHODS: Eighty-eight Sprague Dawley male rats were divided into five groups of eight rats each. Asphyxial CA was induced in all the experimental rats except for the sham group. The rats were sacrificed at 6 hours, 12 hours, one day and two days post-CA. Serum blood urea nitrogen (BUN), creatinine (Crtn) and malondialdehyde from the renal tissues were evaluated. Hematoxylin and eosin and periodic acid-Schiff staining were done to evaluate the renal histopathological changes in the renal cortex. Furthermore, Nrf2/HO-1 immunohistochemistry (ihc) and western blot analysis were performed after CA. RESULTS: The survival rate of rats decreased in a time-dependent manner: 66.6% at 6 hours, 50% at 12 hours, 38.1% in one day, and 25.8% in two days. BUN and serum Crtn markedly increased in CA-operated groups. Histopathological ailments of the renal cortical tissues increased significantly from 6 hours until two days post-CA. Furthermore, Nrf2/HO-1 expression level significantly increased at 6 hours, 12 hours, and one day. CONCLUSIONS: The survival rate decreased time-dependently, and Nrf/HO-1 expression increased from 6 hours with the peak times at 12 hours, and one day post-CA. |
format | Online Article Text |
id | pubmed-8291904 |
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-82919042021-08-03 Changes of renal histopathology and the role of Nrf2/HO-1 in asphyxial cardiac arrest model in rats Jawad, Ali Yoo, Yeo-Jin Yoon, Jae Chol Tian, Weishun Islam, Md Sadikul Lee, Eui-Yong Shin, Ha-Young Kim, So Eun Ahn, Dongchoon Park, Byung-Yong Tae, Hyun-Jin Kim, In-Shik Acta Cir Bras Original Article PURPOSE: To investigate the role of Nrf2/HO-1 in renal histopathological ailments time-dependently in asphyxial cardiac arrest (CA) rat model. METHODS: Eighty-eight Sprague Dawley male rats were divided into five groups of eight rats each. Asphyxial CA was induced in all the experimental rats except for the sham group. The rats were sacrificed at 6 hours, 12 hours, one day and two days post-CA. Serum blood urea nitrogen (BUN), creatinine (Crtn) and malondialdehyde from the renal tissues were evaluated. Hematoxylin and eosin and periodic acid-Schiff staining were done to evaluate the renal histopathological changes in the renal cortex. Furthermore, Nrf2/HO-1 immunohistochemistry (ihc) and western blot analysis were performed after CA. RESULTS: The survival rate of rats decreased in a time-dependent manner: 66.6% at 6 hours, 50% at 12 hours, 38.1% in one day, and 25.8% in two days. BUN and serum Crtn markedly increased in CA-operated groups. Histopathological ailments of the renal cortical tissues increased significantly from 6 hours until two days post-CA. Furthermore, Nrf2/HO-1 expression level significantly increased at 6 hours, 12 hours, and one day. CONCLUSIONS: The survival rate decreased time-dependently, and Nrf/HO-1 expression increased from 6 hours with the peak times at 12 hours, and one day post-CA. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2021-07-19 /pmc/articles/PMC8291904/ /pubmed/34287609 http://dx.doi.org/10.1590/ACB360607 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 Jawad, Ali Yoo, Yeo-Jin Yoon, Jae Chol Tian, Weishun Islam, Md Sadikul Lee, Eui-Yong Shin, Ha-Young Kim, So Eun Ahn, Dongchoon Park, Byung-Yong Tae, Hyun-Jin Kim, In-Shik Changes of renal histopathology and the role of Nrf2/HO-1 in asphyxial cardiac arrest model in rats |
title | Changes of renal histopathology and the role of Nrf2/HO-1 in
asphyxial cardiac arrest model in rats |
title_full | Changes of renal histopathology and the role of Nrf2/HO-1 in
asphyxial cardiac arrest model in rats |
title_fullStr | Changes of renal histopathology and the role of Nrf2/HO-1 in
asphyxial cardiac arrest model in rats |
title_full_unstemmed | Changes of renal histopathology and the role of Nrf2/HO-1 in
asphyxial cardiac arrest model in rats |
title_short | Changes of renal histopathology and the role of Nrf2/HO-1 in
asphyxial cardiac arrest model in rats |
title_sort | changes of renal histopathology and the role of nrf2/ho-1 in
asphyxial cardiac arrest model in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291904/ https://www.ncbi.nlm.nih.gov/pubmed/34287609 http://dx.doi.org/10.1590/ACB360607 |
work_keys_str_mv | AT jawadali changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT yooyeojin changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT yoonjaechol changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT tianweishun changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT islammdsadikul changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT leeeuiyong changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT shinhayoung changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT kimsoeun changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT ahndongchoon changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT parkbyungyong changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT taehyunjin changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats AT kiminshik changesofrenalhistopathologyandtheroleofnrf2ho1inasphyxialcardiacarrestmodelinrats |