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Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism

PURPOSE: To clarify the best protocol for performing remote ischemic conditioning and to minimize the consequences of ischemia and reperfusion syndrome in brain, the present study aimed to evaluate different time protocols and the relation of the organs and the antioxidant effects of this technique....

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Autores principales: Monteiro, Andrew Moraes, Couteiro, Rodrigo Paracampo, da Silva, Dora Fonseca, Trindade, Sérgio Cunha, Silva, Renata Cunha, de Sousa, Luís Fernando Freitas, dos Santos, Deivid Ramos, Freitas, Jofre Jacob da Silva, Brito, Marcus Vinícius Henriques
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/PMC8428670/
https://www.ncbi.nlm.nih.gov/pubmed/34495142
http://dx.doi.org/10.1590/ACB360707
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author Monteiro, Andrew Moraes
Couteiro, Rodrigo Paracampo
da Silva, Dora Fonseca
Trindade, Sérgio Cunha
Silva, Renata Cunha
de Sousa, Luís Fernando Freitas
dos Santos, Deivid Ramos
Freitas, Jofre Jacob da Silva
Brito, Marcus Vinícius Henriques
author_facet Monteiro, Andrew Moraes
Couteiro, Rodrigo Paracampo
da Silva, Dora Fonseca
Trindade, Sérgio Cunha
Silva, Renata Cunha
de Sousa, Luís Fernando Freitas
dos Santos, Deivid Ramos
Freitas, Jofre Jacob da Silva
Brito, Marcus Vinícius Henriques
author_sort Monteiro, Andrew Moraes
collection PubMed
description PURPOSE: To clarify the best protocol for performing remote ischemic conditioning and to minimize the consequences of ischemia and reperfusion syndrome in brain, the present study aimed to evaluate different time protocols and the relation of the organs and the antioxidant effects of this technique. METHODS: The rat’s left femoral artery was clamped with a microvascular clamp in times that ranged from 1 to 5 minutes, according to the corresponding group. After the cycles of remote ischemic conditioning and a reperfusion of 20 minutes, the brain and the left gastrocnemius were collected. The samples were used to measure glutathione peroxidase, glutathione reductase and catalase levels. RESULTS: In the gastrocnemius, the 4-minute protocol increased the catalase concentration compared to the 1-minute protocol, but the latter increased both glutathione peroxidase and glutathione reductase compared to the former. On the other hand, the brain demonstrated higher catalase and glutathione peroxidase in 5-minute group, and the 3-minute group reached higher values of glutathione reductase. CONCLUSIONS: Remote ischemic conditioning increases brain antioxidant capacity in a time-dependent way, while muscle presents higher protection on 1-minute cycles and tends to decrease its defence with longer cycles of intermittent occlusions of the femoral artery.
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spelling pubmed-84286702021-09-16 Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism Monteiro, Andrew Moraes Couteiro, Rodrigo Paracampo da Silva, Dora Fonseca Trindade, Sérgio Cunha Silva, Renata Cunha de Sousa, Luís Fernando Freitas dos Santos, Deivid Ramos Freitas, Jofre Jacob da Silva Brito, Marcus Vinícius Henriques Acta Cir Bras Original Article PURPOSE: To clarify the best protocol for performing remote ischemic conditioning and to minimize the consequences of ischemia and reperfusion syndrome in brain, the present study aimed to evaluate different time protocols and the relation of the organs and the antioxidant effects of this technique. METHODS: The rat’s left femoral artery was clamped with a microvascular clamp in times that ranged from 1 to 5 minutes, according to the corresponding group. After the cycles of remote ischemic conditioning and a reperfusion of 20 minutes, the brain and the left gastrocnemius were collected. The samples were used to measure glutathione peroxidase, glutathione reductase and catalase levels. RESULTS: In the gastrocnemius, the 4-minute protocol increased the catalase concentration compared to the 1-minute protocol, but the latter increased both glutathione peroxidase and glutathione reductase compared to the former. On the other hand, the brain demonstrated higher catalase and glutathione peroxidase in 5-minute group, and the 3-minute group reached higher values of glutathione reductase. CONCLUSIONS: Remote ischemic conditioning increases brain antioxidant capacity in a time-dependent way, while muscle presents higher protection on 1-minute cycles and tends to decrease its defence with longer cycles of intermittent occlusions of the femoral artery. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2021-09-03 /pmc/articles/PMC8428670/ /pubmed/34495142 http://dx.doi.org/10.1590/ACB360707 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
Monteiro, Andrew Moraes
Couteiro, Rodrigo Paracampo
da Silva, Dora Fonseca
Trindade, Sérgio Cunha
Silva, Renata Cunha
de Sousa, Luís Fernando Freitas
dos Santos, Deivid Ramos
Freitas, Jofre Jacob da Silva
Brito, Marcus Vinícius Henriques
Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
title Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
title_full Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
title_fullStr Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
title_full_unstemmed Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
title_short Remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
title_sort remote ischemic conditioning improves rat brain antioxidant defense in a time-dependent mechanism
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428670/
https://www.ncbi.nlm.nih.gov/pubmed/34495142
http://dx.doi.org/10.1590/ACB360707
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